Friedman TB - Search Results

1

Chromosomal locations of three human nuclear genes (RPSM12, TUFM, and AFG3L1) specifying putative components of the mitochondrial gene expression apparatus.

Shah ZH, Migliosi V, Miller SC, Wang A, Friedman TB, Jacobs HT. Shah ZH, et al. Among authors: friedman tb. Genomics. 1998 Mar 15;48(3):384-8. doi: 10.1006/geno.1997.5166. Genomics. 1998. PMID: 9545647

2

A physical map of the mouse shaker-2 region contains many of the genes commonly deleted in Smith-Magenis syndrome (del17p11.2p11.2).

Probst FJ, Chen KS, Zhao Q, Wang A, Friedman TB, Lupski JR, Camper SA. Probst FJ, et al. Among authors: friedman tb. Genomics. 1999 Feb 1;55(3):348-52. doi: 10.1006/geno.1998.5669. Genomics. 1999. PMID: 10049592

3

Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2.

Liang Y, Wang A, Belyantseva IA, Anderson DW, Probst FJ, Barber TD, Miller W, Touchman JW, Jin L, Sullivan SL, Sellers JR, Camper SA, Lloyd RV, Kachar B, Friedman TB, Fridell RA. Liang Y, et al. Among authors: friedman tb. Genomics. 1999 Nov 1;61(3):243-58. doi: 10.1006/geno.1999.5976. Genomics. 1999. PMID: 10552926

4

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

Wang A, Liang Y, Fridell RA, Probst FJ, Wilcox ER, Touchman JW, Morton CC, Morell RJ, Noben-Trauth K, Camper SA, Friedman TB. Wang A, et al. Among authors: friedman tb. Science. 1998 May 29;280(5368):1447-51. doi: 10.1126/science.280.5368.1447. Science. 1998. PMID: 9603736

5

Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2.

Liang Y, Wang A, Probst FJ, Arhya IN, Barber TD, Chen KS, Deshmukh D, Dolan DF, Hinnant JT, Carter LE, Jain PK, Lalwani AK, Li XC, Lupski JR, Moeljopawiro S, Morell R, Negrini C, Wilcox ER, Winata S, Camper SA, Friedman TB. Liang Y, et al. Among authors: friedman tb. Am J Hum Genet. 1998 Apr;62(4):904-15. doi: 10.1086/301786. Am J Hum Genet. 1998. PMID: 9529344 Free PMC article.

6

Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia.

Innis JW, Asher JH Jr, Liang Y, Wang A, Wilke CM, Dierick HA, Kazen-Gillespie K, Sheldon S, Glover TW, Friedman TB. Innis JW, et al. Among authors: friedman tb. Am J Med Genet. 1997 Aug 22;71(3):292-7. Am J Med Genet. 1997. PMID: 9268099 Free article.

7

A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25.

Morell RJ, Friderici KH, Wei S, Elfenbein JL, Friedman TB, Fisher RA. Morell RJ, et al. Among authors: friedman tb. Genomics. 2000 Jan 1;63(1):1-6. doi: 10.1006/geno.1999.6058. Genomics. 2000. PMID: 10662538

8

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

Probst FJ, Fridell RA, Raphael Y, Saunders TL, Wang A, Liang Y, Morell RJ, Touchman JW, Lyons RH, Noben-Trauth K, Friedman TB, Camper SA. Probst FJ, et al. Among authors: friedman tb. Science. 1998 May 29;280(5368):1444-7. doi: 10.1126/science.280.5368.1444. Science. 1998. PMID: 9603735

9

Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner ear.

Peters LM, Belyantseva IA, Lagziel A, Battey JF, Friedman TB, Morell RJ. Peters LM, et al. Among authors: friedman tb. Genomics. 2007 Feb;89(2):197-206. doi: 10.1016/j.ygeno.2006.09.006. Epub 2006 Oct 17. Genomics. 2007. PMID: 17049805 Free PMC article.

10

Effects of Pax3 modifier genes on craniofacial morphology, pigmentation, and viability: a murine model of Waardenburg syndrome variation.

Asher JH Jr, Harrison RW, Morell R, Carey ML, Friedman TB. Asher JH Jr, et al. Among authors: friedman tb. Genomics. 1996 Jun 15;34(3):285-98. doi: 10.1006/geno.1996.0289. Genomics. 1996. PMID: 8786127

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