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Article title matches
- Category:Ush1 (35 bytes)
1: List of pages with the keyword Ush1
Page text matches
- 1uez (3,408 bytes)
10: ...bular function distinguish Usher syndrome type 1 (USH1), Usher syndrome type 2 (USH2) and Usher syndrome... - 1uf1 (3,391 bytes)
10: ...bular function distinguish Usher syndrome type 1 (USH1), Usher syndrome type 2 (USH2) and Usher syndrome... - 1ufx (3,763 bytes)
10: ...bular function distinguish Usher syndrome type 1 (USH1), Usher syndrome type 2 (USH2) and Usher syndrome... - 1x5n (3,632 bytes)
10: ...o blindness.<ref>PMID:10973247</ref> Defects in USH1C are the cause of deafness, autosomal recessive, ...
12: ...a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransducti... - Category:Ush1 (35 bytes)
1: List of pages with the keyword Ush1 - 2kbq (5,360 bytes)
10: ...o blindness.<ref>PMID:10973247</ref> Defects in USH1C are the cause of deafness, autosomal recessive, ...
12: ...a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransducti...
25: ...rotein network called Usher interactome. Harmonin/Ush1C is a master scaffold in the assembly of the Ushe... - 2kbr (5,460 bytes)
10: ...o blindness.<ref>PMID:10973247</ref> Defects in USH1C are the cause of deafness, autosomal recessive, ...
12: ...a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransducti...
25: ...rotein network called Usher interactome. Harmonin/Ush1C is a master scaffold in the assembly of the Ushe... - 2kbs (5,454 bytes)
10: ...o blindness.<ref>PMID:10973247</ref> Defects in USH1C are the cause of deafness, autosomal recessive, ...
12: ...a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransducti...
25: ...rotein network called Usher interactome. Harmonin/Ush1C is a master scaffold in the assembly of the Ushe... - 3k1r (5,483 bytes)
10: ...o blindness.<ref>PMID:10973247</ref> Defects in USH1C are the cause of deafness, autosomal recessive, ...
12: ...a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransducti...
25: ... complex. Mutations in harmonin and Sans found in USH1 patients are shown to destabilize the complex for... - 2l7t (3,845 bytes)
10: ...e type 2 (USH2) and Usher syndrome type 3 (USH3). USH1 is characterized by profound congenital sensorine...
12: ...a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransducti...
15: ... domains in the myosin tail that binds to another USH1 protein, Sans. We report the crystal structure of... - 2lsr (4,822 bytes)
10: ...o blindness.<ref>PMID:10973247</ref> Defects in USH1C are the cause of deafness, autosomal recessive, ...
12: ...a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransducti... - 5f3x (4,772 bytes)
11: ...o blindness.<ref>PMID:10973247</ref> Defects in USH1C are the cause of deafness, autosomal recessive, ...
13: ...a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransducti...
16: ...ons: protocadherin 24 and Harmonin (also known as USH1C or AIE-75), Harmonin and myosin VIIb (MYO7B), Ha...
18: Mechanistic Basis of Organization of the Harmonin/USH1C-Mediated Brush Border Microvilli Tip-Link Comple... - 5tfm (5,461 bytes)
11: ...1DF) [MIM:[https://omim.org/entry/601067 601067]. USH1DF patients are heterozygous for mutations in CDH2...
13: ...s part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransducti... - Harmonin (2,138 bytes)
6: ...rates three Usher syndrome (USH) type proteins to USH1-protein network<ref>PMID:16301216</ref>. Harm an...
10: ...disrupt stereocilia bundles and cause deafness in USH1 patients. - 5vvm (5,429 bytes)
11: ...1DF) [MIM:[https://omim.org/entry/601067 601067]. USH1DF patients are heterozygous for mutations in CDH2...
13: ...s part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransducti... - 5wj8 (5,630 bytes)
11: ...1DF) [MIM:[https://omim.org/entry/601067 601067]. USH1DF patients are heterozygous for mutations in CDH2...
13: ...s part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransducti... - 6kz1 (4,212 bytes)
10: ...bular function distinguish Usher syndrome type 1 (USH1), Usher syndrome type 2 (USH2) and Usher syndrome... - 7ep7 (4,178 bytes)
10: ...bular function distinguish Usher syndrome type 1 (USH1), Usher syndrome type 2 (USH2) and Usher syndrome... - 7x2e (3,177 bytes)
2: ==Structure of USH1C PDZ2 and coiled-coil in complex with CDHR2 C-ter...
11: ...o blindness.<ref>PMID:10973247</ref> Defects in USH1C are the cause of deafness, autosomal recessive, ...
13: ...a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransducti...
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