Segregation analysis of quantitative traits.
Annals of human biology | 2000-01-01 | PMID 10195649
Ginsburg E, Livshits G
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.
Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.
Publications
Page 1126 of 10600
Population structure of two black Venezuelan populations studied through their mating structure and other related variables.
Annals of human biology | 2000-01-01 | PMID 10195651
Castro de Guerra D, Arvelo H, Pinto-Cisternas J
Conserved amino acids in the ligand-binding and tau(i) domains of the peroxisome proliferator-activated receptor alpha are necessary for heterodimerization with RXR.
Molecular and cellular endocrinology | 1999-01-25 | PMID 10195690
Gorla-Bajszczak A, Juge-Aubry C, Pernin A and 2 more
The two amino acid substitutions in the L protein of cpts530/1009, a live-attenuated respiratory syncytial virus candidate vaccine, are independent temperature-sensitive and attenuation mutations.
Vaccine | 1999-03-17 | PMID 10195777
Juhasz K, Whitehead S S, Boulanger C A and 3 more
Is there an advantage to including the nucleoprotein in a rabies glycoprotein subunit vaccine?
Vaccine | 1999-03-17 | PMID 10195792
Drings A, Jallet C, Chambert B and 2 more
Association analysis of sequence variants of GABA(A) alpha6, beta2, and gamma2 gene cluster and alcohol dependence.
Alcoholism, clinical and experimental research | 1999-03-01 | PMID 10195814
Sander T, Ball D, Murray R and 6 more
Genes: GABRA6, GABRB2, GABRG2
Alcoholic pancreatitis and polymorphisms of the variable length polythymidine tract in the cystic fibrosis gene.
Alcoholism, clinical and experimental research | 1999-03-01 | PMID 10195826
Haber P S, Norris M D, Apte M V and 5 more
Genes: CFTR
Positive and negative regulation of IkappaB kinase activity through IKKbeta subunit phosphorylation.
Science (New York, N.Y.) | 1999-04-09 | PMID 10195894
Delhase M, Hayakawa M, Chen Y and 1 more
Abnormal morphogenesis but intact IKK activation in mice lacking the IKKalpha subunit of IkappaB kinase.
Science (New York, N.Y.) | 1999-04-09 | PMID 10195896
Hu Y, Baud V, Delhase M and 5 more
The Pex16p homolog SSE1 and storage organelle formation in Arabidopsis seeds.
Science (New York, N.Y.) | 1999-04-09 | PMID 10195899
Lin Y, Sun L, Nguyen L V and 2 more
Regulation of maternal behavior and offspring growth by paternally expressed Peg3.
Science (New York, N.Y.) | 1999-04-09 | PMID 10195900
Li L, Keverne E B, Aparicio S A and 3 more
Polymorphisms of the tissue factor pathway inhibitor (TFPI) gene in patients with acute coronary syndromes and in healthy subjects : impact of the V264M substitution on plasma levels of TFPI.
Arteriosclerosis, thrombosis, and vascular biology | 1999-04-01 | PMID 10195910
Moatti D, Seknadji P, Galand C and 13 more
Genes: TFPI
Risk of venous thromboembolism and clinical manifestations in carriers of antithrombin, protein C, protein S deficiency, or activated protein C resistance: a multicenter collaborative family study.
Arteriosclerosis, thrombosis, and vascular biology | 1999-04-01 | PMID 10195932
Bucciarelli P, Rosendaal F R, Tripodi A and 6 more
Pleiotropy and genotype by diet interaction in a baboon model for atherosclerosis: a multivariate quantitative genetic analysis of HDL subfractions in two dietary environments.
Arteriosclerosis, thrombosis, and vascular biology | 1999-04-01 | PMID 10195946
Mahaney M C, Blangero J, Rainwater D L and 4 more
Internal transcribed spacer sequence phylogeny of Crambe L. (Brassicaceae): molecular data reveal two Old World disjunctions.
