Your search returned 365 results.

Results
	261.	DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System. [electronic resource] by Sommen, Manou Schrauwen, Isabelle Vandeweyer, Geert Boeckx, Nele Corneveaux, Jason J van den Ende, Jenneke Boudewyns, An De Leenheer, Els Janssens, Sandra Claes, Kathleen Verstreken, Margriet Strenzke, Nicola Predöhl, Friederike Wuyts, Wim Mortier, Geert Bitner-Glindzicz, Maria Moser, Tobias Coucke, Paul Huentelman, Matthew J Van Camp, Guy Producer: 20171215 In: Human mutation vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	262.	A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth. [electronic resource] by Lefèvre, Gaelle Michel, Vincent Weil, Dominique Lepelletier, Léa Bizard, Emilie Wolfrum, Uwe Hardelin, Jean-Pierre Petit, Christine Producer: 20080611 In: Development (Cambridge, England) vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	263.	Outer Retinal Changes Including the Ellipsoid Zone Band in Usher Syndrome 1B due to MYO7A Mutations. [electronic resource] by Sumaroka, Alexander Matsui, Rodrigo Cideciyan, Artur V McGuigan, David B Sheplock, Rebecca Schwartz, Sharon B Jacobson, Samuel G Producer: 20170615 In: Investigative ophthalmology & visual science vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	264.	CLINICAL PRESENTATION AND DISEASE COURSE OF USHER SYNDROME BECAUSE OF MUTATIONS IN MYO7A OR USH2A. [electronic resource] by Testa, Francesco Melillo, Paolo Bonnet, Crystel Marcelli, Vincenzo de Benedictis, Antonella Colucci, Raffaella Gallo, Beatrice Kurtenbach, Anne Rossi, Settimio Marciano, Elio Auricchio, Alberto Petit, Christine Zrenner, Eberhart Simonelli, Francesca Producer: 20180112 In: Retina (Philadelphia, Pa.) vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	265.	Differential distribution of harmonin isoforms and their possible role in Usher-1 protein complexes in mammalian photoreceptor cells. [electronic resource] by Reiners, Jan Reidel, Boris El-Amraoui, Aziz Boëda, Batiste Huber, Irene Petit, Christine Wolfrum, Uwe Producer: 20031120 In: Investigative ophthalmology & visual science vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	266.	Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism. [electronic resource] by Jacobson, Samuel G Cideciyan, Artur V Aleman, Tomas S Sumaroka, Alexander Roman, Alejandro J Gardner, Leigh M Prosser, Haydn M Mishra, Monalisa Bech-Hansen, N Torben Herrera, Waldo Schwartz, Sharon B Liu, Xue-Zhong Kimberling, William J Steel, Karen P Williams, David S Producer: 20080804 In: Human molecular genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	267.	Exploiting decellularized cochleae as scaffolds for inner ear tissue engineering. [electronic resource] by Mellott, Adam J Shinogle, Heather E Nelson-Brantley, Jennifer G Detamore, Michael S Staecker, Hinrich Producer: 20171108 In: Stem cell research & therapy vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	268.	Inhibition of Notch/RBP-J signaling induces hair cell formation in neonate mouse cochleas. [electronic resource] by Yamamoto, Norio Tanigaki, Kenji Tsuji, Masayuki Yabe, Daisuke Ito, Juichi Honjo, Tasuku Producer: 20061211 In: Journal of molecular medicine (Berlin, Germany) vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	269.	Cochleovestibular and ocular features in a Dutch DFNA11 family. [electronic resource] by Bischoff, Anne M L C Pennings, Ronald J E Huygen, Patrick L M Luijendijk, Mirjam W van Wijk, Erwin Cruysberg, Johannes R M Kremer, Hannie Cremers, Cor W R J Producer: 20070628 In: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	270.	Genetic predisposition to calcific aortic stenosis and mitral annular calcification. [electronic resource] by Kutikhin, Anton G Yuzhalin, Arseniy E Brusina, Elena B Ponasenko, Anastasia V Golovkin, Alexey S Barbarash, Olga L Producer: 20151214 In: Molecular biology reports vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	271.	