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 1131 of 10600

Familial context of genetic testing for cancer susceptibility: moderating effect of siblings' test results on psychological distress one to two weeks after BRCA1 mutation testing.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology | 1999-04-01 | PMID 10207644
Smith K R, West J A, Croyle R T and 1 more
Genes: BRCA1
Diagnostic implications of albumin messenger RNA detection and cytokeratin pattern in benign hepatic lesions and biliary cystadenocarcinoma.
Diagnostic molecular pathology : the American journal of surgical pathology, part B | 1998-12-01 | PMID 10207666
D'Errico A, Deleonardi G, Fiorentino M and 2 more
Molecular assessment of clonality leads to the identification of a new germ line TP53 mutation associated with malignant cystosarcoma phyllodes and soft tissue sarcoma.
Diagnostic molecular pathology : the American journal of surgical pathology, part B | 1998-12-01 | PMID 10207667
Bot F J, Sleddens H F, Dinjens W N
Pathogenesis of pituitary tumors.
Endocrinology and metabolism clinics of North America | 1999-03-01 | PMID 10207683
Melmed S
Method for constructing confidently ordered linkage maps.
Genetic epidemiology | 1999-01-01 | PMID 10207715
Broman K W, Weber J L
Recent progress in understanding the genetic susceptibility to osteoporosis.
Genetic epidemiology | 1999-01-01 | PMID 10207717
Zmuda J M, Cauley J A, Ferrell R E
Effects of misclassification on estimates of relative risk in family history studies.
Genetic epidemiology | 1999-01-01 | PMID 10207718
Szatmari P, Jones M B
Inheritance of LDL peak particle diameter: results from a segregation analysis in Israeli families.
Genetic epidemiology | 1999-01-01 | PMID 10207719
Friedlander Y, Kark J D, Sinnreich R and 2 more
Linkage analysis of candidate obesity genes among the Mexican-American population of Starr County, Texas.
Genetic epidemiology | 1999-01-01 | PMID 10207720
Bray M S, Boerwinkle E, Hanis C L
Genes: NPY, LEP, LEPR, UCP1
A genealogical study of Alzheimer disease in the Saguenay region of Quebec.
Genetic epidemiology | 1999-01-01 | PMID 10207721
Vézina H, Heyer E, Fortier I and 3 more
Genes: APOE
Bivariate genetic analysis of fasting insulin and glucose levels.
Genetic epidemiology | 1999-01-01 | PMID 10207722
Snieder H, Boomsma D I, van Doornen L J and 1 more
Etiology of the inflammatory bowel diseases.
International journal of colorectal disease | 1999-02-01 | PMID 10207723
Hugot J P, Zouali H, Lesage S and 1 more
Characterization of anti-hepatitis C virus-positive sera not genotyped by restriction fragment length polymorphism or serology.
Journal of gastroenterology and hepatology | 1999-04-01 | PMID 10207783
Gish R G, Qian K, Brooks L and 4 more
Relationship between the effect of interferon therapy and the change of hepatitis C virus non-structural 5B gene.
Journal of gastroenterology and hepatology | 1999-04-01 | PMID 10207784
Horiike N, Michitaka K, Masumoto T and 3 more
A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria.
Journal of hepatology | 1999-04-01 | PMID 10207799
Brissot P, Moirand R, Jouanolle A M and 4 more
Genes: HFE
Effect of pentoxifylline on early proliferation and phenotypic modulation of fibrogenic cells in two rat models of liver fibrosis and on cultured hepatic stellate cells.
Journal of hepatology | 1999-04-01 | PMID 10207803
Desmoulière A, Xu G, Costa A M and 3 more
Genes: PCNA
[Gly380Arg and Asn540Lys mutations of fibroblast growth factor receptor 3 in achondroplasia and hypochndroplasia in the Spanish population].
Medicina clinica | 1999-03-06 | PMID 10207844
Ezquieta Zubicaray B, Iguacel A O, Varela Junquera J M and 3 more
Genes: FGFR3
Male Rett syndrome variant: application of diagnostic criteria.
