USH1C (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "USH1C" in English language version.

refsWebsite

Global rank English rank

35nih.gov

4^th place

19doi.org

2^nd place

4semanticscholar.org

11^th place

8^th place

2ensembl.org

1,626^th place

1,007^th place

2harvard.edu

18^th place

17^th place

1zenodo.org

621^st place

380^th place

1discovermagazine.com

3,042^nd place

2,171^st place

1medium.com

551^st place

406^th place

discovermagazine.com (Global: 3,042^nd place; English: 2,171^st place)

Katz S (2020). "Why deaf people oppose using gene editing to "cure" deafness". Discover Magazine. Retrieved 2022-05-08.

doi.org (Global: 2^nd place; English: 2^nd place)

Verpy E, Leibovici M, Zwaenepoel I, Liu XZ, Gal A, Salem N, et al. (September 2000). "A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C". Nature Genetics. 26 (1): 51–55. doi:10.1038/79171. PMID 10973247. S2CID 9383331.
Ahmed ZM, Smith TN, Riazuddin S, Makishima T, Ghosh M, Bokhari S, et al. (June 2002). "Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC". Human Genetics. 110 (6): 527–531. doi:10.1007/s00439-002-0732-4. PMID 12107438. S2CID 24276167.
Bitner-Glindzicz M, Lindley KJ, Rutland P, Blaydon D, Smith VV, Milla PJ, et al. (September 2000). "A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene". Nature Genetics. 26 (1): 56–60. doi:10.1038/79178. PMID 10973248. S2CID 2237489.
Gregory FD, Bryan KE, Pangršič T, Calin-Jageman IE, Moser T, Lee A (August 2011). "Harmonin inhibits presynaptic Cav1.3 Ca²⁺ channels in mouse inner hair cells". Nature Neuroscience. 14 (9): 1109–1111. doi:10.1038/nn.2895. PMC 3164920. PMID 21822269.
Gregory FD, Pangrsic T, Calin-Jageman IE, Moser T, Lee A (July 2013). "Harmonin enhances voltage-dependent facilitation of Cav1.3 channels and synchronous exocytosis in mouse inner hair cells". The Journal of Physiology. 591 (13): 3253–3269. doi:10.1113/jphysiol.2013.254367. PMC 3717226. PMID 23613530.
Millán JM, Aller E, Jaijo T, Blanco-Kelly F, Gimenez-Pardo A, Ayuso C (2010-12-23). "An update on the genetics of usher syndrome". Journal of Ophthalmology. 2011 417217. doi:10.1155/2011/417217. PMC 3017948. PMID 21234346.
Grillet N, Xiong W, Reynolds A, Kazmierczak P, Sato T, Lillo C, et al. (May 2009). "Harmonin mutations cause mechanotransduction defects in cochlear hair cells". Neuron. 62 (3): 375–387. doi:10.1016/j.neuron.2009.04.006. PMC 2691393. PMID 19447093.
Boëda B, El-Amraoui A, Bahloul A, Goodyear R, Daviet L, Blanchard S, et al. (December 2002). "Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle". The EMBO Journal. 21 (24): 6689–6699. doi:10.1093/emboj/cdf689. PMC 139109. PMID 12485990.
