Works matching IS 09646906 AND DT 2010 AND VI 19 AND IP 16

Results: 20

PTEN depletion rescues axonal growth defect and improves survival in SMN-deficient motor neurons.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3159, doi. 10.1093/hmg/ddq226
By:
- Ning, Ke;
- Drepper, Carsten;
- Valori, Chiara F.;
- Ahsan, Mansoor;
- Wyles, Matthew;
- Higginbottom, Adrian;
- Herrmann, Thomas;
- Shaw, Pamela;
- Azzouz, Mimoun;
- Sendtner, Michael
Publication type:
Article
Impairment of PGC-1alpha expression, neuropathology and hepatic steatosis in a transgenic mouse model of Huntington's disease following chronic energy deprivation.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3190, doi. 10.1093/hmg/ddq229
By:
- Chaturvedi, Rajnish K.;
- Calingasan, Noel Y.;
- Yang, Lichuan;
- Hennessey, Thomas;
- Johri, Ashu;
- Beal, M. Flint
Publication type:
Article
Lactic acidemia in the pathogenesis of mice carrying mitochondrial DNA with a deletion.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3179, doi. 10.1093/hmg/ddq228
By:
- Ogasawara, Emi;
- Nakada, Kazuto;
- Hayashi, Jun-Ichi
Publication type:
Article
The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3114, doi. 10.1093/hmg/ddq214
By:
- Forlani, Greta;
- Giarda, Elisa;
- Ala, Ugo;
- Di Cunto, Ferdinando;
- Salani, Monica;
- Tupler, Rossella;
- Kilstrup-Nielsen, Charlotte;
- Landsberger, Nicoletta
Publication type:
Article
Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patients.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3124, doi. 10.1093/hmg/ddq215
By:
- Rakovic, Aleksandar;
- Grünewald, Anne;
- Seibler, Philip;
- Ramirez, Alfredo;
- Kock, Norman;
- Orolicki, Slobodanka;
- Lohmann, Katja;
- Klein, Christine
Publication type:
Article
Copy number, linkage disequilibrium and disease association in the FCGR locus.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3282, doi. 10.1093/hmg/ddq216
By:
- Niederer, Heather A.;
- Willcocks, Lisa C.;
- Rayner, Tim F.;
- Yang, Wanling;
- Lau, Yu Lung;
- Williams, Thomas N.;
- Scott, J. Anthony G.;
- Urban, Britta C.;
- Peshu, Norbert;
- Dunstan, Sarah J.;
- Hien, Tran Tinh;
- Phu, Nguyen Hoan;
- Padyukov, Leonid;
- Gunnarsson, Iva;
- Svenungsson, Elisabet;
- Savage, Caroline O.;
- Watts, Richard A.;
- Lyons, Paul A.;
- Clayton, David G.;
- Smith, Kenneth G.C.
Publication type:
Article
The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemias.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3150
By:
- Lilljebjörn, Henrik;
- Soneson, Charlotte;
- Andersson, Anna;
- Heldrup, Jesper;
- Behrendtz, Mikael;
- Kawamata, Norihiko;
- Ogawa, Seishi;
- Koeffler, H. Phillip;
- Mitelman, Felix;
- Johansson, Bertil;
- Fontes, Magnus;
- Fioretos, Thoas
Publication type:
Article
Editorial Board.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. NP, doi. 10.1093/hmg/ddq262
Publication type:
Article
Ubiquilin functions in autophagy and is degraded by chaperone-mediated autophagy.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3219, doi. 10.1093/hmg/ddq231
By:
- Rothenberg, Cara;
- Srinivasan, Deepa;
- Mah, Leann;
- Kaushik, Susmita;
- Peterhoff, Corrine M.;
- Ugolino, Janet;
- Fang, Shengyun;
- Cuervo, Ana Maria;
- Nixon, Ralph A.;
- Monteiro, Mervyn J.