Pediatric neurology | 1999-03-01 | PMID 10207936
Jan M M, Dooley J M, Gordon K E
A set of conserved PCR primers for the analysis of simple sequence repeat polymorphisms in chloroplast genomes of dicotyledonous angiosperms.
Genome | 1999-02-01 | PMID 10207998
Weising K, Gardner R C
Molecular characterization of ribosomal gene variation within and among NORs segregating in specialized populations of chicken.
Genome | 1999-02-01 | PMID 10208002
Delany M E, Krupkin A B
Directed termination of the polymerase chain reaction: kinetics and applications in mutation detection.
Genome | 1999-02-01 | PMID 10208003
Chen J Z, Hebert P D
PCR-based analysis of the intergenic spacers of the Nor loci on the A genomes of Triticum diploids and polyploids.
Genome | 1999-02-01 | PMID 10208005
Sallares R, Brown T A
Microsatellite retrieval in lettuce (Lactuca sativa L.).
Genome | 1999-02-01 | PMID 10208007
van de Wiel C, Arens P, Vosman B
An example of microsatellite length variation in the mitochondrial genome of conifers.
Genome | 1999-02-01 | PMID 10208008
Soranzo N, Provan J, Powell W
Genotype, molecular phenotype, and cognitive phenotype: correlations in fragile X syndrome.
American journal of medical genetics | 1999-04-02 | PMID 10208163
Kaufmann W E, Abrams M T, Chen W and 1 more
Genes: FMR1
Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth.
American journal of medical genetics | 1999-04-02 | PMID 10208166
Parvari R, Mumm S, Galil A and 3 more
Genes: FMR1
Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies.
American journal of medical genetics | 1999-04-02 | PMID 10208177
Jenkins E C, Wen G Y, Kim K S and 10 more
Genes: TAT, FMR1
Leber's hereditary optic neuropathy mitochondrial DNA mutations in familial multiple sclerosis.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie | 1999-04-01 | PMID 10208269
Mojon D S, Fujihara K, Hirano M and 4 more
Genotyping of the prion protein gene at codon 129.
Acta neuropathologica | 1999-04-01 | PMID 10208274
Zimmermann K, Turecek P L, Schwarz H P
Genes: PRNP
Spectroscopic investigation of tertiary fold of staphylococcal protein A to explore its engineering application.
Biomaterials | 1999-04-01 | PMID 10208407
Kikuchi J, Mitsui Y, Asakura T and 3 more
Genes: LPA
Ectopic expression of constitutively activated Ral GTPase inhibits cell shape changes during Drosophila eye development.
Oncogene | 1999-03-18 | PMID 10208418
Sawamoto K, Yamada C, Kishida S and 4 more
Genes: CDC42
Suppression of src-induced transformed phenotype by expression of tropomyosin-1.
Oncogene | 1999-03-18 | PMID 10208425
Prasad G L, Masuelli L, Raj M H and 1 more
Somatic mutation of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanoma.
Oncogene | 1999-03-04 | PMID 10208439
Guldberg P, thor Straten P, Ahrenkiel V and 3 more
Genes: STK11
Susceptibility genes for nicotine dependence: a genome scan and followup in an independent sample suggest that regions on chromosomes 2, 4, 10, 16, 17 and 18 merit further study.
Molecular psychiatry | 1999-03-01 | PMID 10208445
Straub R E, Sullivan P F, Ma Y and 11 more
Genes: NPL
Polymorphisms of the interleukin-1 gene complex in schizophrenia.
Molecular psychiatry | 1999-03-01 | PMID 10208450
Katila H, Hänninen K, Hurme M
Genes: TNF
Mapping susceptibility loci in attention deficit hyperactivity disorder: preferential transmission of parental alleles at DAT1, DBH and DRD5 to affected children.
