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

Results: 21

Reduced NMDAR1 expression in the Sp4 hypomorphic mouse may contribute to endophenotypes of human psychiatric disorders.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3797, doi. 10.1093/hmg/ddq298

By:

Zhou, Xianjin;
Nie, Zhiguo;
Roberts, Amanda;
Zhang, Dongxian;
Sebat, Jonathan;
Malhotra, Dheeraj;
Kelsoe, John R.;
Geyer, Mark A.

Publication type:

Article

Family-based association analysis of 42 hereditary prostate cancer families identifies the Apolipoprotein L3 region on chromosome 22q12 as a risk locus.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3852, doi. 10.1093/hmg/ddq283

By:

Johanneson, Bo;
McDonnell, Shannon K.;
Karyadi, Danielle M.;
Quignon, Pascale;
McIntosh, Laura;
Riska, Shaun M.;
FitzGerald, Liesel M.;
Johnson, Gregory;
Deutsch, Kerry;
Williams, Gabrielle;
Tillmans, Lori S.;
Stanford, Janet L.;
Schaid, Daniel J.;
Thibodeau, Stephen N.;
Ostrander, Elaine A.

Publication type:

Article

Early autophagic response in a novel knock-in model of Huntington disease.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3702, doi. 10.1093/hmg/ddq285

By:

Heng, Mary Y.;
Duong, Duy K.;
Albin, Roger L.;
Tallaksen-Greene, Sara J.;
Hunter, Jesse M.;
Lesort, Mathieu J.;
Osmand, Alex;
Paulson, Henry L.;
Detloff, Peter J.

Publication type:

Article

Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3721, doi. 10.1093/hmg/ddq286

By:

Lee, Yi-Ching;
Huang, Hsun-Yi;
Chang, Chia-Jung;
Cheng, Chao-Hung;
Chen, Yuan-Tsong

Publication type:

Article

Interaction between parkin and mutant glucocerebrosidase variants: a possible link between Parkinson disease and Gaucher disease.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3771, doi. 10.1093/hmg/ddq292

By:

Ron, Idit;
Rapaport, Debora;
Horowitz, Mia

Publication type:

Article

Contents Page.

Published in:: Human Molecular Genetics, 2010, v. 19, n. 19, p. NP, doi. 10.1093/hmg/ddq344
Publication type:: Article

Characterization of the human HSC20, an unusual DnaJ type III protein, involved in iron–sulfur cluster biogenesis.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3816, doi. 10.1093/hmg/ddq301

By:

Uhrigshardt, Helge;
Singh, Anamika;
Kovtunovych, Gennadiy;
Ghosh, Manik;
Rouault, Tracey A.

Publication type:

Article

Systemic transplantation of c-kit+ cells exerts a therapeutic effect in a model of amyotrophic lateral sclerosis.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3782, doi. 10.1093/hmg/ddq293

By:

Corti, Stefania;
Nizzardo, Monica;
Nardini, Martina;
Donadoni, Chiara;
Salani, Sabrina;
Simone, Chiara;
Falcone, Marianna;
Riboldi, Giulietta;
Govoni, Alessandra;
Bresolin, Nereo;
Comi, Giacomo P.

Publication type:

Article

Comprehensive analysis of common genetic variation in 61 genes related to steroid hormone and insulin-like growth factor-I metabolism and breast cancer risk in the NCI breast and prostate cancer cohort consortium†.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3873, doi. 10.1093/hmg/ddq291

By:

Canzian, Federico;
Cox, David G.;
Setiawan, V. Wendy;
Stram, Daniel O.;
Ziegler, Regina G.;
Dossus, Laure;
Beckmann, Lars;
Blanché, Hélène;
Barricarte, Aurelio;
Berg, Christine D.;
Bingham, Sheila;
Buring, Julie;
Buys, Saundra S.;
Calle, Eugenia E.;
Chanock, Stephen J.;
Clavel-Chapelon, Françoise;
DeLancey, John Oliver L.;
Diver, W. Ryan;
Dorronsoro, Miren;
Haiman, Christopher A.

Publication type:

Article

Dysregulation of hypoxia pathways in fumarate hydratase-deficient cells is independent of defective mitochondrial metabolism.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3844, doi. 10.1093/hmg/ddq305

By:

O'Flaherty, Linda;
Adam, Julie;
Heather, Lisa C.;
Zhdanov, Alexander V.;
Chung, Yuen-Li;
Miranda, Melroy X.;
Croft, Joanne;
Olpin, Simon;
Clarke, Kieran;
Pugh, Christopher W.;
Griffiths, John;
Papkovsky, Dmitri;
Ashrafian, Houman;
Ratcliffe, Peter J.;
Pollard, Patrick J.

