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Michael Weston

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Sonia M S Rocha-Sanchez; Laura R Scheetz; Melissa Contreras; Megan Korte; Joann McGee; Michael D Weston; Edward J Walsh
Mature mice lacking Rbl2/p130 gene have supernumerary inner ear hair cells and supporting cells.
Michael D Weston; Marsha L Pierce; Heather C Jensen-Smith; Bernd Fritzsch; Sonia Rocha-Sanchez; Kirk W Beisel; Garrett A Soukup
MicroRNA-183 family expression in hair cell development and requirement of microRNAs for hair cell maintenance and survival.
garrett soukup; Bernd Fritzsch; Marsha L Pierce; Michael D Weston; Israt Jahan; Michael McManus; Brian D Harfe
Residual microRNA expression dictates the extent of inner ear development in conditional Dicer knockout mice.

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All Publications

2011: Sonia M S Rocha-Sanchez; Laura R Scheetz; Melissa Contreras; Megan Korte; Joann McGee; Michael D Weston; Edward J Walsh
Mature mice lacking Rbl2/p130 gene have supernumerary inner ear hair cells and supporting cells.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2011;31(24):8883-93.
2011: Michael D Weston; Marsha L Pierce; Heather C Jensen-Smith; Bernd Fritzsch; Sonia Rocha-Sanchez; Kirk W Beisel; Garrett A Soukup
MicroRNA-183 family expression in hair cell development and requirement of microRNAs for hair cell maintenance and survival.
Developmental dynamics : an official publication of the American Association of Anatomists 2011;240(4):808-19.
2009: garrett soukup; Bernd Fritzsch; Marsha L Pierce; Michael D Weston; Israt Jahan; Michael McManus; Brian D Harfe
Residual microRNA expression dictates the extent of inner ear development in conditional Dicer knockout mice.
Developmental biology 2009;328(2):328-41.
2009: Michael D Weston; garrett soukup
MicroRNAs sound off.
Genome medicine 2009;1(6):59.
2008: Oseremen E Okoruwa; Michael D Weston; Divvya C Sanjeevi; Amanda R Millemon; Bernd Fritzsch; Richard Hallworth; Kirk W Beisel
Evolutionary insights into the unique electromotility motor of mammalian outer hair cells.
Evolution & development 2008;10(3):300-15.
2008: Marsha L Pierce; Michael D Weston; Bernd Fritzsch; Harrison W Gabel; Gary Ruvkun; garrett soukup
MicroRNA-183 family conservation and ciliated neurosensory organ expression.
Evolution & development 2008;10(1):106-13.
2007: Frans P M Cremers; William J Kimberling; Maigi Külm; Arjan de Brouwer; Erwin van Wijk; Heleen te Brinke; Cor W R J Cremers; Lies Hoefsloot; Sandro Banfi; Francesca Simonelli; Johannes C Fleischhauer; Wolfgang Berger; Philip M Kelley; Elene Haralambous; Maria Bitner-Glindzicz; Andrew R Webster; Zubin Saihan; Elfride De Baere; Bart P Leroy; Giuliana Silvestri; Gareth J McKay; Robert K Koenekoop; Jose M Millan; Thomas Rosenberg; Tarja Joensuu; Eeva-Marja Sankila; Dominique Weil; Michael D Weston; Bernd Wissinger; Hannie Kremer
Development of a genotyping microarray for Usher syndrome.
Journal of medical genetics 2007;44(2):153-60.
2006: Michael D Weston; Marsha L Pierce; Sonia M S Rocha-Sanchez; Kirk W Beisel; garrett soukup
MicroRNA gene expression in the mouse inner ear.
Brain research 2006;1111(1):95-104.
2004: Ronald Pennings; Heleen te Brinke; Michael D Weston; Annemarie Claassen; Dana J Orten; Henriëtte H Weekamp; Annelies van Aarem; Patrick Huygen; August F Deutman; Lies Hoefsloot; Frans P M Cremers; Cor W R J Cremers; William J Kimberling; Hannie Kremer
USH2A mutation analysis in 70 Dutch families with Usher syndrome type II.