Molecular psychiatry | 1999-03-01 | PMID 10208453
Daly G, Hawi Z, Fitzgerald M and 1 more
Genes: DBH, DRD5
Primary signet-ring cell carcinoma of the lung: histochemical and immunohistochemical characterization.
Human pathology | 1999-04-01 | PMID 10208457
Hayashi H, Kitamura H, Nakatani Y and 3 more
Assessment and diagnostic utility of the cytotoxic T-lymphocyte phenotype using the specific markers granzyme-B and TIA-1 in esophageal mucosal biopsies.
Human pathology | 1999-04-01 | PMID 10208460
Resnick M B, Finkelstein Y, Weissler A and 2 more
The type of mutation in the low density lipoprotein receptor gene influences the cholesterol-lowering response of the HMG-CoA reductase inhibitor simvastatin in patients with heterozygous familial hypercholesterolaemia.
Atherosclerosis | 1999-03-01 | PMID 10208479
Heath K E, Gudnason V, Humphries S E and 1 more
Genes: LDLR, APOB
P1A1/A2 polymorphism of platelet glycoprotein IIIa and risk of acute coronary syndromes in heterozygous familial hypercholesterolemia.
Atherosclerosis | 1999-03-01 | PMID 10208484
Cenarro A, Casao E, Civeira F and 3 more
Fine mapping of low-density lipoprotein receptor gene by genetic linkage on chromosome 19p13.1-p13.3 and study of the founder effect of four French Canadian low-density lipoprotein receptor gene mutations.
Atherosclerosis | 1999-03-01 | PMID 10208489
Couture P, Morissette J, Gaudet D and 5 more
Genes: LDLR
Contribution of receptor negative versus receptor defective mutations in the LDL-receptor gene to angiographically assessed coronary artery disease among young (25-49 years) versus middle-aged (50-64 years) men.
Atherosclerosis | 1999-03-01 | PMID 10208490
Gaudet D, Vohl M C, Couture P and 5 more
Genes: CAD
Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases.
Atherosclerosis | 1999-03-01 | PMID 10208491
Tsai M Y, Welge B G, Hanson N Q and 7 more
Genes: CAD, PML, CBS, MTHFR
Sensing of cadmium and copper ions by externally exposed ADL, ASE, and ASH neurons elicits avoidance response in Caenorhabditis elegans.
Neuroreport | 1999-03-17 | PMID 10208543
Sambongi Y, Nagae T, Liu Y and 4 more
Increased neuronal damage in apolipoprotein E-deficient mice following global ischaemia.
Neuroreport | 1999-03-17 | PMID 10208557
Horsburgh K, Kelly S, McCulloch J and 3 more
DNA pooling and dense marker maps: a systematic search for genes for cognitive ability.
Neuroreport | 1999-03-17 | PMID 10208558
Hill L, Craig I W, Asherson P and 13 more
Modulation of morphine analgesia in alphaCGRP mutant mice.
Neuroreport | 1999-03-17 | PMID 10208559
Salmon A M, Damaj I, Sekine S and 3 more
The -491AA polymorphism in the APOE gene is associated with increased plasma apoE levels in Alzheimer's disease.
Neuroreport | 1999-03-17 | PMID 10208564
Laws S M, Taddei K, Martins G and 7 more
Genes: APOE
A new GTP-cyclohydrolase I mutation in an unusual dopa-responsive dystonia, familial form.
Neuroreport | 1999-02-25 | PMID 10208576
Brique S, Destée A, Lambert J C and 4 more
Transgenic mice expressing a dominant negative mutant interleukin-1beta converting enzyme show resistance to MPTP neurotoxicity.
Neuroreport | 1999-02-25 | PMID 10208603
Klevenyi P, Andreassen O, Ferrante R J and 3 more
N-acetyltransferase (NAT2) genotype and susceptibility of sporadic Alzheimer's disease.
Pharmacogenetics | 1999-02-01 | PMID 10208637
Rocha L, Garcia C, de Mendonça A and 3 more
Genes: NAT2
CYP2D6 is associated with Parkinson's disease but not with dementia with Lewy Bodies or Alzheimer's disease.
