Banfi S - Search Results

1

Proprioceptor pathway development is dependent on Math1.

Bermingham NA, Hassan BA, Wang VY, Fernandez M, Banfi S, Bellen HJ, Fritzsch B, Zoghbi HY. Bermingham NA, et al. Among authors: banfi s. Neuron. 2001 May;30(2):411-22. doi: 10.1016/s0896-6273(01)00305-1. Neuron. 2001. PMID: 11395003 Free article.

2

Molecular genetics of hereditary ataxias.

Banfi S, Zoghbi HY. Banfi S, et al. Baillieres Clin Neurol. 1994 Aug;3(2):281-95. Baillieres Clin Neurol. 1994. PMID: 7952848 Review.

3

Detection of chimerism in YAC clones.

Banfi S, Zoghbi HY. Banfi S, et al. Methods Mol Biol. 1996;54:115-21. doi: 10.1385/0-89603-313-9:115. Methods Mol Biol. 1996. PMID: 8597782 No abstract available.

4

Cloning and developmental expression analysis of the murine homolog of the spinocerebellar ataxia type 1 gene (Sca1).

Banfi S, Servadio A, Chung M, Capozzoli F, Duvick LA, Elde R, Zoghbi HY, Orr HT. Banfi S, et al. Hum Mol Genet. 1996 Jan;5(1):33-40. doi: 10.1093/hmg/5.1.33. Hum Mol Genet. 1996. PMID: 8789437

5

An easy and rapid method for the detection of chimeric yeast artificial chromosome clones.

Banfi S, Ledbetter SA, Chinault AC, Zoghbi HY. Banfi S, et al. Nucleic Acids Res. 1992 Apr 11;20(7):1814. doi: 10.1093/nar/20.7.1814. Nucleic Acids Res. 1992. PMID: 1579482 Free PMC article.

6

Mice lacking ataxin-1 display learning deficits and decreased hippocampal paired-pulse facilitation.

Matilla A, Roberson ED, Banfi S, Morales J, Armstrong DL, Burright EN, Orr HT, Sweatt JD, Zoghbi HY, Matzuk MM. Matilla A, et al. Among authors: banfi s. J Neurosci. 1998 Jul 15;18(14):5508-16. doi: 10.1523/JNEUROSCI.18-14-05508.1998. J Neurosci. 1998. PMID: 9651231 Free PMC article.

7

Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 Mb.

Banfi S, Chung MY, Kwiatkowski TJ Jr, Ranum LP, McCall AE, Chinault AC, Orr HT, Zoghbi HY. Banfi S, et al. Genomics. 1993 Dec;18(3):627-35. doi: 10.1016/s0888-7543(05)80365-9. Genomics. 1993. PMID: 8307572

8

Identification and characterization of the gene causing type 1 spinocerebellar ataxia.

Banfi S, Servadio A, Chung MY, Kwiatkowski TJ Jr, McCall AE, Duvick LA, Shen Y, Roth EJ, Orr HT, Zoghbi HY. Banfi S, et al. Nat Genet. 1994 Aug;7(4):513-20. doi: 10.1038/ng0894-513. Nat Genet. 1994. PMID: 7951322

9

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

Orr HT, Chung MY, Banfi S, Kwiatkowski TJ Jr, Servadio A, Beaudet AL, McCall AE, Duvick LA, Ranum LP, Zoghbi HY. Orr HT, et al. Among authors: banfi s. Nat Genet. 1993 Jul;4(3):221-6. doi: 10.1038/ng0793-221. Nat Genet. 1993. PMID: 8358429

10

Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset.

Ranum LP, Chung MY, Banfi S, Bryer A, Schut LJ, Ramesar R, Duvick LA, McCall A, Subramony SH, Goldfarb L, et al. Ranum LP, et al. Among authors: banfi s. Am J Hum Genet. 1994 Aug;55(2):244-52. Am J Hum Genet. 1994. PMID: 8037204 Free PMC article.

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