Conducting the embryonic heart: orchestrating development of specialized cardiac tissues.
Trends in cardiovascular medicine | 2000-01-01 | PMID 10189963
Gourdie R G, Kubalak S, Mikawa T
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 1124 of 10600
Gq signaling in cardiac adaptation and maladaptation.
Trends in cardiovascular medicine | 2000-01-01 | PMID 10189964
Dorn G W, Brown J H
[Clinicogenetic study of MEN1: recent physiopathological data and clinical applications. Study Group of Multiple Endocrine Neoplasia (GENEM)].
Annales d'endocrinologie | 1998-01-01 | PMID 10189986
Calender A, Giraud S, Porchet N and 3 more
Genes: MEN1
[Von Hippel-Lindau disease: recent genetic progress and patient management. Francophone Study Group of von Hippel-Lindau Disease (GEFVH)].
Annales d'endocrinologie | 1998-01-01 | PMID 10189987
Richard S, Giraud S, Beroud C and 8 more
Genes: VHL
[Impact of recent oncogenetic progress on the management of high risk breast cancer patients: the example of BRCA1 and BRCA2 genes].
Annales d'endocrinologie | 1998-01-01 | PMID 10189988
Sobol H, Eisinger F, Sauvan R and 3 more
Genes: BRCA1, BRCA2
[INSERM-FNCLCC collective expert's report. Recommendations for management of women having a genetic risk of developing breast and/or ovarian cancer. National Federation of Centers of the Fight Against Cancer].
Annales d'endocrinologie | 1998-01-01 | PMID 10189990
Eisinger F, Alby N, Bremond A and 12 more
Genes: BRCA1, BRCA2
Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia.
Annales d'endocrinologie | 1998-01-01 | PMID 10189991
Fournet J C, Verkarre V, De Lonlay P and 6 more
[Plasmid pCL1 and antimicrobial activity of a strain of Bacillus sp. 62].
Molekuliarnaia genetika, mikrobiologiia i virusologiia | 1999-01-01 | PMID 10190110
Pogosian G P, Nadirova K G, Kaliev A B and 1 more
Recurrence of hepatitis C virus infection after orthotopic liver transplantation: role of genotypes.
The new microbiologica | 1999-01-01 | PMID 10190112
Casino C, Lilli D, Rivanera D and 5 more
Molecular typing of Candida spp. by random amplification of polymorphic DNA and analysis of restriction fragment length polymorphism of ribosomal DNA repeats.
The new microbiologica | 1999-01-01 | PMID 10190116
Cresti S, Posteraro B, Sanguinetti M and 4 more
Use of RAPD-PCR fingerprinting to detect genetic diversity of soil Streptomyces isolates.
The new microbiologica | 1999-01-01 | PMID 10190117
Malkawi H I, Saadoun I, Moumani F A and 1 more
An abnormally long HIV-1 env DNA PCR product due to altered sequences of primer binding sites.
The new microbiologica | 1999-01-01 | PMID 10190118
Boriskin Y S, Sharland M, Booth J C
Mixed-genotype infections of the rodent malaria Plasmodium chabaudi are more infectious to mosquitoes than single-genotype infections.
Parasitology | 1997-08-01 | PMID 10190168
Taylor L H, Walliker D, Read A F
A model for the origins and spread of drug-resistant malaria.
Parasitology | 1997-08-01 | PMID 10190169
Hastings I M
Lack of association between HLA-DRB1 alleles of the major histocompatibility complex and p-ANCA status or clinical characteristics in patients with ulcerative colitis.
Zeitschrift fur Gastroenterologie | 1999-02-01 | PMID 10190246
Folwaczny C, Zahn R, Brünnler G and 5 more
Differing risk factors for cerebral palsy in the presence of mental retardation and epilepsy.
Journal of child neurology | 1999-03-01 | PMID 10190264
Arpino C, Curatolo P, Stazi M A and 2 more
Association of the 677C-->T mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects.
Journal of child neurology | 1999-03-01 | PMID 10190266
Boduroğlu K, Alikaşifoğlu M, Anar B and 1 more
Genetic susceptibility to neurodevelopmental disorders.
Journal of child neurology | 1999-03-01 | PMID 10190270
Ryan S G
Interferon alpha2b differentially affects proliferation of two human renal cell carcinoma cell lines differing in the P-glycoprotein-associated multidrug-resistant phenotype.
