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 1275 of 10600

Transactivation and growth suppression by the gut-enriched Krüppel-like factor (Krüppel-like factor 4) are dependent on acidic amino acid residues and protein-protein interaction.
Nucleic acids research | 2000-03-01 | PMID 10666450
Geiman D E, Ton-That H, Johnson J M and 1 more
Genes: KLF4
Polymorphisms in the large subunit of human RNA polymerase II as target for allele-specific inhibition.
Nucleic acids research | 2000-03-01 | PMID 10666454
ten Asbroek A L, Fluiter K, van Groenigen M and 2 more
The catalytic subunit DNA-dependent protein kinase (DNA-PKcs) facilitates recovery from radiation-induced inhibition of DNA replication.
Nucleic acids research | 2000-03-01 | PMID 10666461
Guan J, DiBiase S, Iliakis G
Genes: ATM, XRCC4
A novel procedure for efficient genotyping of single nucleotide polymorphisms.
Nucleic acids research | 2000-03-01 | PMID 10666474
Sauer S, Lechner D, Berlin K and 4 more
Twenty novel mutations in the alpha-galactosidase A gene causing Fabry disease.
Molecular medicine (Cambridge, Mass.) | 1999-12-01 | PMID 10666480
Topaloglu A K, Ashley G A, Tong B and 4 more
Genetic variation and covariation of parathyroid hormone levels and bone density in the human population.
Calcified tissue international | 2000-03-01 | PMID 10666489
Otremski I, Karasik D, Livshits G
Genes: PTH
Association of bone mineral density with polymorphism of the human calcium-sensing receptor locus.
Calcified tissue international | 2000-03-01 | PMID 10666491
Tsukamoto K, Orimo H, Hosoi T and 7 more
Genes: CASR, PTH
Vitamin D and estrogen receptor polymorphisms and bone mineral changes in postpartum women.
Calcified tissue international | 2000-03-01 | PMID 10666492
Holmberg-Marttila D, Sievänen H, Järvinen T L and 1 more
Genes: VDR
Structural studies of the Msx-1 homeodomain-DNA complex I.
Acta crystallographica. Section D, Biological crystallography | 1999-12-01 | PMID 10666584
DeWees S, Geiger J H
Crystallization of type I chloramphenicol acetyltransferase: an approach based on the concept of ionic strength reducers.
Acta crystallographica. Section D, Biological crystallography | 2000-01-01 | PMID 10666642
Andreeva A E, Borissova B E, Mironova R and 5 more
Genes: CAT
Molecular biology of arrhythmic syndromes.
Current opinion in cardiology | 2000-01-01 | PMID 10666657
Vatta M, Li H, Towbin J A
[Mutagen sensitivity of patients with laryngeal and oropharyngeal carcinoma].
Laryngo- rhino- otologie | 1999-12-01 | PMID 10666694
Kleinsasser N H, Harréus U A, Wallner B C and 1 more
Genes: DBP
Determinants of substitution rates in mammalian genes: expression pattern affects selection intensity but not mutation rate.
Molecular biology and evolution | 2000-01-01 | PMID 10666707
Duret L, Mouchiroud D
[Apert syndrome: clinico-epidemiological analysis of a series of consecutive cases in Spain].
Anales espanoles de pediatria | 1999-12-01 | PMID 10666902
Arroyo Carrera I, Martínez-Frías M L, Marco Pérez J J and 11 more
Genes: FGFR2
[The NADPH-oxidase complex in chronic granulomatous disease: preliminary description of a cluster in Mérida-Venezuela].
Investigacion clinica | 1999-12-01 | PMID 10666954
Salmen S, Berrueta L, Heyworth P and 3 more
A homozygous M694V mutation of the MEFV gene in a patient with periodic fever and thoracic pain.
The Netherlands journal of medicine | 2000-01-01 | PMID 10667038
van de Loosdrecht A A, van der Kleij F G, van Minnen C A and 1 more
Genes: MEFV
Azatyrosine. Mechanism of action for conversion of transformed phenotype to normal.
