Birth prevalence study of the Apert syndrome.
American journal of medical genetics | 1992-03-01 | PMID 1303629
Cohen M M, Kreiborg S, Lammer E J and 5 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 111 of 10600
Complementation of Saccharomyces cerevisiae auxotrophic mutants by Arabidopsis thaliana cDNAs.
The Plant journal : for cell and molecular biology | 1992-05-01 | PMID 1303803
Minet M, Dufour M E, Lacroute F
[Studies on human cervical carcinoma cell line. II. Establishment of HGPRT- cell line CC-80IAR2 and its biological characteristics].
Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae | 1992-12-01 | PMID 1303821
Wang R
Retinoma and phthisis bulbi of retinoblastoma. 1. Clinical and genetic analysis.
Yan ke xue bao = Eye science | 1992-09-01 | PMID 1303868
Zhang Q, Chen Y, Wu Z and 4 more
Is cadmium genotoxic?
IARC scientific publications | 1992-01-01 | PMID 1303963
Rossman T G, Roy N K, Lin W C
High frequencies in African and non-African populations of independent mutations in the mannose binding protein gene.
Human molecular genetics | 1992-12-01 | PMID 1304173
Lipscombe R J, Sumiya M, Hill A V and 4 more
Genes: MBP, GAA
HLA and complement C4 studies in psoriasis vulgaris.
The National medical journal of India | 2000-01-01 | PMID 1304260
Chablani U A, Contractor N M, Gadgil R B
Structural analysis of wild-type and mutant yeast calmodulins by limited proteolysis and electrospray ionization mass spectrometry.
Protein science : a publication of the Protein Society | 1992-04-01 | PMID 1304352
Brockerhoff S E, Edmonds C G, Davis T N
Guanidine derivatives restore activity to carboxypeptidase lacking arginine-127.
Protein science : a publication of the Protein Society | 1992-04-01 | PMID 1304353
Phillips M A, Hedstrom L, Rutter W J
Amino acid binding by the class I aminoacyl-tRNA synthetases: role for a conserved proline in the signature sequence.
Protein science : a publication of the Protein Society | 1992-05-01 | PMID 1304356
Burbaum J J, Schimmel P
Amino acid sequence of fibrolase, a direct-acting fibrinolytic enzyme from Agkistrodon contortrix contortrix venom.
Protein science : a publication of the Protein Society | 1992-05-01 | PMID 1304358
Randolph A, Chamberlain S H, Chu H L and 3 more
Characterization of REC104, a gene required for early meiotic recombination in the yeast Saccharomyces cerevisiae.
Developmental genetics | 1992-01-01 | PMID 1304422
Galbraith A M, Malone R E
Variance component analysis of bristle characters in local populations of Drosophila melanogaster.
Idengaku zasshi | 1992-12-01 | PMID 1304769
Ichinose M, Tachida H, Mukai T
Quantitative genetic study on sexual difference in emigration behavior of Drosophila melanogaster in a natural population.
Idengaku zasshi | 1992-12-01 | PMID 1304770
Mikasi K
Acute myelogenous leukemia with T-cell features.
Bulletin du cancer | 1992-01-01 | PMID 1304836
Ribrag V, Bayle C, Brault P and 3 more
Structure of a stabilizing disulfide bridge mutant that closes the active-site cleft of T4 lysozyme.
Protein science : a publication of the Protein Society | 1992-01-01 | PMID 1304882
Jacobson R H, Matsumura M, Faber H R and 1 more
Modeling the effects of mutations on the denatured states of proteins.
Protein science : a publication of the Protein Society | 1992-02-01 | PMID 1304903
Shortle D, Chan H S, Dill K A
In vitro effects of Chelidonium majus L. alkaloid thiophosphoric acid conjugates (Ukrain) on the phenotype of normal human lymphocytes.
Drugs under experimental and clinical research | 1992-01-01 | PMID 1305038
Slesak B, Nowicky J W, Harłozinska A
Comparison of lethal mutations of Drosophila melanogaster with D. simulans when detected by the attached-X method.
Genetica | 1992-01-01 | PMID 1305124
Inoue Y
Effects on ADH activity and distribution, following selection for tolerance to ethanol in Drosophila melanogaster.
