Antigenic and S-1 genomic characterization of the Delaware variant serotype of infectious bronchitis virus.
Avian diseases | 2000-01-01 | PMID 9356713
Gelb J, Keeler C L, Nix W A and 2 more
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
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Publications
Page 911 of 10600
Estrogen receptor gene polymorphism and bone mineral density at the lumbar spine of pre- and postmenopausal women.
Bone | 1997-11-01 | PMID 9356730
Mizunuma H, Hosoi T, Okano H and 8 more
Functional vasopressin V1 type receptors are present in variant as well as classical forms of small-cell carcinoma.
Peptides | 1997-01-01 | PMID 9357056
North W G, Fay M J, Longo K and 1 more
Validation of the five-drug "Pittsburgh cocktail" approach for assessment of selective regulation of drug-metabolizing enzymes.
Clinical pharmacology and therapeutics | 1997-10-01 | PMID 9357387
Frye R F, Matzke G R, Adedoyin A and 2 more
Isoniazid acetylation metabolic ratio during maturation in children.
Clinical pharmacology and therapeutics | 1997-10-01 | PMID 9357388
Pariente-Khayat A, Rey E, Gendrel D and 6 more
Induction of CYP2D6 in pregnancy.
Clinical pharmacology and therapeutics | 1997-10-01 | PMID 9357391
Wadelius M, Darj E, Frenne G and 1 more
UKPDS 25: autoantibodies to islet-cell cytoplasm and glutamic acid decarboxylase for prediction of insulin requirement in type 2 diabetes. UK Prospective Diabetes Study Group.
Lancet (London, England) | 1997-11-01 | PMID 9357409
Turner R, Stratton I, Horton V and 6 more
Immune system genes in multiple sclerosis: genetic association and linkage analyses on TCR beta, IGH, IFN-gamma and IL-1ra/IL-1 beta loci.
Journal of neuroimmunology | 1997-10-01 | PMID 9357444
Wansen K, Pastinen T, Kuokkanen S and 4 more
Genes: IGH
Effect of retroviral transduction on human endothelial cell phenotype and adhesion to Dacron vascular grafts.
Journal of vascular surgery | 1997-10-01 | PMID 9357471
Jankowski R J, Severyn D A, Vorp D A and 1 more
Chromosomal mutations and chromosome loss measured in a new human-hamster hybrid cell line, ALC: studies with colcemid, ultraviolet irradiation, and 137Cs gamma-rays.
Mutation research | 1997-10-06 | PMID 9357544
Kraemer S M, Waldren C A
Spectrum of spontaneous and 2,4,6-trinitrotoluene (TNT)-induced mutations in Salmonella typhimurium strains with different nitroreductase and O-acetyltransferase activities.
Mutation research | 1997-10-06 | PMID 9357547
Väätänen A K, Ridanpää M, Norppa H and 1 more
Euglena gracilis as an eukaryotic test organism for detecting mutagens and antimutagens.
Mutation research | 1997-09-18 | PMID 9357556
Foltínová P, Grones J
Development of a mouse model for studying in vivo T-cell receptor mutations.
Mutation research | 1997-09-18 | PMID 9357560
Umeki S, Suzuki T, Kusunoki Y and 3 more
Using data mining to characterize DNA mutations by patient clinical features.
Proceedings : a conference of the American Medical Informatics Association. AMIA Fall Symposium | 1997-01-01 | PMID 9357627
Evans S, Lemon S J, Deters C and 4 more
Abnormal regulation of HGP by hyperglycemia in mice with a disrupted glucokinase allele.
The American journal of physiology | 1997-10-01 | PMID 9357804
Rossetti L, Chen W, Hu M and 3 more
Differential effect of pp120 on insulin endocytosis by two variant insulin receptor isoforms.
The American journal of physiology | 1997-10-01 | PMID 9357811
Li Calzi S, Choice C V, Najjar S M
Biosynthesis of sulfated extracellular matrices by alveolar type II cells increases with time in culture.
