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- Hepatitis
B virus genotypes in the United
States: results of a nationwide
study.
- Outbreak
of Acinetobacter baumannii bacteremia
in a neonatal intensive care unit:
clinical implications and genotyping
analysis.
- Mutations
in mitochondrial aldehyde dehydrogenase
(ALDH2) change cofactor affinity
and segregate with voluntary alcohol
consumption in rats.
- Possibility
of using DNA chip technology for
diagnosis of human papillomavirus.
- Bacteria
and granulation tissue associated
with Montgomery T-tubes.
- Early
virological response at week 12
has positive predictive value for
end of treatment response for hepatitis
C virus genotype 4 chronic active
hepatitis cases treated with combination
therapy of pegylated interferon
plus ribavirin.
- Genotyping
of hepatitis C virus isolates from
Saudi patients by analysis of sequences
from PCR-amplified core region of
te virus genome.
- The
association of cyclin D1 (A870G)
polymorphism with susceptibility
to esophageal and cardiac cancer
in north Chinese population
- A
rapid method for manual or automated
purification of fluorescently labeled
nucleic acids for sequencing, genotyping,
and microarrays.
- The
relevance of alternative RNA splicing
to pharmacogenomics.
- Association
study of the vitamin D: 1alpha-hydroxylase
(CYP1alpha) gene and type 2 diabetes
mellitus in a Polish population.
- The
genetic characteristic of HLA-DRB1
locus in the Jiangsu-Zhejiang-Shanghai
Han population and a comparison
of its frequency distribution with
that of other populations
- Listeria
monocytogenes occurrence and characterization
in meat-producing plants.
- Protective
association of genetic variation
in alcohol dehydrogenase with alcohol
dependence in Native American Mission
Indians.
- Polymorphism
of monocyte chemoattractant protein
1 in Crohn's disease.
- Molecular
haplotype determination using allele-specific
PCR and pyrosequencing technology.
- Close
genetic linkage between HLA and
congenital adrenal hyperplasia (21-hydroxylase
deficiency).
- Study
of MICA alleles in 201 African Americans
by multiplexed single nucleotide
extension (MSNE) typing.
- Association
of CTLA-4 with systemic sclerosis
in Japanese patients.
- The
M235T variant of the angiotensinogen
gene and the body mass index are
useful markers for prevention of
hypertension in pregnancy: a tree-based
analysis of gene-environment interaction.
- Association
of estrogen receptor gene polymorphism
with cerebral infarction, a case-control
study
- Molecular
and quantitative analyses of Malassezia
microflora on the skin of atopic
dermatitis patients and genotyping
of M. globosa DNA
- Replicative
fitness of protease inhibitor-resistant
mutants of human immunodeficiency
virus type 1.
- Association
of the platelet glycoprotein Ia
C807T gene polymorphism with nonfatal
myocardial infarction in younger
patients.
- Determinants
of postprandial lipemia in obese
women.
- TNFA
and TNFB polymorphisms in myasthenia
gravis.
- Cross-colonisation
with Pseudomonas aeruginosa of patients
in an intensive care unit.
- Discrimination
of subtype B and non-subtype B strains
of human immunodeficiency virus
type 1 by serotyping: correlation
with genotyping.
- Genotyping
of the prion protein gene at codon
129.
- Susceptibility
genes for nicotine dependence: a
genome scan and followup in an independent
sample suggest that regions on chromosomes
2, 4, 10, 16, 17 and 18 merit further
study.
- Cytochrome
P4502D6 (debrisoquine 4-hydroxylase)
and Parkinson's disease in Chinese
and Caucasians.
- Tuberculosis
in an indigenous young white south
Wales population.
- abst
12
- Increased
frequency of G-protein beta 3-subunit
825 T allele in dialyzed patients
with type 2 diabetes.
- Comparison
of specific and random priming in
the reverse transcriptase polymerase
chain reaction for genotyping group
A rotaviruses.
- Autosomal
dominant Stargardt-like macular
dystrophy: I. Clinical characterization,
longitudinal follow-up, and evidence
for a common ancestry in families
linked to chromosome 6q14.
- Molecular
screening of potential HNPCC patients
using a multiplex microsatellite
PCR system.
- Genotype-phenotype
relationships in studies of a polymorphism
in NAD(P)H:quinone oxidoreductase
1.
- Epidemiological
typing of Streptococcus pneumoniae
from various sources in Sweden and
India using Box A PCR fingerprinting.
- Functional
significance of a C-->A polymorphism
in intron 1 of the cytochrome P450
CYP1A2 gene tested with caffeine.