The unconventional myosin CRINKLED and its mammalian orthologue MYO7A regulate caspases in their signalling roles. [electronic resource] by Orme, Mariam H Liccardi, Gianmaria Moderau, Nina Feltham, Rebecca Wicky-John, Sidonie Tenev, Tencho Aram, Lior Wilson, Rebecca Bianchi, Katiuscia Morris, Otto Monteiro Domingues, Celia Robertson, David Tare, Meghana Wepf, Alexander Williams, David Bergmann, Andreas Gstaiger, Matthias Arama, Eli Ribeiro, Paulo S Meier, Pascal Producer: 20160727 In: Nature communications vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	272.	Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex. [electronic resource] by Küssel-Andermann, P El-Amraoui, A Safieddine, S Nouaille, S Perfettini, I Lecuit, M Cossart, P Wolfrum, U Petit, C Producer: 20010104 In: The EMBO journal vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	273.	Erratum: analysis of DNA elements that modulate myosin VIIa expression in humans. [electronic resource] by Orten, D J Weston, M D Kelley, P M Cremers, C W Wagenaar, M Jacobson, S G Kimberling, W J Producer: 20000120 In: Human mutation vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	274.	Modulation of Wnt Signaling Enhances Inner Ear Organoid Development in 3D Culture. [electronic resource] by DeJonge, Rachel E Liu, Xiao-Ping Deig, Christopher R Heller, Stefan Koehler, Karl R Hashino, Eri Producer: 20170804 In: PloS one vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	275.	Targeted next generation sequencing in Italian patients with Usher syndrome: phenotype-genotype correlations. [electronic resource] by Eandi, Chiara M Dallorto, Laura Spinetta, Roberta Micieli, Maria Pia Vanzetti, Mario Mariottini, Alessandro Passerini, Ilaria Torricelli, Francesca Alovisi, Camilla Marchese, Cristiana Producer: 20190703 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	276.	Assessment of differential gene expression in vestibular epithelial cell types using microarray analysis. [electronic resource] by Cristobal, Ricardo Wackym, P Ashley Cioffi, Joseph A Erbe, Christy B Roche, Joseph P Popper, Paul Producer: 20050512 In: Brain research. Molecular brain research vol. 133 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	277.	Lentiviral gene replacement therapy of retinas in a mouse model for Usher syndrome type 1B. [electronic resource] by Hashimoto, T Gibbs, D Lillo, C Azarian, S M Legacki, E Zhang, X-M Yang, X-J Williams, D S Producer: 20070629 In: Gene therapy vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	278.	The genetic dissection of [electronic resource] by Lu, Ye Zhou, Diana King, Rebecca Zhu, Shuang Simpson, Claire L Jones, Byron C Zhang, Wenbo Geisert, Eldon E Lu, Lu Producer: 20181112 In: Molecular vision vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	279.	Mitochondrial DNA variants mediate energy production and expression levels for CFH, C3 and EFEMP1 genes: implications for age-related macular degeneration. [electronic resource] by Kenney, M Cristina Chwa, Marilyn Atilano, Shari R Pavlis, Janelle M Falatoonzadeh, Payam Ramirez, Claudio Malik, Deepika Hsu, Tiffany Woo, Grace Soe, Kyaw Nesburn, Anthony B Boyer, David S Kuppermann, Baruch D Jazwinski, S Michal Miceli, Michael V Wallace, Douglas C Udar, Nitin Producer: 20130708 In: PloS one vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	280.	Detecting novel genetic mutations in Chinese Usher syndrome families using next-generation sequencing technology. [electronic resource] by Qu, Ling-Hui Jin, Xin Xu, Hai-Wei Li, Shi-Ying Yin, Zheng-Qin Producer: 20150406 In: Molecular genetics and genomics : MGG vol. 290 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 365 results.