The American journal of physiology | 1997-10-01 | PMID 9357860
Sannes P L, Khosla J, Peters B P
Role of the constriction loop in the gating of outer membrane porin PhoE of Escherichia coli.
FEBS letters | 1997-10-06 | PMID 9357991
Eppens E F, Saint N, Van Gelder P and 2 more
Glutathione S-transferase M1 gene polymorphism and susceptibility to endometriosis in a French population.
Molecular human reproduction | 1997-09-01 | PMID 9358003
Baranova H, Bothorishvilli R, Canis M and 6 more
Genes: GSTM1
The spectrum of beta-thalassaemia mutations in the Lebanon.
Human heredity | 2000-01-01 | PMID 9358011
Zahed L, Talhouk R, Saleh M and 3 more
Angiotensin-converting enzyme deletion polymorphism is associated with hypertension in a Sikh population.
Human heredity | 2000-01-01 | PMID 9358012
Mastana S, Nunn J
Genes: ACE
Molecular and cytogenetic investigations of the fragile X region including the Frax A and Frax E CGG trinucleotide repeat sequences in families multiplex for autism and related phenotypes.
Human heredity | 2000-01-01 | PMID 9358013
Gurling H M, Bolton P F, Vincent J and 2 more
Ethnic differences in the HFE codon 282 (Cys/Tyr) polymorphism.
Human heredity | 2000-01-01 | PMID 9358014
Beckman L E, Saha N, Spitsyn V and 2 more
Genes: HFE
Linkage analysis of manic depression (bipolar affective disorder) in Icelandic and British kindreds using markers on the short arm of chromosome 18.
Human heredity | 2000-01-01 | PMID 9358015
Kalsi G, Smyth C, Brynjolfsson J and 7 more
Investigation of complement C4B deficiency in schizophrenia.
Human heredity | 2000-01-01 | PMID 9358016
Schroers R, Nöthen M M, Rietschel M and 7 more
Haptoglobin polymorphism in Korean patients with cardiovascular diseases.
Human heredity | 2000-01-01 | PMID 9358017
Hong S H, Kang B Y, Lim J H and 4 more
Paternity analysis in cases of father-daughter incest using multiallelic loci.
Human heredity | 2000-01-01 | PMID 9358018
Cifuentes O L, Jorquera G H
A CA repeat in the first intron of the CFTR gene.
Human heredity | 2000-01-01 | PMID 9358019
Moulin D S, Smith A N, Harris A
Genes: CFTR
Association between allele 1 of T102C polymorphism, 5-hydroxytryptamine 2a receptor gene and schizophrenia in Chinese males in Singapore.
Human heredity | 2000-01-01 | PMID 9358020
Tay A H, Lim L C, Lee W L and 3 more
The sequences of hypF, hypC and hypD complete the hyp gene cluster required for hydrogenase activity in Bradyrhizobium japonicum.
Gene | 1997-10-15 | PMID 9358044
Olson J W, Maier R J
The Azotobacter vinelandii alg8 and alg44 genes are essential for alginate synthesis and can be transcribed from an algD-independent promoter.
Gene | 1997-10-15 | PMID 9358065
Mejía-Ruíz H, Guzmán J, Moreno S and 2 more
Sequencing analysis of prion genes from red deer and camel.
Gene | 1997-10-15 | PMID 9358067
Kaluz S, Kaluzova M, Flint A P
The ETS family member ERM contains an alpha-helical acidic activation domain that contacts TAFII60.
Nucleic acids research | 1997-11-15 | PMID 9358152
Defossez P A, Baert J L, Monnot M and 1 more
Genes: TBP
Higher fidelity of RNA-dependent DNA mispair extension by M184V drug-resistant than wild-type reverse transcriptase of human immunodeficiency virus type 1.
