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	81.	siRNA targeting Hes5 augments hair cell regeneration in aminoglycoside-damaged mouse utricle. [electronic resource] by Jung, Jae Yun Avenarius, Matt R Adamsky, Swetlana Alpert, Evgenia Feinstein, Elena Raphael, Yehoash Producer: 20131101 In: Molecular therapy : the journal of the American Society of Gene Therapy vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	82.	Identification of novel variants in the Myosin VIIA gene of patients with nonsyndromic hearing loss from Taiwan. [electronic resource] by Su, Mao-Chang Yang, Jiann-Jou Su, Ching-Chyuan Hsin, Chung-Han Li, Shuan-Yow Producer: 20090826 In: International journal of pediatric otorhinolaryngology vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	83.	Targeted next generation sequencing identified a novel mutation in MYO7A causing Usher syndrome type 1 in an Iranian consanguineous pedigree. [electronic resource] by Kooshavar, Daniz Razipour, Masoumeh Movasat, Morteza Keramatipour, Mohammad Producer: 20180116 In: International journal of pediatric otorhinolaryngology vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	84.	Human myosin VIIa is a very slow processive motor protein on various cellular actin structures. [electronic resource] by Sato, Osamu Komatsu, Satoshi Sakai, Tsuyoshi Tsukasaki, Yoshikazu Tanaka, Ryosuke Mizutani, Takeomi Watanabe, Tomonobu M Ikebe, Reiko Ikebe, Mitsuo Producer: 20170706 In: The Journal of biological chemistry vol. 292 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	85.	Retinal gene therapy with a large MYO7A cDNA using adeno-associated virus. [electronic resource] by Lopes, V S Boye, S E Louie, C M Boye, S Dyka, F Chiodo, V Fofo, H Hauswirth, W W Williams, D S Producer: 20131101 In: Gene therapy vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	86.	Identification of a MYO7A mutation in a large Chinese DFNA11 family and genotype-phenotype review for DFNA11. [electronic resource] by Li, Lina Yuan, Hu Wang, Hongyang Guan, Jing Lan, Lan Wang, Dayong Zong, Liang Liu, Qiong Han, Bing Huang, Deliang Wang, Qiuju Producer: 20180926 In: Acta oto-laryngologica vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	87.	Water Waves to Sound Waves: Using Zebrafish to Explore Hair Cell Biology. [electronic resource] by Pickett, Sarah B Raible, David W Producer: 20200413 In: Journal of the Association for Research in Otolaryngology : JARO vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	88.	Functional analysis of splicing mutations in MYO7A and USH2A genes. [electronic resource] by Jaijo, T Aller, E Aparisi, M J García-García, G Hernan, I Gamundi, M J Nájera, C Carballo, M Millán, J M Producer: 20110524 In: Clinical genetics vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	89.	Screen for usher syndrome 1B mutations in the ovine myosin VIIa gene. [electronic resource] by Slatter, Tania Azarian, Sassan M Tebbutt, Scott Maw, Marion Williams, David S Producer: 20040804 In: Advances in experimental medicine and biology vol. 533 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	90.	Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review. [electronic resource] by Beheshtian, Maryam Babanejad, Mojgan Azaiez, Hela Bazazzadegan, Niloofar Kolbe, Diana Sloan-Heggen, Christina Arzhangi, Sanaz Booth, Kevin Mohseni, Marzieh Frees, Kathy Azizi, Mohammad Hossein Daneshi, Ahmad Farhadi, Mohammad Kahrizi, Kimia Smith, Richard Jh Najmabadi, Hossein Producer: 20170228 In: Archives of Iranian medicine vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	91.	Two Finnish USH1B patients with three novel mutations in myosin VIIA. [electronic resource] by Vastinsalo, Hanna Isosomppi, Juha Aittakorpi, Anne Sankila, Eeva-Marja Producer: 20061211 In: Molecular vision vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	92.	Myosin VIIa Supports Spermatid/Organelle Transport and Cell Adhesion During Spermatogenesis in the Rat Testis. [electronic resource] by Wen, Qing Wu, Siwen Lee, Will M Wong, Chris K C Lui, Wing-Yee Silvestrini, Bruno Cheng, C Yan Producer: 20191209 In: Endocrinology vol. 160 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	93.	Hereditary familial vestibular degenerative diseases. [electronic resource] by Sun, J C Van Alphen, A M Wagenaar, M Huygen, P Hoogenraad, C C Hasson, T Koekkoek, S K Bohne, B A De Zeeuw, C I Producer: 20011207 In: Annals of the New York Academy of Sciences vol. 942 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	94.	Novel compound heterozygous mutations in MYO7A Associated with Usher syndrome 1 in a Chinese family. [electronic resource] by Gao, Xue Wang, Guo-Jian Yuan, Yong-Yi Xin, Feng Han, Ming-Yu Lu, Jing-Qiao Zhao, Hui Yu, Fei Xu, Jin-Cao Zhang, Mei-Guang Dong, Jiang Lin, Xi Dai, Pu Producer: 20151105 In: PloS one vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	95.	Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type I. [electronic resource] by Oshima, A Jaijo, T Aller, E Millan, J M Carney, C Usami, S Moller, C Kimberling, W J Producer: 20080715 In: Human mutation vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	96.	Identification of three novel mutations in the MYO7A gene. [electronic resource] by Cuevas, J M Espinós, C Millán, J M Sánchez, F Trujillo, M J Ayuso, C Beneyto, M Nájera, C Producer: 19990812 In: Human mutation vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	97.	The molecular regulation of organelle transport in mammalian retinal pigment epithelial cells. [electronic resource] by Futter, Clare E Producer: 20060622 In: Pigment cell research vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	98.	Mutations in myosin VIIA (MYO7A) and usherin (USH2A) in Spanish patients with Usher syndrome types I and II, respectively. [electronic resource] by Nájera, Carmen Beneyto, Magdalena Blanca, José Aller, Elena Fontcuberta, Ana Millán, José María Ayuso, Carmen Producer: 20020805 In: Human mutation vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	99.	Expression of myosin VIIA in the developing chick inner ear neurons. [electronic resource] by Nguyen, Kristi Hall, Amanda L Jones, Jennifer M Producer: 20160908 In: Gene expression patterns : GEP vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	100.	The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A). [electronic resource] by Kelley, P M Weston, M D Chen, Z Y Orten, D J Hasson, T Overbeck, L D Pinnt, J Talmadge, C B Ing, P Mooseker, M S Corey, D Sumegi, J Kimberling, W J Producer: 19970623 In: Genomics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 365 results.