Pharmacogenetics | 1999-02-01 | PMID 10208640
Atkinson A, Singleton A B, Steward A and 7 more
The frequency and distribution of thiopurine methyltransferase alleles in Caucasian and Asian populations.
Pharmacogenetics | 1999-02-01 | PMID 10208641
Collie-Duguid E S, Pritchard S C, Powrie R H and 4 more
Genes: TPMT
The effect of genetic polymorphisms in CYP2C9 on sulphamethoxazole N-hydroxylation.
Pharmacogenetics | 1999-02-01 | PMID 10208642
Gill H J, Tjia J F, Kitteringham N R and 3 more
Pharmacokinetics of chlorpheniramine, phenytoin, glipizide and nifedipine in an individual homozygous for the CYP2C9*3 allele.
Pharmacogenetics | 1999-02-01 | PMID 10208645
Kidd R S, Straughn A B, Meyer M C and 3 more
Detection of the GSTM1*0 allele by long polymerase chain reaction.
Pharmacogenetics | 1999-02-01 | PMID 10208647
Kerb R, Brockmöller J, Sachse C and 1 more
Genes: GSTM1, GSTM2
Association of arylamine N-acetyltransferases NAT1 and NAT2 genotypes to laryngeal cancer risk.
Pharmacogenetics | 1999-02-01 | PMID 10208649
Henning S, Cascorbi I, Münchow B and 2 more
Genes: NAT2, NAT1
Pitfalls in N-acetyltransferase 2 genotyping.
Pharmacogenetics | 1999-02-01 | PMID 10208651
Cascorbi I, Roots I
Genes: NAT2
Defects in tracheoesophageal and lung morphogenesis in Nkx2.1(-/-) mouse embryos.
Developmental biology | 1999-05-01 | PMID 10208743
Minoo P, Su G, Drum H and 2 more
Dynein-dynactin function and sensory axon growth during Drosophila metamorphosis: A role for retrograde motors.
Developmental biology | 1999-05-01 | PMID 10208745
Murphey R K, Caruccio P C, Getzinger M and 2 more
The Caenorhabditis elegans mel-11 myosin phosphatase regulatory subunit affects tissue contraction in the somatic gonad and the embryonic epidermis and genetically interacts with the Rac signaling pathway.
Developmental biology | 1999-05-01 | PMID 10208747
Wissmann A, Ingles J, Mains P E
Solid-phase sequence scanning for drug resistance detection in tuberculosis.
Molecular and cellular probes | 1999-04-01 | PMID 10208797
Head S R, Parikh K, Rogers Y H and 3 more
In vitro codon-reading specificities of unmodified tRNA molecules with different anticodons on the sequence background of Escherichia coli tRNASer.
Biochemical and biophysical research communications | 1999-04-21 | PMID 10208840
Takai K, Takaku H, Yokoyama S
Genes: AGA, CGA
IRF-1 is an essential mediator in IFN-gamma-induced cell cycle arrest and apoptosis of primary cultured hepatocytes.
Biochemical and biophysical research communications | 1999-04-21 | PMID 10208842
Kano A, Haruyama T, Akaike T and 1 more
The novel sarcomeric protein telethonin exhibits developmental and functional regulation.
Biochemical and biophysical research communications | 1999-04-21 | PMID 10208846
Mason P, Bayol S, Loughna P T
Fabry disease: identification of novel alpha-galactosidase A mutations and molecular carrier detection by use of fluorescent chemical cleavage of mismatches.
Biochemical and biophysical research communications | 1999-04-21 | PMID 10208848
Germain D P, Poenaru L
Genes: GLA
Repression of hepatitis B virus X gene expression by hammerhead ribozymes.
Biochemical and biophysical research communications | 1999-04-21 | PMID 10208856
Kim Y K, Junn E, Park I and 3 more
Transcription of the human thyrotropin-releasing hormone receptor gene-analysis of basal promoter elements and glucocorticoid response elements.