Annals of the New York Academy of Sciences | 1999-01-01 | PMID 10667209
Monden Y, Hamano Takaku F, Shindo Okada N and 1 more
Molecular abnormalities associated with secretory carcinomas of the breast.
Human pathology | 1999-12-01 | PMID 10667421
Maitra A, Tavassoli F A, Albores-Saavedra J and 7 more
Genes: BRCA1
Genetic polymorphism of CYP genes, alone or in combination, as a risk modifier of tobacco-related cancers.
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 10667460
Bartsch H, Nair U, Risch A and 3 more
Genes: GSTM1
Molecular genetics and epidemiology of the NAT1 and NAT2 acetylation polymorphisms.
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 10667461
Hein D W, Doll M A, Fretland A J and 6 more
Genes: NAT2, NAT1
GSTT1 and GSTM1 null genotypes and the risk of gastric cancer: a case-control study in a Chinese population.
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 10667466
Setiawan V W, Zhang Z F, Yu G P and 8 more
Genes: GSTT1, GSTM1
Behavioral risk factors among women presenting for genetic testing.
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 10667468
Emmons K M, Kalkbrenner K J, Klar N and 3 more
Genes: BRCA1, BRCA2
A case-control study of galactose consumption and metabolism in relation to ovarian 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 10667469
Cramer D W, Greenberg E R, Titus-Ernstoff L and 4 more
Genes: GALT
Cancer risk estimates for family members of a population-based family registry for breast and ovarian 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 10667470
Ziogas A, Gildea M, Cohen P and 11 more
A splicing mutation in the hydroxymethylbilane synthase gene in a Japanese family with acute intermittent porphyria.
Clinical biochemistry | 1999-08-01 | PMID 10667475
Maeda N, Horie Y, Sasaki Y and 6 more
Genes: AIP, HMBS
Lipoprotein-genotype associations in Trinidadian neonates.
Clinical biochemistry | 1999-08-01 | PMID 10667478
Hegele R A, Ban M R, Busch C P and 2 more
Genes: AGT, WRN, APOE
The HRAS1 minisatellite locus and risk of ovarian cancer.
Cancer research | 2000-01-15 | PMID 10667571
Weitzel J N, Ding S, Larson G P and 5 more
Genes: BRCA1
Association of vitamin D receptor gene polymorphism with prostate cancer and benign prostatic hyperplasia in a Japanese population.
Cancer research | 2000-01-15 | PMID 10667581
Habuchi T, Suzuki T, Sasaki R and 11 more
Genes: VDR
Mutations in the retinoblastoma-related gene RB2/p130 in lung tumors and suppression of tumor growth in vivo by retrovirus-mediated gene transfer.
Cancer research | 2000-01-15 | PMID 10667590
Claudio P P, Howard C M, Pacilio C and 12 more
Genetic alterations disrupting the nuclear localization of the retinoblastoma-related gene RB2/p130 in human tumor cell lines and primary tumors.
Cancer research | 2000-01-15 | PMID 10667591
Cinti C, Claudio P P, Howard C M and 6 more
Induced micronucleus frequencies in peripheral lymphocytes as a screening test for carriers of a BRCA1 mutation in breast cancer families.
Cancer research | 2000-01-15 | PMID 10667592
Rothfuss A, Schütz P, Bochum S and 5 more
Genes: BRCA1
Atm deficiency causes an increased frequency of intrachromosomal homologous recombination in mice.
Cancer research | 2000-01-15 | PMID 10667593
Bishop A J, Barlow C, Wynshaw-Boris A J and 1 more
Genes: ATM
Inherited predisposition to pancreatic adenocarcinoma: role of family history and germ-line p16, BRCA1, and BRCA2 mutations.