Journal of cancer research and clinical oncology | 1999-01-01 | PMID 10190320
Frank M H, Pomer S
World distribution of the T833C/844INS68 CBS in cis double mutation: a reliable anthropological marker.
Human genetics | 1999-02-01 | PMID 10190322
Pepe G, Vanegas O C, Rickards O and 7 more
Genes: CBS, MTHFR
Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibility.
Human genetics | 1999-02-01 | PMID 10190323
Semprini S, Capon F, Bovolenta S and 7 more
Supravalvular aortic stenosis: a splice site mutation within the elastin gene results in reduced expression of two aberrantly spliced transcripts.
Human genetics | 1999-02-01 | PMID 10190324
Urbán Z, Michels V V, Thibodeau S N and 3 more
Identification and characterization of mutations in patients with holocarboxylase synthetase deficiency.
Human genetics | 1999-02-01 | PMID 10190325
Aoki Y, Li X, Sakamoto O and 8 more
Nucleotide sequence diversity in non-coding regions of ALDH2 as revealed by restriction enzyme and SSCP analysis.
Human genetics | 1999-02-01 | PMID 10190330
Peterson R J, Goldman D, Long J C
Genes: ALDH2
Effect of the stromelysin-1 promoter on efficacy of pravastatin in coronary atherosclerosis and restenosis.
The American journal of cardiology | 1999-03-15 | PMID 10190398
de Maat M P, Jukema J W, Ye S and 9 more
Increase in radiation-induced HPRT gene mutation frequency after nonthermal exposure to nonionizing 60 Hz electromagnetic fields.
Radiation research | 1999-04-01 | PMID 10190502
Walleczek J, Shiu E C, Hahn G M
Restoration of mutant TP53 to normal TP53 function by glycerol as a chemical chaperone.
Radiation research | 1999-04-01 | PMID 10190503
Ohnishi T, Ohnishi K, Wang X and 2 more
A new mutation in the elastin gene causing supravalvular aortic stenosis.
The American journal of cardiology | 1999-04-01 | PMID 10190538
Boeckel T, Dierks A, Vergopoulos A and 8 more
Effect of hMSH6 cDNA expression on the phenotype of mismatch repair-deficient colon cancer cell line HCT15.
Carcinogenesis | 1999-03-01 | PMID 10190549
Lettieri T, Marra G, Aquilina G and 4 more
Cytotoxic and mutagenic response of mismatch repair-defective human cancer cells exposed to a food-associated heterocyclic amine.
Carcinogenesis | 1999-03-01 | PMID 10190551
Glaab W E, Skopek T R
Inhibition of benzo[a]pyrene-induced mutagenesis by (-)-epigallocatechin gallate in the lung of rpsL transgenic mice.
Carcinogenesis | 1999-03-01 | PMID 10190556
Muto S, Yokoi T, Gondo Y and 4 more
Hprt mutant frequency and aromatic DNA adduct level in non-smoking and smoking lung cancer patients and population controls.
Carcinogenesis | 1999-03-01 | PMID 10190559
Hou S M, Yang K, Nyberg F and 3 more
In situ detection of mutated hepatitis B virus in microdissected, formalin-fixed liver tissues from patients with chronic hepatitis B.
Journal of hepatology | 1999-03-01 | PMID 10190715
Kojima N, Horiike N, Michitaka K and 1 more
Familial primary biliary cirrhosis reassessed: a geographically-based population study.
Journal of hepatology | 1999-03-01 | PMID 10190721
Jones D E, Watt F E, Metcalf J V and 2 more
Overcoming bcl-2- and p53-mediated resistance in prostate cancer.
Seminars in oncology | 1999-02-01 | PMID 10190792
DiPaola R S, Aisner J
Mutational analysis and genotype-phenotype correlation of 29 unrelated Japanese patients with X-linked adrenoleukodystrophy.
Archives of neurology | 1999-03-01 | PMID 10190819
Takano H, Koike R, Onodera O and 2 more
Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn.
The Journal of pediatrics | 1999-04-01 | PMID 10190918
Monaghan G, McLellan A, McGeehan A and 7 more
Phenotypic spectrum and management issues in Kabuki syndrome.
The Journal of pediatrics | 1999-04-01 | PMID 10190924
Kawame H, Hannibal M C, Hudgins L and 1 more
The prothrombin gene variant 20210A in venous and arterial thromboembolism.
