Skvorak AB - Search Results

1

Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21.

Greinwald JH Jr, Scott DA, Marietta JR, Carmi R, Manaligod J, Ramesh A, Zbar RI, Kraft ML, Elbedour K, Yairi Y, Musy M, Skvorak AB, Van Camp G, Srisailapathy CR, Lovett M, Morton CC, Sheffield VC, Smith RJ. Greinwald JH Jr, et al. Among authors: skvorak ab. Genome Res. 1997 Sep;7(9):879-86. doi: 10.1101/gr.7.9.879. Genome Res. 1997. PMID: 9314493 Free article.

2

Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness.

Skvorak AB, Weng Z, Yee AJ, Robertson NG, Morton CC. Skvorak AB, et al. Hum Mol Genet. 1999 Mar;8(3):439-52. doi: 10.1093/hmg/8.3.439. Hum Mol Genet. 1999. PMID: 9949203

3

Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9.

Robertson NG, Skvorak AB, Yin Y, Weremowicz S, Johnson KR, Kovatch KA, Battey JF, Bieber FR, Morton CC. Robertson NG, et al. Among authors: skvorak ab. Genomics. 1997 Dec 15;46(3):345-54. doi: 10.1006/geno.1997.5067. Genomics. 1997. PMID: 9441737

4

Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans.

Vahava O, Morell R, Lynch ED, Weiss S, Kagan ME, Ahituv N, Morrow JE, Lee MK, Skvorak AB, Morton CC, Blumenfeld A, Frydman M, Friedman TB, King MC, Avraham KB. Vahava O, et al. Among authors: skvorak ab. Science. 1998 Mar 20;279(5358):1950-4. doi: 10.1126/science.279.5358.1950. Science. 1998. PMID: 9506947

5

Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice.

Avraham KB, Hasson T, Sobe T, Balsara B, Testa JR, Skvorak AB, Morton CC, Copeland NG, Jenkins NA. Avraham KB, et al. Among authors: skvorak ab. Hum Mol Genet. 1997 Aug;6(8):1225-31. doi: 10.1093/hmg/6.8.1225. Hum Mol Genet. 1997. PMID: 9259267

6

An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1).

Skvorak AB, Robertson NG, Yin Y, Weremowicz S, Her H, Bieber FR, Beisel KW, Lynch ED, Beier DR, Morton CC. Skvorak AB, et al. Genomics. 1997 Dec 1;46(2):191-9. doi: 10.1006/geno.1997.5026. Genomics. 1997. PMID: 9417906

7

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness.

Karet FE, Finberg KE, Nelson RD, Nayir A, Mocan H, Sanjad SA, Rodriguez-Soriano J, Santos F, Cremers CW, Di Pietro A, Hoffbrand BI, Winiarski J, Bakkaloglu A, Ozen S, Dusunsel R, Goodyer P, Hulton SA, Wu DK, Skvorak AB, Morton CC, Cunningham MJ, Jha V, Lifton RP. Karet FE, et al. Among authors: skvorak ab. Nat Genet. 1999 Jan;21(1):84-90. doi: 10.1038/5022. Nat Genet. 1999. PMID: 9916796

8

Monoclonal antibodies to yeast poly(A) polymerase (PAP) provide evidence for association of PAP with cleavage factor I.

Kessler MM, Zhelkovsky AM, Skvorak A, Moore CL. Kessler MM, et al. Biochemistry. 1995 Feb 7;34(5):1750-9. doi: 10.1021/bi00005a032. Biochemistry. 1995. PMID: 7849035

9

Oxidation of rat insulin II, but not I, leads to anomalous elution profiles upon HPLC analysis of insulin-related peptides.

Gross D, Skvorak A, Hendrick G, Weir G, Villa-Komaroff L, Halban P. Gross D, et al. FEBS Lett. 1988 Dec 5;241(1-2):205-8. doi: 10.1016/0014-5793(88)81062-7. FEBS Lett. 1988. PMID: 3058512 Free article.

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