Cancer research | 2000-01-15 | PMID 10667595
Lal G, Liu G, Schmocker B and 5 more
Genes: BRCA1, BRCA2
Deregulation of the p14ARF/MDM2/p53 pathway is a prerequisite for human astrocytic gliomas with G1-S transition control gene abnormalities.
Cancer research | 2000-01-15 | PMID 10667596
Ichimura K, Bolin M B, Goike H M and 3 more
Genes: MDM2, CDK4
The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect.
Cancer research | 2000-01-15 | PMID 10667598
Berneburg M, Clingen P H, Harcourt S A and 6 more
Effect of CYP2E1 induction by ethanol on the immunotoxicity and genotoxicity of extended low-level benzene exposure.
Journal of toxicology and environmental health. Part A | 2000-02-11 | PMID 10667633
Daiker D H, Shipp B K, Schoenfeld H A and 4 more
A pigment-binding protein essential for regulation of photosynthetic light harvesting.
Nature | 2000-01-27 | PMID 10667783
Li X P, Björkman O, Shih C and 4 more
DNA-bound structures and mutants reveal abasic DNA binding by APE1 and DNA repair coordination [corrected].
Nature | 2000-01-27 | PMID 10667800
Mol C D, Izumi T, Mitra S and 1 more
Problems and perspectives of phenotyping for drug-metabolizing enzymes in man.
International journal of clinical pharmacology and therapeutics | 2000-01-01 | PMID 10667830
Zaigler M, Tantcheva-Poór I, Fuhr U
Analysis of point mutation in exon 2 of CYP2E1 gene in renal cell/urothelial cancer patients in comparison with control population.
International journal of clinical pharmacology and therapeutics | 2000-01-01 | PMID 10667834
Farker K, Lehmann M H, Kästner R and 4 more
Functional characterization of glycosylation-deficient human P-glycoprotein using a vaccinia virus expression system.
The Journal of membrane biology | 2000-02-01 | PMID 10667916
Gribar J J, Ramachandra M, Hrycyna C A and 2 more
The Saccharomyces cerevisiae Cdc14 phosphatase is implicated in the structural organization of the nucleolus.
Biology of the cell | 1999-12-01 | PMID 10668096
de Almeida A, Raccurt I, Peyrol S and 1 more
Genes: GAR1, NOP2
A nuclear function for the tumor suppressor BRCA1.
Histology and histopathology | 2000-01-01 | PMID 10668218
Monteiro A N, Birge R B
Genes: BRCA1
Genomic imprinting and Beckwith-Wiedemann syndrome.
Histology and histopathology | 2000-01-01 | PMID 10668219
Hatada I, Mukai T
[Possible genetic causes for late complications of diabetes mellitus].
Medizinische Klinik (Munich, Germany : 1983) | 2000-01-15 | PMID 10668342
Klemm T, Paschke R
Genes: ACE
Protein folding and deficiencies caused by dominant-negative mutants of hormones.
Vitamins and hormones | 2000-01-01 | PMID 10668393
Dannies P S
HIV protease: enzyme function and drug resistance.
Vitamins and hormones | 2000-01-01 | PMID 10668400
Gulnik S, Erickson J W, Xie D
Oncogenic activating mutations in the neu/erbB-2 oncogene are involved in the induction of mammary tumors.
Annals of the New York Academy of Sciences | 1999-01-01 | PMID 10668481
Chan R, Muller W J, Siegel P M
Cyclooxygenase-deficient mice. A summary of their characteristics and susceptibilities to inflammation and carcinogenesis.
Annals of the New York Academy of Sciences | 1999-01-01 | PMID 10668482
Langenbach R, Loftin C D, Lee C and 1 more
The role of COX-2 in intestinal cancer.
Annals of the New York Academy of Sciences | 1999-01-01 | PMID 10668484
Williams C, Shattuck-Brandt R L, DuBois R N
Genes: APC
Mutations in the gene encoding the alpha-subunit of the Gs protein in molar pregnancy.
