Early loss of heterozygosity on 17q in ovarian cancer. The Abe Ovarian Cancer Genetics Group.
Oncogene | 1992-10-01 | PMID 1408149
Eccles D M, Russell S E, Haites N E and 7 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 143 of 10600
Mutational analysis of Max: role of basic, helix-loop-helix/leucine zipper domains in DNA binding, dimerization and regulation of Myc-mediated transcriptional activation.
Oncogene | 1992-10-01 | PMID 1408152
Reddy C D, Dasgupta P, Saikumar P and 3 more
Strategies for constructing a guinea pig organ of Corti cDNA library and its potential use.
Otolaryngologic clinics of North America | 1992-10-01 | PMID 1408189
Wilcox E R
Epidemiology of childhood diabetes in the Baltic area.
Nordisk medicin | 1992-01-01 | PMID 1408719
Tuomilehto J
An abasic site analogue activates a c-Ha-ras gene by a point mutation at modified and adjacent positions.
Nucleic acids research | 1992-09-11 | PMID 1408742
Kamiya H, Suzuki M, Komatsu Y and 7 more
Spontaneous chromosome rearrangements in the protozoan Giardia lamblia: estimation of mutation rates.
Nucleic acids research | 1992-09-11 | PMID 1408754
Le Blancq S M, Korman S H, Van der Ploeg L H
Construction of human XRCC1 minigenes that fully correct the CHO DNA repair mutant EM9.
Nucleic acids research | 1992-09-11 | PMID 1408759
Caldecott K W, Tucker J D, Thompson L H
Genes: XRCC1
Detection of single base differences using biotinylated nucleotides with very long linker arms.
Nucleic acids research | 1992-09-25 | PMID 1408798
Livak K J, Hobbs F W, Zagursky R J
Genes: APOE
DNA diversity among clinical isolates of Helicobacter pylori detected by PCR-based RAPD fingerprinting.
Nucleic acids research | 1992-10-11 | PMID 1408828
Akopyanz N, Bukanov N O, Westblom T U and 2 more
Evolutionary somatic cell changes in cervical tumour progression quantitatively evaluated with morphological, histochemical and kinetic parameters.
Pathology, research and practice | 1992-06-01 | PMID 1409071
Mariuzzi G, Sisti S, Santinelli A and 2 more
Age-related modification of average volume and anisotropy of vascular smooth muscle cells.
Pathology, research and practice | 1992-06-01 | PMID 1409102
Mauriello A, Orlandi A, Palmieri G and 3 more
Molecular basis of type IA (tyrosinase negative) oculocutaneous albinism.
Pigment cell research | 1992-01-01 | PMID 1409426
King R A, Oetting W S
Identification of mutations in the pigment cell-specific gene located at the brown locus in mouse.
Pigment cell research | 1992-01-01 | PMID 1409444
Shibahara S, Tomita Y, Yoshizawa M and 2 more
Molecular bases of tyrosinase-negative oculocutaneous albinism: a single base insertion or a missense point mutation in the tyrosinase gene.
Pigment cell research | 1992-01-01 | PMID 1409445
Tomita Y, Takeda A, Matsunaga J and 3 more
[Molecular bases of cardiac aging].
Presse medicale (Paris, France : 1983) | 1992-07-22 | PMID 1409472
Carrier L, Chassagne C, Boheler K R and 1 more
A point mutation that decreases the thermal stability of human interferon gamma.
Protein engineering | 1992-04-01 | PMID 1409545
Lunn C A, Fossetta J, Murgolo N and 3 more
A point mutation of human interferon gamma abolishes receptor recognition.
Protein engineering | 1992-04-01 | PMID 1409546
Lunn C A, Fossetta J, Dalgarno D and 5 more
Early regional specification for a molecular neuronal phenotype in the rat neocortex.
Proceedings of the National Academy of Sciences of the United States of America | 1992-10-01 | PMID 1409580
Arimatsu Y, Miyamoto M, Nihonmatsu I and 4 more
Centromere DNA mutations induce a mitotic delay in Saccharomyces cerevisiae.
Proceedings of the National Academy of Sciences of the United States of America | 1992-10-01 | PMID 1409584
Spencer F, Hieter P
A strategy for making synthetic peptide vaccines.