Molecular phylogenetics and evolution | 1999-04-01 | PMID 10196078
Francisco-Ortega J, Fuertes-Aguilar J, Gómez-Campo C and 2 more
Evolution of a mitochondrial cytochrome b gene sequence in the species-rich genus sebastes (Teleostei, Scorpaenidae) and its utility in testing the monophyly of the subgenus Sebastomus.
Molecular phylogenetics and evolution | 1999-04-01 | PMID 10196083
Rocha-Olivares A, Kimbrell C A, Eitner B J and 1 more
Molecular evolution, systematics, and zoogeography of the rockfish subgenus Sebastomus (Sebastes, Scorpaenidae) based on mitochondrial cytochrome b and control region sequences.
Molecular phylogenetics and evolution | 1999-04-01 | PMID 10196084
Rocha-Olivares A, Rosenblatt R H, Vetter R D
Phylogenetic relationships of the New World monkeys (Primates, platyrrhini) based on nuclear G6PD DNA sequences.
Molecular phylogenetics and evolution | 1999-04-01 | PMID 10196085
von Dornum M, Ruvolo M
Single-locus tests of microsatellite evolution: multi-step mutations and constraints on allele size.
Molecular phylogenetics and evolution | 1999-04-01 | PMID 10196086
Nielsen R, Palsbøll P J
Methods of assaying Bcl-2 and Bax family proteins in yeast.
Methods (San Diego, Calif.) | 1999-04-01 | PMID 10196100
Xu Q, Jürgensmeier J M, Reed J C
Use of gene knockouts in cultured cells to study apoptosis.
Methods (San Diego, Calif.) | 1999-04-01 | PMID 10196101
Lahti J M
Interactions of CcdB with DNA gyrase. Inactivation of Gyra, poisoning of the gyrase-DNA complex, and the antidote action of CcdA.
The Journal of biological chemistry | 1999-04-16 | PMID 10196173
Bahassi E M, O'Dea M H, Allali N and 3 more
Proliferative defect and embryonic lethality in mice homozygous for a deletion in the p110alpha subunit of phosphoinositide 3-kinase.
The Journal of biological chemistry | 1999-04-16 | PMID 10196176
Bi L, Okabe I, Bernard D J and 2 more
Transcomplementation between different types of respiration-deficient mitochondria with different pathogenic mutant mitochondrial DNAs.
The Journal of biological chemistry | 1999-04-16 | PMID 10196206
Takai D, Isobe K, Hayashi J
Interaction between the nucleotide exchange factor Mge1 and the mitochondrial Hsp70 Ssc1.
The Journal of biological chemistry | 1999-04-16 | PMID 10196216
Sakuragi S, Liu Q, Craig E
Disruption of YHC8, a member of the TSR1 gene family, reveals its direct involvement in yeast protein translocation.
The Journal of biological chemistry | 1999-04-16 | PMID 10196219
Mamoun C B, Beckerich J M, Gaillardin C and 1 more
Genes: TSR1
CD40 ligand mutants responsible for X-linked hyper-IgM syndrome associate with wild type CD40 ligand.
The Journal of biological chemistry | 1999-04-16 | PMID 10196221
Seyama K, Osborne W R, Ochs H D
Regions of Byr4, a regulator of septation in fission yeast, that bind Spg1 or Cdc16 and form a two-component GTPase-activating protein with Cdc16.
The Journal of biological chemistry | 1999-04-16 | PMID 10196225
Furge K A, Cheng Q C, Jwa M and 3 more
Highly potent RANTES analogues either prevent CCR5-using human immunodeficiency virus type 1 infection in vivo or rapidly select for CXCR4-using variants.
Journal of virology | 1999-05-01 | PMID 10196243
Mosier D E, Picchio G R, Gulizia R J and 6 more
Genes: CCR5, CXCR4, MIP
Evolution and biological characterization of human immunodeficiency virus type 1 subtype E gp120 V3 sequences following horizontal and vertical virus transmission in a single family.
