Works matching IS 09646906 AND DT 2010 AND VI 19 AND IP 3

Results: 19

Life course variations in the associations between FTO and MC4R gene variants and body size.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 545, doi. 10.1093/hmg/ddp504

By:

Hardy, Rebecca;
Wills, Andrew K.;
Wong, Andrew;
Elks, Cathy E.;
Wareham, Nicholas J.;
Loos, Ruth J.F.;
Kuh, Diana;
Ong, Ken K.

Publication type:

Article

Sox10 gain-of-function causes XX sex reversal in mice: implications for human 22q-linked disorders of sex development.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 506, doi. 10.1093/hmg/ddp520

By:

Polanco, Juan Carlos;
Wilhelm, Dagmar;
Davidson, Tara-Lynne;
Knight, Deon;
Koopman, Peter

Publication type:

Article

Cover Page.

Published in:: Human Molecular Genetics, 2010, v. 19, n. 3, p. NP, doi. 10.1093/hmg/ddp574
Publication type:: Article

Effects of 2,4-diaminoquinazoline derivatives on SMN expression and phenotype in a mouse model for spinal muscular atrophy.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 454, doi. 10.1093/hmg/ddp510

By:

Butchbach, Matthew E.R.;
Singh, Jasbir;
Þorsteinsdóttir, Margrét;
Saieva, Luciano;
Slominski, Elzbieta;
Thurmond, John;
Andrésson, Thorkell;
Zhang, Jun;
Edwards, Jonathan D.;
Simard, Louise R.;
Pellizzoni, Livio;
Jarecki, Jill;
Burghes, Arthur H.M.;
Gurney, Mark E.

Publication type:

Article

The COPD genetic association compendium: a comprehensive online database of COPD genetic associations.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 526, doi. 10.1093/hmg/ddp519

By:

Castaldi, Peter J.;
Cho, Michael H.;
Cohn, Matthew;
Langerman, Fawn;
Moran, Sienna;
Tarragona, Nestor;
Moukhachen, Hala;
Venugopal, Radhika;
Hasimja, Delvina;
Kao, Esther;
Wallace, Byron;
Hersh, Craig P.;
Bagade, Sachin;
Bertram, Lars;
Silverman, Edwin K.;
Trikalinos, Thomas A.

Publication type:

Article

A novel form of cell type-specific partial IFN-γR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 434, doi. 10.1093/hmg/ddp507

By:

Kong, Xiao-Fei;
Vogt, Guillaume;
Chapgier, Ariane;
Lamaze, Christophe;
Bustamante, Jacinta;
Prando, Carolina;
Fortin, Anny;
Puel, Anne;
Feinberg, Jacqueline;
Zhang, Xin-Xin;
Gonnord, Pauline;
Pihkala-Saarinen, Ulla M.;
Arola, Mikko;
Moilanen, Petra;
Abel, Laurent;
Korppi, Matti;
Boisson-Dupuis, Stéphanie;
Casanova, Jean-Laurent

Publication type:

Article

A genome-wide association study identifies GLT6D1 as a susceptibility locus for periodontitis.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 553, doi. 10.1093/hmg/ddp508

By:

Schaefer, Arne S.;
Richter, Gesa M.;
Nothnagel, Michael;
Manke, Thomas;
Dommisch, Henrik;
Jacobs, Gunnar;
Arlt, Alexander;
Rosenstiel, Philip;
Noack, Barbara;
Groessner-Schreiber, Birte;
Jepsen, Søren;
Loos, Bruno G.;
Schreiber, Stefan

Publication type:

Article

Integrative genomics identifies DSCR1 (RCAN1) as a novel NFAT-dependent mediator of phenotypic modulation in vascular smooth muscle cells.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 468, doi. 10.1093/hmg/ddp511

By:

Lee, Monica Y.;
Garvey, Sean M.;
Baras, Alex S.;
Lemmon, Julia A.;
Gomez, Maria F.;
Schoppee Bortz, Pamela D.;
Daum, Guenter;
LeBoeuf, Renee C.;
Wamhoff, Brian R.