Endocrine | 1999-08-01 | PMID 10668646
Garon G, LeHoux J G, Bessette P
The association between APOE and dementia does not seem to be mediated by vascular factors.
Neurology | 2000-01-25 | PMID 10668701
Prince M, Lovestone S, Cervilla J and 4 more
Genes: APOE
E4 allele dosage does not predict cholinergic activity or synapse loss in Alzheimer's disease.
Neurology | 2000-01-25 | PMID 10668702
Corey-Bloom J, Tiraboschi P, Hansen L A and 5 more
Genes: APOE
Cholinergic dysfunction in diseases with Lewy bodies.
Neurology | 2000-01-25 | PMID 10668703
Tiraboschi P, Hansen L A, Alford M and 5 more
Genes: APOE
APOE epsilon4 does not predict mortality, cognitive decline, or dementia in the oldest old.
Neurology | 2000-01-25 | PMID 10668704
Juva K, Verkkoniemi A, Viramo P and 4 more
Genes: APOE
Early-life risk factors and the development of Alzheimer's disease.
Neurology | 2000-01-25 | PMID 10668705
Moceri V M, Kukull W A, Emanuel I and 2 more
Genes: APOE
Lu 25-109, a muscarinic agonist, fails to improve cognition in Alzheimer's disease. Lu25-109 Study Group.
Neurology | 2000-01-25 | PMID 10668706
Thal L J, Forrest M, Loft H and 1 more
Lack of association of the alpha2-macroglobulin locus on chromosome 12 in AD.
Neurology | 2000-01-25 | PMID 10668708
Gibson A M, Singleton A B, Smith G and 7 more
Genes: APOE
Alpha2 macroglobulin and the risk of Alzheimer's disease.
Neurology | 2000-01-25 | PMID 10668709
Dodel R C, Du Y, Bales K R and 18 more
Genes: APOE
Alpha2-macroglobulin polymorphism is not associated with AD or AD-type neuropathology in the Japanese.
Neurology | 2000-01-25 | PMID 10668711
Sodeyama N, Yamada M, Itoh Y and 4 more
Genes: APOE
An interrupted 34-CAG repeat SCA-2 allele in patients with sporadic spinocerebellar ataxia.
Neurology | 2000-01-25 | PMID 10668721
Costanzi-Porrini S, Tessarolo D, Abbruzzese C and 3 more
Atypical Friedreich ataxia phenotype associated with a novel missense mutation in the X25 gene.
Neurology | 2000-01-25 | PMID 10668723
De Michele G, Filla A, Cavalcanti F and 8 more
Genes: GAA
A kindred with Parkinson's disease not showing genetic linkage to established loci.
Neurology | 2000-01-25 | PMID 10668726
Gwinn-Hardy K A, Crook R, Lincoln S and 4 more
Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A gene.
Neurology | 2000-01-25 | PMID 10668728
Chabriat H, Vahedi K, Clark C A and 5 more
Mutation causing von Willebrand's disease in Scottish Terriers.
Journal of veterinary internal medicine | 2000-01-01 | PMID 10668811
Venta P J, Li J, Yuzbasiyan-Gurkan V and 2 more
Familial protein-losing enteropathy and protein-losing nephropathy in Soft Coated Wheaten Terriers: 222 cases (1983-1997).
Journal of veterinary internal medicine | 2000-01-01 | PMID 10668820
Littman M P, Dambach D M, Vaden S L and 1 more
Genes: PLN
CYP3A4 allelic variants with amino acid substitutions in exons 7 and 12: evidence for an allelic variant with altered catalytic activity.
Clinical pharmacology and therapeutics | 2000-01-01 | PMID 10668853
Sata F, Sapone A, Elizondo G and 6 more
Deficient cotinine formation from nicotine is attributed to the whole deletion of the CYP2A6 gene in humans.
Clinical pharmacology and therapeutics | 2000-01-01 | PMID 10668854
Nakajima M, Yamagishi S, Yamamoto H and 3 more
Sequence variation of ribosomal internal transcribed spacers (ITS) in commercially important Phytoseiidae mites.