- N-acetyltransferase-2,
glutathione S-transferase M1, alcohol
dehydrogenase, and cytochrome P450IIE1
genotypes in alcoholic liver cirrhosis:
a case-control study.
- Microdissection-based
analysis of mature ovarian teratoma.
- Determinants
of peak bone mass: clinical and
genetic analyses in a young female
Canadian cohort.
- DNA
sequence variation and molecular
genotyping of natural killer leukocyte
immunoglobulin-like receptor, LILRA3.
- Studies
on identification of circumsporozoite
protein genotyping of Plasmodium
vivax
- Linkage
analysis in haemophilia A: simultaneous
genotyping of two polymorphisms
of the human factor VIII gene using
induced heteroduplex formation.
- Confirmation
of linkage of type 1 hereditary
sensory neuropathy to human chromosome
9q22.
- Detection
and genotyping of bovine diarrhea
virus by reverse transcription-polymerase
chain amplification of the 5' untranslated
region.
- Pyrin/marenostrin
mutations in familial Mediterranean
fever.
- Characterization
of Saccharomyces cerevisiae strains
from spontaneously fermented maize
dough by profiles of assimilation,
chromosome polymorphism, PCR and
MAL genotyping.
- Epidemiologic
and molecular investigation of outbreaks
of hepatitis C virus infection on
a pediatric oncology service.
- Microsatellite
instability and defects in mismatch
repair proteins: a new aetiology
for Sertoli cell-only syndrome.
- Cytochrome
P450 2D6 (CYP2D6) genotyping on
postmortem blood as a supplementary
tool for interpretation of forensic
toxicological results.
- Age
of onset in Huntington disease:
sex specific influence of apolipoprotein
E genotype and normal CAG repeat
length.
- Determination
of mutacin activity and detection
of mutA genes in Streptococcus mutans
genotypes from caries-free and caries-active
children.
- Characterization
of a novel alpha-mannosidosis-causing
mutation and its use in leukocyte
genotyping after bone marrow transplantation.
- Glycosylase
mediated polymorphism detection
(GMPD)--a novel process for genetic
analysis.
- Severe
skeletal complications in Japanese
patients with type 1 Gaucher disease.
- Diagnostic
Detection and Direct Genotyping
of Borrelia burgdor feri Regular
by Polymerase Chain Reaction in
Cerebrospinal Fluid in Lyme Neuroborreliosis.
- Spinocerebellar
ataxia type 6: evidence for a strong
founder effect among German families.
- Neurobiological
correlates of a putative risk allele
for Alzheimer's disease on chromosome
12q.
- Homogeneous
genotyping assays for single nucleotide
polymorphisms with fluorescence
resonance energy transfer detection.
- Genotyping
single nucleotide polymorphisms
by primer extension and high performance
liquid chromatography.
- Selective
genotyping for the role of 5-HT2A,
5-HT2C, and GABA alpha 6 receptors
and the serotonin transporter in
the level of response to alcohol:
a pilot study.
- Identification
of the mutation in the alkaptonuria
mouse model. Mutations in brief
no. 216. Online.
- A
multiplex methylation PCR assay
for identification of uniparental
disomy of chromosome 7.
- Flushing
response and its role in alcohol
disease in Siberian populations.
- Two
novel superantigens found in both
group A and group C Streptococcus.
- Inherited
Thrombophilia due to Factor V Leiden
Mutation.
- A
new biallelic polymorphism in intron
1 of the CHRNA4 gene may cause erroneous
genotyping of a closely linked CA
repeat marker.
- Autosomal
dominant Stargardt-like macular
dystrophy segregating in a large
Canadian family.
- The
length of the CTLA-4 microsatellite
(AT)N-repeat affects the risk for
type 1 diabetes. Diabetes Incidence
in Sweden Study Group.
- Influence
of non-MHC genes on lymphocyte response
to Mycobacterium tuberculosis antigens
& tuberculin reactive status
in pulmonary tuberculosis.
- Relationships
of TP53 codon 72 and HRAS1 polymorphisms
with lung cancer risk in an ethnically
diverse population.
- Single
nucleotide polymorphisms in cytochrome
P450 genes from barley.
- Pollination
in the marine realm: microsatellites
reveal high outcrossing rates and
multiple paternity in eelgrass Zostera
marina.
- Use
of a novel outbred by inbred F1
cross to detect genetic markers
for growth.
- Protective
role against restenosis from an
interleukin-1 receptor antagonist
gene polymorphism in patients treated
with coronary stenting.
- Evaluation
of a new hepatitis C virus sequencing
assay as a routine method for genotyping.