Nucleic acids research | 1997-11-15 | PMID 9358162
Hsu M, Inouye P, Rezende L and 4 more
Both the polypyrimidine tract and the 3' splice site function prior to the first step of splicing in fission yeast.
Nucleic acids research | 1997-11-15 | PMID 9358179
Romfo C M, Wise J A
Trade-off between false positives and false negatives in the linkage analysis of complex traits.
Genetic epidemiology | 1997-01-01 | PMID 9358264
Todorov A A, Rao D C
Sample size required for predefined linkage decision quality.
Genetic epidemiology | 1997-01-01 | PMID 9358266
Ginsburg E K, Axenovich T I
Evaluation of different lymphoid tissue sources for the construction of human immunoglobulin gene libraries.
Immunotechnology : an international journal of immunological engineering | 1997-10-01 | PMID 9358272
Yip Y L, Hawkins N J, Clark M A and 1 more
X-linked severe combined immunodeficiency in a family of Cardigan Welsh corgis.
Journal of the American Animal Hospital Association | 2000-01-01 | PMID 9358416
Pullen R P, Somberg R L, Felsburg P J and 1 more
Epidermolysis bullosa: a spectrum of clinical phenotypes explained by molecular heterogeneity.
Molecular medicine today | 1997-10-01 | PMID 9358473
Uitto J, Pulkkinen L, McLean W H
Clinical application of preimplantation diagnosis for myotonic dystrophy.
Prenatal diagnosis | 1997-10-01 | PMID 9358572
Sermon K, Lissens W, Joris H and 5 more
Prenatal diagnosis of trisomy 9: cytogenetic, fish, and DNA studies.
Prenatal diagnosis | 1997-10-01 | PMID 9358573
Van den Berg C, Ramlakhan S K, Van Opstal D and 3 more
Mutation analysis for prenatal diagnosis of hereditary tyrosinaemia type 1.
Prenatal diagnosis | 1997-10-01 | PMID 9358577
Mustonen A, Ploos van Amstel H K, Berger R and 3 more
Genetic landmarks for defects in mouse neural tube closure.
Teratology | 1997-09-01 | PMID 9358605
Harris M J, Juriloff D M
Gene frequencies of the HPA-1 and HPA-2 platelet antigen alleles among the Amerindians.
Vox sanguinis | 1997-01-01 | PMID 9358621
Covas D T, Delgado M, Zeitune M M and 3 more
Genotyping of the human platelet antigen-1 by ELISA detection of allele-specific amplicons.
Vox sanguinis | 1997-01-01 | PMID 9358622
Müller T H, Döscher A, Schunter F
Systemic activation of the vascular endothelial growth factor receptor KDR/flk-1 selectively triggers endothelial cells with an angiogenic phenotype.
The American journal of pathology | 1997-11-01 | PMID 9358746
Ortéga N, Jonca F, Vincent S and 3 more
Genes: KDR
Characterization of tumor-infiltrating T lymphocytes in B-cell lymphomas of mucosa-associated lymphoid tissue.
The American journal of pathology | 1997-11-01 | PMID 9358761
Koulis A, Diss T, Isaacson P G and 1 more
Genetic progression and heterogeneity in intraductal papillary-mucinous neoplasms of the pancreas.
The American journal of pathology | 1997-11-01 | PMID 9358771
Fujii H, Inagaki M, Kasai S and 4 more
Genetic factors in osteoporosis. What are the implications for prevention and treatment?
