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Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndrome.
Published in:
eLife, 2021, p. 1, doi. 10.7554/eLife.67361
By:
- Sethna, Saumil;
- Zein, Wadih M.;
- Riaz, Sehar;
- Giese, Arnaud P. J.;
- Schultz, Julie M.;
- Duncan, Todd;
- Hufnagel, Robert B.;
- Brewer, Carmen C.;
- Griffith, Andrew J.;
- Redmond, T. Michael;
- Riazuddin, Saima;
- Friedman, Thomas B.;
- Ahmed, Zubair M.
Publication type:
Article
Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome.
Published in:
Clinical Genetics, 2021, v. 99, n. 2, p. 226, doi. 10.1111/cge.13868
By:
- Wafa, Talah T.;
- Faridi, Rabia;
- King, Kelly A.;
- Zalewski, Christopher;
- Yousaf, Rizwan;
- Schultz, Julie M.;
- Morell, Robert J.;
- Muskett, Julie;
- Turriff, Amy;
- Tsilou, Ekaterini;
- Griffith, Andrew J.;
- Friedman, Thomas B.;
- Zein, Wadih M.;
- Brewer, Carmen C.
Publication type:
Article
Noncoding Microdeletion in Mouse Hgf Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyndromic Deafness DFNB39.
Published in:
Journal of Neuroscience, 2020, v. 40, n. 15, p. 2976, doi. 10.1523/JNEUROSCI.2278-19.2020
By:
- Morell, Robert J.;
- Olszewski, Rafal;
- Tona, Risa;
- Leitess, Samuel;
- Wafa, Talah T.;
- Taukulis, Ian;
- Schultz, Julie M.;
- Thomason, Elizabeth J.;
- Richards, Keri;
- Whitley, Brittany N.;
- Hill, Connor;
- Saunders, Thomas;
- Starost, Matthew F.;
- Fitzgerald, Tracy;
- Wilson, Elizabeth;
- Takahiro Ohyama;
- Friedman, Thomas B.;
- Hoa, Michael
Publication type:
Article
Genetic Analysis through OtoSeq of Pakistani Families Segregating Prelingual Hearing Loss.
Published in:
Otolaryngology-Head & Neck Surgery, 2013, v. 149, n. 3, p. 478, doi. 10.1177/0194599813493075
By:
- Shahzad, Mohsin;
- Sivakumaran, Theru A.;
- Qaiser, Tanveer A.;
- Schultz, Julie M.;
- Hussain, Zawar;
- Flanagan, Megan;
- Bhinder, Munir A.;
- Kissell, Diane;
- Greinwald, John H.;
- Khan, Shaheen N.;
- Friedman, Thomas B.;
- Zhang, Kejian;
- Riazuddin, Saima;
- Riazuddin, Sheikh;
- Ahmed, Zubair M.
Publication type:
Article

Found: 4

Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndrome.

Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome.

Noncoding Microdeletion in Mouse Hgf Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyndromic Deafness DFNB39.

Genetic Analysis through OtoSeq of Pakistani Families Segregating Prelingual Hearing Loss.