- Small-subunit
rRNA genotyping of rhizobia nodulating
Australian Acacia spp.
- Multiplex
allele-specific target amplification
based on PCR suppression.
- New
approaches for genotyping of Helicobacter
pylori based on amplification of
polymorphisms in intergenic DNA
regions and at the insertion site
of the cag pathogenicity island.
- Lower
levels of N-acetylaspartate in multiple
sclerosis patients with the apolipoprotein
E epsilon4 allele.
- Cheap,
accurate and rapid allele frequency
estimation of single nucleotide
polymorphisms by primer extension
and DHPLC in DNA pools.
- Automated,
PCR-RFLP genotyping of the urokinase
gene.
- Linkage
of rheumatoid arthritis to insulin-dependent
diabetes mellitus loci: evidence
supporting a hypothesis for the
existence of common autoimmune susceptibility
loci.
- Familial
idiopathic scoliosis: evidence of
an X-linked susceptibility locus.
- Prevalence
and genotypes of hepatitis C virus
infection among drug addicts and
blood donors in Thailand.
- Molecular
analysis of plasma alpha 1,3-fucosyltransferase
deficiency and development of the
methods for its genotyping.
- Distribution
of hepatitis C virus genotypes in
patients with chronic hepatitis
C in northern Estonia.
- Genetic
mapping of quantitative trait loci
governing longevity of Caenorhabditis
elegans in recombinant-inbred progeny
of a Bergerac-BO x RC301 interstrain
cross.
- Comprehensive
mutation screening in a cystic fibrosis
center.
- DNA
sequencing and genotyping by transcriptional
synthesis of chain-terminated RNA
ladders and MALDI-TOF mass spectrometry.
- Fine
mapping of the SLEB2 locus involved
in susceptibility to systemic lupus
erythematosus.
- Relationships
of testicular iron and ferritin
concentrations with testicular weight
and sperm production in boars.
- Genotyping
system of GBV-C/HGV type 1 to type
4 by the polymerase chain reaction
using type-specific primers and
geographical distribution of viral
genotypes.
- Lack
of evidence of a specific role for
C4A gene deficiency in determining
disease susceptibility among C4-deficient
patients with systemic lupus erythematosus
(SLE).
- HLA
class II typing of whole genome
amplified mouth swab DNA.
- Genotyping
of human papillomavirus genotyes
in cervical scrapes by line probe
assay
- Blood
group genotyping in a population
of highly diverse ancestry.
- Molecular
characterization of strains of Human
herpesvirus 8 from Japan, Argentina
and Kuwait.
- Detection
and genotyping of GBV-C/HGV variants
in China.
- DNA
from buccal swabs recruited by mail:
evaluation of storage effects on
long-term stability and suitability
for multiplex polymerase chain reaction
genotyping.
- A
nuclear-mitochondrial DNA interaction
affecting hearing impairment in
mice.
- Linkage
of benign familial infantile convulsions
to chromosome 16p12-q12 suggests
allelism to the infantile convulsions
and choreoathetosis syndrome.
- Phenotype
analysis of cytochrome P450 2C19
in Chinese subjects with mephenytoin
S/R enantiomeric ratio in urine
measured by chiral GC.
- The
genomic revolution: is the real
risk under-investment rather than
bankrupt health care systems?
- Structural
characterization of a new variant
of the CYP2A6 gene (CYP2A6*1B) apparently
diagnosed as heterozygotes of CYP2A6*1A
and CYP2A6*4C.
- Genetic
polymorphisms of biotransformation
enzymes: allele frequencies in the
population of the Czech Republic.
- Association
of Eotaxin gene family with asthma
and serum total IgE.
- Association
of thymidylate synthase gene polymorphism
with its mRNA and protein expression
and with prognosis in gastric cancer.
- Genotyping
of feline MHC (FLA) class II DRB
by PCR-RFLP method using group-specific
primers.
- Conversion
of capillary electrophoresis microchip
genotyping data for analysis with
Genetic Profiler software.
- Genetic
polymorphism of IL-12 p40 gene in
immune-mediated disease.
- The
clinical expression of hemochromatosis
in Oslo, Norway. Excessive oral
iron intake may lead to secondary
hemochromatosis even in HFE C282Y
mutation negative subjects.
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204
- Comparative
genotyping of Candida albicans bloodstream
and nonbloodstream isolates at a
polymorphic microsatellite locus.
- Comparison
of human immunodeficiency virus
type 1 RNA sequence heterogeneity
in cerebrospinal fluid and plasma.