Journal of virology | 1999-05-01 | PMID 10196244
Sato H, Shiino T, Kodaka N and 5 more
Enrichment of a precore-minus mutant of duck hepatitis B virus in experimental mixed infections.
Journal of virology | 1999-05-01 | PMID 10196253
Zhang Y Y, Summers J
Genetic divergence with emergence of novel phenotypic variants of equine arteritis virus during persistent infection of stallions.
Journal of virology | 1999-05-01 | PMID 10196259
Hedges J F, Balasuriya U B, Timoney P J and 2 more
Intrastrain variants of herpes simplex virus type 1 isolated from a neonate with fatal disseminated infection differ in the ICP34.5 gene, glycoprotein processing, and neuroinvasiveness.
Journal of virology | 1999-05-01 | PMID 10196279
Bower J R, Mao H, Durishin C and 5 more
Selection of RNA replicons capable of persistent noncytopathic replication in mammalian cells.
Journal of virology | 1999-05-01 | PMID 10196280
Frolov I, Agapov E, Hoffman T A and 4 more
Genetic studies exposing the splicing events involved in herpes simplex virus type 1 latency-associated transcript production during lytic and latent infection.
Journal of virology | 1999-05-01 | PMID 10196281
Alvira M R, Goins W F, Cohen J B and 1 more
Genes: LAT
Frequent detection of escape from cytotoxic T-lymphocyte recognition in perinatal human immunodeficiency virus (HIV) type 1 transmission: the ariel project for the prevention of transmission of HIV from mother to infant.
Journal of virology | 1999-05-01 | PMID 10196293
Wilson C C, Brown R C, Korber B T and 13 more
High-level variability in the ORF-K1 membrane protein gene at the left end of the Kaposi's sarcoma-associated herpesvirus genome defines four major virus subtypes and multiple variants or clades in different human populations.
Journal of virology | 1999-05-01 | PMID 10196312
Zong J C, Ciufo D M, Alcendor D J and 14 more
Genetic and phenotypic changes accompanying the emergence of epizootic subtype IC Venezuelan equine encephalitis viruses from an enzootic subtype ID progenitor.
Journal of virology | 1999-05-01 | PMID 10196323
Wang E, Barrera R, Boshell J and 6 more
Immunization with a live, attenuated simian immunodeficiency virus vaccine leads to restriction of viral diversity in Rhesus macaques not protected from pathogenic challenge.
Journal of virology | 1999-05-01 | PMID 10196343
Sodora D L, Sheridan K E, Marx P A and 1 more
The human HLA-A*0201 allele, expressed in hamster cells, is not a high-affinity receptor for adenovirus type 5 fiber.
Journal of virology | 1999-05-01 | PMID 10196358
Davison E, Kirby I, Elliott T and 1 more
Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1.
Human molecular genetics | 1999-05-01 | PMID 10196361
Xue Y, Gao X, Lindsell C E and 7 more
Genes: JAG1
Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A).
Human molecular genetics | 1999-05-01 | PMID 10196363
Allikmets R, Raskind W H, Hutchinson A and 3 more
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study.
Human molecular genetics | 1999-05-01 | PMID 10196369
Philippe A, Martinez M, Guilloud-Bataille M and 12 more
Mismatch repair gene defects contribute to the genetic basis of double primary cancers of the colorectum and endometrium.
Human molecular genetics | 1999-05-01 | PMID 10196371
Millar A L, Pal T, Madlensky L and 9 more
Impaired synaptic plasticity in mice carrying the Huntington's disease mutation.
Human molecular genetics | 1999-05-01 | PMID 10196373
Usdin M T, Shelbourne P F, Myers R M and 1 more
Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations.
Human molecular genetics | 1999-05-01 | PMID 10196376
Tamanini F, Bontekoe C, Bakker C E and 7 more
Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s).
Human molecular genetics | 1999-05-01 | PMID 10196377
Weiler T, Bashir R, Anderson L V and 9 more
Genes: DYSF
Extremely complex repeat shuffling during germline mutation at human minisatellite B6.7.
