Apoptosis in a Fas-resistant, T-cell receptor-sensitive human leukaemic T-cell clone.
Immunology | 1997-03-01 | PMID 9155645
Delehanty L L, Payne J A, Farrow S N 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 849 of 10600
Genetic heterogeneity in sporadic colorectal adenomas.
The Journal of pathology | 1997-03-01 | PMID 9155713
Saraga E, Bautista D, Dorta G and 7 more
Phenotype and maturation rate of oocytes of chimaeric mice produced from two strains that differ in oocyte quality.
Journal of reproduction and fertility | 1997-03-01 | PMID 9155737
Wabik-Sliz B
Changes in the hemagglutinin molecule of influenza type A (H3N2) virus associated with increased virulence for mice.
Archives of virology | 1997-01-01 | PMID 9155874
Hartley C A, Reading P C, Ward A C and 1 more
Growth ability of auxiliary gene mutants of human immunodeficiency virus types 1 and 2 in unstimulated peripheral blood mononuclear cells.
Archives of virology | 1997-01-01 | PMID 9155882
Tokunaga K, Ishimoto A, Ikuta K and 1 more
Cyclosporin inhibits intercellular adhesion molecule-1 expression and reduces mast cell numbers in the asebia mouse model of chronic skin inflammation.
The British journal of dermatology | 1997-04-01 | PMID 9155951
Oran A, Marshall J S, Kondo S and 2 more
Hypothesis testing in evolutionary inference.
Journal of theoretical biology | 1997-04-21 | PMID 9156079
Brookfield J F
Continuous stability and evolutionary convergence.
Journal of theoretical biology | 1997-04-07 | PMID 9156083
Eshel I, Motro U, Sansone E
The evolutionary dynamics of selfish replicators: a two-level selection model.
Journal of theoretical biology | 1997-04-07 | PMID 9156087
Godelle B, Reboud X
Molecular and cellular biology of prostate cancer.
Cancer metastasis reviews | 1997-06-01 | PMID 9156279
Lalani el-N, Laniado M E, Abel P D
Nephropathic cystinosis (CTNS-LSB): construction of a YAC contig comprising the refined critical region on chromosome 17p13.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9156315
Peters U, Senger G, Rählmann M and 8 more
Genes: CTNS
Characterisation of five missense mutations in the cystathionine beta-synthase gene from three patients with B6-nonresponsive homocystinuria.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9156316
Dawson P A, Cox A J, Emmerson B T and 3 more
Genes: CBS
Erythrocyte glucose-6-phosphate dehydrogenase deficiency in Poland--a study on the 563 and 1311 mutations of the G6PD gene.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9156317
Jabłońska-Skwiecińska E, Zimowski J G, Kłopocka J and 3 more
Mitochondrial DNA and Y chromosome-specific polymorphisms in the Seminole Tribe of Florida.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9156318
Huoponen K, Torroni A, Wickman P R and 4 more
Association of extracolonic manifestations of familial adenomatous polyposis with acetylation phenotype in a large FAP kindred.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9156320
Scott R J, Taeschner W, Heinimann K and 6 more
Genes: FAP, APC, NAT2
Population studies of human deoxyribonuclease I polymorphism.
Human heredity | 2000-01-01 | PMID 9156322
Yasuda T, Takeshita H, Iida R and 2 more
Genes: DNASE1
Data on six short-tandem repeat polymorphisms in an autochthonous Basque population.
Human heredity | 2000-01-01 | PMID 9156324
Iriondo M, Barbero M C, Izagirre N and 1 more
Phenylketonuria mutations and linked haplotypes in the Lithuanian population: origin of the most common R408W mutation.
Human heredity | 2000-01-01 | PMID 9156326
Giannattasio S, Jurgelevicius V, Lattanzio P and 3 more
Genes: PAH
Pressor and hormonal responses to angiotensin I infusion in healthy subjects of different angiotensin-converting enzyme genotypes.
Journal of cardiovascular pharmacology | 1997-04-01 | PMID 9156358
Chadwick I G, O'Toole L, Morice A H and 3 more
Genes: ACE
The genetic testing of children for cancer susceptibility: ethical, legal, and social issues.
Behavioral sciences & the law | 1996-01-01 | PMID 9156420
Patenaude A F
An alternative splice variant of the mouse TRH receptor mRNA is the major form expressed in the mouse pituitary gland.
Journal of molecular endocrinology | 1996-04-01 | PMID 9156522
Jones K E, Brubaker J H, Chin W W
Genes: TRH
Discrimination between normal wildtype and carriers of coagulation factor V Leiden mutation by the activated protein C resistance test in the presence of factor V deficient plasma.