Proceedings of the National Academy of Sciences of the United States of America | 1992-10-01 | PMID 1409595
Ogasawara K, Naruse H, Itoh Y and 5 more
Uncoupling gene activity from chromatin structure: promoter mutations can inactivate transcription of the yeast HSP82 gene without eliminating nucleosome-free regions.
Proceedings of the National Academy of Sciences of the United States of America | 1992-10-01 | PMID 1409619
Lee M S, Garrard W T
Cloning of an apparent splice variant of the rat N-methyl-D-aspartate receptor NMDAR1 with altered sensitivity to polyamines and activators of protein kinase C.
Proceedings of the National Academy of Sciences of the United States of America | 1992-10-01 | PMID 1409641
Durand G M, Gregor P, Zheng X and 3 more
Selective expression of human X chromosome-linked green opsin genes.
Proceedings of the National Academy of Sciences of the United States of America | 1992-10-15 | PMID 1409688
Winderickx J, Battisti L, Motulsky A G and 1 more
Genetic analysis of the interaction between bacteriophage T7 DNA polymerase and Escherichia coli thioredoxin.
Proceedings of the National Academy of Sciences of the United States of America | 1992-10-15 | PMID 1409697
Himawan J S, Richardson C C
Chronic stress induces strain-dependent sensitization to the behavioral effects of amphetamine in the mouse.
Pharmacology, biochemistry, and behavior | 1992-09-01 | PMID 1409819
Badiani A, Cabib S, Puglisi-Allegra S
A rapid thin layer chromatographic procedure to identify poor and extensive oxidative drug metabolizers in man using dextromethorphan.
Die Pharmazie | 1992-05-01 | PMID 1409826
De Zeeuw R A, Eikema D, Franke J P and 1 more
The use of CXB recombinant inbred mice to detect quantitative trait loci in behavior.
Physiology & behavior | 1992-09-01 | PMID 1409902
Neiderhiser J M, Plomin R, McClearn G E
Genotype-dependent involvement of limbic areas in spatial learning and postlesion recovery.
Physiology & behavior | 1992-09-01 | PMID 1409912
Ammassari-Teule M, Fagioli S, Rossi-Arnaud C
["New cytology" and diagnosis of malignant tumors].
La Revue de medecine interne | 2000-01-01 | PMID 1410873
Seigneurin D, Piaton E
AB0 and Lewis blood groups in reactive arthritis.
Rheumatology international | 1992-01-01 | PMID 1411088
Tertti R, Järvinen H, Lahesmaa R and 2 more
Demography of genotypes: failure of the limited life-span paradigm in Drosophila melanogaster.
Science (New York, N.Y.) | 1992-10-16 | PMID 1411541
Curtsinger J W, Fukui H H, Townsend D R and 1 more
Idiopathic dilated cardiomyopathy: lack of association between circulating organ-specific cardiac antibodies and HLA-DR antigens.
Tissue antigens | 1992-05-01 | PMID 1412410
Caforio A L, Martinetti M, Schwarz G and 7 more
The HLA DQB1*0502 allele is neutrally associated with insulin-dependent diabetes mellitus in the Sardinian population.
Tissue antigens | 1992-05-01 | PMID 1412411
Muntoni F, Congia M, Cucca F and 7 more
Population and family studies of HLA-DR4 by use of oligonucleotide typing.
Tissue antigens | 1992-05-01 | PMID 1412412
Reed E, Lupu F, McManus P and 2 more
HLA antigens in Tlingit Indians with rheumatoid arthritis.
Tissue antigens | 1992-08-01 | PMID 1412417
Nelson J L, Boyer G, Templin D and 6 more
HLA-DP polymorphism in Sudanese controls and patients with insulin-dependent diabetes mellitus.
Tissue antigens | 1992-08-01 | PMID 1412418
Magzoub M M, Stephens H A, Sachs J A and 4 more
Two new HLA DRB1 alleles found in African Americans: implications for balancing selection at positions 57 and 86.
Tissue antigens | 1992-08-01 | PMID 1412419
Apple R J, Erlich H A
[The role of the genotype in the development of suppurative inflammatory complications in trauma to the facial bones].
Stomatologiia | 2000-01-01 | PMID 1412541
Grigor'iants L A, Zuev V P, Pospelov L E and 3 more
Utility of a one-point (3-hour postdose) plasma metabolic ratio as a phenotyping test using metoprolol in two east Asian populations.