Human molecular genetics | 1999-05-01 | PMID 10196378
Tamaki K, May C A, Dubrova Y E and 1 more
Germline BRCA1 alterations in a population-based series of ovarian cancer cases.
Human molecular genetics | 1999-05-01 | PMID 10196379
Janezic S A, Ziogas A, Krumroy L M and 8 more
Genes: BRCA1
Analysis of myocilin mutations in 1703 glaucoma patients from five different populations.
Human molecular genetics | 1999-05-01 | PMID 10196380
Fingert J H, Héon E, Liebmann J M and 16 more
DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children.
Human molecular genetics | 1999-05-01 | PMID 10196382
Fisher P J, Turic D, Williams N M and 12 more
Genes: MSX1
Transchromosomal mouse embryonic stem cell lines and chimeric mice that contain freely segregating segments of human chromosome 21.
Human molecular genetics | 1999-05-01 | PMID 10196383
Hernandez D, Mee P J, Martin J E and 2 more
Alterations in the CSB gene in three Italian patients with the severe form of Cockayne syndrome (CS) but without clinical photosensitivity.
Human molecular genetics | 1999-05-01 | PMID 10196384
Colella S, Nardo T, Mallery D and 5 more
Practical applications of immunohistochemistry in hematolymphoid neoplasms.
Annals of diagnostic pathology | 1999-04-01 | PMID 10196391
Chu P G, Chang K L, Arber D A and 1 more
Genes: ALK
Characterisation of XlCdc1, a Xenopus homologue of the small (PolD2) subunit of DNA polymerase delta; identification of ten conserved regions I-X based on protein sequence comparisons across ten eukaryotic species.
Gene | 1999-04-01 | PMID 10196469
Reynolds N, MacNeill S A
Allelic recombination and linkage disequilibrium within Msp-1 of Plasmodium falciparum, the malignant human malaria parasite.
Gene | 1999-04-01 | PMID 10196473
Sakihama N, Kimura M, Hirayama K and 5 more
Genomic organization of the human fibroblast growth factor receptor 2 (FGFR2) gene and comparative analysis of the human FGFR gene family.
Gene | 1999-04-01 | PMID 10196476
Zhang Y, Gorry M C, Post J C and 1 more
Genes: FGFR2
Genetic dissection of Alzheimer's disease and related dementias: amyloid and its relationship to tau.
Nature neuroscience | 1998-09-01 | PMID 10196523
Hardy J, Duff K, Hardy K G and 2 more
Double strand break rejoining by the Ku-dependent mechanism of non-homologous end-joining.
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie | 2000-01-01 | PMID 10196660
Jeggo P, Singleton B, Beamish H and 1 more
Induction of genetic instability by ionizing radiation.
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie | 2000-01-01 | PMID 10196663
Little J B
Association and linkage analysis of candidate chromosomal regions in multiple sclerosis: indication of disease genes in 12q23 and 7ptr-15.
European journal of human genetics : EJHG | 2000-01-01 | PMID 10196692
Xu C, Dai Y, Fredrikson S and 1 more
Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients.
European journal of human genetics : EJHG | 2000-01-01 | PMID 10196695
Moncla A, Malzac P, Voelckel M A and 7 more
Analysis of the trinucleotide CAG repeat from the human mitochondrial DNA polymerase gene in healthy and diseased individuals.
European journal of human genetics : EJHG | 2000-01-01 | PMID 10196696
Rovio A, Tiranti V, Bednarz A L and 8 more
Genes: POLG
Study of three intragenic polymorphisms in the Machado-Joseph disease gene (MJD1) in relation to genetic instability of the (CAG)n tract.
European journal of human genetics : EJHG | 2000-01-01 | PMID 10196697
Maciel P, Gaspar C, Guimarães L and 8 more
Tracing past population migrations: genealogy of steroid 21-hydroxylase (CYP21) gene mutations in Finland.