Genetica | 1992-01-01 | PMID 1305125
Kerver J W, Wolf W, Kamping A and 1 more
Epidemiological models of carcinogenesis: the example of bladder cancer.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology | 2000-01-01 | PMID 1306098
Vineis P
Prospective study of Lewis antigen alterations in the gastric precancerous process.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology | 2000-01-01 | PMID 1306106
Torrado J, Correa P, Ruiz B and 2 more
Determination of CYP1A2 and NAT2 phenotypes in human populations by analysis of caffeine urinary metabolites.
Pharmacogenetics | 1992-06-01 | PMID 1306111
Butler M A, Lang N P, Young J F and 7 more
Genes: NAT2
The ability to 4-hydroxylate debrisoquine is related to recurrence of bladder cancer.
Pharmacogenetics | 1992-06-01 | PMID 1306112
Fleming C M, Kaisary A, Wilkinson G R and 2 more
The novel bilirubin/phenol UDP-glucuronosyltransferase UGT1 gene locus: implications for multiple nonhemolytic familial hyperbilirubinemia phenotypes.
Pharmacogenetics | 1992-06-01 | PMID 1306114
Owens I S, Ritter J K
Molecular genetics of human aldehyde dehydrogenase.
Pharmacogenetics | 1992-08-01 | PMID 1306115
Yoshida A
Genes: ALDH2
Guinea pig or rabbit lung flavin-containing monooxygenases with distinct mobilities in SDS-PAGE are allelic variants that differ at only two positions.
Pharmacogenetics | 1992-10-01 | PMID 1306120
Nikbakht K N, Lawton M P, Philpot R M
Genes: SDS
Genotyping human polymorphic arylamine N-acetyltransferase: identification of new slow allotypic variants.
Pharmacogenetics | 1992-10-01 | PMID 1306121
Hickman D, Risch A, Camilleri J P and 1 more
Interindividual variability of coumarin 7-hydroxylation in healthy volunteers.
Pharmacogenetics | 1992-10-01 | PMID 1306122
Rautio A, Kraul H, Kojo A and 2 more
Structural basis of the butyrylcholinesterase H-variant segregating in two Danish families.
Pharmacogenetics | 1992-10-01 | PMID 1306123
Jensen F S, Bartels C F, La Du B N
A methodological investigation on the estimation of the S-mephenytoin hydroxylation phenotype using the urinary S/R ratio.
Pharmacogenetics | 1992-10-01 | PMID 1306124
Tybring G, Bertilsson L
Metabolic cytochrome P450 genotypes and assessment of individual susceptibility to lung cancer.
Pharmacogenetics | 1992-12-01 | PMID 1306126
Hirvonen A, Husgafvel-Pursiainen K, Anttila S and 3 more
Genetic changes in breast carcinomas in an Icelandic population.
Pharmacogenetics | 1992-12-01 | PMID 1306132
Eyfjörd J E, Thorlacius S
Detection of DNA variation in cancer.
Pharmacogenetics | 1992-12-01 | PMID 1306133
Hovig E, Smith-Sørensen B, Uitterlinden A G and 1 more
Exclusion probabilities of red cell antigen systems for Chinese.
Zhonghua Minguo wei sheng wu ji mian yi xue za zhi = Chinese journal of microbiology and immunology | 1992-02-01 | PMID 1306147
Sun C F, Tsao K C, Teh C H
Genes: ABO, CPE
The phenotype and gene frequencies of human platelet specific antigens among Chinese in Taiwan.
Zhonghua Minguo wei sheng wu ji mian yi xue za zhi = Chinese journal of microbiology and immunology | 1992-02-01 | PMID 1306149
Tsao K C, Sun C F, Lai N C
Expression of the PMP-22 gene in Trembler mutant mice: comparison with the other myelin protein genes.
Developmental neuroscience | 1992-01-01 | PMID 1306159
Bascles L, Bonnet J, Garbay B
[Analysis of oncogenes and suppressor genes in lung cancer and bronchial lesions from high risk group].
Nihon Kyobu Shikkan Gakkai zasshi | 1992-12-01 | PMID 1306237
Awaya Y, Hiyama K, Yamakido M
Genes: TRA
DNA repair pathways in mammalian cells analyzed by isolation of ACNU-sensitive Chinese hamster ovary cells.
The Tohoku journal of experimental medicine | 1992-10-01 | PMID 1306296
Numata M, Hata H, Tohda H and 2 more
Role of c-Myc on erythroid differentiation.