- Prognostic
value of genomic alterations in
minimal residual cancer cells purified
from the blood of breast cancer
patients.
- Mapping
of the CYP1A1, SSTR1 and TTF1 genes
to pig chromosome 7q refines the
porcine-human comparative map.
- Restriction
analysis of Bordetella pertussis
DNA isolated from patients with
whooping cough in 1968 and 1995-98
and B. pertussis used for production
of national vaccine strains
- Rapid
genotyping of paraoxonase 55 and
192 mutations by melting point analysis
using real time PCR technology.
- ABO
genotyping by PCR-direct sequencing
method
- Foot
and mouth disease in livestock and
reduced cryptosporidiosis in humans,
England and Wales.
- Transplantation
in miniature swine. I. Fixation
of the major histocompatibility
complex.
- Polymorphism
of the N-acetyltransferase (NAT2),
smoking and the potential risk of
periodontal disease.
- Allelic
variants of the thiopurine S-methyltransferase
deficiency in patients with ulcerative
colitis and in healthy controls.
- FcgammaRIIIA-158V
and rheumatoid arthritis: a confirmation
study.
- Demonstration
of thiopurine methyltransferase
activity in the erythrocytes of
cats.
- Spoligotyping
and polymorphic GC-rich repetitive
sequence fingerprinting of mycobacterium
tuberculosis strains having few
copies of IS6110.
- Genotyping
of rotaviruses in environmental
water and stool samples in Southern
Switzerland by nucleotide sequence
analysis of 189 base pairs at the
5' end of the VP7 gene.
- A
high-throughput MS-PCR method on
MADGE gels for ANG II type-1 receptor
A1166C polymorphism.
- Evaluation
of the role of MHC class II alleles,
haplotypes and selected amino acid
sequences in primary sclerosing
cholangitis.
- Genotypes
and phenotypes for apolipoprotein
E and Alzheimer disease in the Honolulu-Asia
aging study.
- Distinct
distribution of rare us kshv genotypes
in south texas. Implications for
kshv epidemiology and evolution.
- Prevalence
of human papillomavirus DNA in different
histological subtypes of cervical
adenocarcinoma.
- Major
genes regulating total serum immunoglobulin
E levels in families with asthma.
- Identification
of missense, nonsense, and deletion
mutations in the GRHPR gene in patients
with primary hyperoxaluria type
II (PH2).
- Does
APO epsilon4 correlate with MRI
changes in Alzheimer's disease?
- Comparison
of two hepatitis C virus typing
assays in a Tunisian population
- Is
there an association between angiotensin-converting
enzyme gene variants and chronic
nonproductive cough?
- DNA
typing for HLA-A, B antigens by
polymerase chain reaction with sequence-specific
primers and clinical application
- The
efficiency of genetic analysis of
DNA from aged siblings to detect
chromosomal regions implicated in
longevity.
- Arylamine
N-acetyltransferase 2 polymorphism
in the ethnic populations of South
India.
- Identification
of a novel recombinant allele in
three unrelated Italian Gaucher
patients: implications for prognosis
and genetic counseling.
- Glutathione
S-transferase polymorphisms and
skin cancer after renal transplantation.
- D2
dopamine receptor gene polymorphisms
among African-Americans and Mexican-Americans:
a lung cancer case-control study.
- VP7
and VP4 genotypes among rotavirus
strains recovered from children
with gastroenteritis over a 3-year
period in Valencia, Spain.
- Confirmation
of an excess of the high enzyme
activity COMT val allele in heroin
addicts in a family-based haplotype
relative risk study.
- Microsatellite
genotyping of post-PCR fluorescently
labeled markers.
- A
variant within the DNA repair gene
XRCC3 is associated with the development
of melanoma skin cancer.
- Construction
of a high-throughput rat genetic
mapping system with 466 arbitrarily
primed-representational difference
analysis markers.
- Application
of the PCR-APLP method to determine
ABO genotypes in forensic samples
- Asn540Lys
mutation in fibroblast growth factor
receptor 3 and phenotype in hypochondroplasia.
- Lack
of association of CCR2-64I and CCR5-Delta
32 with type 1 diabetes and latent
autoimmune diabetes in adults.
- Association
between polymorphisms in caspase
recruitment domain containing protein
15 and allergy in two German populations.
- Genotyping
of clinical and chicken isolates
of Campylobacter jejuni and Campylobacter
coli.
- Polymorphic
microsatellite markers identified
in individual Plasmodium falciparum
oocysts from wild-caught Anopheles
mosquitoes.
- The
calpain small subunit gene is essential:
its inactivation results in embryonic
lethality.