Haematologica | 1999-04-01 | PMID 10190951
Vicente V, González-Conejero R, Rivera J and 1 more
Microsatellite loci in wild-type and inbred Strongylocentrotus purpuratus.
Developmental biology | 1999-04-15 | PMID 10191043
Cameron R A, Leahy P S, Britten R J and 1 more
Z/AP, a double reporter for cre-mediated recombination.
Developmental biology | 1999-04-15 | PMID 10191045
Lobe C G, Koop K E, Kreppner W and 3 more
Murine fibroblast growth factor receptor 1alpha isoforms mediate node regression and are essential for posterior mesoderm development.
Developmental biology | 1999-04-15 | PMID 10191046
Xu X, Li C, Takahashi K and 3 more
Notchspl is deficient for inductive processes in the eye, and E(spl)D enhances split by interfering with proneural activity.
Developmental biology | 1999-04-15 | PMID 10191054
Nagel A C, Preiss A
Mutations in the zebrafish unmask shared regulatory pathways controlling the development of catecholaminergic neurons.
Developmental biology | 1999-04-15 | PMID 10191060
Guo S, Wilson S W, Cooke S and 3 more
Evolution of the ribosomal RNA internal transcribed spacer one (ITS-1) in cichlid fishes of the Lake Victoria region.
Molecular phylogenetics and evolution | 1999-03-01 | PMID 10191071
Booton G C, Kaufman L, Chandler M and 3 more
Relationships among the cyclostome braconid (Hymenoptera: Braconidae) subfamilies inferred from a mitochondrial tRNA gene rearrangement.
Molecular phylogenetics and evolution | 1999-03-01 | PMID 10191072
Dowton M
A genetic linkage map of microsatellites in the domestic cat (Felis catus).
Genomics | 1999-04-01 | PMID 10191079
Menotti-Raymond M, David V A, Lyons L A and 4 more
Functional characterization of the human PAX3 gene regulatory region.
Genomics | 1999-04-01 | PMID 10191090
Okladnova O, Syagailo Y V, Tranitz M and 4 more
Genes: PAX3
Mapping of a cadherin gene cluster to a region of chromosome 5 subject to frequent allelic loss in carcinoma.
Genomics | 1999-04-01 | PMID 10191097
Chalmers I J, Höfler H, Atkinson M J
Genotype-phenotype correlations in neuronal ceroid lipofuscinosis due to palmitoyl-protein thioesterase deficiency.
Molecular genetics and metabolism | 1999-04-01 | PMID 10191107
Hofmann S L, Das A K, Yi W and 2 more
Genes: NCL, CLN3
The molecular basis of GROD-storing neuronal ceroid lipofuscinoses in Scotland.
Molecular genetics and metabolism | 1999-04-01 | PMID 10191109
Stephenson J B, Greene N D, Leung K Y and 8 more
Reevaluation of neuronal ceroid lipofuscinoses: atypical juvenile onset may be the result of CLN2 mutations.
Molecular genetics and metabolism | 1999-04-01 | PMID 10191110
Wisniewski K E, Kaczmarski A, Kida E and 5 more
Genes: CLN3
Investigation of Batten disease with the yeast Saccharomyces cerevisiae.
Molecular genetics and metabolism | 1999-04-01 | PMID 10191120
Pearce D A, Sherman F
Genes: CLN3
Studies of pH regulation by Btn1p, the yeast homolog of human Cln3p.
Molecular genetics and metabolism | 1999-04-01 | PMID 10191121
Pearce D A, Nosel S A, Sherman F
Genes: CLN3
Genetic and physical mapping of the CLN6 gene on chromosome 15q21-23.
Molecular genetics and metabolism | 1999-04-01 | PMID 10191123
Sharp J D, Wheeler R B, Lake B D and 3 more
Genes: CLN6
Progress toward the cloning of CLN6, the gene underlying a variant LINCL.
Molecular genetics and metabolism | 1999-04-01 | PMID 10191124
Auger K J, Ajene A, Lerner T
Genes: CLN6, NCL
A new locus for variant late infantile neuronal ceroid lipofuscinosis-CLN7.
Molecular genetics and metabolism | 1999-04-01 | PMID 10191125
Wheeler R B, Sharp J D, Mitchell W A and 4 more
Genes: CLN5, CLN6
An early-onset congenic strain of the motor neuron degeneration (mnd) mouse.