The Tohoku journal of experimental medicine | 1992-10-01 | PMID 1306305
Ohmori Y, Tanabe J, Terashima M and 3 more
Molecular genetics of the human cytochrome P450-dependent monooxygenases.
The Tohoku journal of experimental medicine | 1992-10-01 | PMID 1306335
Wolf C R, Smith C A, Smith G and 4 more
[Molecular pathology of inherited Glanzmann's thrombasthenia. Report of 11 cases].
Zhonghua nei ke za zhi | 1992-10-01 | PMID 1306460
Ruan C G, Gu J M, Li J Y
Molecular basis of insulin resistance.
Hormone research | 1992-01-01 | PMID 1306516
Clauser E, Leconte I, Auzan C
The thyroid hormone receptors: molecular basis of thyroid hormone resistance.
Hormone research | 1992-01-01 | PMID 1306518
De Nayer P
G-protein oncogenes in acromegaly.
Hormone research | 1992-01-01 | PMID 1306524
Spada A, Vallar L
Phenotype frequencies of the class II (DR, DQ) DNA alleles by the patterns of sequence-specific primer mixtures (SSPM) in four different populations and the probable haplotypes between DRB1 allele and DQB1 allele.
Clinical transplants | 1992-01-01 | PMID 1306720
Park M S, Tonai R
[The biological mechanisms of a congenital predisposition to alcoholism].
Fiziologicheskii zhurnal imeni I.M. Sechenova | 1992-12-01 | PMID 1306754
Anokhina I P, Vekshina N L, Kuznetsova M N and 4 more
Molecular biology of disorders of sex differentiation.
Hormone research | 1992-01-01 | PMID 1306840
Sultan C, Lobaccaro J M, Belon C and 2 more
Genes: SRY
The presence of two different infantile Tay-Sachs disease mutations in a Cajun population.
American journal of human genetics | 1992-11-01 | PMID 1307230
McDowell G A, Mules E H, Fabacher P and 2 more
Mutations in the candidate gene for Norrie disease.
Human molecular genetics | 1992-10-01 | PMID 1307245
Berger W, van de Pol D, Warburg M and 7 more
Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype.
Human molecular genetics | 1992-10-01 | PMID 1307246
Shelbourne P, Winqvist R, Kunert E and 7 more
Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome.
Human molecular genetics | 1992-10-01 | PMID 1307250
Batch J A, Williams D M, Davies H R and 4 more
Segregation of the fragile X mutation from an affected male to his normal daughter.
Human molecular genetics | 1992-10-01 | PMID 1307252
Willems P J, Van Roy B, De Boulle K and 6 more
Hemoglobin H disease in children.
Journal of the Medical Association of Thailand = Chotmaihet thangphaet | 1992-11-01 | PMID 1307383
Wongchanchailert M, Laosombat V, Maipang M
Colonization of infant mice with flagellar variants of Campylobacter jejuni.
Acta microbiologica Hungarica | 1992-01-01 | PMID 1307436
Diker K S, Hascelik G, Diker S
Multiple enlargements in the right inverted terminal repeat of the DNA of canine adenovirus type 2.
Acta microbiologica Hungarica | 1992-01-01 | PMID 1307439
Fejér G, Berencsi G, Ruzsics Z and 3 more
[Genetic diagnosis of phenylketonuria: identification of the mutations of phenylalanine hydroxylase gene by PCR direct sequencing].
Rinsho byori. The Japanese journal of clinical pathology | 1992-10-01 | PMID 1307609
Yamashita K, Takarada Y, Otsuka N and 3 more
Genes: PAH, TAT
Genes involved in androgen biosynthesis and the male phenotype.
Hormone research | 1992-01-01 | PMID 1307739
Waterman M R, Keeney D S
Role of the androgen receptor in male sexual differentiation.
Hormone research | 1992-01-01 | PMID 1307741
Batch J A, Williams D M, Davies H R and 4 more
Testicular adrenal-like tissue in a patient with 17 alpha-hydroxylase deficiency.
Hormone research | 1992-01-01 | PMID 1307744
García-Mayor R V, Sopeña B, Fluiters E and 4 more
[Phenotype analysis of mononuclear cells from endomyocardial biopsy specimens in patients with viral myocarditis and dilated cardiomyopathy].
Zhonghua xin xue guan bing za zhi | 1992-12-01 | PMID 1307978
Li W
Genes: EMB
Nucleotide sequence of the 18S ribosomal ribonucleic acid gene from two teleosts and two sharks and their molecular phylogeny.
