Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74.

[1]  J. Ervasti,et al.  β-Actin and γ-Actin Are Each Dispensable for Auditory Hair Cell Development But Required for Stereocilia Maintenance , 2010, PLoS genetics.

[2]  Mohsin Shahzad,et al.  Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79. , 2010, American journal of human genetics.

[3]  S. Novoselov,et al.  Regulation of selenoproteins and methionine sulfoxide reductases A and B1 by age, calorie restriction, and dietary selenium in mice. , 2010, Antioxidants & redox signaling.

[4]  Richard Weindruch,et al.  Age-related hearing loss in C57BL/6J mice is mediated by Bak-dependent mitochondrial apoptosis , 2009, Proceedings of the National Academy of Sciences.

[5]  Samson Jamesdaniel,et al.  Age-related changes in antioxidant enzymes related to hydrogen peroxide metabolism in rat inner ear , 2009, Neuroscience Letters.

[6]  Richard J. Salvi,et al.  A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice , 2009, Neurobiology of Aging.

[7]  S. Riazuddin,et al.  DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2‐q15 , 2009, Clinical genetics.

[8]  J. Ervasti,et al.  γ-Actin is required for cytoskeletal maintenance but not development , 2009, Proceedings of the National Academy of Sciences.

[9]  H. Nicolini,et al.  Methionine sulfoxide reductase: A novel schizophrenia candidate gene , 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[10]  Rebecca F. Halperin,et al.  GRM7 variants confer susceptibility to age-related hearing impairment. , 2009, Human molecular genetics.

[11]  B. Godley,et al.  Mitochondrial DNA damage and its potential role in retinal degeneration , 2008, Progress in Retinal and Eye Research.

[12]  T. Wienker,et al.  Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait. , 2008, American journal of human genetics.

[13]  J. Rochet,et al.  Methionine sulfoxide reductase A protects dopaminergic cells from Parkinson's disease-related insults. , 2008, Free radical biology & medicine.

[14]  Joe G Hollyfield,et al.  Oxidative damage–induced inflammation initiates age-related macular degeneration , 2008, Nature Medicine.

[15]  T. Wienker,et al.  The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment. , 2008, Human molecular genetics.

[16]  N. Brot,et al.  Methionine Sulfoxide Reductase A and a Dietary Supplement S-Methyl-L-Cysteine Prevent Parkinson's-Like Symptoms , 2007, The Journal of Neuroscience.

[17]  Hongyan Jiang,et al.  Oxidative imbalance in the aging inner ear , 2007, Neurobiology of Aging.

[18]  T. Wienker,et al.  The Contribution of GJB2 (Connexin 26) 35delG to Age-Related Hearing Impairment and Noise-Induced Hearing Loss , 2007, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

[19]  C. Franceschi,et al.  Apoptosis remodeling in immunosenescence: implications for strategies to delay ageing. , 2007, Current medicinal chemistry.

[20]  T. Wienker,et al.  Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment , 2007, Journal of Medical Genetics.

[21]  A. Forge,et al.  Tricellulin is a tight-junction protein necessary for hearing. , 2006, American journal of human genetics.

[22]  C. Morton,et al.  Newborn hearing screening--a silent revolution. , 2006, The New England journal of medicine.

[23]  V. Gladyshev,et al.  Different Catalytic Mechanisms in Mammalian Selenocysteine- and Cysteine-Containing Methionine-R-Sulfoxide Reductases , 2005, PLoS biology.

[24]  Hong-Xiu Yu,et al.  Insights into the role of the metal binding site in methionine‐R‐sulfoxide reductases B , 2005, Protein science : a publication of the Protein Society.

[25]  D. Sagher,et al.  Methionine sulfoxide reductases B1, B2, and B3 are present in the human lens and confer oxidative stress resistance to lens cells. , 2005, Investigative ophthalmology & visual science.

[26]  R. Truscott.  Age-related nuclear cataract-oxidation is the key. , 2005, Experimental eye research.

[27]  S. Heinemann,et al.  Heterogeneity and function of mammalian MSRs: enzymes for repair, protection and regulation. , 2005, Biochimica et biophysica acta.

[28]  L. Tranebjaerg,et al.  The calcium-binding aspartate/glutamate carriers, citrin and aralar1, are new substrates for the DDP1/TIMM8a-TIMM13 complex. , 2004, Human molecular genetics.

[29]  V. Gladyshev,et al.  Characterization of mouse endoplasmic reticulum methionine-R-sulfoxide reductase. , 2004, Biochemical and biophysical research communications.

[30]  A. Griffith,et al.  Genetic insights into the morphogenesis of inner ear hair cells , 2004, Nature Reviews Genetics.

[31]  E. Fransen,et al.  A Novel Z-Score–Based Method to Analyze Candidate Genes for Age-Related Hearing Impairment , 2004, Ear and hearing.

[32]  V. Gladyshev,et al.  Methionine sulfoxide reduction in mammals: characterization of methionine-R-sulfoxide reductases. , 2003, Molecular biology of the cell.

[33]  P. Sieving,et al.  PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23. , 2003, Human molecular genetics.

[34]  A. Griffith,et al.  Human nonsyndromic sensorineural deafness. , 2003, Annual review of genomics and human genetics.

[35]  S. Leal,et al.  Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26) , 2003 .

[36]  V. Gladyshev,et al.  Reaction Mechanism, Evolutionary Analysis, and Role of Zinc in Drosophila Methionine-R-sulfoxide Reductase* , 2002, The Journal of Biological Chemistry.

[37]  B. Matthews,et al.  Peptide methionine sulfoxide reductase: structure, mechanism of action, and biological function. , 2002, Archives of biochemistry and biophysics.

[38]  E. Stadtman,et al.  Methionine sulfoxide reductase (MsrA) is a regulator of antioxidant defense and lifespan in mammals , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[39]  S. Riazuddin,et al.  Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. , 2001, American journal of human genetics.

[40]  N. Segil,et al.  Deafness due to degeneration of cochlear neurons in caspase-3-deficient mice. , 2001, Biochemical and biophysical research communications.

[41]  M. Boulton,et al.  The role of oxidative stress in the pathogenesis of age-related macular degeneration. , 2000, Survey of ophthalmology.

[42]  B. Hamel,et al.  A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness–dystonia–optic atrophy syndrome , 2000, European Journal of Human Genetics.

[43]  G. Moonen,et al.  Oxidative stress-induced apoptosis of cochlear sensory cells: otoprotective strategies , 2000, International Journal of Developmental Neuroscience.

[44]  W. Markesbery,et al.  Decrease in Peptide Methionine Sulfoxide Reductase in Alzheimer's Disease Brain , 1999, Journal of neurochemistry.

[45]  S. Merchant,et al.  Human deafness dystonia syndrome is a mitochondrial disease. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[46]  G. Richardson,et al.  Nonsyndromic hearing impairment is associated with a mutation in DFNA5 , 1998, Nature Genetics.

[47]  D. Vetrie,et al.  A novel X–linked gene, DDP, shows mutations in families with deafness (DFN–1), dystonia, mental deficiency and blindness , 1996, Nature Genetics.

[48]  J Punch,et al.  The prevalence of hearing impairment. , 1983, ASHA.

[49]  S. Leal,et al.  Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26). , 2003, American journal of human genetics.

[50]  Diane C. Thompson,et al.  Newborn Hearing Screening , 2001 .

[51]  Malou M-Louise Haine,et al.  Van Laer N. , 1986 .