Drugs & aging | 1997-11-01 | PMID 9359020
Keen R W, Kelly P J
Genes: VDR
Mutations in Hirschsprung disease: when does a mutation contribute to the phenotype.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9359036
Hofstra R M, Osinga J, Buys C H
Genes: EDN3, EDNRB, GDNF, RET
Two new mutations in the glucose-6-phosphatase gene cause glycogen storage disease in Hungarian patients.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9359038
Parvari R, Lei K J, Szonyi L and 3 more
Relationship between mutation genotype and biochemical phenotype in a heterogeneous Spanish phenylketonuria population.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9359039
Desviat L R, Pérez B, García M J and 9 more
Genes: PAH
Estimating recessive disease allele frequency based on genetic maps.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9359040
Haghighi F, Ott J
BOR and BO syndromes are allelic defects of EYA1.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9359046
Vincent C, Kalatzis V, Abdelhak S and 5 more
Genes: EYA1
Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9359047
Bidaud C, Salomon R, Van Camp G and 9 more
Genes: EDN3, EDNRB, GDNF, RET
Nasal T/natural killer (NK)-cell lymphomas are derived from Epstein-Barr virus-infected cytotoxic lymphocytes of both NK- and T-cell lineage.
International journal of cancer | 1997-11-04 | PMID 9359478
Chiang A K, Chan A C, Srivastava G and 1 more
Polymorphisms of HPA-1 through 6 on platelet membrane glycoprotein receptors are not a genetic risk factor for myocardial infarction in the Japanese population.
The American journal of cardiology | 1997-11-01 | PMID 9359557
Hato T, Minamoto Y, Fukuyama T and 1 more
Genetic and biochemical studies on ommochrome genesis in an albino strain of a terrestrial isopod, Armadillidium vulgare.
Pigment cell research | 1997-10-01 | PMID 9359622
Hasegawa Y, Negishi S, Naito J and 4 more
HIV type 1 subtypes, coreceptor usage, and CCR5 polymorphism.
AIDS research and human retroviruses | 1997-11-01 | PMID 9359654
Zhang L, Carruthers C D, He T and 5 more
Genes: CCR5, CXCR4, CCR3
Diversity of full-length subtype E HIV type 1 env sequences in early seroconvertors from northern Thailand.
AIDS research and human retroviruses | 1997-11-01 | PMID 9359664
Yu X F, Wang Z, Beyrer C and 3 more
Suppression of a CFTR premature stop mutation in a bronchial epithelial cell line.
Nature medicine | 1997-11-01 | PMID 9359706
Bedwell D M, Kaenjak A, Benos D J and 6 more
Genes: CFTR
Osteopetrosis in mice lacking NF-kappaB1 and NF-kappaB2.
Nature medicine | 1997-11-01 | PMID 9359707
Iotsova V, Caamaño J, Loy J and 3 more
Low detection rate and maternal provenance of hepatitis B virus S gene mutants in cases of failed postnatal immunoprophylaxis in England and Wales.
The Journal of infectious diseases | 1997-11-01 | PMID 9359739
Ngui S L, O'Connell S, Eglin R P and 2 more
The incidence and genetic variability of small round-structured viruses in outbreaks of gastroenteritis in The Netherlands.
The Journal of infectious diseases | 1997-11-01 | PMID 9359742
Vinjé J, Altena S A, Koopmans M P
Zidovudine-resistant human immunodeficiency virus type 1 strains subcultured in the presence of both lamivudine and quinoxaline HBY 097 retain marked sensitivity to HBY 097 but not to lamivudine.
The Journal of infectious diseases | 1997-11-01 | PMID 9359746
Balzarini J, Pelemans H, Riess G and 4 more
The DNA damage-recognition problem in human and other eukaryotic cells: the XPA damage binding protein.
The Biochemical journal | 1997-11-15 | PMID 9359827
Cleaver J E, States J C
Genes: XPA
A structure/function analysis of Rat7p/Nup159p, an essential nucleoporin of Saccharomyces cerevisiae.
Journal of cell science | 1997-12-01 | PMID 9359887
Del Priore V, Heath C, Snay C and 4 more
Yeast functional assay of the p53 gene status in human cell lines maintained in our laboratory.
Acta medica Okayama | 1997-10-01 | PMID 9359923
Mihara K, Miyazaki M, Kondo T and 6 more
Genes: GAL
Expanded CAG/CTG repeats in bipolar disorder: no correlation with phenotypic measures of illness severity.