Experimental & applied acarology | 1999-11-01 | PMID 10668860
Navajas M, Lagnel J, Fauvel G and 1 more
Sequence variations in the Boophilus microplus Bm86 locus and implications for immunoprotection in cattle vaccinated with this antigen.
Experimental & applied acarology | 1999-11-01 | PMID 10668863
García-García J C, Gonzalez I L, González D M and 9 more
Development of low-dose streptozotocin-induced diabetes in ICAM-1-deficient mice.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme | 1999-12-01 | PMID 10668914
Martin S, Vinke A, Heidenthal E and 2 more
Utility of the predictors of coronary heart disease mortality in a longitudinal study of elderly Finnish men aged 65 to 84 years is dependent on context defined by Apo E genotype and area of residence.
Clinical genetics | 1999-11-01 | PMID 10668927
Stengård J H, Kardia S L, Tervahauta M and 3 more
Association between polymorphism of the cholecystokinin gene and idiopathic Parkinson's disease.
Clinical genetics | 1999-11-01 | PMID 10668930
Fujii C, Harada S, Ohkoshi N and 4 more
Genes: CCK
Phenotype vs genotype in the evolution of astrocytic brain tumors.
Toxicologic pathology | 2000-01-01 | PMID 10669004
Kleihues P, Ohgaki H
Genes: EGFR, MDM2, PTEN
Sensitization of the adenylyl cyclase system in cloned kappa-opioid receptor-transfected cells following sustained agonist treatment: A chimeric study using G protein alpha(i)2/alpha(q) subunits.
Japanese journal of pharmacology | 1999-12-01 | PMID 10669040
Nakagawa T, Ozawa T, Watanabe T and 2 more
Mutational analysis of X-linked amelogenesis imperfecta in multiple families.
Archives of oral biology | 2000-01-01 | PMID 10669095
Hart S, Hart T, Gibson C and 1 more
The Twirler mouse, a model for the study of cleft lip and palate.
Archives of oral biology | 2000-01-01 | PMID 10669096
Gong S G, White N J, Sakasegawa A Y
Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease.
Thrombosis and haemostasis | 2000-01-01 | PMID 10669148
Renner W, Köppel H, Brodmann M and 5 more
Thirty-three novel mutations in the protein C gene. French INSERM network on molecular abnormalities responsible for protein C and protein S.
Thrombosis and haemostasis | 2000-01-01 | PMID 10669160
Alhenc-Gelas M, Gandrille S, Aubry M L and 1 more
Genes: PROC
Homozygosity for the protein S Heerlen allele is associated with type I PS deficiency in a thrombophilic pedigree with multiple risk factors.
Thrombosis and haemostasis | 2000-01-01 | PMID 10669162
Espinosa-Parrilla Y, Navarro G, Morell M and 3 more
Genes: PROS1
Von Willebrand Disease type 2M "Vicenza" in Italian and German patients: identification of the first candidate mutation (G3864A; R1205H) in 8 families.
Thrombosis and haemostasis | 2000-01-01 | PMID 10669167
Schneppenheim R, Federici A B, Budde U and 8 more
Genes: VWF
Mutations in the protein kinase-binding domain of the NS5A protein in patients infected with hepatitis C virus type 1a are associated with treatment response.
The Journal of infectious diseases | 2000-02-01 | PMID 10669323
Sarrazin C, Berg T, Lee J H and 4 more
Presence of human immunodeficiency virus (HIV) type 1, group M, non-B subtypes, Bronx, New York: a sentinel site for monitoring HIV genetic diversity in the United States.
The Journal of infectious diseases | 2000-02-01 | PMID 10669328
Weidle P J, Ganea C E, Irwin K L and 8 more
Effect of zidovudine resistance mutations on virologic response to treatment with zidovudine-lamivudine-ritonavir: genotypic analysis of human immunodeficiency virus type 1 isolates from AIDS clinical trials group protocol 315.ACTG Protocol 315 Team.