European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies | 1997-01-01 | PMID 9156566
Reuner K H, Litfin F, Patscheke H
Control of glucose transport by GLUT1: regulated secretion in an unexpected environment.
Bioscience reports | 1995-12-01 | PMID 9156574
Widnell C C
Chloride channels and cystic fibrosis of the pancreas.
Bioscience reports | 1995-12-01 | PMID 9156582
Gray M A, Winpenny J P, Verdon B and 2 more
Genes: CFTR
Lung cancer risk in relation to the CYP2E1 Rsa I genetic polymorphism among African-Americans and Caucasians in Los Angeles County.
Pharmacogenetics | 1996-04-01 | PMID 9156693
London S J, Daly A K, Cooper J and 4 more
Evaluation of caffeine as a test drug for CYP1A2, NAT2 and CYP2E1 phenotyping in man by in vivo versus in vitro correlations.
Pharmacogenetics | 1996-04-01 | PMID 9156694
Fuhr U, Rost K L, Engelhardt R and 8 more
Genes: NAT2
Genotyping of the polymorphic N-acetyltransferase (NAT2*) gene locus in two native African populations.
Pharmacogenetics | 1996-04-01 | PMID 9156695
Deloménie C, Sica L, Grant D M and 2 more
Genes: NAT2
Simultaneous characterization of glutathione S-transferase M1 and T1 polymorphisms by polymerase chain reaction in American whites and blacks.
Pharmacogenetics | 1996-04-01 | PMID 9156696
Chen C L, Liu Q, Relling M V
Genes: GSTM1, GSTT1
[Genetic diagnosis, classification and clinical hereditary ataxia disease entities].
Fortschritte der Neurologie-Psychiatrie | 1997-02-01 | PMID 9157050
Schöls L, Riess O, Amoiridis G and 3 more
Systemic lupus erythematosus with nephritis is strongly associated with the TNFB*2 homozygote in the Korean population.
Human immunology | 1996-03-01 | PMID 9157084
Kim T G, Kim H Y, Lee S H and 5 more
A computerized method to predict the discriminatory properties for class II sequencing based typing.
Human immunology | 1996-03-01 | PMID 9157086
Rozemuller E H, Tilanus M G
Polymorphism of HLA-DRB, -DQA1, and -DQB1 in rheumatoid arthritis in Asian Indians: association with DRB1*0405 and DRB1*1001.
Human immunology | 1996-03-01 | PMID 9157087
Taneja V, Giphart M J, Verduijn W and 3 more
The role of HLA-DR-DR and HLA-DR-DP interactions in genetic susceptibility to rheumatoid arthritis.
Human immunology | 1996-03-01 | PMID 9157088
Perdriger A, Guggenbuhl P, Chales G and 5 more
An association in non-insulin-dependent diabetes mellitus subjects between susceptibility to retinopathy and tumor necrosis factor polymorphism.
Human immunology | 1996-03-01 | PMID 9157089
Hawrami K, Hitman G A, Rema M and 4 more
Genes: TNF
A novel DR beta 1*03 allele identified by polymerase chain reaction-restriction fragment length polymorphism.
Human immunology | 1996-03-01 | PMID 9157090
Fenske B, Lemieux J, Hoar D and 2 more
PilP, a pilus biogenesis lipoprotein in Neisseria gonorrhoeae, affects expression of PilQ as a high-molecular-mass multimer.
Molecular microbiology | 1997-02-01 | PMID 9157238
Drake S L, Sandstedt S A, Koomey M
The dual role of Apl in prophage induction of coliphage 186.
Molecular microbiology | 1997-02-01 | PMID 9157239
Reed M R, Shearwin K E, Pell L M and 1 more
The com locus controls genetic transformation in Streptococcus pneumoniae.
Molecular microbiology | 1997-02-01 | PMID 9157240
Cheng Q, Campbell E A, Naughton A M and 2 more
Integration host factor stimulates both FimB- and FimE-mediated site-specific DNA inversion that controls phase variation of type 1 fimbriae expression in Escherichia coli.
Molecular microbiology | 1997-02-01 | PMID 9157242
Blomfield I C, Kulasekara D H, Eisenstein B I
Construction and analysis of a recombination-deficient (radA) mutant of Haloferax volcanii.
Molecular microbiology | 1997-02-01 | PMID 9157249
Woods W G, Dyall-Smith M L
Genes: RAD51
Interspecies recombination, and phylogenetic distortions, within the glutamine synthetase and shikimate dehydrogenase genes of Neisseria meningitidis and commensal Neisseria species.