Biological psychiatry | 1997-11-15 | PMID 9359972
Craddock N, McKeon P, Moorhead S and 8 more
Genes: TNR
Depression and dementia in relation to apolipoprotein E polymorphism in a population sample age 75+.
Biological psychiatry | 1997-11-15 | PMID 9359975
Forsell Y, Corder E H, Basun H and 3 more
Genes: APOE
Neuroreceptor subunit genes and the genetic susceptibility to Gilles de la Tourette syndrome.
Biological psychiatry | 1997-11-15 | PMID 9359981
Brett P M, Curtis D, Robertson M M and 1 more
Hereditary defect in biosynthesis of aldosterone: aldosterone synthase deficiency 1964-1997.
The Journal of clinical endocrinology and metabolism | 1997-11-01 | PMID 9360501
Peter M, Fawaz L, Drop S L and 2 more
Phenotype: genotype relationships in growth hormone insensitivity syndrome.
The Journal of clinical endocrinology and metabolism | 1997-11-01 | PMID 9360502
Woods K A, Dastot F, Preece M A and 7 more
Genes: GHR
Mosaicism due to a somatic mutation of the androgen receptor gene determines phenotype in androgen insensitivity syndrome.
The Journal of clinical endocrinology and metabolism | 1997-11-01 | PMID 9360511
Holterhus P M, Brüggenwirth H T, Hiort O and 4 more
Autosomal dominant neurohypophyseal diabetes insipidus associated with a missense mutation encoding Gly23-->Val in neurophysin II.
The Journal of clinical endocrinology and metabolism | 1997-11-01 | PMID 9360520
Gagliardi P C, Bernasconi S, Repaske D R
Genes: AVP
Novel compound heterozygous mutations of growth hormone (GH) receptor gene in a patient with GH insensitivity syndrome.
The Journal of clinical endocrinology and metabolism | 1997-11-01 | PMID 9360529
Kaji H, Nose O, Tajiri H and 6 more
Abnormalities of apolipoprotein E in the acquired immunodeficiency syndrome.
The Journal of clinical endocrinology and metabolism | 1997-11-01 | PMID 9360533
Grunfeld C, Doerrler W, Pang M and 3 more
Effect of variations in plasma magnesium concentration on resistance to insulin-mediated glucose disposal in nondiabetic subjects.
The Journal of clinical endocrinology and metabolism | 1997-11-01 | PMID 9360541
Rosolova H, Mayer O, Reaven G
A single amino acid substitution in the putative redox partner-binding site of P450c17 as cause of isolated 17,20-lyase deficiency.
The Journal of clinical endocrinology and metabolism | 1997-11-01 | PMID 9360545
Biason-Lauber A, Leiberman E, Zachmann M
Three novel mutations and a de novo deletion mutation of the DAX-1 gene in patients with X-linked adrenal hypoplasia congenita.
The Journal of clinical endocrinology and metabolism | 1997-11-01 | PMID 9360549
Nakae J, Abe S, Tajima T and 6 more
Somatic mutations in the thyrotropin receptor gene and not in the Gs alpha protein gene in 31 toxic thyroid nodules.
The Journal of clinical endocrinology and metabolism | 1997-11-01 | PMID 9360556
Führer D, Holzapfel H P, Wonerow P and 2 more
Genes: TSHR
Cooperativity of folding of the apomyoglobin pH 4 intermediate studied by glycine and proline mutations.
Nature structural biology | 1997-11-01 | PMID 9360609
Luo Y, Kay M S, Baldwin R L
Identification and characterization of two polymorphic Ya5 Alu repeats.
Mutation research | 1997-09-01 | PMID 9360633
Arcot S S, DeAngelis M M, Sherry S T and 5 more
The design of a new mutation model for active genes: expression of the Escherichia coli lac operon in mammalian cells.
