Walsh CA - Search Results

1

Comment on "Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens".

Yu F, Hill RS, Schaffner SF, Sabeti PC, Wang ET, Mignault AA, Ferland RJ, Moyzis RK, Walsh CA, Reich D. Yu F, et al. Among authors: walsh ca. Science. 2007 Apr 20;316(5823):370. doi: 10.1126/science.316.5823.370a. Science. 2007. PMID: 17446375

2

Regulation of cerebral cortical size by control of cell cycle exit in neural precursors.

Chenn A, Walsh CA. Chenn A, et al. Among authors: walsh ca. Science. 2002 Jul 19;297(5580):365-9. doi: 10.1126/science.1074192. Science. 2002. PMID: 12130776

3

Autosomal recessive form of periventricular heterotopia.

Sheen VL, Topçu M, Berkovic S, Yalnizoglu D, Blatt I, Bodell A, Hill RS, Ganesh VS, Cherry TJ, Shugart YY, Walsh CA. Sheen VL, et al. Among authors: walsh ca. Neurology. 2003 Apr 8;60(7):1108-12. doi: 10.1212/01.wnl.0000055898.00349.02. Neurology. 2003. PMID: 12682315

4

Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain.

Ferland RJ, Cherry TJ, Preware PO, Morrisey EE, Walsh CA. Ferland RJ, et al. Among authors: walsh ca. J Comp Neurol. 2003 May 26;460(2):266-79. doi: 10.1002/cne.10654. J Comp Neurol. 2003. PMID: 12687690

5

Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex.

Sheen VL, Ganesh VS, Topcu M, Sebire G, Bodell A, Hill RS, Grant PE, Shugart YY, Imitola J, Khoury SJ, Guerrini R, Walsh CA. Sheen VL, et al. Among authors: walsh ca. Nat Genet. 2004 Jan;36(1):69-76. doi: 10.1038/ng1276. Epub 2003 Nov 30. Nat Genet. 2004. PMID: 14647276

6

G protein-coupled receptor-dependent development of human frontal cortex.

Piao X, Hill RS, Bodell A, Chang BS, Basel-Vanagaite L, Straussberg R, Dobyns WB, Qasrawi B, Winter RM, Innes AM, Voit T, Ross ME, Michaud JL, Déscarie JC, Barkovich AJ, Walsh CA. Piao X, et al. Among authors: walsh ca. Science. 2004 Mar 26;303(5666):2033-6. doi: 10.1126/science.1092780. Science. 2004. PMID: 15044805

7

Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome.

Ferland RJ, Eyaid W, Collura RV, Tully LD, Hill RS, Al-Nouri D, Al-Rumayyan A, Topcu M, Gascon G, Bodell A, Shugart YY, Ruvolo M, Walsh CA. Ferland RJ, et al. Among authors: walsh ca. Nat Genet. 2004 Sep;36(9):1008-13. doi: 10.1038/ng1419. Epub 2004 Aug 22. Nat Genet. 2004. PMID: 15322546

8

EMX2-independent familial schizencephaly: clinical and genetic analyses.

Tietjen I, Erdogan F, Currier S, Apse K, Chang BS, Hill RS, Lee CK, Walsh CA. Tietjen I, et al. Among authors: walsh ca. Am J Med Genet A. 2005 Jun 1;135(2):166-70. doi: 10.1002/ajmg.a.30734. Am J Med Genet A. 2005. PMID: 15887302

9

Early asymmetry of gene transcription in embryonic human left and right cerebral cortex.

Sun T, Patoine C, Abu-Khalil A, Visvader J, Sum E, Cherry TJ, Orkin SH, Geschwind DH, Walsh CA. Sun T, et al. Among authors: walsh ca. Science. 2005 Jun 17;308(5729):1794-8. doi: 10.1126/science.1110324. Epub 2005 May 12. Science. 2005. PMID: 15894532 Free PMC article.

10

Characterization of Rho-GDIgamma and Rho-GDIalpha mRNA in the developing and mature brain with an analysis of mice with targeted deletions of Rho-GDIgamma.

Ferland RJ, Li X, Buhlmann JE, Bu X, Walsh CA, Lim B. Ferland RJ, et al. Among authors: walsh ca. Brain Res. 2005 Aug 23;1054(1):9-21. doi: 10.1016/j.brainres.2005.04.088. Brain Res. 2005. PMID: 16054116

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