PMC Links for OMIM (Select 607557) - PMC

Select item 47226161.

Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans

Nari Ryu, Borum Sagong, Hong-Joon Park, Min-A Kim, Kyu-Yup Lee, Jae Young Choi, Un-Kyung Kim

BMC Med Genet. 2016; 17: 6. Published online 2016 Jan 22. doi: 10.1186/s12881-016-0269-3

PMCID:: PMC4722616

Abstract Article PDF–1.7M

Select item 28102052.

Unmyelinated Low Threshold Mechanoreceptors are Required for Injury-induced Mechanical Hypersensitivity

Rebecca P. Seal, Xidao Wang, Yun Guan, Srinivasa N. Raja, C. Jeffery Woodbury, Allan I. Basbaum, Robert H. Edwards

Nature. Author manuscript; available in PMC 2010 Jun 3.

Published in final edited form as: Nature. 2009 Dec 3; 462(7273): 651–655. Published online 2009 Nov 15. doi: 10.1038/nature08505

PMCID:: PMC2810205

Abstract Article PDF–929K

Select item 24950733.

Impairment of SLC17A8 Encoding Vesicular Glutamate Transporter-3, VGLUT3, Underlies Nonsyndromic Deafness DFNA25 and Inner Hair Cell Dysfunction in Null Mice

Jérôme Ruel, Sarah Emery, Régis Nouvian, Tiphaine Bersot, Bénédicte Amilhon, Jana M. Van Rybroek, Guy Rebillard, Marc Lenoir, Michel Eybalin, Benjamin Delprat, Theru A. Sivakumaran, Bruno Giros, Salah El Mestikawy, Tobias Moser, Richard J.H. Smith, Marci M. Lesperance, Jean-Luc Puel

Am J Hum Genet. 2008 Aug 8; 83(2): 278–292. Published online 2008 Aug 1. doi: 10.1016/j.ajhg.2008.07.008

PMCID:: PMC2495073

Abstract Article PDF–1.5M

Select item 22932834.

Sensorineural Deafness and Seizures in Mice Lacking Vesicular Glutamate Transporter 3

Rebecca P. Seal, Omar Akil, Eunyoung Yi, Christopher M. Weber, Lisa Grant, Jong Yoo, Amanda Clause, Karl Kandler, Jeffrey L Noebels, Elisabeth Glowatzki, Lawrence R. Lustig, Robert H. Edwards

Neuron. Author manuscript; available in PMC 2009 Jan 24.

Published in final edited form as: Neuron. 2008 Jan 24; 57(2): 263–275. doi: 10.1016/j.neuron.2007.11.032

PMCID:: PMC2293283

Abstract Article PDF–2.2M

Select item 12349225.

DFNA25, a Novel Locus for Dominant Nonsyndromic Hereditary Hearing Impairment, Maps to 12q21-24

Charles C. Greene, Pamella M. McMillan, Susan E. Barker, Purnima Kurnool, Margaret I. Lomax, Margit Burmeister, Marci M. Lesperance

Am J Hum Genet. 2001 Jan; 68(1): 254–260. Published online 2000 Dec 11. doi: 10.1086/316925

PMCID:: PMC1234922

Abstract Article PDF–235K

Select item 10842136.

Molecular cloning and functional characterization of human vesicular glutamate transporter 3

Shigeo Takamori, Pari Malherbe, Clemens Broger, Reinhard Jahn

EMBO Rep. 2002 Aug 15; 3(8): 798–803. doi: 10.1093/embo-reports/kvf159

PMCID:: PMC1084213

Abstract Article PDF–368K

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from OMIM

Items: 6

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity