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Beginning of a molecular era in hearing and deafness.
Published in:
Clinical Genetics, 2000, p. 39, doi. 10.1034/j.1399-0004.2000.57SI04.x
By:
- Robertson, Nahid G.;
- Morton, Cynthia C.
Publication type:
Article
Beginning of a molecular era in hearing and deafness.
Published in:
Clinical Genetics, 1999, v. 57, p. 39, doi. 10.1034/j.1399-0004.2000.57si04.x
By:
- Robertson, Nahid G;
- Morton, Cynthia C
Publication type:
Article
Beginning of a molecular era in hearing and deafness.
Published in:
Clinical Genetics, 1999, v. 55, n. 3, p. 149, doi. 10.1034/j.1399-0004.1999.550303.x
By:
- Robertson, Nahid G;
- Morton, Cynthia C
Publication type:
Article
Cochlin in normal middle ear and abnormal middle ear deposits in DFNA9 and Coch (G88E/G88E) mice.
Published in:
2014
By:
- Robertson, Nahid G;
- O'Malley, Jennifer T;
- Ong, Cheng Ai;
- Giersch, Anne B S;
- Shen, Jun;
- Stankovic, Konstantina M;
- Morton, Cynthia C
Publication type:
journal article
Characterization of an abundant COL9A1 transcript in the cochlea with a novel 3' UTR: Expression studies and detection of miRNA target sequence.
Published in:
2006
By:
- Sivakumaran, Theru A.;
- Resendes, Barbara L.;
- Robertson, Nahid G.;
- Giersch, Anne B. S.;
- Morton, Cynthia C.
Publication type:
journal article
Isolation from cochlea of a novel human intronless gene with predominant fetal expression.
Published in:
2004
By:
- Resendes, Barbara L.;
- Kuo, Sharon F.;
- Robertson, Nahid G.;
- Giersch, Anne B.S.;
- Honrubia, Dynio;
- Ohara, Osamu;
- Adams, Joe C.;
- Morton, Cynthia C.
Publication type:
journal article
Corrigendum: Loss of LDAH associated with prostate cancer and hearing loss.
Published in:
Human Molecular Genetics, 2019, v. 28, n. 10, p. 1753, doi. 10.1093/hmg/ddz036
By:
- Currall, Benjamin B;
- Chen, Ming;
- Sallari, Richard C;
- Cotter, Maura;
- Wong, Kristen E;
- Robertson, Nahid G;
- Penney, Kathryn L;
- Lunardi, Andrea;
- Reschke, Markus;
- Hickox, Ann E;
- Yin, Yanbo;
- Wong, Garrett T;
- Fung, Jacqueline;
- Brown, Kerry K;
- Williamson, Robin E;
- Sinnott-Armstrong, Nicholas A;
- Kammin, Tammy;
- Ivanov, Andrew;
- Zepeda-Mendoza, Cinthya J;
- Shen, Jun
Publication type:
Article
Loss of LDAH associated with prostate cancer and hearing loss.
Published in:
Human Molecular Genetics, 2018, v. 27, n. 24, p. 4194, doi. 10.1093/hmg/ddy310
By:
- Currall, Benjamin B;
- Chen, Ming;
- Sallari, Richard C;
- Cotter, Maura;
- Wong, Kristen E;
- Robertson, Nahid G;
- Penney, Kathryn L;
- Lunardi, Andrea;
- Reschke, Markus;
- Hickox, Ann E
Publication type:
Article
Cochlin Deficiency Protects Against Noise-Induced Hearing Loss.
Published in:
Frontiers in Molecular Neuroscience, 2021, v. 13, p. 1, doi. 10.3389/fnmol.2021.670013
By:
- Seist, Richard;
- Landegger, Lukas D.;
- Robertson, Nahid G.;
- Vasilijic, Sasa;
- Morton, Cynthia C.;
- Stankovic, Konstantina M.
Publication type:
Article
Identification of Pathogenic Mechanisms of COCH Mutations, Abolished Cochlin Secretion, and Intracellular Aggregate Formation: Genotype-Phenotype Correlations in DFNA9 Deafness and Vestibular Disorder.
Published in:
Human Mutation, 2014, v. 35, n. 12, p. 1506, doi. 10.1002/humu.22701
By:
- Bae, Seung‐Hyun;
- Robertson, Nahid G.;
- Cho, Hyun‐Ju;
- Morton, Cynthia C.;
- Jung, Da Jung;
- Baek, Jeong‐In;
- Choi, Soo‐Young;
- Lee, Jaetae;
- Lee, Kyu‐Yup;
- Kim, Un‐Kyung
Publication type:
Article
A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 21, p. 3426, doi. 10.1093/hmg/ddn236
By:
- Robertson, Nahid G.;
- Jones, Sherri M.;
- Sivakumaran, Theru A.;
- Giersch, Anne B.S.;
- Jurado, Sara A.;
- Call, Linda M.;
- Miller, Constance E.;
- Maison, Stéphane F.;
- Liberman, M. Charles;
- Morton, Cynthia C.
