Robertson NG - Search Results

1

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

Bhattacharya SK, Rockwood EJ, Smith SD, Bonilha VL, Crabb JS, Kuchtey RW, Robertson NG, Peachey NS, Morton CC, Crabb JW. Bhattacharya SK, et al. Among authors: robertson ng. J Biol Chem. 2005 Feb 18;280(7):6080-4. doi: 10.1074/jbc.M411233200. Epub 2004 Dec 3. J Biol Chem. 2005. PMID: 15579465 Free PMC article.

2

Mapping and characterization of a novel human myc-like (MYCLK1) sequence.

Robertson NG, Morton CC. Robertson NG, et al. Genomics. 1992 Jun;13(2):449-51. doi: 10.1016/0888-7543(92)90269-x. Genomics. 1992. PMID: 1612604

3

Expression and localization of COL2A1 mRNA and type II collagen in human fetal cochlea.

Khetarpal U, Robertson NG, Yoo TJ, Morton CC. Khetarpal U, et al. Among authors: robertson ng. Hear Res. 1994 Sep;79(1-2):59-73. doi: 10.1016/0378-5955(94)90127-9. Hear Res. 1994. PMID: 7806485

4

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. Genomics. 1997 Dec 15;46(3):345-54. doi: 10.1006/geno.1997.5067. Genomics. 1997. PMID: 9441737

5

Beginning of a molecular era in hearing and deafness.

Robertson NG, Morton CC. Robertson NG, et al. Clin Genet. 1999 Mar;55(3):149-59. doi: 10.1034/j.1399-0004.1999.550303.x. Clin Genet. 1999. PMID: 10334469 Review. No abstract available.

6

Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9.

Robertson NG, Resendes BL, Lin JS, Lee C, Aster JC, Adams JC, Morton CC. Robertson NG, et al. Hum Mol Genet. 2001 Oct 15;10(22):2493-500. doi: 10.1093/hmg/10.22.2493. Hum Mol Genet. 2001. PMID: 11709536

7

Subcellular localisation, secretion, and post-translational processing of normal cochlin, and of mutants causing the sensorineural deafness and vestibular disorder, DFNA9.

Robertson NG, Hamaker SA, Patriub V, Aster JC, Morton CC. Robertson NG, et al. J Med Genet. 2003 Jul;40(7):479-86. doi: 10.1136/jmg.40.7.479. J Med Genet. 2003. PMID: 12843317 Free PMC article.

8

Isolation from cochlea of a novel human intronless gene with predominant fetal expression.

Resendes BL, Kuo SF, Robertson NG, Giersch AB, Honrubia D, Ohara O, Adams JC, Morton CC. Resendes BL, et al. Among authors: robertson ng. J Assoc Res Otolaryngol. 2004 Jun;5(2):185-202. doi: 10.1007/s10162-003-4042-x. J Assoc Res Otolaryngol. 2004. PMID: 15357420 Free PMC article.

9

Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorder.

Makishima T, Rodriguez CI, Robertson NG, Morton CC, Stewart CL, Griffith AJ. Makishima T, et al. Among authors: robertson ng. Hum Genet. 2005 Oct;118(1):29-34. doi: 10.1007/s00439-005-0001-4. Epub 2005 Oct 28. Hum Genet. 2005. PMID: 16078052

10

A novel DFNA9 mutation in the vWFA2 domain of COCH alters a conserved cysteine residue and intrachain disulfide bond formation resulting in progressive hearing loss and site-specific vestibular and central oculomotor dysfunction.

Street VA, Kallman JC, Robertson NG, Kuo SF, Morton CC, Phillips JO. Street VA, et al. Among authors: robertson ng. Am J Med Genet A. 2005 Dec 1;139A(2):86-95. doi: 10.1002/ajmg.a.30980. Am J Med Genet A. 2005. PMID: 16261627

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

39 results

Search Page

Filters