- Disease-related
conditions in relatives of patients
with hemochromatosis.
- FISSR-PCR:
a simple and sensitive assay for
highthroughput genotyping and genetic
mapping.
- Genotyping
of alcohol dehydrogenase type 2
and 3 using a two-buffer polyacrylamide
gel electrophoresis system.
- Quality
and quantity of DNA isolated from
frozen urine in population-based
research.
- Analysis
of cDNA coding MHC class II beta
chain of the chimpanzee (Pan troglodytes).
- NAD(P)H:
quinone oxidoreductase 1 (NQO1)
C609T polymorphism and the risk
of eight cancers for Japanese.
- Efficiency
of single-nucleotide polymorphism
haplotype estimation from pooled
DNA.
- Fine
mapping of a quantitative trait
locus for twinning rate using combined
linkage and linkage disequilibrium
mapping.
- Microplate
array diagonal gel electrophoresis
for cohort studies of microsatellite
loci.
- The
combination of several polymorphic
amino acid residues in the DQalpha
and DQbeta chains forms a domain
structure pattern and is associated
with insulin-dependent diabetes
mellitus.
- A
whole genome screen for linkage
disequilibrium in multiple sclerosis
confirms disease associations with
regions previously linked to susceptibility.
- A
potential role for the XRCC2 R188H
polymorphic site in DNA-damage repair
and breast cancer.
- Hb
H hydrops fetalis syndrome associated
with the interaction of two common
determinants of alpha thalassaemia
(--MED/(alpha)TSaudi(alpha)).
- Relationship
of polymorphisms of the Interleukin-1
gene cluster to occurrence and severity
of rheumatoid arthritis.
- Single
nucleotide polymorphism (SNP) discovery
in porcine expressed genes.
- Sharing
of a conserved haplotype suggests
a susceptibility gene for multiple
sclerosis at chromosome 17p11.
- Ocular
developmental abnormalities and
glaucoma associated with interstitial
6p25 duplications and deletions.
- Association
of HMG-CoA reductase gene polymorphism
with levels of lipids
- Organic
solvent exposure, genes, and risk
of neuropsychological impairment.
- Internal
quality control of PCR-based genotyping
methods in research studies and
patient diagnostics.
- Molecular
identification of food-borne and
water-borne protozoa.
- Therapy
and risk-stratification in hypertrophic
cardiomyopathy - a current survey
- Absence
of age effect on meiotic recombination
between human X and Y chromosomes.
- Distribution
of bovine lymphocyte antigen (BoLA-DRB3)
alleles in Brazilian dairy Gir cattle
(Bos indicus).
- Allele
and genotype frequencies of polymorphic
cytochromes P450 (CYP2C9, CYP2C19,
CYP2E1) and dihydropyrimidine dehydrogenase
(DPYD) in the Egyptian population.
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267
- Melting
curve SNP (McSNP) genotyping: a
useful approach for diallelic genotyping
in forensic science.
- Genotypic
exploration of a hospital neonatal
outbreak due to Klebsiella pneumoniae
producing extended-spectrum-betalactamase
- DNA
diagnosis by capillary electrophoresis
and microfabricated electrophoretic
devices.
- HLA-DRB
genotyping in Gilles de la Tourette
patients and their parents.
- High-throughput
genotyping of single nucleotide
polymorphisms using new biplex invader
technology.
- Rapid
genotyping of loci involved in antifolate
drug resistance in Plasmodium falciparum
by primer extension.
- Constructing
universal multiplex PCR systems
for comparative genotyping.
- Molecular
genetic characteristics of Mycobacterium
tuberculosis isolated from patients
operated on for pulmonary tuberculosis
- Comparison
of ITS profiling, REP- and ERIC-PCR
of Salmonella Enteritidis isolates
from Poland.
- Universal,
robust, highly quantitative SNP
allele frequency measurement in
DNA pools.
- Meat
consumption, cigarette smoking,
and genetic susceptibility in the
etiology of colorectal cancer: results
from a Dutch prospective study.
- Low
prevalence of antiretroviral drug
resistance among HIV-1 seroconverters
in London, 1984-1991.
- Report
on the Fourth International Granulocyte
Immunology Workshop: progress toward
quality assessment.
- Isolation
and molecular characterization of
Toxoplasma gondii from chickens
and ducks from Egypt.
- Type-specific
antibody for hepatitis C virus detected
by use of NS-4 peptide and hepatitis
C virus genome in Korea.