Molecular genetics and metabolism | 1999-04-01 | PMID 10191135
Messer A, Manley K, Plummer J A
Genes: NCL
Ultrastructural and electrophysiological correlation of the genotypes of NCL.
Molecular genetics and metabolism | 1999-04-01 | PMID 10191136
Williams R E, Boyd S, Lake B D
Genes: NCL
Estimation of mutation frequencies in normal mammalian cells and the development of cancer.
Seminars in cancer biology | 1998-12-01 | PMID 10191175
Turker M S
On the origin of multiple mutations in human cancers.
Seminars in cancer biology | 1998-12-01 | PMID 10191176
Jackson A L, Loeb L A
Hypermutability and silent mutations in human carcinogenesis.
Seminars in cancer biology | 1998-12-01 | PMID 10191177
Strauss B S
Evolution and the inevitability of human cancer.
Seminars in cancer biology | 1998-12-01 | PMID 10191178
Simpson A J, Camargo A A
Prevalence and changes in hepatitis C virus genotypes among multitransfused persons with hemophilia. The Multicenter Hemophilia Cohort Study.
The Journal of infectious diseases | 1999-05-01 | PMID 10191205
Eyster M E, Sherman K E, Goedert J J and 2 more
Association of major histocompatibility complex determinants with the development of symptomatic and asymptomatic genital herpes simplex virus type 2 infections.
The Journal of infectious diseases | 1999-05-01 | PMID 10191207
Lekstrom-Himes J A, Hohman P, Warren T and 5 more
Genotypic resistance and the treatment of HIV-1 infection in Espírito Santo, Brazil.
The Journal of infectious diseases | 1999-05-01 | PMID 10191233
Pilcher C D, Perkins M D, Fiscus S A and 6 more
Prediction and experimental testing of Bacillus acidocaldarius thioredoxin stability.
The Biochemical journal | 1999-04-15 | PMID 10191261
Pedone E, Cannio R, Saviano M and 2 more
Lipoprotein lipase activity is decreased in a large cohort of patients with coronary artery disease and is associated with changes in lipids and lipoproteins.
Journal of lipid research | 1999-04-01 | PMID 10191298
Henderson H E, Kastelein J J, Zwinderman A H and 8 more
Genes: LPL, CAD
Glutamate receptor expression regulates quantal size and quantal content at the Drosophila neuromuscular junction.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 1999-04-15 | PMID 10191319
DiAntonio A, Petersen S A, Heckmann M and 1 more
Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 1999-04-15 | PMID 10191337
Carter R J, Lione L A, Humby T and 5 more
The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
Genetic counseling (Geneva, Switzerland) | 1999-01-01 | PMID 10191425
McDonald-McGinn D M, Kirschner R, Goldmuntz E and 19 more
Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11.
Genetic counseling (Geneva, Switzerland) | 1999-01-01 | PMID 10191426
Marino B, Digilio M C, Toscano A and 2 more
Chromosome 22q11 deletions in patients with selected outflow tract malformations.
Genetic counseling (Geneva, Switzerland) | 1999-01-01 | PMID 10191427
Frohn-Mulder I M, Wesby Swaay E, Bouwhuis C and 4 more
22q11 deletion in DGS/VCFS monozygotic twins with discordant phenotypes.
Genetic counseling (Geneva, Switzerland) | 1999-01-01 | PMID 10191428
Vincent M C, Heitz F, Tricoire J and 4 more
The deletions of 22q11--the Portuguese experience.
Genetic counseling (Geneva, Switzerland) | 1999-01-01 | PMID 10191429
Gaspar I M, Lourenço M T, Reis M I and 4 more
The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome.
Genetic counseling (Geneva, Switzerland) | 1999-01-01 | PMID 10191430
Van Esch H, Groenen P, Fryns J P and 2 more
Abdominal lymphatic dysplasia and 22q11 microdeletion.
Genetic counseling (Geneva, Switzerland) | 1999-01-01 | PMID 10191431
Mansir T, Lacombe D, Lamireau T and 5 more
Retrospective analysis of feeding and speech disorders in 50 patients with velo-cardio-facial syndrome.
Genetic counseling (Geneva, Switzerland) | 1999-01-01 | PMID 10191432
Rommel N, Vantrappen G, Swillen A and 3 more
The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.
Genetic counseling (Geneva, Switzerland) | 1999-01-01 | PMID 10191433
Swillen A, Devriendt K, Legius E and 4 more
Behavior problems and personality aspects of 40 children with velo-cardio-facial syndrome.