Molecular microbiology | 1997-02-01 | PMID 9157250
Zhou J, Bowler L D, Spratt B G
The qmeA (ts) mutation of Escherichia coli is localized in the fabI gene, which encodes enoyl-ACP reductase.
Research in microbiology | 1996-10-01 | PMID 9157486
Kleerebezem M, Heutink M, de Cock H and 1 more
[Mechanisms and consequences of genetic mutations].
La Revue du praticien | 1997-01-15 | PMID 9157512
Vidaud M
[Genetic diseases and unstable expansions of trinucleotide repeats].
La Revue du praticien | 1997-01-15 | PMID 9157513
Mandel J L
[Animal models of hereditary diseases].
La Revue du praticien | 1997-01-15 | PMID 9157514
Montagutelli X, Guénet J L
HLA class II profile: a weak determinant of factor VIII inhibitor development in severe haemophilia A. UKHCDO Inhibitor Working Party.
Thrombosis and haemostasis | 1997-02-01 | PMID 9157572
Hay C R, Ollier W, Pepper L and 7 more
HLA genotype of patients with severe haemophilia A due to intron 22 inversion with and without inhibitors of factor VIII.
Thrombosis and haemostasis | 1997-02-01 | PMID 9157573
Oldenburg J, Picard J K, Schwaab R and 3 more
A common thrombomodulin amino acid dimorphism is associated with myocardial infarction.
Thrombosis and haemostasis | 1997-02-01 | PMID 9157575
Norlund L, Holm J, Zöller B and 1 more
Genes: EGF
Molecular characterization of a type I quantitative factor V deficiency in a thrombosis patient that is "pseudo homozygous" for activated protein C resistance.
Thrombosis and haemostasis | 1997-02-01 | PMID 9157576
Guasch J F, Lensen R P, Bertina R M
Genes: APC
Factor V Leiden is not common in children with portal vein thrombosis.
Thrombosis and haemostasis | 1997-02-01 | PMID 9157577
Seixas C A, Hessel G, Ribeiro C C and 2 more
Evaluation of original and modified APC-resistance tests in unselected outpatients with clinically suspected thrombosis and in healthy controls.
Thrombosis and haemostasis | 1997-02-01 | PMID 9157592
Svensson P J, Zöller B, Dahlbäck B
Genes: APC
PAI-1 concentrations in first-degree relatives of patients with non-insulin-dependent diabetes: metabolic and genetic associations.
Thrombosis and haemostasis | 1997-02-01 | PMID 9157596
Mansfield M W, Stickland M H, Grant P J
Plasminogen-dependent and -independent proteolytic activity of murine endothelioma cells with targeted inactivation of fibrinolytic genes.
Thrombosis and haemostasis | 1997-02-01 | PMID 9157597
Lijnen H R, Wagner E F, Collen D
[A new system of prolonged genetic instability induced by N-ethyl-N-nitrosourea in Drosophila melanogaster].
TSitologiia i genetika | 2000-01-01 | PMID 9157641
Shcherbata H R, Maksymiv D V
[The criterion of lactation stability in cows].
TSitologiia i genetika | 2000-01-01 | PMID 9157642
Vinnichuk D T, Oleĭnik L A
[The DNA diagnosis of a familial case of Kennedy's spinal and bulbar amyotrophy].
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova | 1997-01-01 | PMID 9157759
Petrukhin A S, Zavadenko N N, Petrukhin A A and 1 more
Associations between diet and the hyperapobetalipoproteinemia phenotype expression in children and young adults: the Cardiovascular Risk in Young Finns Study.
Arteriosclerosis, thrombosis, and vascular biology | 1997-05-01 | PMID 9157943
Nuotio I O, Raitakari O T, Porkka K V and 3 more
Differences in the phenotype between children with familial defective apolipoprotein B-100 and familial hypercholesterolemia.
Arteriosclerosis, thrombosis, and vascular biology | 1997-05-01 | PMID 9157944
Pimstone S N, Defesche J C, Clee S M and 3 more
Segregation analysis of plasma apolipoprotein B levels in familial combined hyperlipidemia.
Arteriosclerosis, thrombosis, and vascular biology | 1997-05-01 | PMID 9157945
Bredie S J, van Drongelen J, Kiemeney L A and 3 more
Five frequent polymorphisms of the PAI-1 gene: lack of association between genotypes, PAI activity, and triglyceride levels in a healthy population.
Arteriosclerosis, thrombosis, and vascular biology | 1997-05-01 | PMID 9157947
Henry M, Chomiki N, Scarabin P Y and 9 more
Shared and unique genetic effects among seven HDL phenotypes.