Publication type:
Article
Identification of a new NEMO/TRAF6 interface affected in incontinentia pigmenti pathology.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3138, doi. 10.1093/hmg/ddq222
By:
- Gautheron, Jérémie;
- Pescatore, Alessandra;
- Fusco, Francesca;
- Esposito, Elio;
- Yamaoka, Shoji;
- Agou, Fabrice;
- Ursini, Matilde Valeria;
- Courtois, Gilles
Publication type:
Article
Cover Page.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. NP, doi. 10.1093/hmg/ddq261
Publication type:
Article
Mutant HSPB8 causes motor neuron-specific neurite degeneration.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3254, doi. 10.1093/hmg/ddq234
By:
- Irobi, Joy;
- Almeida-Souza, Leonardo;
- Asselbergh, Bob;
- De Winter, Vicky;
- Goethals, Sofie;
- Dierick, Ines;
- Krishnan, Jyothsna;
- Timmermans, Jean-Pierre;
- Robberecht, Wim;
- De Jonghe, Peter;
- Van Den Bosch, Ludo;
- Janssens, Sophie;
- Timmerman, Vincent
Publication type:
Article
Genome-wide identification of mouse congenital heart disease loci.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3105, doi. 10.1093/hmg/ddq211
By:
- Kamp, Anna;
- Peterson, Michael A.;
- Svenson, Karen L.;
- Bjork, Bryan C.;
- Hentges, Kathryn E.;
- Rajapaksha, Tharinda W.;
- Moran, Jennifer;
- Justice, Monica J.;
- Seidman, Jon G.;
- Seidman, Christine E.;
- Moskowitz, Ivan P.;
- Beier, David R.
Publication type:
Article
Neurotoxic effects of TDP-43 overexpression in C. elegans.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3206, doi. 10.1093/hmg/ddq230
By:
- Ash, Peter E.A.;
- Zhang, Yong-Jie;
- Roberts, Christine M.;
- Saldi, Tassa;
- Hutter, Harald;
- Buratti, Emanuele;
- Petrucelli, Leonard;
- Link, Christopher D.
Publication type:
Article
Contents Page.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. NP, doi. 10.1093/hmg/ddq260
Publication type:
Article
Drug screening to identify suppressors of GFAP expression.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3169, doi. 10.1093/hmg/ddq227
By:
- Cho, Woosung;
- Brenner, Michael;
- Peters, Noel;
- Messing, Albee
Publication type:
Article
Site-directed gene repair of the dystrophin gene mediated by PNA–ssODNs.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3266, doi. 10.1093/hmg/ddq235
By:
- Kayali, Refik;
- Bury, Frederic;
- Ballard, McIver;
- Bertoni, Carmen
Publication type:
Article
Subscription Page.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. NP, doi. 10.1093/hmg/ddq263
Publication type:
Article
Integrative gene–tissue microarray-based approach for identification of human disease biomarkers: application to amyotrophic lateral sclerosis.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3233, doi. 10.1093/hmg/ddq232
By:
- Kudo, Lili C.;
- Parfenova, Liubov;
- Vi, Nancy;
- Lau, Kimbley;
- Pomakian, Justine;
- Valdmanis, Paul;
- Rouleau, Guy A.;
- Vinters, Harry V.;
- Wiedau-Pazos, Martina;
- Karsten, Stanislav L.
Publication type:
Article
Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 16, p. 3295, doi. 10.1093/hmg/ddq221
By:
- Corneveaux, Jason J.;
- Myers, Amanda J.;
- Allen, April N.;
- Pruzin, Jeremy J.;
- Ramirez, Manuel;
- Engel, Anzhelika;
- Nalls, Michael A.;
- Chen, Kewei;
- Lee, Wendy;
- Chewning, Kendria;
- Villa, Stephen E.;
- Meechoovet, Hunsar B.;
- Gerber, Jill D.;
- Frost, Danielle;
- Benson, Hollie L.;
- O'Reilly, Sean;
- Chibnik, Lori B.;
- Shulman, Joshua M.;
- Singleton, Andrew B.;
- Craig, David W.
Publication type:
Article