Genetic counseling (Geneva, Switzerland) | 1999-01-01 | PMID 10191434
Heineman-de Boer J A, Van Haelst M J, Cordia-de Haan M and 1 more
[Brain malformation and apoptosis].
No to hattatsu = Brain and development | 1999-03-01 | PMID 10191635
Mizuguchi M
Linkage disequilibrium, mutational analysis and natural selection in the repetitive region of the clock gene, period, in Drosophila melanogaster.
Genetical research | 1997-04-01 | PMID 10191718
Rosato E, Peixoto A A, Costa R and 1 more
[Myocardiopathy and isolated glucocorticoid deficit with ACTH resistance: a fortuitous association?].
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie | 1999-03-01 | PMID 10191895
Vigneron P, Cabrol S, Tillous-Borde I and 5 more
[Prion diseases in pediatrics].
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie | 1999-03-01 | PMID 10191898
Sol-Caubel I, Castela F, Brousse V and 4 more
Genes: PRNP
[Ontogeny of the immune system].
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie | 1999-01-01 | PMID 10191919
Millet V, Lacroze V, Bodiou A C and 3 more
Metabolic risk factors for coronary heart disease: current and future prospects.
Current opinion in cardiology | 1999-03-01 | PMID 10191978
Wilson P W
Rolling circle amplification of DNA immobilized on solid surfaces and its application to multiplex mutation detection.
Genetic analysis : biomolecular engineering | 1999-04-01 | PMID 10191983
Hatch A, Sano T, Misasi J and 1 more
Genes: BRCA1
PCR based targeted genomic and cDNA differential display.
Genetic analysis : biomolecular engineering | 1999-04-01 | PMID 10191986
Broude N E, Storm N, Malpel S and 4 more
[Vascular disease and cellular activation: exploration of cell adhesion phenotype by quantitative flow cytometry].
Journal des maladies vasculaires | 1999-02-01 | PMID 10192030
Latger V, Dumas D, Lecompte T and 2 more
Genetic analysis of three South African horse breeds.
Journal of the South African Veterinary Association | 1998-12-01 | PMID 10192084
Cothran E G, van Dyk E
Significant differences in the interleukin-1beta and interleukin-1 receptor antagonist gene polymorphisms in a Hungarian population with inflammatory bowel disease.
Scandinavian journal of gastroenterology | 1999-02-01 | PMID 10192196
Nemetz A, Köpe A, Molnár T and 6 more
A sex difference and no effect of ApoE type on the amount of cytoskeletal alterations in the nucleus basalis of Meynert in Alzheimer's disease.
Neurobiology of aging | 2000-01-01 | PMID 10192208
Salehi A, Gonzalez Martinez V, Swaab D F
Targeted cleavage of RNA molecules by human RNase P using minimized external guide sequences.
Antisense & nucleic acid drug development | 1999-02-01 | PMID 10192292
Werner M, Rosa E, Al Emran O and 2 more
Lack of evidence for antisense suppression in the fungal plant pathogen Ustilago maydis.
Antisense & nucleic acid drug development | 1999-02-01 | PMID 10192295
Keon J P, Owen J W, Hargreaves J A
Plasma carotenoids, glutathione S-transferase M1 and T1 genetic polymorphisms, and risk of hepatocellular carcinoma: independent and interactive effects.
American journal of epidemiology | 1999-04-01 | PMID 10192309
Yu M W, Chiu Y H, Chiang Y C and 6 more
Factor V Arg506Gln mutation is not associated with cardiovascular mortality in older women.
American journal of epidemiology | 1999-04-01 | PMID 10192314
Roest M, Banga J D, Tempelman M J and 4 more
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Nature genetics | 1999-04-01 | PMID 10192385
Yasunaga S, Grati M, Cohen-Salmon M and 6 more
Genes: OTOF, FER
A human IFNGR1 small deletion hotspot associated with dominant susceptibility to mycobacterial infection.
Nature genetics | 1999-04-01 | PMID 10192386
Jouanguy E, Lamhamedi-Cherradi S, Lammas D and 19 more
Genes: IFNGR1
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
Nature genetics | 1999-04-01 | PMID 10192387
Koob M D, Moseley M L, Schut L J and 4 more
Independent regulation of the two Pax5 alleles during B-cell development.
Nature genetics | 1999-04-01 | PMID 10192389
Nutt S L, Vambrie S, Steinlein P and 4 more