Publication type:

Article

Locus category based analysis of a large genome-wide association study of rheumatoid arthritis.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3863, doi. 10.1093/hmg/ddq304

By:

Freudenberg, Jan;
Lee, Annette T.;
Siminovitch, Katherine A.;
Amos, Christopher I.;
Ballard, David;
Li, Wentian;
Gregersen, Peter K.

Publication type:

Article

Deducing the pathogenic contribution of recessive ABCA4 alleles in an outbred population.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3693, doi. 10.1093/hmg/ddq284

By:

Schindler, Emily I.;
Nylen, Erik L.;
Ko, Audrey C.;
Affatigato, Louisa M.;
Heggen, Andrew C.;
Wang, Kai;
Sheffield, Val C.;
Stone, Edwin M.

Publication type:

Article

Cover Page.

Published in:: Human Molecular Genetics, 2010, v. 19, n. 19, p. NP, doi. 10.1093/hmg/ddq345
Publication type:: Article

Activation of FoxO by LRRK2 induces expression of proapoptotic proteins and alters survival of postmitotic dopaminergic neuron in Drosophila.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3747, doi. 10.1093/hmg/ddq289

By:

Kanao, Tomoko;
Venderova, Katerina;
Park, David S.;
Unterman, Terry;
Lu, Bingwei;
Imai, Yuzuru

Publication type:

Article

Genome-wide association analysis identifies multiple loci related to resting heart rate.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3885, doi. 10.1093/hmg/ddq303

By:

Eijgelsheim, Mark;
Newton-Cheh, Christopher;
Sotoodehnia, Nona;
de Bakker, Paul I.W.;
Müller, Martina;
Morrison, Alanna C.;
Smith, Albert V.;
Isaacs, Aaron;
Sanna, Serena;
Dörr, Marcus;
Navarro, Pau;
Fuchsberger, Christian;
Nolte, Ilja M.;
de Geus, Eco J.C.;
Estrada, Karol;
Hwang, Shih-Jen;
Bis, Joshua C.;
Rückert, Ina-Maria;
Alonso, Alvaro;
Launer, Lenore J.

Publication type:

Article

The Rps23rg gene family originated through retroposition of the ribosomal protein s23 mRNA and encodes proteins that decrease Alzheimer's β-amyloid level and tau phosphorylation.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3835, doi. 10.1093/hmg/ddq302

By:

Huang, Xiumei;
Chen, Yaomin;
Li, Wu-Bo;
Cohen, Stanley N.;
Liao, Francesca-Fang;
Li, Limin;
Xu, Huaxi;
Zhang, Yun-wu

Publication type:

Article

TRAF6 promotes atypical ubiquitination of mutant DJ-1 and alpha-synuclein and is localized to Lewy bodies in sporadic Parkinson's disease brains.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3759, doi. 10.1093/hmg/ddq290

By:

Zucchelli, Silvia;
Codrich, Marta;
Marcuzzi, Federica;
Pinto, Milena;
Vilotti, Sandra;
Biagioli, Marta;
Ferrer, Isidro;
Gustincich, Stefano

Publication type:

Article

Loss of the Parkinson's disease-linked gene DJ-1 perturbs mitochondrial dynamics.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3734, doi. 10.1093/hmg/ddq288

By:

Irrcher, I.;
Aleyasin, H.;
Seifert, E.L.;
Hewitt, S.J.;
Chhabra, S.;
Phillips, M.;
Lutz, A.K.;
Rousseaux, M.W.C.;
Bevilacqua, L.;
Jahani-Asl, A.;
Callaghan, S.;
MacLaurin, J.G.;
Winklhofer, K.F.;
Rizzu, P.;
Rippstein, P.;
Kim, R.H.;
Chen, C.X.;
Fon, E.A.;
Slack, R.S.;
Harper, M.E.

Publication type:

Article

Mutant WDR36 directly affects axon growth of retinal ganglion cells leading to progressive retinal degeneration in mice.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 19, p. 3806, doi. 10.1093/hmg/ddq299

By:

Chi, Zai-Long;
Yasumoto, Fumie;
Sergeev, Yuri;
Minami, Masayoshi;
Obazawa, Minoru;
Kimura, Itaru;
Takada, Yuichiro;
Iwata, Takeshi

Publication type:

Article

Editorial Board.

Published in:: Human Molecular Genetics, 2010, v. 19, n. 19, p. NP, doi. 10.1093/hmg/ddq346
Publication type:: Article

Subscription Page.

Published in:: Human Molecular Genetics, 2010, v. 19, n. 19, p. NP, doi. 10.1093/hmg/ddq347
Publication type:: Article