Tempel BL - Search Results

1

Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathies.

Street VA, Goldy JD, Golden AS, Tempel BL, Bird TD, Chance PF. Street VA, et al. Among authors: tempel bl. Am J Hum Genet. 2002 Jan;70(1):244-50. doi: 10.1086/337943. Epub 2001 Nov 16. Am J Hum Genet. 2002. PMID: 11713717 Free PMC article.

2

Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C.

Street VA, Bennett CL, Goldy JD, Shirk AJ, Kleopa KA, Tempel BL, Lipe HP, Scherer SS, Bird TD, Chance PF. Street VA, et al. Among authors: tempel bl. Neurology. 2003 Jan 14;60(1):22-6. doi: 10.1212/wnl.60.1.22. Neurology. 2003. PMID: 12525712

3

Physical mapping of potassium channel gene clusters on mouse chromosomes three and six.

Street VA, Tempel BL. Street VA, et al. Among authors: tempel bl. Genomics. 1997 Aug 15;44(1):110-7. doi: 10.1006/geno.1997.4799. Genomics. 1997. PMID: 9286706

4

Physical and genetic maps of the deafwaddler region on distal mouse Chr 6.

McKee-Johnson JW, Street VA, Erford SK, Robinson LC, Tempel BL. McKee-Johnson JW, et al. Among authors: tempel bl. Genomics. 1998 May 1;49(3):371-7. doi: 10.1006/geno.1998.5274. Genomics. 1998. PMID: 9615221

5

Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice.

Street VA, McKee-Johnson JW, Fonseca RC, Tempel BL, Noben-Trauth K. Street VA, et al. Among authors: tempel bl. Nat Genet. 1998 Aug;19(4):390-4. doi: 10.1038/1284. Nat Genet. 1998. PMID: 9697703

6

Molecular genetic analysis of distal mouse chromosome 6 defines gene order and positions of the deafwaddler and opisthotonos mutations.

Street VA, Robinson LC, Erford SK, Tempel BL. Street VA, et al. Among authors: tempel bl. Genomics. 1995 Sep 1;29(1):123-30. doi: 10.1006/geno.1995.1222. Genomics. 1995. PMID: 8530061

7

Genomic structure, sequence, and physiological expression of mKv 1.5, a mouse potassium channel gene.

Street VA, Hopkins WF, Tempel BL. Street VA, et al. Among authors: tempel bl. Epilepsy Res Suppl. 1996;12:165-75. Epilepsy Res Suppl. 1996. PMID: 9302515 No abstract available.

8

Resistance to noise-induced hearing loss in 129S6 and MOLF mice: identification of independent, overlapping, and interacting chromosomal regions.

Street VA, Kujawa SG, Manichaikul A, Broman KW, Kallman JC, Shilling DJ, Iwata AJ, Robinson LC, Robbins CA, Li J, Liberman MC, Tempel BL. Street VA, et al. Among authors: tempel bl. J Assoc Res Otolaryngol. 2014 Oct;15(5):721-38. doi: 10.1007/s10162-014-0472-x. Epub 2014 Jun 21. J Assoc Res Otolaryngol. 2014. PMID: 24952082 Free PMC article.

9

Cloning, sequence and chromosomal localization of MK6, a murine potassium channel gene.

Migeon MB, Street VA, Demas VP, Tempel BL. Migeon MB, et al. Among authors: tempel bl. Epilepsy Res Suppl. 1992;9:173-80; discussion 180-1. Epilepsy Res Suppl. 1992. PMID: 1285906 No abstract available.

10

The type 1 inositol 1,4,5-trisphosphate receptor gene is altered in the opisthotonos mouse.

Street VA, Bosma MM, Demas VP, Regan MR, Lin DD, Robinson LC, Agnew WS, Tempel BL. Street VA, et al. Among authors: tempel bl. J Neurosci. 1997 Jan 15;17(2):635-45. doi: 10.1523/JNEUROSCI.17-02-00635.1997. J Neurosci. 1997. PMID: 8987786 Free PMC article.

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