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
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
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
Cover Page.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 19, p. NP, doi. 10.1093/hmg/ddq345
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
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
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