Human mutation 2004;24(2):185.
2004: Michael D Weston; Mirjam W J Luijendijk; Kurt D Humphrey; Claes Möller; William J Kimberling
Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.
American journal of human genetics 2004;74(2):357-66.
2003: Ronald Pennings; Patrick Huygen; Michael D Weston; Annelies van Aarem; Michiel Wagenaar; William J Kimberling; Cor W R J Cremers
Pure tone hearing thresholds and speech recognition scores in Dutch patients carrying mutations in the USH2A gene.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2003;24(1):58-63.
2002: Dali Huang; James D Eudy; Eva Uzvolgyi; Jack R Davis; Catherine B Talmadge; Dalyir Pretto; Michael D Weston; Janae E Lehman; Ming Zhou; Thomas A Seemayer; Iqbal Ahmad; William J Kimberling; Janos Sumegi
Identification of the mouse and rat orthologs of the gene mutated in Usher syndrome type IIA and the cellular source of USH2A mRNA in retina, a target tissue of the disease.
Genomics 2002;80(2):195-203.
2002: Lisa M Astuto; Julie M Bork; Michael D Weston; James W Askew; R R Fields; Dana J Orten; S J Ohliger; Sheikh Amer Riazuddin; Robert J Morell; Shaheen Khan; S Riazuddin; Hannie Kremer; Peter Van Hauwe; CG Moller; Cor W R J Cremers; C Ayuso; John R Heckenlively; Klaus Rohrschneider; Ulrich H M Spandau; J Greenberg; Rajkumar Ramesar; William Reardon; P Bitoun; J Millan; R Legge; Thomas B Friedman; William J Kimberling
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.
American journal of human genetics 2002;71(2):262-75.
2002: Lisa M Astuto; Philip M Kelley; James W Askew; Michael D Weston; Richard J H Smith; Abdulrahman Alswaid; Mona Al-Rakaf; William J Kimberling
Searching for evidence of DFNB2.
American journal of medical genetics 2002;109(4):291-7.
2001: B Dreyer; Lisbeth Tranebjaerg; Vigdis Brox; T Rosenberg; Claes Möller; M Beneyto; Michael D Weston; William J Kimberling; C W Cremers; Xue Zhong Liu; Oivind Nilssen
A common ancestral origin of the frequent and widespread 2299delG USH2A mutation.
American journal of human genetics 2001;69(1):228-34.
2001: Bart P Leroy; J A Aragon-Martin; Michael D Weston; David A R Bessant; Catherine Willis; Andrew R Webster; Alan C Bird; William J Kimberling; Annette M Payne; Shomi S Bhattacharya
Spectrum of mutations in USH2A in British patients with Usher syndrome type II.
Experimental eye research 2001;72(5):503-9.
2000: Lisa M Astuto; Michael D Weston; C A Carney; Denise M Hoover; Cor W R J Cremers; Michiel Wagenaar; CG Moller; Richard J H Smith; S Pieke-Dahl; J Greenberg; Rajkumar Ramesar; SG Jacobson; C Ayuso; John R Heckenlively; M Tamayo; M B Gorin; William Reardon; William J Kimberling
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.
American journal of human genetics 2000;67(6):1569-74.
2000: B Dreyer; Lisbeth Tranebjaerg; T Rosenberg; Michael D Weston; William J Kimberling; Oivind Nilssen
Identification of novel USH2A mutations: implications for the structure of USH2A protein.
European journal of human genetics : EJHG 2000;8(7):500-6.
2000: Avital Adato; Michael D Weston; A Berry; William J Kimberling; A Bonne-Tamir
Three novel mutations and twelve polymorphisms identified in the USH2A gene in Israeli USH2 families.
Human mutation 2000;15(4):388.