- Study
on application of CODIS loci to
excluding paternity
- Spontaneous
remission of B-cell chronic lymphocytic
leukemia associated with T lymphocytic
hyperplasia in bone marrow.
- The
single nucleotide polymorphism T1128C
in the signal peptide of neuropeptide
Y (NPY) was not identified in a
Korean population.
- Patient-to-patient
transmission of nosocomial malaria
in Italy.
- Association
of functional polymorphisms of matrix
metalloproteinase (MMP)-1 and MMP-3
genes with colorectal cancer.
- Disease
surveillance in recombining pathogens:
multilocus genotypes identify sources
of human Coccidioides infections.
- Clinical
utility of total HCV core antigen
quantification: a new indirect marker
of HCV replication.
- Genome
scan for loci involved in cleft
lip with or without cleft palate,
in Chinese multiplex families.
- Single-step
assays to analyze CYP2D6 gene polymorphisms
in Asians: allele frequencies and
a novel *14B allele in mainland
Chinese.
- Simultaneous
analysis of five genetic risk factors
in Polish patients with Alzheimer's
disease.
- Virulence
genes in Helicobacter pylori strains
from West Bengal residents with
overt H. pylori-associated disease
and healthy volunteers.
- A
novel locus for autosomal dominant
nuclear cataract mapped to chromosome
2p12 in a Pakistani family.
- Prevalence
and clinical features of skin diseases
in chronic HCV infection. A prospective
study in 96 patients.
- HLA
and cytokine gene polymorphisms
in biliary atresia.
- The
CD14-260 C --> T promoter polymorphism
co-segregates with the tumor necrosis
factor-alpha (TNF-alpha)-308 G -->
A polymorphism and is associated
with the interleukin-1 beta (IL-1
beta) synthesis capacity of human
leukocytes.
- Colonization
of germ-free transgenic mice with
genotyped Helicobacter pylori strains
from a case-control study of gastric
cancer reveals a correlation between
host responses and HsdS components
of type I restriction-modification
systems.
- Investigation
of an anaerobic microbial community
associated with a corneal ulcer
by denaturing gradient gel electrophoresis
and 16S rDNA sequence analysis.
- Use
of PCR-RFLP for genotyping 16S rRNA
and characterizing bacteria cultured
from halibut fry.
- A
first-generation linkage disequilibrium
map of human chromosome 22.
- Catalog
of 605 single-nucleotide polymorphisms
(SNPs) among 13 genes encoding human
ATP-binding cassette transporters:
ABCA4, ABCA7, ABCA8, ABCD1, ABCD3,
ABCD4, ABCE1, ABCF1, ABCG1, ABCG2,
ABCG4, ABCG5, and ABCG8.
- The
maternally transcribed gene p57(KIP2)
(CDNK1C) is abnormally expressed
in both androgenetic and biparental
complete hydatidiform moles.
- Pheno-
and genotyping the prescription
of drugs metabolized by CYP2D6.
- Novel
double promoter approach for identification
of transgenic animals: A tool for
in vivo analysis of gene function
and development of gene-based therapies.
- Distribution
of emm genotypes and superantigen
genes of Streptococcus pyogenes
isolated in Japan, 1994-9.
- A
natural history of melanomas and
dysplastic nevi: an atlas of lesions
in melanoma-prone families.
- Catalog
of 238 variations among six human
genes encoding solute carriers (
hSLCs) in the Japanese population.
- Integrated
platform for detection of DNA sequence
variants using capillary array electrophoresis.
- Preimplantation
genetic diagnosis for single gene
disorders: experience with five
single gene disorders.
- The
diabetes-prone NZO/HlLt strain.
I. Immunophenotypic comparison to
the related NZB/BlNJ and NZW/LacJ
strains.
- A
candidate gene study in low HDL-cholesterol
families provides evidence for the
involvement of the APOA2 gene and
the APOA1C3A4 gene cluster.
- Apolipoprotein(a)
gene polymorphism in the Korean
population: is there any relevance
to essential hypertension?
- Clustering
of cancer-related mutations in a
subset of BRCA1 alleles: a study
in the Spanish population.
- Slow
acetylator genotypes as a possible
risk factor for infectious mononucleosis-like
syndrome induced by salazosulfapyridine.
- Detection
and quantification of insertion/deletion
variations by allele-specific real-time
PCR: application for genotyping
and chimerism analysis.
- Association
between pre-excitation syndrome
and 7q3 D7S505 pseudonym gene
- A
cryptic clonal line of the loach
Misgurnus anguillicaudatus (Teleostei:
Cobitidae) evidenced by induced
gynogenesis, interspecific hybridization,
microsatellite genotyping and multilocus
DNA fingerprinting.