Biochemical and biophysical research communications | 1999-04-21 | PMID 10208868
Høvring P I, Matre V, Fjeldheim A K and 2 more
Genes: TRHR, CAT
Antigenic heterogeneity of the hepatitis C virus NS4 protein as modeled with synthetic peptides.
Virology | 1999-04-25 | PMID 10208931
Chang J C, Seidel C, Ofenloch B and 3 more
Hereditary pancreatitis and mutation of the trypsinogen gene.
Archives of disease in childhood | 1999-05-01 | PMID 10208958
Weber P, Keim V, Zimmer K P
Identification of two major histocompatibility complex class Ib genes, Q7 and Q9, as the Ped gene in the mouse.
Biology of reproduction | 1999-05-01 | PMID 10208972
Wu L, Feng H, Warner C M
Defects in the germ line and gonads of mice lacking connexin43.
Biology of reproduction | 1999-05-01 | PMID 10208994
Juneja S C, Barr K J, Enders G C and 1 more
Mgm101p is a novel component of the mitochondrial nucleoid that binds DNA and is required for the repair of oxidatively damaged mitochondrial DNA.
The Journal of cell biology | 1999-04-19 | PMID 10209025
Meeusen S, Tieu Q, Wong E and 4 more
Targeted gene disruption reveals an adhesin indispensable for pathogenicity of Blastomyces dermatitidis.
The Journal of experimental medicine | 1999-04-19 | PMID 10209038
Brandhorst T T, Wüthrich M, Warner T and 1 more
Signal transducer and activator of transcription (STAT)5 activation by BCR/ABL is dependent on intact Src homology (SH)3 and SH2 domains of BCR/ABL and is required for leukemogenesis.
The Journal of experimental medicine | 1999-04-19 | PMID 10209040
Nieborowska-Skorska M, Wasik M A, Slupianek A and 4 more
Genes: BCR
The transmembrane sequence of human histocompatibility leukocyte antigen (HLA)-C as a determinant in inhibition of a subset of natural killer cells.
The Journal of experimental medicine | 1999-04-19 | PMID 10209043
Davis D M, Mandelboim O, Luque I and 3 more
Extended duration of DH-JH rearrangement in immunoglobulin heavy chain transgenic mice: implications for regulation of allelic exclusion.
The Journal of experimental medicine | 1999-04-19 | PMID 10209046
Chang Y, Bosma M J, Bosma G C
Deficiency in CD22, a B cell-specific inhibitory receptor, is sufficient to predispose to development of high affinity autoantibodies.
The Journal of experimental medicine | 1999-04-19 | PMID 10209047
O'Keefe T L, Williams G T, Batista F D and 1 more
Genes: BCR
The Pds1 anaphase inhibitor and Mec1 kinase define distinct checkpoints coupling S phase with mitosis in budding yeast.
Current biology : CB | 1999-04-08 | PMID 10209118
Clarke D J, Segal M, Mondésert G and 1 more
F-box/WD-repeat proteins pop1p and Sud1p/Pop2p form complexes that bind and direct the proteolysis of cdc18p.
Current biology : CB | 1999-04-08 | PMID 10209119
Wolf D A, McKeon F, Jackson P K
The GRIP domain - a novel Golgi-targeting domain found in several coiled-coil proteins.
Current biology : CB | 1999-04-08 | PMID 10209120
Munro S, Nichols B J
Genes: EEA1
A novel Rab6-interacting domain defines a family of Golgi-targeted coiled-coil proteins.
Current biology : CB | 1999-04-08 | PMID 10209123
Barr F A
A novel Golgi-localisation domain shared by a class of coiled-coil peripheral membrane proteins.
Current biology : CB | 1999-04-08 | PMID 10209125
Kjer-Nielsen L, Teasdale R D, van Vliet C and 1 more
Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33.
Journal of neurology, neurosurgery, and psychiatry | 1999-05-01 | PMID 10209165
Gabreëls-Festen A, van Beersum S, Eshuis L and 4 more
The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases.