Therapeutic drug monitoring | 1992-06-01 | PMID 1412602
Sohn D R, Kusaka M, Shin S G and 3 more
Haloperidol disposition is dependent on the debrisoquine hydroxylation phenotype: increased plasma levels of the reduced metabolite in poor metabolizers.
Therapeutic drug monitoring | 1992-06-01 | PMID 1412613
Llerena A, Dahl M L, Ekqvist B and 1 more
Thromboxane augmentation of alloreactive T cell function.
Transplantation | 1992-09-01 | PMID 1412730
Ruiz P, Rey L, Spurney R and 2 more
The time course of cell-mediated lympholysis in rat hepatic allograft recipients pretreated with a single donor-specific blood transfusion.
Transplantation | 1992-09-01 | PMID 1412734
Katsumori T, Yamaguchi Y, Mori K and 6 more
Genes: DST
Replication capacities of natural and artificial precore stop codon mutants of hepatitis B virus: relevance of pregenome encapsidation signal.
Virology | 1992-11-01 | PMID 1413504
Tong S P, Li J S, Vitvitski L and 1 more
Phylogenetic analysis of alphaviruses in the Venezuelan equine encephalitis complex and identification of the source of epizootic viruses.
Virology | 1992-11-01 | PMID 1413507
Weaver S C, Bellew L A, Rico-Hesse R
Mutational analysis of the monopartite geminivirus beet curly top virus.
Virology | 1992-11-01 | PMID 1413511
Stanley J, Latham J R, Pinner M S and 2 more
cis-acting elements for in trans complementation of replication-defective mutant of tobacco mosaic virus.
Virology | 1992-11-01 | PMID 1413517
Ogawa T, Watanabe Y, Okada Y
The coat protein of white clover mosaic potexvirus has a role in facilitating cell-to-cell transport in plants.
Virology | 1992-11-01 | PMID 1413520
Forster R L, Beck D L, Guilford P J and 3 more
[Age changes in brain monoamine oxidase in mice from four lines].
Voprosy meditsinskoi khimii | 2000-01-01 | PMID 1413646
Voĭtenko N N
Expression of red cell antigens C and c on neonatal and adult erythrocytes. A flow-cytometric analysis.
Vox sanguinis | 1992-01-01 | PMID 1413664
DePalma L
[Intermediate lymphocytic lymphoma].
Wiadomosci lekarskie (Warsaw, Poland : 1960) | 1992-02-01 | PMID 1413789
Kończalik P, Hyjek E
Mutational activation of RAS and GSP oncogenes in differentiated thyroid cancer and their biological implications.
World journal of surgery | 2000-01-01 | PMID 1413827
Goretzki P E, Lyons J, Stacy-Phipps S and 6 more
The value of measurement of ras oncogenes and nuclear DNA analysis in the diagnosis of Hürthle cell tumors of the thyroid.
World journal of surgery | 2000-01-01 | PMID 1413844
Schark C, Fulton N, Yashiro T and 6 more
The attenuation phenotype conferred by the M gene of the influenza A/Ann Arbor/6/60 cold-adapted virus (H2N2) on the A/Korea/82 (H3N2) reassortant virus results from a gene constellation effect.
Virus research | 1992-09-01 | PMID 1413993
Subbarao E K, Perkins M, Treanor J J and 1 more
[The adhesive properties of S and R mutants of Salmonella minnesota during batch cultivation].
Zhurnal mikrobiologii, epidemiologii i immunobiologii | 1992-01-01 | PMID 1414109
Voskun S E, Novikova L F, Golubev O A
HbH disease in Sardinia: molecular, hematological and clinical aspects.
Acta haematologica | 1992-01-01 | PMID 1414154
Galanello R, Aru B, Dessì C and 7 more
Alpha 1-antitrypsin-deficiency-related emphysema.
The Journal of the American Board of Family Practice | 2000-01-01 | PMID 1414450
Barker A F
Oculo-dento-digital syndrome (Gorlin's syndrome): clinical and genetical report of a new family.
Acta neurologica | 1992-04-01 | PMID 1414553
Battisti C, Palmeri S, Federico A
Treatment of refractory familial hypercholesterolemia by low-density lipoprotein apheresis using an automated dextran sulfate cellulose adsorption system. The Liposorber Study Group.
The American journal of cardiology | 1992-10-15 | PMID 1414897
Gordon B R, Kelsey S F, Bilheimer D W and 7 more
Can the genetic factors influence the treatment of systemic hypertension? The case of the renin-angiotensin-aldosterone system.