European journal of human genetics : EJHG | 2000-01-01 | PMID 10196702
Levo A, Jääskeläinen J, Sistonen P and 3 more
Mortality risk in men is associated with a common mutation in the methylene-tetrahydrofolate reductase gene (MTHFR).
European journal of human genetics : EJHG | 2000-01-01 | PMID 10196703
Heijmans B T, Gussekloo J, Kluft C and 5 more
Genes: MTHFR
Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies.
European journal of human genetics : EJHG | 2000-01-01 | PMID 10196705
Ryynänen M, Heinonen S, Makkonen M and 3 more
Genes: FMR1
Asynchronous replication of alleles in genomes carrying an extra autosome.
European journal of human genetics : EJHG | 2000-01-01 | PMID 10196707
Amiel A, Korenstein A, Gaber E and 1 more
Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss.
European journal of human genetics : EJHG | 2000-01-01 | PMID 10196713
Alloisio N, Morlé L, Bozon M and 7 more
Genes: TECTA
Haplotypes and mutations of the PAH locus in Egyptian families with PKU.
European journal of human genetics : EJHG | 2000-01-01 | PMID 10196714
Effat L, Kuzmin A, Kasem N and 7 more
Genes: PAH
Experimentally observed germline mutations at human micro- and minisatellite loci.
European journal of human genetics : EJHG | 2000-01-01 | PMID 10196715
Sajantila A, Lukka M, Syvänen A C
Sources of error in lung densitometry with CT.
Investigative radiology | 1999-04-01 | PMID 10196723
Stoel B C, Vrooman H A, Stolk J and 1 more
Isolation and characterization of two glycerol-fermenting clostridial strains from a pilot scale anaerobic digester treating high lipid-content slaughterhouse waste.
Journal of applied microbiology | 1999-03-01 | PMID 10196746
Jarvis G N, Strömpl C, Moore E R and 1 more
Genotypic and phenotypic relationships in Burkholderia cepacia isolated from cystic fibrosis patients and the environment.
Journal of applied microbiology | 1999-03-01 | PMID 10196751
Wigley P, Burton N F
Genetic diversity among dairy lactococcal strains investigated by polymerase chain reaction with three arbitrary primers.
Journal of applied microbiology | 1999-03-01 | PMID 10196756
Mangin I, Corroler D, Reinhardt A and 1 more
An improved system for selection of forward mutations in an Escherichia coli supF gene carried by plasmids.
Journal of radiation research | 1998-12-01 | PMID 10196781
Obata F, Nunoshiba T, Hashimoto-Gotoh T and 1 more
Early onset cerebellar ataxia and preservation of tendon reflexes: clinical phenotypes associated with GAA trinucleotide repeat expanded and non-expanded genotypes.
Journal of the peripheral nervous system : JPNS | 1999-01-01 | PMID 10197066
De Castro M, Cruz-Martínez A, Vílchez J J and 4 more
Genes: GAA
A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients.
Clinical endocrinology | 1998-11-01 | PMID 10197076
Kemp E H, Ajjan R A, Husebye E S and 6 more
Beta 3-adrenoreceptor gene polymorphism and leptin. Lack of relationship in type 2 diabetic patients.
Clinical endocrinology | 1998-11-01 | PMID 10197086
Vendrell J, Gutierrez C, Broch M and 3 more
The prevalence of allergic rhinosinusitis: a review.
The Journal of laryngology and otology | 1998-11-01 | PMID 10197137
Jones N S, Carney A S, Davis A
The vestigial gene of Drosophila melanogaster is involved in the formation of the peripheral nervous system: genetic interactions with the scute gene.
Journal of neurogenetics | 1998-03-01 | PMID 10197159
Zider A, Paumard-Rigal S, Frouin I and 1 more
Genetic polymorphism of the angiotensin-converting enzyme (ACE) in asthmatic patients.