Publication type:

Article

Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 535, doi. 10.1093/hmg/ddp522

By:

Perry, John R.B.;
Weedon, Michael N.;
Langenberg, Claudia;
Jackson, Anne U.;
Lyssenko, Valeriya;
Sparsø, Thomas;
Thorleifsson, Gudmar;
Grallert, Harald;
Ferrucci, Luigi;
Maggio, Marcello;
Paolisso, Giuseppe;
Walker, Mark;
Palmer, Colin N.A.;
Payne, Felicity;
Young, Elizabeth;
Herder, Christian;
Narisu, Narisu;
Morken, Mario A.;
Bonnycastle, Lori L.;
Owen, Katharine R.

Publication type:

Article

Drosophila models of peroxisomal biogenesis disorder: peroxins are required for spermatogenesis and very-long-chain fatty acid metabolism.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 494, doi. 10.1093/hmg/ddp518

By:

Chen, Haiyang;
Liu, Zhonghua;
Huang, Xun

Publication type:

Article

Genetic structure of a unique admixed population: implications for medical research.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 411, doi. 10.1093/hmg/ddp505

By:

Patterson, Nick;
Petersen, Desiree C.;
van der Ross, Richard E.;
Sudoyo, Herawati;
Glashoff, Richard H.;
Marzuki, Sangkot;
Reich, David;
Hayes, Vanessa M.

Publication type:

Article

Editorial Board.

Published in:: Human Molecular Genetics, 2010, v. 19, n. 3, p. NP, doi. 10.1093/hmg/ddp576
Publication type:: Article

Overexpression of Hr links excessive induction of Wnt signaling to Marie Unna hereditary hypotrichosis.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 445, doi. 10.1093/hmg/ddp509

By:

Kim, Jeong-Ki;
Kim, Eunmin;
Baek, In-Cheol;
Kim, Bong-Kyu;
Cho, A-Ri;
Kim, Tae-Yoon;
Song, Chang-Woo;
Seong, Je Kyung;
Yoon, Jong-Bok;
Stenn, Kurt S.;
Parimoo, Satish;
Yoon, Sungjoo Kim

Publication type:

Article

Contents Page.

Published in:: Human Molecular Genetics, 2010, v. 19, n. 3, p. NP, doi. 10.1093/hmg/ddp572
Publication type:: Article

Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 420, doi. 10.1093/hmg/ddp506

By:

Murray, Lyndsay M.;
Lee, Sheena;
Bäumer, Dirk;
Parson, Simon H.;
Talbot, Kevin;
Gillingwater, Thomas H.

Publication type:

Article

Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 517, doi. 10.1093/hmg/ddp517

By:

Calafell, Francesc;
Almasy, Laura;
Sabater-Lleal, Maria;
Buil, Alfonso;
Mordillo, Carolina;
Ramírez-Soriano, Anna;
Sikora, Martin;
Souto, Juan Carlos;
Blangero, John;
Fontcuberta, Jordi;
Soria, José Manuel

Publication type:

Article

Tsc/mTORC1 signaling in oocytes governs the quiescence and activation of primordial follicles.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 397, doi. 10.1093/hmg/ddp483

By:

Adhikari, Deepak;
Zheng, Wenjing;
Shen, Yan;
Gorre, Nagaraju;
Hämäläinen, Tuula;
Cooney, Austin J.;
Huhtaniemi, Ilpo;
Lan, Zi-Jian;
Liu, Kui

Publication type:

Article

Subscription Page.

Published in:: Human Molecular Genetics, 2010, v. 19, n. 3, p. NP, doi. 10.1093/hmg/ddp578
Publication type:: Article

Involvement of a novel preimplantation-specific gene encoding the high mobility group box protein Hmgpi in early embryonic development.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 3, p. 480, doi. 10.1093/hmg/ddp512

By:

Yamada, Mitsutoshi;
Hamatani, Toshio;
Akutsu, Hidenori;
Chikazawa, Nana;
Kuji, Naoaki;
Yoshimura, Yasunori;
Umezawa, Akihiro

Publication type:

Article