Siemens J, Kazmierczak P, Reynolds A, Sticker M, Littlewood-Evans A, Müller U (November 2002). "The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions". Proceedings of the National Academy of Sciences of the United States of America. 99 (23): 14946–14951. Bibcode:2002PNAS...9914946S. doi:10.1073/pnas.232579599. PMC 137525. PMID 12407180.
Yu IM, Planelles-Herrero VJ, Sourigues Y, Moussaoui D, Sirkia H, Kikuti C, et al. (June 2017). "Myosin 7 and its adaptors link cadherins to actin". Nature Communications. 8 (1) 15864. Bibcode:2017NatCo...815864Y. doi:10.1038/ncomms15864. PMC 5493754. PMID 28660889.
Lentz J, Savas S, Ng SS, Athas G, Deininger P, Keats B (February 2005). "The USH1C 216G-->A splice-site mutation results in a 35-base-pair deletion". Human Genetics. 116 (3): 225–227. doi:10.1007/s00439-004-1217-4. PMID 15578223. S2CID 31987210.
Wang L, Kempton JB, Jiang H, Jodelka FM, Brigande AM, Dumont RA, et al. (May 2020). "Fetal antisense oligonucleotide therapy for congenital deafness and vestibular dysfunction". Nucleic Acids Research. 48 (9): 5065–5080. doi:10.1093/nar/gkaa194. PMC 7229850. PMID 32249312.
Reiners J, Nagel-Wolfrum K, Jürgens K, Märker T, Wolfrum U (July 2006). "Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease". Experimental Eye Research. 83 (1): 97–119. doi:10.1016/j.exer.2005.11.010. PMID 16545802.
de Joya EM, Colbert BM, Tang PC, Lam BL, Yang J, Blanton SH, et al. (April 2021). "Usher Syndrome in the Inner Ear: Etiologies and Advances in Gene Therapy". International Journal of Molecular Sciences. 22 (8): 3910. doi:10.3390/ijms22083910. PMC 8068832. PMID 33920085.
Locher H, Frijns JH, van Iperen L, de Groot JC, Huisman MA, Chuva de Sousa Lopes SM (October 2013). "Neurosensory development and cell fate determination in the human cochlea". Neural Development. 8 (1) 20. doi:10.1186/1749-8104-8-20. PMC 3854452. PMID 24131517.
Ponnath A, Depreux FF, Jodelka FM, Rigo F, Farris HE, Hastings ML, Lentz JJ (February 2018). "Rescue of Outer Hair Cells with Antisense Oligonucleotides in Usher Mice Is Dependent on Age of Treatment". Journal of the Association for Research in Otolaryngology. 19 (1): 1–16. doi:10.1007/s10162-017-0640-x. PMC 5783922. PMID 29027038.
Shnerson A, Willott JF (February 1980). "Ontogeny of the acoustic startle response in C57BL/6J mouse pups". Journal of Comparative and Physiological Psychology. 94 (1): 36–40. doi:10.1037/h0077648. PMID 7372853.
Pan B, Askew C, Galvin A, Heman-Ackah S, Asai Y, Indzhykulian AA, et al. (March 2017). "Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c". Nature Biotechnology. 35 (3): 264–272. doi:10.1038/nbt.3801. PMC 5340578. PMID 28165476.
Gonçalves GA, Paiva RM (2017). "Gene therapy: advances, challenges and perspectives". Einstein. 15 (3): 369–375. doi:10.1590/S1679-45082017RB4024. PMC 5823056. PMID 29091160.