Arteriosclerosis, thrombosis, and vascular biology | 1997-05-01 | PMID 9157948
Comuzzie A G, Rainwater D L, Blangero J and 3 more
Adenovirus-mediated transfer of a dominant-negative H-ras suppresses neointimal formation in balloon-injured arteries in vivo.
Arteriosclerosis, thrombosis, and vascular biology | 1997-05-01 | PMID 9157953
Ueno H, Yamamoto H, Ito S and 2 more
The insulin-like growth factor II receptor gene is mutated in genetically unstable cancers of the endometrium, stomach, and colorectum.
Cancer research | 1997-05-15 | PMID 9157973
Ouyang H, Shiwaku H O, Hagiwara H and 8 more
Localization of the multiple endocrine neoplasia type I (MEN1) gene based on tumor loss of heterozygosity analysis.
Cancer research | 1997-05-15 | PMID 9157974
Emmert-Buck M R, Lubensky I A, Dong Q and 13 more
Genes: MEN1, PYGM
DNA damage-associated dysregulation of the cell cycle and apoptosis control in cells with germ-line p53 mutation.
Cancer research | 1997-05-15 | PMID 9157982
Goi K, Takagi M, Iwata S and 16 more
Mutational activation of pp60(c-src) leads to a tumorigenic phenotype in a preneoplastic Syrian hamster embryo cell line.
Cancer research | 1997-05-15 | PMID 9157992
Lansing T J, Turk B F, Kanner S B and 1 more
A persistent double-strand break destabilizes human DNA in yeast and can lead to G2 arrest and lethality.
Cancer research | 1997-05-15 | PMID 9157993
Bennett C B, Snipe J R, Resnick M A
Concerted nonsyntenic allelic losses in hyperploid hepatocellular carcinoma as determined by a high-resolution allelotype.
Cancer research | 1997-05-15 | PMID 9157995
Boige V, Laurent-Puig P, Fouchet P and 8 more
Somatic mutational mechanisms involved in intestinal tumor formation in Min mice.
Cancer research | 1997-05-15 | PMID 9157997
Shoemaker A R, Luongo C, Moser A R and 2 more
Genes: APC
Creation of human alkyltransferases resistant to O6-benzylguanine.
Cancer research | 1997-05-15 | PMID 9157998
Christians F C, Dawson B J, Coates M M and 1 more
Disrupted IGF2 promoter control by silencing of promoter P1 in human hepatocellular carcinoma.
Cancer research | 1997-05-15 | PMID 9158004
Li X, Nong Z, Ekström C and 8 more
Genes: IGF2
Autologous lymphokine-activated killer cell therapy of Epstein-Barr virus-positive and -negative lymphoproliferative disorders arising in organ transplant recipients.
Transplantation | 1997-05-15 | PMID 9158009
Nalesnik M A, Rao A S, Furukawa H and 8 more
Humoral response to defined Plasmodium falciparum antigens in cerebral and uncomplicated malaria and their relationship to parasite genotype.
The American journal of tropical medicine and hygiene | 1997-04-01 | PMID 9158053
Al-Yaman F, Genton B, Reeder J C and 3 more
Evidence that recurrent Plasmodium falciparum infection is caused by recrudescence of resistant parasites.
The American journal of tropical medicine and hygiene | 1997-04-01 | PMID 9158054
Al-Yaman F, Genton B, Reeder J C and 2 more
A genetic study of a melanization response to Sephadex beads in Plasmodium-refractory and -susceptible strains of Anopheles gambiae.
The American journal of tropical medicine and hygiene | 1997-04-01 | PMID 9158056
Gorman M J, Paskewitz S M
Inheritance of larval resistance to permethrin in Aedes aegypti and association with sex ratio distortion and life history variation.
The American journal of tropical medicine and hygiene | 1997-04-01 | PMID 9158058
Mebrahtu Y B, Norem J, Taylor M
Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA).
Human molecular genetics | 1997-05-01 | PMID 9158138
Morell R, Spritz R A, Ho L and 4 more
Genes: MITF, TYR
Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2.
Human molecular genetics | 1997-05-01 | PMID 9158139
Litt M, Carrero-Valenzuela R, LaMorticella D M and 4 more
Genes: CRYBB2
Homozygous alpha6 integrin mutation in junctional epidermolysis bullosa with congenital duodenal atresia.
Human molecular genetics | 1997-05-01 | PMID 9158140
Pulkkinen L, Kimonis V E, Xu Y and 3 more
Genes: ITGA6
Structure and sequence variation at the human leptin receptor gene in lean and obese Pima Indians.
