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Items: 8

1.

COMT Val158Met genotype influences neurodegeneration within dopamine-innervated brain structures.

Gennatas ED, Cholfin JA, Zhou J, Crawford RK, Sasaki DA, Karydas A, Boxer AL, Bonasera SJ, Rankin KP, Gorno-Tempini ML, Rosen HJ, Kramer JH, Weiner M, Miller BL, Seeley WW.

Neurology. 2012 May 22;78(21):1663-9. doi: 10.1212/WNL.0b013e3182574fa1. Epub 2012 May 9.

2.

Genetic regulation of prefrontal cortex development and function.

Cholfin JA, Rubenstein JL.

Novartis Found Symp. 2007;288:165-73; discussion 173-7, 276-81. Review.

PMID:
18494258
3.

Frontal cortex subdivision patterning is coordinately regulated by Fgf8, Fgf17, and Emx2.

Cholfin JA, Rubenstein JL.

J Comp Neurol. 2008 Jul 10;509(2):144-55. doi: 10.1002/cne.21709.

4.

Abnormal social behaviors in mice lacking Fgf17.

Scearce-Levie K, Roberson ED, Gerstein H, Cholfin JA, Mandiyan VS, Shah NM, Rubenstein JL, Mucke L.

Genes Brain Behav. 2008 Apr;7(3):344-54. Epub 2007 Oct 1.

5.

Patterning of frontal cortex subdivisions by Fgf17.

Cholfin JA, Rubenstein JL.

Proc Natl Acad Sci U S A. 2007 May 1;104(18):7652-7. Epub 2007 Apr 18.

6.

New neurons follow the flow of cerebrospinal fluid in the adult brain.

Sawamoto K, Wichterle H, Gonzalez-Perez O, Cholfin JA, Yamada M, Spassky N, Murcia NS, Garcia-Verdugo JM, Marin O, Rubenstein JL, Tessier-Lavigne M, Okano H, Alvarez-Buylla A.

Science. 2006 Feb 3;311(5761):629-32. Epub 2006 Jan 12.

7.

The SCA12 mutation as a rare cause of spinocerebellar ataxia.

Cholfin JA, Sobrido MJ, Perlman S, Pulst SM, Geschwind DH.

Arch Neurol. 2001 Nov;58(11):1833-5.

PMID:
11708992
8.

SCA8 repeat expansions in ataxia: a controversial association.

Sobrido MJ, Cholfin JA, Perlman S, Pulst SM, Geschwind DH.

Neurology. 2001 Oct 9;57(7):1310-2.

PMID:
11591855

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