Publication type:
Article
Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 7, p. 1071, doi. 10.1093/hmg/ddl022
By:
- Robertson, Nahid G.;
- Cremers, Cor W.R.J.;
- Huygen, Patrick L.M.;
- Ikezono, Tetsuo;
- Krastins, Bryan;
- Kremer, Hannie;
- Kuo, Sharon F.;
- Liberman, M. Charles;
- Merchant, Saumil N.;
- Miller, Constance E.;
- Nadol, Joseph B.;
- Sarracino, David A.;
- Verhagen, Wim I.M.;
- Morton, Cynthia C.
Publication type:
Article
Inner ear localization of mRNAand protein products of COCH, mutated in the sensorineuraldeafness and vestibular disorder, DFNA9.
Published in:
Human Molecular Genetics, 2001, v. 10, n. 22, p. 2493, doi. 10.1093/hmg/10.22.2493
By:
- Robertson, Nahid G.;
- Resendes, BarbaraL.;
- Lin, Jason S.;
- Lee, Charles;
- Aster, JonC.;
- Adams, Joe C.;
- Morton, CynthiaC.
Publication type:
Article
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.
Published in:
Human Molecular Genetics, 2001, v. 10, n. 3, p. 195, doi. 10.1093/hmg/10.3.195
By:
- Wayne, Sigrid;
- Robertson, Nahid G.;
- DeClau, Frank;
- Chen, Nancy;
- Verhoeven, Kristien;
- Prasad, Sai;
- Tranebjärg, Lisbeth;
- Morton, Cynthia C.;
- Ryan, Allen F.;
- Camp, Guy;
- Smith, Richard J.H.
Publication type:
Article
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction.
Published in:
Nature Genetics, 1998, v. 20, n. 3, p. 299, doi. 10.1038/3118
By:
- Robertson, Nahid G.;
- Lu, Leonard;
- Heller, Stefan;
- Merchant, Saumil N.;
- Eavey, Roland D.;
- McKenna, Michael;
- Nadol, Joseph B.;
- Miyamoto, Richard T.;
- Linthicum, Frederick H.;
- Lubianca Neto, José F.;
- Hudspeth, A.J.;
- Seidman, Christine E.;
- Morton, Cynthia C.;
- Seidman, J.G.
Publication type:
Article
Histopathology of the Human Inner Ear in the p.L114P COCH Mutation (DFNA9).
Published in:
2016
By:
- Burgess, Barbara J.;
- O''Malley, Jennifer T.;
- Kamakura, Takefumi;
- Kristiansen, Kris;
- Robertson, Nahid G.;
- Morton, Cynthia C.;
- Nadol Jr., Joseph B.
Publication type:
journal article
High prevalence of symptoms of Meniere's disease in three families with a mutation on the COCH gene.
Published in:
Human Molecular Genetics, 1999, v. 8, n. 8, p. 1425, doi. 10.1093/hmg/8.8.1425
By:
- Fransen, Erik;
- Verstreken, Margriet;
- Verhagen, Wim I. M.;
- Wuyts, Floris L.;
- Huygen, Patrick L. M.;
- D'Haese, Patrick;
- Robertson, Nahid G.;
- Morton, Cynthia C.;
- McGuirt, Wyman T.;
- Smith, Richard J. H.;
- Declau, Frank;
- Heyning, Paul H. Van de;
- Camp, Guy Van
Publication type:
Article
Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness.
Published in:
Human Molecular Genetics, 1999, v. 8, n. 3, p. 439, doi. 10.1093/hmg/8.3.439
By:
- Skvorak, Anne B.;
- Weng, Zhiping;
- Yee, Andrew J.;
- Robertson, Nahid G.;
- Morton, Cynthia C.
Publication type:
Article
A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects.
Published in:
Human Molecular Genetics, 1999, v. 8, n. 2, p. 361, doi. 10.1093/hmg/8.2.361
By:
- de Kok, Yvette J. M.;
- Bom, Steven J. H.;
- Brunt, Tibor M.;
- Kemperman, Martijn H.;
- van Beusekom, Ellen;
- van der Velde-Visser, Saskia D.;
- Robertson, Nahid G.;
- Morton, Cynthia C.;
- Huygen, Patrick L. M.;
- Verhagen, Wim I. M.;
- Brunner, Han G.;
- Cremers, Cor W. R. J.;
- Cremers, Frans P. M.
Publication type:
Article

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