Human molecular genetics | 1997-05-01 | PMID 9158141
Thompson D B, Ravussin E, Bennett P H and 1 more
Genes: LEPR
Mutations causing achondroplasia and thanatophoric dysplasia alter bFGF-induced calcium signals in human diploid fibroblasts.
Human molecular genetics | 1997-05-01 | PMID 9158142
Nguyen H B, Estacion M, Gargus J J
Genes: FGFR3, FGFR1
The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype?
Human molecular genetics | 1997-05-01 | PMID 9158144
Andresen B S, Bross P, Udvari S and 16 more
Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families.
Human molecular genetics | 1997-05-01 | PMID 9158145
Cancel G, Dürr A, Didierjean O and 21 more
alpha-Mannosidosis: functional cloning of the lysosomal alpha-mannosidase cDNA and identification of a mutation in two affected siblings.
Human molecular genetics | 1997-05-01 | PMID 9158146
Nilssen O, Berg T, Riise H M and 6 more
Congenital myasthenic syndromes due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene: identification and functional characterization of six new mutations.
Human molecular genetics | 1997-05-01 | PMID 9158150
Ohno K, Quiram P A, Milone M and 9 more
Mutations in different functional domains of the human muscle acetylcholine receptor alpha subunit in patients with the slow-channel congenital myasthenic syndrome.
Human molecular genetics | 1997-05-01 | PMID 9158151
Croxen R, Newland C, Beeson D and 4 more
Reduced penetrance of the Huntington's disease mutation.
Human molecular genetics | 1997-05-01 | PMID 9158152
McNeil S M, Novelletto A, Srinidhi J and 7 more
Molecular defects in Sanfilippo syndrome type A.
Human molecular genetics | 1997-05-01 | PMID 9158154
Blanch L, Weber B, Guo X H and 2 more
Mouse pale ear (ep) is homologous to human Hermansky-Pudlak syndrome and contains a rare 'AT-AC' intron.
Human molecular genetics | 1997-05-01 | PMID 9158155
Feng G H, Bailin T, Oh J and 1 more
Estimating Y chromosome specific microsatellite mutation frequencies using deep rooting pedigrees.
Human molecular genetics | 1997-05-01 | PMID 9158156
Heyer E, Puymirat J, Dieltjes P and 2 more
Identification of functionally important regions of the muscular chloride channel CIC-1 by analysis of recessive and dominant myotonic mutations.
Human molecular genetics | 1997-05-01 | PMID 9158157
Wollnik B, Kubisch C, Steinmeyer K and 1 more
Genes: CIC
Missense mutations in exon 6 of the survival motor neuron gene in patients with spinal muscular atrophy (SMA).
Human molecular genetics | 1997-05-01 | PMID 9158159
Hahnen E, Schönling J, Rudnik-Schöneborn S and 3 more
Expression rate of vinculin isoforms in human aortocoronary saphenous vein grafts.
International journal of cardiology | 1997-04-18 | PMID 9158163
Brinck U, Mirzaie M, Korabiowska M and 1 more
Lipid abnormalities in Greek patients with coronary artery disease.
International journal of cardiology | 1997-04-18 | PMID 9158172
Elisaf M S, Siamopoulos K C, Tselegarides T J and 5 more
Genes: CAD
Non-insulin-dependent diabetes mellitus.
British medical bulletin | 1997-01-01 | PMID 9158288
Hales C N
Absence of p53 mutations in squamous carcinomas of the tongue in nonsmoking and nondrinking patients younger than 40 years.
Archives of otolaryngology--head & neck surgery | 1997-05-01 | PMID 9158397
Sorensen D M, Lewark T M, Haney J L and 3 more
Genes: CGA
Restoration of the G1 checkpoint and the apoptotic pathway mediated by wild-type p53 sensitizes squamous cell carcinoma of the head and neck to radiotherapy.
Archives of otolaryngology--head & neck surgery | 1997-05-01 | PMID 9158398
Chang E H, Jang Y J, Hao Z and 7 more
Cytokine production by subsets of CD4 memory T cells differing in P-glycoprotein expression: effects of aging.
The journals of gerontology. Series A, Biological sciences and medical sciences | 1997-05-01 | PMID 9158547
Bining N, Miller R A
Apolipoprotein E polymorphism and silent microangiopathy-related cerebral damage. Results of the Austrian Stroke Prevention Study.
Stroke | 1997-05-01 | PMID 9158631
Schmidt R, Schmidt H, Fazekas F and 5 more
Genetic susceptibility to experimental cerebral aneurysm formation in the rat.
Stroke | 1997-05-01 | PMID 9158647
Coutard M, Osborne-Pellegrin M