Publications

Casein kinase id mutations in familial migraine and advanced sleep phase.

Brennan KC, Bates EA, Shapiro RE, Zyuzin J, Hallows WC, Huang Y, Lee HY, Jones CR, Fu YH, Charles AC, Ptácek LJ

2013
Loss of Gsx1 and Gsx2 function rescues distinct phenotypes in Dlx1/2 mutants.

Wang B, Long JE, Flandin P, Pla R, Waclaw RR, Campbell K, Rubenstein JL

2013
Stimulating the Prefrontal Cortex to Undo Stimulant Addiction.

Vikaas S. Sohal

2013
Abstract A08: Systematic identification of genetic vulnerabilities synergizing with proteasome and IRE1 inhibition in multiple myeloma cells using ultra-complex shRNA libraries.

Diego Acosta-Alvear, Martin Kampmann, Michael C. Bassik, Crystal P. Lee, Marc A. Shuman, Jonathan S. Weissman, Peter Walter

2013
Abstract PR06: Systematic genetic interaction maps reveal synthetic-lethal vulnerabilities in leukemia and multiple myeloma.

Martin Kampmann, Diego Acosta-Alvear, Michael C. Bassik, Yuwen Chen, Peter Walter, Jonathan S. Weissman

2013
Nuclear localization of the mitochondrial factor HIGD1A during metabolic stress.

Ameri K, Rajah AM, Nguyen V, Sanders TA, Jahangiri A, Delay M, Donne M, Choi HJ, Tormos KV, Yeghiazarians Y, Jeffrey SS, Rinaudo PF, Rowitch DH, Aghi M, Maltepe E

2013
Episodic neurologic disorders: syndromes, genes, and mechanisms.

Russell JF, Fu YH, Ptácek LJ

2013
Episodic neurologic disorders: syndromes, genes, and mechanisms.

Russell JF, Fu YH, Ptácek LJ

2013
Mutations in protein N-arginine methyltransferases are not the cause of FTLD-FUS.

Ravenscroft TA, Baker MC, Rutherford NJ, Neumann M, Mackenzie IR, Josephs KA, Boeve BF, Petersen R, Halliday GM, Kril J, van Swieten JC, Seeley WW, Dickson DW, Rademakers R

2013
Mutations in protein N-arginine methyltransferases are not the cause of FTLD-FUS.

Ravenscroft TA, Baker MC, Rutherford NJ, Neumann M, Mackenzie IR, Josephs KA, Boeve BF, Petersen R, Halliday GM, Kril J, van Swieten JC, Seeley WW, Dickson DW, Rademakers R

2013

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