Works matching IS 09646906 AND DT 2008 AND VI 17 AND IP 4

Results: 14

High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 4, p. 617

By:

Kato, Norihiro;
Miyata, Toshiyuki;
Tabara, Yasuharu;
Katsuya, Tomohiro;
Yanai, Kazuyuki;
Hanada, Hironori;
Kamide, Kei;
Nakura, Jun;
Kohara, Katsuhiko;
Takeuchi, Fumihiko;
Mano, Hiroyuki;
Yasunami, Michio;
Kimura, Akinori;
Kita, Yoshikuni;
Ueshima, Hirotsugu;
Nakayama, Tomohiro;
Soma, Masayoshi;
Hata, Akira;
Fujioka, Akihiro;
Kawano, Yuhei

Publication type:

Article

KH-type splicing regulatory protein interacts with survival motor neuron protein and is misregulated in spinal muscular atrophy.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 4, p. 506

By:

Tadesse, Helina;
Deschênes-Furry, Julie;
Boisvenue, Sophie;
Côté, Jocelyn

Publication type:

Article

Zebrafish model of holoprosencephaly demonstrates a key role for TGIF in regulating retinoic acid metabolism.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 4, p. 525, doi. 10.1093/hmg/ddm328

By:

Gongal, Patricia A.;
Waskiewicz, Andrew J.

Publication type:

Article

FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 4, p. 490, doi. 10.1093/hmg/ddm326

By:

Berry, Fred B.;
Skarie, Jonathan M.;
Mirzayans, Farideh;
Fortin, Yannick;
Hudson, Thomas J.;
Raymond, Vincent;
Link, Brian A.;
Walter, Michael A.

Publication type:

Article

Common variation in the ABO glycosyltransferase is associated with susceptibility to severe Plasmodium falciparum malaria.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 4, p. 567, doi. 10.1093/hmg/ddm331

By:

Fry, Andrew E.;
Griffiths, Michael J.;
Auburn, Sarah;
Diakite, Mahamadou;
Forton, Julian T.;
Green, Angela;
Richardson, Anna;
Wilson, Jonathan;
Jallow, Muminatou;
Sisay-Joof, Fatou;
Pinder, Margaret;
Peshu, Norbert;
Williams, Thomas N.;
Marsh, Kevin;
Molyneux, Malcolm E.;
Taylor, Terrie E.;
Rockett, Kirk A.;
Kwiatkowski, Dominic P.

Publication type:

Article

Recombination rates of genes expressed in human tissues.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 4, p. 577, doi. 10.1093/hmg/ddm332

By:

Kato, Mamoru;
Miya, Fuyuki;
Kanemura, Yonehiro;
Tanaka, Toshihiro;
Nakamura, Yusuke;
Tsunoda, Tatsuhiko

Publication type:

Article

Strong evidence that GNB1L is associated with schizophrenia.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 4, p. 555, doi. 10.1093/hmg/ddm330

By:

Williams, Nigel M.;
Glaser, Beate;
Norton, Nadine;
Williams, Hywel;
Pierce, Timothy;
Moskvina, Valentina;
Monks, Stephen;
Del Favero, Jurgen;
Goossens, Dirk;
Rujescu, Dan;
Giegling, Ina;
Kirov, George;
Craddock, Nicholas;
Murphy, Kieran C.;
O'Donovan, Michael C.;
Owen, Michael J.

Publication type:

Article

Identification of TRAF6-dependent NEMO polyubiquitination sites through analysis of a new NEMO mutation causing incontinentia pigmenti.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 4, p. 639

By:

Sebban-Benin, Hélène;
Pescatore, Alessandra;
Fusco, Francesca;
Pascuale, Valérie;
Gautheron, Jérémie;
Yamaoka, Shoji;
Moncla, Anne;
Ursini, Matilde Valeria;
Courtois, Gilles

Publication type:

Article

Pink1 Parkinson mutations, the Cdc37/Hsp90 chaperones and Parkin all influence the maturation or subcellular distribution of Pink1.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 4, p. 602, doi. 10.1093/hmg/ddm334

By:

Weihofen, Andreas;
Ostaszewski, Beth;
Minami, Yasufumi;
Selkoe, Dennis J.

Publication type:

Article

Mouse Fkbp8 activity is required to inhibit cell death and establish dorso-ventral patterning in the posterior neural tube.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 4, p. 587, doi. 10.1093/hmg/ddm333

By:

Wong, Rebecca Lee Yean;
Wlodarczyk, Bogdan J.;
Min, Kyung Soo;
Scott, Melissa L.;
Kartiko, Susan;
Yu, Wei;
Merriweather, Michelle Y.;
Vogel, Peter;
Zambrowicz, Brian P.;
Finnell, Richard H.

Publication type:

Article

The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 4, p. 539, doi. 10.1093/hmg/ddm329

By:

Dobrowolski, Radoslaw;
Sasse, Philipp;
Schrickel, Jan W.;
Watkins, Marcus;
Kim, Jung-Sun;
Rackauskas, Mindaugas;
Troatz, Clemens;
Ghanem, Alexander;
Tiemann, Klaus;
Degen, Joachim;
Bukauskas, Feliksas F.;
Civitelli, Roberto;
Lewalter, Thorsten;
Fleischmann, Bernd K.;
Willecke, Klaus

Publication type:

Article

Recurrent 16p11.2 microdeletions in autism.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 4, p. 628

By:

Kumar, Ravinesh A.;
KaraMohamed, Samer;
Sudi, Jyotsna;
Conrad, Donald F.;
Brune, Camille;
Badner, Judith A.;
Gilliam, T. Conrad;
Nowak, Norma J.;
Cook, Edwin H.;
Dobyns, William B.;
Christian, Susan L.

Publication type:

Article

ER and oxidative stresses are common mediators of apoptosis in both neurodegenerative and non-neurodegenerative lysosomal storage disorders and are alleviated by chemical chaperones.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 4, p. 469, doi. 10.1093/hmg/ddm324

By:

Wei, Hui;
Kim, Sung-Jo;
Zhang, Zhongjian;
Tsai, Pei-Chih;
Wisniewski, Krystyna E.;
Mukherjee, Anil B.

Publication type:

Article

The diabetes-linked transcription factor Pax4 is expressed in human pancreatic islets and is activated by mitogens and GLP-1.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 4, p. 478

By:

Brun, Thierry;
He, Kai Hui Hu;
Lupi, Roberto;
Boehm, Bernhard;
Wojtusciszyn, Anne;
Sauter, Nadine;
Donath, Marc;
Marchetti, Piero;
Maedler, Kathrin;
Gauthier, Benoit R.

Publication type:

Article