Molecular marine biology and biotechnology | 1992-06-01 | PMID 1308203
Bernardi G, Sordino P, Powers D A
Direct sequencing of mitochondrial DNA detects highly divergent haplotypes in blue marlin (Makaira nigricans).
Molecular marine biology and biotechnology | 1992-06-01 | PMID 1308204
Finnerty J R, Block B A
The gel test: some problems and solutions.
Transfusion medicine (Oxford, England) | 1992-06-01 | PMID 1308208
de Figueiredo M, Lima M, Morais S and 2 more
Genes: ABO
[Influence of lovastatin on serum lipids in patients with primary hyperlipidemia and phenotype IIa and IIB. II. Changes of lipid composition of plasma lipoprotein fractions after lovastatin administration].
Przeglad lekarski | 1992-01-01 | PMID 1308286
Idzior-Waluś B
[Changes in the level of certain hemostatic factors during treatment with lovastatin in patients with primary hyperlipoproteinemia and phenotype IIa and IIb].
Przeglad lekarski | 1992-01-01 | PMID 1308287
Idzior-Waluś B
GMS syndrome: a new dominant condition with goniodysgenesis, mental retardation, and short stature.
American journal of medical genetics | 1992-01-01 | PMID 1308345
Kupchik G S, Ludman M D, Raab E L and 1 more
Phenotypically dissimilar hypophosphatasia in two sibships.
American journal of medical genetics | 1992-01-01 | PMID 1308350
Macfarlane J D, Kroon H M, van der Harten J J
Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes.
American journal of medical genetics | 1992-01-01 | PMID 1308352
Collins F A, Murphy D L, Reiss A L and 7 more
Genes: MAOA, MAOB
Ectopia lentis and aortic root dilatation in congenital contractural arachnodactyly.
American journal of medical genetics | 1992-01-01 | PMID 1308360
Bawle E, Quigg M H
Stable ring chromosome 21: molecular and clinical definition of the lesion.
American journal of medical genetics | 1992-01-01 | PMID 1308361
Falik-Borenstein T C, Pribyl T M, Pulst S M and 6 more
Genes: CBS
De Barsy syndrome: report of a case, literature review, and elastin gene expression studies of the skin.
American journal of medical genetics | 1992-01-01 | PMID 1308362
Karnes P S, Shamban A T, Olsen D R and 2 more
Alagille syndrome with de novo del(20) (p11.2).
American journal of medical genetics | 1992-01-01 | PMID 1308363
Teebi A S, Murthy D S, Ismail E A and 1 more
Cockayne syndrome: review of 140 cases.
American journal of medical genetics | 1992-01-01 | PMID 1308368
Nance M A, Berry S A
Progressive bilateral nasal alar collapse: a dominantly inherited trait.
American journal of medical genetics | 1992-01-01 | PMID 1308370
Cole H, Bodurtha J, Salbert B A and 1 more
Agonadism in a 46,XY patient with CHARGE association.
American journal of medical genetics | 1992-01-01 | PMID 1308372
Kushnick T, Wiley J E, Palmer S M
Genes: ZFY
[Phenotypic expression variation of isovaleric acidemia in Argentinian patients. A long term follow-up].
Medicina | 1992-01-01 | PMID 1308904
Dodelson de Kremer R, Depetris de Boldini C, Paschini de Capra A and 2 more
Cloning and expression of the defective genes in delta-aminolevulinate dehydratase porphyria: compound heterozygosity in this hereditary liver disease.
Transactions of the Association of American Physicians | 1992-01-01 | PMID 1309003
Sassa S, Ishida N, Fujita H and 4 more
Genes: ALAD
Energy-dependent processes involved in reduced drug accumulation in multidrug-resistant human lung cancer cell lines without P-glycoprotein expression.
Cancer research | 1992-01-01 | PMID 1309222
Versantvoort C H, Broxterman H J, Pinedo H M and 4 more
ras transformation of simian virus 40-immortalized rat hepatocytes: an in vitro model of hepatocarcinogenesis.
Cancer research | 1992-01-01 | PMID 1309223
Fang X J, Flowers M, Keating A and 2 more
Genes: ALB
Three pathways of Epstein-Barr virus gene activation from EBNA1-positive latency in B lymphocytes.
Journal of virology | 1992-01-01 | PMID 1309242
Rowe M, Lear A L, Croom-Carter D and 2 more
Deletion of the VP16 open reading frame of herpes simplex virus type 1.