- High-throughput
genetic screening using matrix-assisted
laser desorption/ionization mass
spectrometry.
- Typing
of human isolates of Streptococcus
agalactiae (group B streptococcus,
GBS) strains from Zimbabwe.
- Association
between Bcl-2 gene polymorphism
with systemic lupus erythematosus
- Molecular
epidemiology of malaria in cameroon.
IX. Characteristics of recrudescent
and persistent Plasmodium falciparum
infections after chloroquine or
amodiaquine treatment in children.
- Study
on the forensic application of ABO
genotyping by PCR-RFLP
- Re-sequencing
of multiple single nucleotide polymorphisms
by liquid chromatography-electrospray
ionization mass spectrometry.
- Antibody-based
approach to high-volume genotyping
for MIC-1 polymorphism.
- Follow-up
of 68 children with congenital adrenal
hyperplasia due to 21-hydroxylase
deficiency: relevance of genotype
for management.
- SNP
genotyping on pooled DNAs: comparison
of genotyping technologies and a
semi automated method for data storage
and analysis.
- An
efficient haplotyping method with
DNA pools.
- Foci
of tick-borne diseases in southwest
Germany.
- Evidence
for environmental influence on CYP2D6-catalysed
debrisoquine hydroxylation as demonstrated
by phenotyping and genotyping of
Ethiopians living in Ethiopia or
in Sweden.
- Clonal
mixing in the soldier-producing
aphid Pemphigus spyrothecae (Hemiptera:
Aphididae).
- Infantile-onset
ascending hereditary spastic paralysis
is associated with mutations in
the alsin gene.
- Phenotyping
and genotyping of Sporothrix schenckii
isolates according to geographic
origin and clinical form of Sporotrichosis.
- Association
of HLA-DQ and HLA-DR alleles with
susceptibility or resistance to
HIV-1 infection among the population
of Chaco Province, Argentina.
- Relation
of the G protein beta3-subunit polymorphism
with left ventricle structure and
function.
- IL-1beta
gene polymorphisms influence hepatitis
B vaccination.
- Smoking
and tardive dyskinesia: lack of
involvement of the CYP1A2 gene.
- Simultaneous
genotyping of single nucleotide
polymorphisms in the IL-1 gene complex
by multiplex polymerase chain reaction-restriction
fragment length polymorphism.
- Assessing
the efficacy of a ram-genotyping
programme to reduce susceptibility
to scrapie in Great Britain.
- Identification
of 779 genetic variations in eight
genes encoding members of the ATP-binding
cassette, subfamily C (ABCC/MRP/CFTR.
- A
study of the relationship between
MICA gene and systemic lupus erythematosus
- Azathioprine
therapy and adverse drug reactions
in patients with inflammatory bowel
disease: impact of thiopurine S-methyltransferase
polymorphism.
- A
catalogue of polymorphisms related
to xenobiotic metabolism and cancer
susceptibility.
- Angiotensin-converting
enzyme genotype and outcome in pediatric
IgA nephropathy.
- GSTM1,
GSTT1 and GSTP1 polymorphisms and
lung cancer risk.
- Simultaneous
identification of ryanodine receptor
1 (RYR1) and estrogen receptor (ESR)
genotypes with the multiplex PCR-RFLP
method in Polish Large White and
Polish Landrace pigs.
- 906
variations among 27 genes encoding
cytochrome P450 (CYP) enzymes and
aldehyde dehydrogenases (ALDHs)
in the Japanese population.
- Human
neutrophil antigen-4a gene frequencies
in an Australian population, determined
by a new polymerase chain reaction
method using sequence-specific primers.
- N-acetyltransferase
2 genotype-related sulfapyridine
acetylation and its adverse events.
- Evidence
for a gene influencing heart rate
on chromosome 4 among hypertensives.
- Genome-wide
multipoint linkage analyses of multiplex
schizophrenia pedigrees from the
oceanic nation of Palau.
- Association
analysis of childhood absence epilepsy
by microsatellite DNA.
- Incidence,
prevalence, and clearance of type-specific
human papillomavirus infections:
The Young Women's Health Study.
- Nosocomial
hepatitis C virus infection in a
renal transplantation center.
- Beta-cell
dysfunction in late-onset diabetic
subjects carrying homozygous mutation
in transcription factors NeuroD1
and Pax4.
- High
prevalence of human papillomavirus
(HPV) infections and high frequency
of multiple HPV genotypes in human
immunodeficiency virus-infected
women in Brazil.