The American journal of cardiology | 1992-10-29 | PMID 1414920
Corvol P, Jeunemaitre X, Charru A and 1 more
Molecular basis of beta thalassemia in the south of Thailand.
American journal of hematology | 1992-11-01 | PMID 1415194
Laosombat V, Fucharoen S P, Panich V and 7 more
Genotype-phenotype relationships in human red/green color-vision defects: molecular and psychophysical studies.
American journal of human genetics | 1992-10-01 | PMID 1415215
Deeb S S, Lindsey D T, Hibiya Y and 4 more
Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhere.
American journal of human genetics | 1992-10-01 | PMID 1415216
Northrup H, Kwiatkowski D J, Roach E S and 6 more
Significant linkage disequilibrium between the Huntington disease gene and the loci D4S10 and D4S95 in the Dutch population.
American journal of human genetics | 1992-10-01 | PMID 1415218
Skraastad M I, Van de Vosse E, Belfroid R and 5 more
Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathy.
American journal of human genetics | 1992-10-01 | PMID 1415219
Sweeney M G, Davis M B, Lashwood A and 3 more
A double mutation in exon 6 of the beta-hexosaminidase alpha subunit in a patient with the B1 variant of Tay-Sachs disease.
American journal of human genetics | 1992-10-01 | PMID 1415222
Ainsworth P J, Coulter-Mackie M B
Gaucher disease: A G+1----A+1 IVS2 splice donor site mutation causing exon 2 skipping in the acid beta-glucosidase mRNA.
American journal of human genetics | 1992-10-01 | PMID 1415223
He G S, Grabowski G A
Identification of two different point mutations associated with the fluoride-resistant phenotype for human butyrylcholinesterase.
American journal of human genetics | 1992-10-01 | PMID 1415224
Nogueira C P, Bartels C F, McGuire M C and 7 more
Lipoprotein(a) in women twins: heritability and relationship to apolipoprotein(a) phenotypes.
American journal of human genetics | 1992-10-01 | PMID 1415225
Austin M A, Sandholzer C, Selby J V and 3 more
Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I.
American journal of human genetics | 1992-10-01 | PMID 1415226
Zhang Z P, Lindstedt M, Falk G and 3 more
Genes: CGA
Inter- and intrafamilial heterogeneity: effective sampling strategies and comparison of analysis methods.
American journal of human genetics | 1992-10-01 | PMID 1415227
Durner M, Greenberg D A, Hodge S E
Testing Hardy-Weinberg equilibrium on allelic data from VNTR loci.
American journal of human genetics | 1992-11-01 | PMID 1415252
Geisser S, Johnson W
Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox).
American journal of human genetics | 1992-11-01 | PMID 1415254
de Boer M, de Klein A, Hossle J P and 4 more
Different mosaicism frequencies for proximal and distal Duchenne muscular dystrophy (DMD) mutations indicate difference in etiology and recurrence risk.
American journal of human genetics | 1992-11-01 | PMID 1415256
Passos-Bueno M R, Bakker E, Kneppers A L and 5 more
Genes: DMD
Evidence for increased prevalence of SRY mutations in XY females with complete rather than partial gonadal dysgenesis.
American journal of human genetics | 1992-11-01 | PMID 1415266
Hawkins J R, Taylor A, Goodfellow P N and 3 more
Genes: SRY
Independence of VNTR alleles defined as floating bins.
American journal of human genetics | 1992-11-01 | PMID 1415268
Weir B S
Five years experience of predictive testing for myotonic dystrophy using linked DNA markers.
American journal of medical genetics | 1992-08-01 | PMID 1415325
Reardon W, Floyd J L, Myring J and 3 more
VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies?
American journal of medical genetics | 1992-08-01 | PMID 1415330
Porteous M E, Cross I, Burn J
VACTERL or MURCS association in a girl with neurenteric cyst and identical thoracic malformations in the father: a case of gonosomal mosaicism?
American journal of medical genetics | 1992-08-01 | PMID 1415331
Orstavik K H, Steen-Johnsen J, Foerster A and 3 more
Oculoauriculovertebral anomaly: segregation analysis.
American journal of medical genetics | 1992-08-01 | PMID 1415339
Kaye C I, Martin A O, Rollnick B R and 6 more
Callosal agenesis, iris coloboma, and megacolon in a Brazilian boy with Rubinstein-Taybi syndrome.