Journal of virology | 1992-01-01 | PMID 1309245
Weinheimer S P, Boyd B A, Durham S K and 2 more
Construction and properties of a mutant of herpes simplex virus type 1 with glycoprotein H coding sequences deleted.
Journal of virology | 1992-01-01 | PMID 1309250
Forrester A, Farrell H, Wilkinson G and 3 more
The UL5 gene of herpes simplex virus type 1: isolation of a lacZ insertion mutant and association of the UL5 gene product with other members of the helicase-primase complex.
Journal of virology | 1992-01-01 | PMID 1309255
Zhu L A, Weller S K
The six conserved helicase motifs of the UL5 gene product, a component of the herpes simplex virus type 1 helicase-primase, are essential for its function.
Journal of virology | 1992-01-01 | PMID 1309257
Zhu L A, Weller S K
Evidence that the herpes simplex virus immediate early protein ICP27 acts post-transcriptionally during infection to regulate gene expression.
Virology | 1992-01-01 | PMID 1309283
Smith I L, Hardwicke M A, Sandri-Goldin R M
Reaction of the nucleotide analogue 2-[(4-bromo-2,3-dioxobutyl)thio]adenosine 2',5'-bisphosphate at the coenzyme site of wild-type and mutant NADP(+)-specific glutamate dehydrogenases from Salmonella typhimurium.
Archives of biochemistry and biophysics | 1992-01-01 | PMID 1309291
Haeffner-Gormley L, Chen Z D, Zalkin H and 1 more
Ki-ras oncogene activation in preinvasive pancreatic cancer.
Gastroenterology | 1992-01-01 | PMID 1309358
Lemoine N R, Jain S, Hughes C M and 4 more
Dietary arginine influences Rous sarcoma growth in a major histocompatibility B complex progressor genotype.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.) | 1992-01-01 | PMID 1309397
Taylor R L, Austic R E, Dietert R R
Hepatitis B virus. New and evolving issues.
Digestive diseases and sciences | 1992-01-01 | PMID 1309448
Yoffe B, Noonan C A
The human beta 3-adrenergic receptor: relationship with atypical receptors.
The American journal of clinical nutrition | 1992-01-01 | PMID 1309479
Emorine L J, Fève B, Pairault J and 5 more
A temperature-sensitive CHO-K1 cell mutant (tsTM13) defective in chromosome decondensation and spindle deconstruction in M phase.
Experimental cell research | 1992-02-01 | PMID 1309502
Tsuji H, Matsudo Y, Ajiro K and 6 more
The pgpA and pgpB genes of Escherichia coli are not essential: evidence for a third phosphatidylglycerophosphate phosphatase.
Journal of bacteriology | 1992-01-01 | PMID 1309518
Funk C R, Zimniak L, Dowhan W
Construction and application of plasmid- and transposon-based promoter-probe vectors for Streptomyces spp. that employ a Vibrio harveyi luciferase reporter cassette.
Journal of bacteriology | 1992-01-01 | PMID 1309525
Sohaskey C D, Im H, Schauer A T
Roles of the orlA, tsE, and bimG genes of Aspergillus nidulans in chitin synthesis.
Journal of bacteriology | 1992-01-01 | PMID 1309526
Borgia P T
Involvement of Fis protein in replication of the Escherichia coli chromosome.
Journal of bacteriology | 1992-01-01 | PMID 1309527
Filutowicz M, Ross W, Wild J and 1 more
The oriT region of the conjugative transfer system of plasmid pCU1 and specificity between it and the mob region of other N tra plasmids.
Journal of bacteriology | 1992-01-01 | PMID 1309528
Paterson E S, Iyer V N
Identification of the gene (aroK) encoding shikimic acid kinase I of Escherichia coli.
Journal of bacteriology | 1992-01-01 | PMID 1309529
Løbner-Olesen A, Marinus M G
The basic region of myogenin cooperates with two transcription activation domains to induce muscle-specific transcription.
Molecular and cellular biology | 1992-01-01 | PMID 1309591
Schwarz J J, Chakraborty T, Martin J and 2 more
Differential splicing in the extracellular region of fibroblast growth factor receptor 1 generates receptor variants with different ligand-binding specificities.
Molecular and cellular biology | 1992-01-01 | PMID 1309595
Werner S, Duan D S, de Vries C and 3 more
Genes: FGFR1