2000: Michael D Weston; James D Eudy; S Fujita; S Yao; Shin-ichi Usami; Cor W R J Cremers; J Greenberg; Rajkumar Ramesar; martini alessandro; CG Moller; Richard J H Smith; Janos Sumegi; William J Kimberling; J Greenburg
Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa.
American journal of human genetics 2000;66(4):1199-210.
2000: Dana J Orten; Michael D Weston; Philip M Kelley; Cor W R J Cremers; Michiel Wagenaar; SG Jacobson; William J Kimberling
Erratum: analysis of DNA elements that modulate myosin VIIa expression in humans.
Human mutation 2000;15(1):114-5.
1999: Dana J Orten; Michael D Weston; Philip M Kelley; Cor W R J Cremers; Michiel Wagenaar; SG Jacobson; William J Kimberling
Analysis of DNA elements that modulate myosin VIIA expression in humans.
Human mutation 1999;14(4):354.
1999: Shin-ichi Usami; Satoko Abe; Michael D Weston; Hideichi Shinkawa; G Van Camp; William J Kimberling
Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations.
Human genetics 1999;104(2):188-92.
1998: Satoko Abe; Shin-ichi Usami; Hideichi Shinkawa; Michael D Weston; L D Overbeck; Denise M Hoover; Judith B Kenyon; S Horai; William J Kimberling
Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.
European journal of human genetics : EJHG 1998;6(6):563-9.
1998: James D Eudy; S Yao; Michael D Weston; M Ma-Edmonds; Catherine B Talmadge; J J Cheng; William J Kimberling; Janos Sumegi
Isolation of a gene encoding a novel member of the nuclear receptor superfamily from the critical region of Usher syndrome type IIa at 1q41.
Genomics 1998;50(3):382-4.
1998: James D Eudy; Michael D Weston; S Yao; Denise M Hoover; Heidi L Rehm; M Ma-Edmonds; Denise Yan; Iqbal Ahmad; J J Cheng; C Ayuso; Cor W R J Cremers; S Davenport; CG Moller; Catherine B Talmadge; Kirk W Beisel; M Tamayo; Cynthia C Morton; Anand Swaroop; William J Kimberling; Janos Sumegi
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Science (New York, N.Y.) 1998;280(5370):1753-7.
1998: S Kumar; William J Kimberling; Michael D Weston; B G Schaefer; M A Berg; Henri Marres; Cor W R J Cremers
Identification of three novel mutations in human EYA1 protein associated with branchio-oto-renal syndrome.
Human mutation 1998;11(6):443-9.
1997: James D Eudy; M Ma-Edmonds; S F Yao; Catherine B Talmadge; Philip M Kelley; Michael D Weston; William J Kimberling; Janos Sumegi
Isolation of a novel human homologue of the gene coding for echinoderm microtubule-associated protein (EMAP) from the Usher syndrome type 1a locus at 14q32.
Genomics 1997;43(1):104-6.
1997: Philip M Kelley; Michael D Weston; Z Y Chen; Dana J Orten; Tama Hasson; L D Overbeck; J Pinnt; Catherine B Talmadge; P Ing; Mark S Mooseker; D Corey; Janos Sumegi; William J Kimberling
The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A).
Genomics 1997;40(1):73-9.
1996: Michael D Weston; Philip M Kelley; L D Overbeck; Michiel Wagenaar; Dana J Orten; Tama Hasson; Z Y Chen; David P Corey; Mark S Mooseker; Janos Sumegi; Cor W R J Cremers; C Moller; S G Jacobson; M B Gorin; William J Kimberling
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.
American journal of human genetics 1996;59(5):1074-83.
1996: Janos Sumegi; J Y Wang; D K Zhen; James D Eudy; Catherine B Talmadge; B F Li; P Berglund; Michael D Weston; S F Yao; M Ma-Edmonds; L Overbeck; Philip M Kelley; Eugene R Zabarovsky; Eva Uzvolgyi; Eric J Stanbridge; George Klein; William J Kimberling
The construction of a yeast artificial chromosome (YAC) contig in the vicinity of the Usher syndrome type IIa (USH2A) gene in 1q41.
