Literature DB >> 10337628

Mapping of the otogelin gene (OTGN) to mouse chromosome 7 and human chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18.

M Cohen-Salmon1, M G Mattei, C Petit.   

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Year:  1999        PMID： 10337628     DOI： 10.1007/s003359901033

Source DB:  PubMed          Journal:  Mamm Genome        ISSN： 0938-8990            Impact factor:   2.957


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  6 in total

1.  Similar phenotypes caused by mutations in OTOG and OTOGL.

Authors:  Anne M M Oonk; Joop M Leijendeckers; Patrick L M Huygen; Margit Schraders; Miguel del Campo; Ignacio del Castillo; Mustafa Tekin; Ilse Feenstra; Andy J Beynon; Henricus P M Kunst; Ad F M Snik; Hannie Kremer; Ronald J C Admiraal; Ronald J E Pennings
Journal:  Ear Hear       Date:  2014 May-Jun       Impact factor: 3.570

2.  Clinical characteristics with long-term follow-up of four Okinawan families with moderate hearing loss caused by an OTOG variant.

Authors:  Akira Ganaha; Tadashi Kaname; Kumiko Yanagi; Tetsuya Tono; Teruyuki Higa; Mikio Suzuki
Journal:  Hum Genome Var       Date:  2019-08-13

3.  A new Otogelin ENU mouse model for autosomal-recessive nonsyndromic moderate hearing impairment.

Authors:  Carole El Hakam Kamareddin; Laetitia Magnol; Veronique Blanquet
Journal:  Springerplus       Date:  2015-11-25

4.  A secretory cell type develops alongside multiciliated cells, ionocytes and goblet cells, and provides a protective, anti-infective function in the frog embryonic mucociliary epidermis.

Authors:  Eamon Dubaissi; Karine Rousseau; Robert Lea; Ximena Soto; Siddarth Nardeosingh; Axel Schweickert; Enrique Amaya; David J Thornton; Nancy Papalopulu
Journal:  Development       Date:  2014-03-05       Impact factor: 6.868

5.  A reverse genetic approach identifies an ancestral frameshift mutation in RP1 causing recessive progressive retinal degeneration in European cattle breeds.

Authors:  Pauline Michot; Sabine Chahory; Andrew Marete; Cécile Grohs; Dimitri Dagios; Elise Donzel; Abdelhak Aboukadiri; Marie-Christine Deloche; Aurélie Allais-Bonnet; Matthieu Chambrial; Sarah Barbey; Lucie Genestout; Mekki Boussaha; Coralie Danchin-Burge; Sébastien Fritz; Didier Boichard; Aurélien Capitan
Journal:  Genet Sel Evol       Date:  2016-08-10       Impact factor: 4.297

6.  Characterization of rare spindle and root cell transcriptional profiles in the stria vascularis of the adult mouse cochlea.

Authors:  Shoujun Gu; Rafal Olszewski; Ian Taukulis; Zheng Wei; Daniel Martin; Robert J Morell; Michael Hoa
Journal:  Sci Rep       Date:  2020-10-22       Impact factor: 4.996
  6 in total

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