Respiratory medicine | 1998-12-01 | PMID 10197222
Tomita H, Sato S, Matsuda R and 4 more
Genes: ACE
Mesenchymal tumors of the gastrointestinal tract: a paradise for acronyms (STUMP, GIST, GANT, and now GIPACT), implication of c-kit in genesis, and yet another of the many emerging roles of the interstitial cell of Cajal in the pathogenesis of gastrointestinal diseases?
Advances in anatomic pathology | 1999-01-01 | PMID 10197236
Chan J K
Lipoprotein (a) and apolipoprotein E epsilon 4 as independent risk factors for ischemic stroke.
Journal of cardiovascular risk | 1999-02-01 | PMID 10197285
Peng D Q, Zhao S P, Wang J L
Genetic polymorphism of platelet glycoprotein IIIa in patients with acute myocardial infarction and acute ischaemic stroke.
Journal of cardiovascular risk | 1999-02-01 | PMID 10197287
Kekomäki S, Hämäläinen L, Kauppinen-Mäkelin R and 3 more
Identification of novel bladder tumour suppressor genes.
Electrophoresis | 1999-02-01 | PMID 10197433
Knowles M A
Mosaic analysis with a repressible cell marker for studies of gene function in neuronal morphogenesis.
Neuron | 1999-03-01 | PMID 10197526
Lee T, Luo L
Synaptic targeting of the postsynaptic density protein PSD-95 mediated by lipid and protein motifs.
Neuron | 1999-03-01 | PMID 10197530
Craven S E, El-Husseini A E, Bredt D S
Genes: PSD
Calmodulin is the Ca2+ sensor for Ca2+ -dependent inactivation of L-type calcium channels.
Neuron | 1999-03-01 | PMID 10197534
Peterson B Z, DeMaria C D, Adelman J P and 1 more
NMDAR channel segments forming the extracellular vestibule inferred from the accessibility of substituted cysteines.
Neuron | 1999-03-01 | PMID 10197535
Beck C, Wollmuth L P, Seeburg P H and 2 more
Architecture of a K+ channel inner pore revealed by stoichiometric covalent modification.
Neuron | 1999-03-01 | PMID 10197536
Lu T, Nguyen B, Zhang X and 1 more
Caspase-8 is required for cell death induced by expanded polyglutamine repeats.
Neuron | 1999-03-01 | PMID 10197541
Sánchez I, Xu C J, Juo P and 3 more
Genes: FADD
Insights from Bcl-2 and Myc: malignancy involves abrogation of apoptosis as well as sustained proliferation.
Cancer research | 1999-04-01 | PMID 10197581
Cory S, Vaux D L, Strasser A and 2 more
The role of chimeric paired box transcription factors in the pathogenesis of pediatric rhabdomysarcoma.
Cancer research | 1999-04-01 | PMID 10197585
Barr F G
Genes: PAX3, PAX7
Developmental basis of retinal-specific induction of cancer by RB mutation.
Cancer research | 1999-04-01 | PMID 10197588
Gallie B L, Campbell C, Devlin H and 2 more
The phenotypes associated with ret mutations in the multiple endocrine neoplasia type 2 syndrome.
Cancer research | 1999-04-01 | PMID 10197589
Ponder B A
Genes: RET
BRCA1, BRCA2, and Rad51 operate in a common DNA damage response pathway.
Cancer research | 1999-04-01 | PMID 10197592
Chen J J, Silver D, Cantor S and 2 more
Genes: BRCA1, BRCA2
Tissue structure, nuclear organization, and gene expression in normal and malignant breast.
Cancer research | 1999-04-01 | PMID 10197593
Bissell M J, Weaver V M, Lelièvre S A and 3 more
Allelotype of gastric adenocarcinoma.
Cancer research | 1999-04-01 | PMID 10197609
Yustein A S, Harper J C, Petroni G R and 3 more
Beta-catenin mutations are more frequent in small colorectal adenomas than in larger adenomas and invasive carcinomas.
Cancer research | 1999-04-01 | PMID 10197610
Samowitz W S, Powers M D, Spirio L N and 3 more
Genes: APC