- Absence
of mutation in the NOD2/CARD15 gene
among 483 Japanese patients with
Crohn's disease.
- Data
mining of public SNP databases for
the selection of intragenic SNPs.
- A
hospital-associated outbreak of
Legionnaires' disease caused by
Legionella pneumophila serogroup
1 is characterized by stable genetic
fingerprinting but variable monoclonal
antibody patterns.
- Altered
expression of Lewis antigen on tissue
and erythrocytes in gastric cancer
patients.
- PCR-RFLP
based molecular typing of enteroviruses
isolated from patients with aseptic
meningitis in Korea.
- Evaluation
of multiple presenilin 2 SNPs for
association with early-onset sporadic
Alzheimer disease.
- A
7-year follow-up study of cases
with dementia to identify predictors
of mortality
- iFRET:
an improved fluorescence system
for DNA-melting analysis.
- Identification
of common disease related genes
by means of genome-wide SNP typing
- Immunoglobulin
kappa light chain gene alleles are
not associated with primary Sjogren's
syndrome.
- Thiopurine
methyltransferase phenotype and
genotype in relation to azathioprine
therapy in autoimmune hepatitis.
- Single
nucleotide polymorphism detection:
allelic discrimination using TaqMan.
- Detection
and genotyping of astroviruses from
children with acute gastroenteritis
from Goiania, Goias, Brazil.
- How
does Trypanosoma equiperdum fit
into the Trypanozoon group? A cluster
analysis by RAPD and multiplex-endonuclease
genotyping approach.
- Genotyping
of essential hypertension single-nucleotide
polymorphisms by a homogeneous PCR
method with universal energy transfer
primers.
- cagA
and vacA in strains of Helicobacter
pylori from ulcer and non-ulcerative
dyspepsia patients.
- Antiretroviral
drug resistance among HIV-1 infected
children failing treatment.
- Eotaxin
gene single nucleotide polymorphisms
in the promoter and exon regions
are not associated with susceptibility
to atopic dermatitis, but two of
them in the promoter region are
associated with serum IgE levels
in patients with atopic dermatitis.
- High
throughput parallel synthesis of
oligonucleotides with 1536 channel
synthesizer.
- Comparative
use of faecal egg count reduction
test, egg hatch assay and beta-tubulin
codon 200 genotyping in small strongyles
(cyathostominae) before and after
benzimidazole treatment.
- A
general likelihood approach to trait-based
multipoint linkage analysis in large
groFedex of half-sibs and super sisters.
- Power
and sample size calculations for
case-control genetic association
tests when errors are present: application
to single nucleotide polymorphisms.
- ChickRH6:
a chicken whole-genome radiation
hybrid panel.
- Rapid
detection of the CCR2-V64I, CCR5-A59029G
and SDF1-G801A polymorphisms by
tetra-primer PCR.
- Discrepant
results in the interpretation of
HIV-1 drug-resistance genotypic
data among widely used algorithms.
- Polymorphisms
of TLR4: rapid genotyping and reduced
response to lipopolysaccharide of
TLR4 mutant alleles.
- The
use of real-time PCR with fluorogenic
probes for the rapid selection of
mutant neuroectodermal grafts.
- Skeletal
remains presumed submerged in water
for three years identified using
PCR-STR analysis.
- Blood
group genotyping facilitates transfusion
of beta-thalassemia patients.
- Weak
linkage at 4p16 to predisposition
for human neuroblastoma.
- Novel
single nucleotide polymorphisms
in the 3'-UTR of the TGFbetaRI and
TGFbetaRIII genes.
- No
association between obsessive-compulsive
disorder and the 5-HT(1Dbeta) receptor
gene.
- Alterations
in Plasmodium falciparum genotypes
during sequential infections suggest
the presence of strain specific
immunity.
- Mutant
Thermotoga neapolitana DNA polymerase
I: altered catalytic properties
for non-templated nucleotide addition
and incorporation of correct nucleotides.
- Prevalence
of S315T mutation within the katG
gene in isoniazid-resistant clinical
Mycobacterium tuberculosis isolates
from Dubai and Beirut.
- abst
37
- Evaluation
of NQO1 gene expression and variant
allele in human NSCLC tumors and
matched normal lung tissue.
- abst
381
- Detection
of single nucleotide polymorphisms
using electrospray ionization mass
spectrometry: validation of a one-well
assay and quantitative pooling studies.
- Application
of multiplex PCR in genotyping of
hepatitis B virus prevailing in
Guangdong Province of China
- Genetic
variation of the nine Profiler Plus
loci in Russians.
- Valine-alanine
manganese superoxide
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