Genomics 1996;35(1):79-86.
1995: Catherine B Talmadge; D K Zhen; J Y Wang; P Berglund; B F Li; Michael D Weston; William J Kimberling; Eugene R Zabarovsky; Eric J Stanbridge; George Klein
Construction and characterization of a NotI linking library from human chromosome region 1q25-qter.
Genomics 1995;29(1):105-14.
1995: William J Kimberling; Michael D Weston; C Möller; A van Aarem; Cor W R J Cremers; Janos Sumegi; P S Ing; C Connolly; martini alessandro; M Milani
Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41.
American journal of human genetics 1995;56(1):216-23.
1994: Michael D Weston; William J Kimberling
Dinucleotide repeat polymorphism for D1S70 (CRI-L461) on chromosome 1q41.
Human molecular genetics 1994;3(7):1212.
1994: Michael D Weston; D K Zhen; Janos Sumegi; William J Kimberling
Dinucleotide repeat polymorphism in the TGFB2 gene.
Human molecular genetics 1994;3(7):1211.
1994: Michael D Weston; D K Zhen; Janos Sumegi; William J Kimberling
Dinucleotide repeat polymorphism at D1S556.
Human molecular genetics 1994;3(7):1211.
1993: S Pieke Dahl; William J Kimberling; M B Gorin; Michael D Weston; J M Furman; A Pikus; C Möller
Genetic heterogeneity of Usher syndrome type II.
Journal of medical genetics 1993;30(10):843-8.
1993: S P Dahl; Michael D Weston; L D Overbeck; K L Evans; D J Porteous; William J Kimberling
Dinucleotide repeat polymorphism at the human olfactory marker protein (OMP) locus on chromosome 11q13.5 near tyrosinase (TYR).
Human molecular genetics 1993;2(6):822.
1993: L D Overbeck; Michael D Weston; William J Kimberling; G A Evans
Dinucleotide (CT)n (CA)n repeat polymorphism for D11S787 on chromosome 11q13.4.
Human molecular genetics 1993;2(5):611.
1992: William J Kimberling; C G Möller; S Davenport; I A Priluck; P H Beighton; J Greenberg; W Reardon; Michael D Weston; J B Kenyon; J A Grunkemeyer
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11.
Genomics 1992;14(4):988-94.
1992: L D Overbeck; Michael D Weston; William J Kimberling; D H Johnson
A new highly polymorphic dinucleotide (CT)n repeat polymorphism D1S158 on chromosome 1q isolated by microdissection.
Human molecular genetics 1992;1(2):141.
1991: S Pieke Dahl; Michael D Weston; William J Kimberling; J B Kenyon; Yin Yao Shugart; R J Smith
Report on attempts to localize Usher syndrome type 1 by linkage analysis to selected candidate regions.
Annals of the New York Academy of Sciences 1991;630():298-300.
1991: Michael D Weston; William J Kimberling; C G Möller; S Pieke Dahl; R J Smith; martini alessandro; M Milani
A progress report on the localization of Usher syndrome type II to chromosome 1q.
Annals of the New York Academy of Sciences 1991;630():284-7.
1991: William J Kimberling; Michael D Weston; S Pieke Dahl; J B Kenyon; Yin Yao Shugart; C Moller; S L Davenport; martini alessandro; M Milani; R J Smith
Genetic studies of Usher syndrome.
Annals of the New York Academy of Sciences 1991;630():167-75.
1990: William J Kimberling; Michael D Weston; C Möller; S L Davenport; Yin Yao Shugart; I A Priluck; martini alessandro; M Milani; R J Smith
Localization of Usher syndrome type II to chromosome 1q.
Genomics 1990;7(2):245-9.
1989: William J Kimberling; C G Möller; S L Davenport; G Lund; T J Grissom; I Priluck; V White; Michael D Weston; K Biscone-Halterman; P E Brookhouser
Usher syndrome: clinical findings and gene localization studies.
The Laryngoscope 1989;99(1):66-72.