American journal of medical genetics | 1992-08-01 | PMID 1415341
Guion-Almeida M L, Richieri-Costa A
Lacrimo-auriculo-dento-digital syndrome: evidence for lower limb involvement and severe congenital renal anomalies.
American journal of medical genetics | 1992-08-01 | PMID 1415342
Bamforth J S, Kaurah P
Acrocallosal syndrome: report of a Brazilian girl.
American journal of medical genetics | 1992-08-01 | PMID 1415343
Guion-Almeida M L, Richieri-Costa A
Overlap between Majewski and hydrolethalus syndromes: a report of two cases.
American journal of medical genetics | 1992-08-01 | PMID 1415345
Sharma A K, Phadke S, Chandra K and 4 more
King syndrome: a genetically heterogenous phenotype due to congenital myopathies.
American journal of medical genetics | 1992-08-01 | PMID 1415346
Chitayat D, Hodgkinson K A, Ginsburg O and 2 more
Clinical variability and genetic heterogeneity within the Acadian Usher population.
American journal of medical genetics | 1992-08-01 | PMID 1415347
Smith R J, Pelias M Z, Daiger S P and 3 more
New autosomal recessive syndrome of sparse hair, osteopenia, and mental retardation in Mennonite sisters.
American journal of medical genetics | 1992-08-01 | PMID 1415349
Kaler S G, Garrity A M, Stern H J and 5 more
Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia.
American journal of medical genetics | 1992-08-01 | PMID 1415350
Chemke J, Carmi R, Galil A and 3 more
Ullrich-Turner syndrome with a small ring X chromosome and presence of mental retardation.
American journal of medical genetics | 1992-08-01 | PMID 1415351
Van Dyke D L, Wiktor A, Palmer C G and 6 more
A stem cell niche theory of intestinal crypt maintenance based on a study of somatic mutation in colonic mucosa.
The American journal of pathology | 1992-10-01 | PMID 1415475
Williams E D, Lowes A P, Williams D and 1 more
Whole body insulin sensitivity in Osborne-Mendel and S 5B/Pl rats eating a low- or high-fat diet.
The American journal of physiology | 1992-10-01 | PMID 1415789
Buchanan T A, Fisler J S, Underberger S and 2 more
Molecular mechanisms of tumor formation.
American journal of surgery | 1992-10-01 | PMID 1415950
Samara G, Hurwitz M, Sawicki M and 1 more
Determining the effect of inducible protein phosphorylation on the DNA-binding activity of transcription factors.
Analytical biochemistry | 1992-06-01 | PMID 1416026
Papavassiliou A G, Bohmann K, Bohmann D
Genetic linkage analysis between protein polymorphisms and the FecB major gene in sheep.
Animal genetics | 1992-01-01 | PMID 1416247
Tate M L, Manly H C, Dodds K G and 1 more
Genes: HBB
Temperature gradient gel electrophoresis: detection of a single base substitution in the cattle beta-lactoglobulin gene.
Animal genetics | 1992-01-01 | PMID 1416248
Tee M K, Moran C, Nicholas F W
A new transferrin allele in Australian goats.
Animal genetics | 1992-01-01 | PMID 1416252
Vankan D M, Bell K
Bovine and ovine DNA microsatellites from the EMBL and GENBANK databases.
Animal genetics | 1992-01-01 | PMID 1416254
Moore S S, Barendse W, Berger K T and 2 more
Identification of halothane gene carriers by use of in vivo 31P nuclear magnetic resonance spectroscopy in pigs.
American journal of veterinary research | 1992-09-01 | PMID 1416381
Geers R, Decanniere C, Villé H and 6 more
[Recurrent familial amyotrophic neuralgia of the brachial plexus. Report of a family and review of the literature].
Anales espanoles de pediatria | 1992-07-01 | PMID 1416523
Zuazo Zamalloa E, Pomposo Bolumburu I, Garaizár Axpe C and 1 more
The influence of HLA-DRB1 genes on disease severity in rheumatoid arthritis.
Annals of internal medicine | 1992-11-15 | PMID 1416553
Weyand C M, Hicok K C, Conn D L and 1 more
[Oculocutaneous albinism].
Annales de pediatrie | 1992-09-01 | PMID 1416662
Lacour J P, Ortonne J P