Journal of neurology, neurosurgery, and psychiatry | 1999-05-01 | PMID 10209184
Morris H R, Janssen J C, Bandmann O and 4 more
Determinants of potassium channel assembly localised within the cytoplasmic C-terminal domain of Kv2.1.
Biochimica et biophysica acta | 1999-04-14 | PMID 10209222
Bentley G N, Brooks M A, O'Neill C A and 1 more
Transcriptional regulation of the squalene synthase gene (ERG9) in the yeast Saccharomyces cerevisiae.
Biochimica et biophysica acta | 1999-04-14 | PMID 10209263
Kennedy M A, Barbuch R, Bard M
Genes: HAP1
Amino acid residues of heparin cofactor II required for stimulation of thrombin inhibition by sulphated polyanions.
Biochimica et biophysica acta | 1999-04-12 | PMID 10209287
Colwell N S, Grupe M J, Tollefsen D M
Structural characterization, stability and fatty acid-binding properties of two French genetic variants of human serum albumin.
Biochimica et biophysica acta | 1999-04-12 | PMID 10209294
Minchiotti L, Kragh-Hansen U, Nielsen H and 3 more
Ibd1p, a possible spindle pole body associated protein, regulates nuclear division and bud separation in Saccharomyces cerevisiae.
Biochimica et biophysica acta | 1999-04-01 | PMID 10209303
Lee J, Hwang H S, Kim J and 1 more
Infrequent bax gene mutations in B-cell lymphomas.
The Journal of pathology | 1998-12-01 | PMID 10209486
Peng H, Aiello A, Packham G and 2 more
Surface phenotype analysis of CD16+ monocytes from leukapheresis collections for peripheral blood progenitors.
Clinical and experimental immunology | 1999-04-01 | PMID 10209505
Tanaka M, Honda J, Imamura Y and 3 more
Disease-associated autoantibodies and HLA-DQB1 genotypes in children with newly diagnosed insulin-dependent diabetes mellitus (IDDM). The Childhood Diabetes in Finland Study Group.
Clinical and experimental immunology | 1999-04-01 | PMID 10209508
Sabbah E, Savola K, Kulmala P and 7 more
The effects of extracorporeal whole body hyperthermia on the functional and phenotypic features of canine peripheral blood mononuclear cells (PBMC).
Clinical and experimental immunology | 1999-04-01 | PMID 10209525
Kearns R J, Ringler S, Krakowka S and 3 more
Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt-losing congenital adrenal hyperplasia caused by steroid 21-hydroxylase deficiency.
Clinical endocrinology | 1998-12-01 | PMID 10209571
Koppens P F, Hoogenboezem T, Drop S L and 2 more
Production of avirulent Mycobacterium bovis strains by illegitimate recombination with deoxyribonucleic acid fragments containing an interrupted ahpC gene.
Tubercle and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease | 1997-01-01 | PMID 10209677
Wilson T, Wards B J, White S J and 3 more
Multiple transcription factors of the FNR family in denitrifying Pseudomonas stutzeri: characterization of four fnr-like genes, regulatory responses and cognate metabolic processes.
Molecular microbiology | 1999-03-01 | PMID 10209742
Vollack K U, Härtig E, Körner H and 1 more
Modelling in Escherichia coli of mutations in mitoribosomal protein S12: novel mutant phenotypes of rpsL.
Molecular microbiology | 1999-03-01 | PMID 10209746
Toivonen J M, Boocock M R, Jacobs H T
Amino acid residue Ala-62 in the FimH fimbrial adhesin is critical for the adhesiveness of meningitis-associated Escherichia coli to collagens.
Molecular microbiology | 1999-03-01 | PMID 10209747
Pouttu R, Puustinen T, Virkola R and 3 more
Escherichia coli nusG mutations that block transcription termination by coliphage HK022 Nun protein.
Molecular microbiology | 1999-03-01 | PMID 10209750
Burova E, Hung S C, Chen J and 4 more