Works matching IS 03406717 AND DT 2001 AND VI 108 AND IP 3

Results: 17

A method for sex assignment in mixed samples.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 267, doi. 10.1007/s004390100478

By:

Falconi, Mirella;
Pelotti, Susi;
Pappalardo, Giuseppe

Publication type:

Article

Increased reproductive success of MHC class II heterozygous males among free-ranging rhesus macaques.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 249, doi. 10.1007/s004390100485

By:

Sauermann, Ulrike;
Nürnberg, Peter;
Bercovitch, Fred B.;
Berard, John D.;
Trefilov, Andrea;
Widdig, Anja;
Kessler, Matt;
Schmidtke, Jörg;
Krawczak, Michael

Publication type:

Article

Carrier rate of APC I1307K is not increased in inflammatory bowel disease patients of Ashkenazi Jewish origin.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 205, doi. 10.1007/s004390100474

By:

Silverberg, Mark S.;
Clelland, Catherine;
Murphy, Janet E.;
Steinhart, A. Hillary;
McLeod, Robin S.;
Greenberg, Gordon R.;
Cohen, Zane;
Siminovitch, Katherine A.

Publication type:

Article

The missense Glu298Asp variant of the endothelial nitric oxide synthase gene is strongly associated with placental abruption.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 181, doi. 10.1007/s004390000454

By:

Yoshimura, Toshihiro;
Yoshimura, Michihiro;
Tabata, Ai;
Yasue, Hirofumi;
Okamura, Hitoshi

Publication type:

Article

De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 269, doi. 10.1007/s004390100484

By:

Janecke, Andreas R.;
Nekahm, Doris;
Löffler, Judith;
Hirst-Stadlmann, Almut;
Müller, Thomas;
Utermann, Gerd

Publication type:

Article

CFTR gene mutations – including three novel nucleotide substitutions – and haplotype background in patients with asthma, disseminated bronchiectasis and chronic obstructive pulmonary disease.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 216, doi. 10.1007/s004390100467

By:

Tzetis, Maria;
Efthymiadou, Alexandra;
Strofalis, Stefanos;
Psychou, Photini;
Dimakou, Aikaterini;
Pouliou, Eleni;
Dodounakis, Stavros;
Kanavakis, Emmanuel

Publication type:

Article

Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 237, doi. 10.1007/s004390100469

By:

Neerman-Arbez, M.;
de Moerloose, P.;
Honsberger, A.;
Parlier, G.;
Arnuti, B.;
Biron, C.;
Borg, J.-Y.;
Eber, S.;
Meili, E.;
Peter-Salonen, K.;
Ripoll, L.;
Vervel, C.;
d'Oiron, R.;
Staeger, P.;
Antonarakis, S. E.;
Morris, M. A.

Publication type:

Article

Elite swimmers and the D allele of the ACE I/D polymorphism.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 230, doi. 10.1007/s004390100466

By:

Woods, David;
Hickman, Michelle;
Jamshidi, Yalda;
Brull, David;
Vassiliou, Vassilis;
Jones, Alun;
Humphries, Steve;
Montgomery, Hugh

Publication type:

Article

A single nucleotide polymorphism (SNP) in the leptin receptor is associated with BMI, fat mass and leptin levels in postmenopausal Caucasian women.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 233, doi. 10.1007/s004390100468

By:

Quinton, Naomi;
Lee, Allison J.;
Ross, Richard J. M.;
Eastell, Richard;
Blakemore, Alexandra I. F.

Publication type:

Article

A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH).

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 199, doi. 10.1007/s004390100459

By:

Nietzel, Angela;
Rocchi, Mariano;
Starke, Heike;
Heller, Anita;
Fiedler, Wolfgang;
Wlodarska, Iwona;
Loncarevic, Ivan F.;
Beensen, Volkmar;
Claussen, Uwe;
Liehr, Thomas

Publication type:

Article

SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids: SMN2 is unique to Homo sapiens.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 255, doi. 10.1007/s004390100473

By:

Rochette, C. F.;
Gilbert, N.;
Simard, L. R.

Publication type:

Article

Characterisation of SMN hybrid genes in Spanish SMA patients: de novo, homozygous and compound heterozygous cases.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 222, doi. 10.1007/s004390000452

By:

Cuscó, Ivon;
Barceló, María J.;
del Rio, Elisabeth;
Martín, Yolanda;
Hernández-Chico, Concepción;
Bussaglia, Elena;
Baiget, Montserrat;
Tizzano, Eduardo F.

Publication type:

Article

Cross-sectional study on cytokine polymorphisms, cytokine production after T-cell stimulation and clinical parameters in a random sample of a German population.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 241, doi. 10.1007/s004390100464

By:

Nieters, Alexandra;
Brems, Stefanie;
Becker, Nikolaus

Publication type:

Article

Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 194, doi. 10.1007/s004390100463

By:

Carrieri, Giuseppina;
Bonafè, Massimiliano;
De Luca, Maria;
Rose, Giuseppina;
Varcasia, Ottavia;
Bruni, Amalia;
Maletta, Raffaele;
Nacmias, Benedetta;
Sorbi, Sandro;
Corsonello, Francesco;
Feraco, Emidio;
Andreev, Kirill F.;
Yashin, Anatoli I.;
Franceschi, Claudio;
De Benedictis, Giovanna

Publication type:

Article

Analysis of the CC chemokine receptor 5 (CCR5) delta-32 polymorphism in inflammatory bowel disease.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 190, doi. 10.1007/s004390100462

By:

Rector, Annabel;
Vermeire, Severine;
Thoelen, Inge;
Keyaerts, Els;
Struyf, Frank;
Vlietinck, Robert;
Rutgeerts, Paul;
Van Ranst, Marc

Publication type:

Article

Complex segregation analysis of Parkinson's disease in the Finnish population.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 184, doi. 10.1007/s004390100470

By:

Moilanen, J. S.;
Autere, J. M.;
Myllylä, V. V.;
Majamaa, K.

Publication type:

Article

Genomic organization, chromosomal localization, alternative splicing, and isoforms of the human synaptosome-associated protein-23 gene implicated in vesicle-membrane fusion processes.

Published in:

Human Genetics, 2001, v. 108, n. 3, p. 211, doi. 10.1007/s004390100480

By:

Lazo, Pedro A.;
Nadal, Marga;
Ferrer, Milagros;
Area, Estela;
Hernández-Torres, Javier;
Nabokina, Svetlana M.;
Mollinedo, Faustino;
Estivill, Xavier

Publication type:

Article