Mutation research | 1997-09-01 | PMID 9360635
van Sloun P P, Lohman P H, Vrieling H
Genes: LTK
Search for DNA sequence variations using a MutS-based technology.
Mutation research | 1997-09-01 | PMID 9360636
Bellanné-Chantelot C, Beaufils S, Hourdel V and 6 more
Detection of a point mutation (A to G) in exon 5 of the murine Mgf gene defines a novel allele at the Steel locus with a weak phenotype.
Mutation research | 1997-09-01 | PMID 9360640
Graw J, Neuhäuser-Klaus A, Pretsch W
Expression of the yeast NAM9 gene coding for mitochondrial ribosomal protein.
Acta biochimica Polonica | 1997-01-01 | PMID 9360714
Boguta M, Chacińska A, Murawski M and 1 more
Molecular cloning and expression in Escherichia coli of a gene coding for bovine S100A1 protein and its Glu32-->Gln and Glu73-->Gln mutants.
Acta biochimica Polonica | 1997-01-01 | PMID 9360716
Bolewska K, Kozłowska H, Goch G and 2 more
Identifying infertile homozygous Inverdale (FecXI) ewe lambs on the basis of genotype differences in reproductive hormone concentrations.
Animal reproduction science | 1997-07-01 | PMID 9360768
McLeod B J, Fenton L F, Davis G H and 3 more
Hepatitis C virus in infants and children.
Current opinion in pediatrics | 1997-10-01 | PMID 9360832
Thaler M M
Enriched SSCP: a highly sensitive method for the detection of unknown mutations. Application to the molecular diagnosis of lung cancer in sputum samples.
Diagnostic molecular pathology : the American journal of surgical pathology, part B | 1997-08-01 | PMID 9360839
Marchetti A, Buttitta F, Carnicelli V and 4 more
The pattern of p53 and p21WAF1/CIP1 immunoreactivity in non-Hodgkin's lymphomas predicts p53 gene status.
Diagnostic molecular pathology : the American journal of surgical pathology, part B | 1997-08-01 | PMID 9360843
Mansukhani M M, Osborne B M, Zhong J and 1 more
Convenient, nonradioactive, heteroduplex-based methods for identifying recurrent mutations in the BRCA1 and BRCA2 genes.
Diagnostic molecular pathology : the American journal of surgical pathology, part B | 1997-08-01 | PMID 9360844
Mansukhani M M, Nastiuk K L, Hibshoosh H and 3 more
Genes: BRCA1, BRCA2
Oligoclonal peripheral T-cell lymphocytosis as a result of aberrant T-cell development in a cortical thymoma.
Diagnostic molecular pathology : the American journal of surgical pathology, part B | 1997-08-01 | PMID 9360846
de Jong D, Richel D J, Schenkeveld C and 2 more
Recovery of replication-competent HIV despite prolonged suppression of plasma viremia.
Science (New York, N.Y.) | 1997-11-14 | PMID 9360926
Wong J K, Hezareh M, Günthard H F and 4 more
Identification of a reservoir for HIV-1 in patients on highly active antiretroviral therapy.
Science (New York, N.Y.) | 1997-11-14 | PMID 9360927
Finzi D, Hermankova M, Pierson T and 12 more
daf-16: An HNF-3/forkhead family member that can function to double the life-span of Caenorhabditis elegans.
Science (New York, N.Y.) | 1997-11-14 | PMID 9360933
Lin K, Dorman J B, Rodan A and 1 more
Familial hypercholesterolemia and familial defective apolipoprotein B-100: comparison of the phenotypic expression In 116 cases.
European journal of medical research | 1996-05-24 | PMID 9360938
Brugger D, Schuster H, Zöllner N
Genes: LDLR, CAD
Agonist-receptor-arrestin, an alternative ternary complex with high agonist affinity.
The Journal of biological chemistry | 1997-11-14 | PMID 9360951
Gurevich V V, Pals-Rylaarsdam R, Benovic J L and 2 more