Robertson NG - Search Results

1

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.

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

Testis-specific expression of the human MYCL2 gene.

Robertson NG, Pomponio RJ, Mutter GL, Morton CC. Robertson NG, et al. Nucleic Acids Res. 1991 Jun 11;19(11):3129-37. doi: 10.1093/nar/19.11.3129. Nucleic Acids Res. 1991. PMID: 1711681 Free PMC article.

4

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

5

Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening.

Robertson NG, Khetarpal U, Gutiérrez-Espeleta GA, Bieber FR, Morton CC. Robertson NG, et al. Genomics. 1994 Sep 1;23(1):42-50. doi: 10.1006/geno.1994.1457. Genomics. 1994. PMID: 7829101

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. Among authors: robertson ng. Genomics. 1997 Dec 1;46(2):191-9. doi: 10.1006/geno.1997.5026. Genomics. 1997. PMID: 9417906

7

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

8

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction.

Robertson NG, Lu L, Heller S, Merchant SN, Eavey RD, McKenna M, Nadol JB Jr, Miyamoto RT, Linthicum FH Jr, Lubianca Neto JF, Hudspeth AJ, Seidman CE, Morton CC, Seidman JG. Robertson NG, et al. Nat Genet. 1998 Nov;20(3):299-303. doi: 10.1038/3118. Nat Genet. 1998. PMID: 9806553

9

A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects.

de Kok YJ, Bom SJ, Brunt TM, Kemperman MH, van Beusekom E, van der Velde-Visser SD, Robertson NG, Morton CC, Huygen PL, Verhagen WI, Brunner HG, Cremers CW, Cremers FP. de Kok YJ, et al. Among authors: robertson ng. Hum Mol Genet. 1999 Feb;8(2):361-6. doi: 10.1093/hmg/8.2.361. Hum Mol Genet. 1999. PMID: 9931344

10

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. Among authors: robertson ng. Hum Mol Genet. 1999 Mar;8(3):439-52. doi: 10.1093/hmg/8.3.439. Hum Mol Genet. 1999. PMID: 9949203

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