The Journal of infectious diseases | 2000-02-01 | PMID 10669331
Kuritzkes D R, Sevin A, Young B and 8 more
Genital tract human immunodeficiency virus type 1 (HIV-1) shedding and inflammation and HIV-1 env diversity in perinatal HIV-1 transmission.
The Journal of infectious diseases | 2000-02-01 | PMID 10669339
Panther L A, Tucker L, Xu C and 3 more
Genetic evidence for the role of the Lv locus in early susceptibility but not IL-10 synthesis in experimental coccidioidomycosis in C57BL mice.
The Journal of infectious diseases | 2000-02-01 | PMID 10669355
Fierer J, Walls L, Kirkland T N
Selection of multiresistant hepatitis B virus during sequential nucleoside-analogue therapy.
The Journal of infectious diseases | 2000-02-01 | PMID 10669360
Mutimer D, Pillay D, Cook P and 6 more
Human immunodeficiency virus-infected persons with mutations conferring resistance to zidovudine show reduced virologic responses to hydroxyurea and stavudine-lamivudine.
The Journal of infectious diseases | 2000-02-01 | PMID 10669364
Montaner J S, Mo T, Raboud J M and 5 more
Secretor polymorphism and human immunodeficiency virus infection in Senegalese women.
The Journal of infectious diseases | 2000-02-01 | PMID 10669366
Ali S, Niang M A, N'doye I and 4 more
Genes: FUT2
Antiretroviral resistance mutations in human immunodeficiency virus type 1 reverse transcriptase and protease from paired cerebrospinal fluid and plasma samples.
The Journal of infectious diseases | 2000-02-01 | PMID 10669367
Venturi G, Catucci M, Romano L and 4 more
Stability of Borrelia burgdorferi outer surface protein C under immune selection pressure.
The Journal of infectious diseases | 2000-02-01 | PMID 10669369
Hodzic E, Feng S, Barthold S W
Evidence for DNA loss as a determinant of genome size.
Science (New York, N.Y.) | 2000-02-11 | PMID 10669421
Petrov D A, Sangster T A, Johnston J S and 2 more
Modifications of seizure susceptibility in Drosophila.
Journal of neurophysiology | 2000-02-01 | PMID 10669511
Kuebler D, Tanouye M A
Mapping susceptibility genes for asthma and allergy.
The Journal of allergy and clinical immunology | 2000-02-01 | PMID 10669527
Howard T D, Meyers D A, Bleecker E R
Strategies for analyzing genotype-phenotype relationships in asthma.
The Journal of allergy and clinical immunology | 2000-02-01 | PMID 10669528
Wiesch D G, Meyers D A
The pharmacogenetics of beta2-adrenergic receptors: relevance to asthma.
The Journal of allergy and clinical immunology | 2000-02-01 | PMID 10669529
Liggett S B
Dose-dependent changes in the spectrum of mutations induced by ionizing radiation.
Radiation research | 2000-03-01 | PMID 10669553
Schwartz J L, Jordan R, Sun J and 2 more
High levels of gene flow and heterozygote excess characterize Rhizoctonia solani AG-1 IA (Thanatephorus cucumeris) from Texas.
Fungal genetics and biology : FG & B | 1999-12-01 | PMID 10669581
Rosewich U L, Pettway R E, McDonald B A and 1 more
Evidence that MRas1 and MRas3 proteins are associated with distinct cellular functions during growth and morphogenesis in the fungus Mucor racemosus.
Fungal genetics and biology : FG & B | 1999-12-01 | PMID 10669583
Roze L V, Mahanti N, Mehigh R and 2 more
Bacteriophage P22 Abc2 protein binds to RecC increases the 5' strand nicking activity of RecBCD and together with lambda bet, promotes Chi-independent recombination.
Journal of molecular biology | 2000-02-18 | PMID 10669596
Murphy K C