ensembl.org (Global: 1,626^th place; English: 1,007^th place)

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000006611 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000030838 – Ensembl, May 2017

harvard.edu (Global: 18^th place; English: 17^th place)

ui.adsabs.harvard.edu

Siemens J, Kazmierczak P, Reynolds A, Sticker M, Littlewood-Evans A, Müller U (November 2002). "The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions". Proceedings of the National Academy of Sciences of the United States of America. 99 (23): 14946–14951. Bibcode:2002PNAS...9914946S. doi:10.1073/pnas.232579599. PMC 137525. PMID 12407180.
Yu IM, Planelles-Herrero VJ, Sourigues Y, Moussaoui D, Sirkia H, Kikuti C, et al. (June 2017). "Myosin 7 and its adaptors link cadherins to actin". Nature Communications. 8 (1) 15864. Bibcode:2017NatCo...815864Y. doi:10.1038/ncomms15864. PMC 5493754. PMID 28660889.

medium.com (Global: 551^st place; English: 406^th place)

futurehuman.medium.com

Mullin E (2021-01-26). "Gene therapy could end deafness. Should it?". Future Human. Retrieved 2022-05-08.

nih.gov (Global: 4^th place; English: 4^th place)

pubmed.ncbi.nlm.nih.gov

Verpy E, Leibovici M, Zwaenepoel I, Liu XZ, Gal A, Salem N, et al. (September 2000). "A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C". Nature Genetics. 26 (1): 51–55. doi:10.1038/79171. PMID 10973247. S2CID 9383331.
Ahmed ZM, Smith TN, Riazuddin S, Makishima T, Ghosh M, Bokhari S, et al. (June 2002). "Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC". Human Genetics. 110 (6): 527–531. doi:10.1007/s00439-002-0732-4. PMID 12107438. S2CID 24276167.
Bitner-Glindzicz M, Lindley KJ, Rutland P, Blaydon D, Smith VV, Milla PJ, et al. (September 2000). "A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene". Nature Genetics. 26 (1): 56–60. doi:10.1038/79178. PMID 10973248. S2CID 2237489.
Gregory FD, Bryan KE, Pangršič T, Calin-Jageman IE, Moser T, Lee A (August 2011). "Harmonin inhibits presynaptic Cav1.3 Ca²⁺ channels in mouse inner hair cells". Nature Neuroscience. 14 (9): 1109–1111. doi:10.1038/nn.2895. PMC 3164920. PMID 21822269.
Gregory FD, Pangrsic T, Calin-Jageman IE, Moser T, Lee A (July 2013). "Harmonin enhances voltage-dependent facilitation of Cav1.3 channels and synchronous exocytosis in mouse inner hair cells". The Journal of Physiology. 591 (13): 3253–3269. doi:10.1113/jphysiol.2013.254367. PMC 3717226. PMID 23613530.
Millán JM, Aller E, Jaijo T, Blanco-Kelly F, Gimenez-Pardo A, Ayuso C (2010-12-23). "An update on the genetics of usher syndrome". Journal of Ophthalmology. 2011 417217. doi:10.1155/2011/417217. PMC 3017948. PMID 21234346.
Grillet N, Xiong W, Reynolds A, Kazmierczak P, Sato T, Lillo C, et al. (May 2009). "Harmonin mutations cause mechanotransduction defects in cochlear hair cells". Neuron. 62 (3): 375–387. doi:10.1016/j.neuron.2009.04.006. PMC 2691393. PMID 19447093.
Boëda B, El-Amraoui A, Bahloul A, Goodyear R, Daviet L, Blanchard S, et al. (December 2002). "Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle". The EMBO Journal. 21 (24): 6689–6699. doi:10.1093/emboj/cdf689. PMC 139109. PMID 12485990.
Siemens J, Kazmierczak P, Reynolds A, Sticker M, Littlewood-Evans A, Müller U (November 2002). "The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions". Proceedings of the National Academy of Sciences of the United States of America. 99 (23): 14946–14951. Bibcode:2002PNAS...9914946S. doi:10.1073/pnas.232579599. PMC 137525. PMID 12407180.
Yu IM, Planelles-Herrero VJ, Sourigues Y, Moussaoui D, Sirkia H, Kikuti C, et al. (June 2017). "Myosin 7 and its adaptors link cadherins to actin". Nature Communications. 8 (1) 15864. Bibcode:2017NatCo...815864Y. doi:10.1038/ncomms15864. PMC 5493754. PMID 28660889.
Lentz J, Savas S, Ng SS, Athas G, Deininger P, Keats B (February 2005). "The USH1C 216G-->A splice-site mutation results in a 35-base-pair deletion". Human Genetics. 116 (3): 225–227. doi:10.1007/s00439-004-1217-4. PMID 15578223. S2CID 31987210.
Wang L, Kempton JB, Jiang H, Jodelka FM, Brigande AM, Dumont RA, et al. (May 2020). "Fetal antisense oligonucleotide therapy for congenital deafness and vestibular dysfunction". Nucleic Acids Research. 48 (9): 5065–5080. doi:10.1093/nar/gkaa194. PMC 7229850. PMID 32249312.
Reiners J, Nagel-Wolfrum K, Jürgens K, Märker T, Wolfrum U (July 2006). "Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease". Experimental Eye Research. 83 (1): 97–119. doi:10.1016/j.exer.2005.11.010. PMID 16545802.
de Joya EM, Colbert BM, Tang PC, Lam BL, Yang J, Blanton SH, et al. (April 2021). "Usher Syndrome in the Inner Ear: Etiologies and Advances in Gene Therapy". International Journal of Molecular Sciences. 22 (8): 3910. doi:10.3390/ijms22083910. PMC 8068832. PMID 33920085.
Locher H, Frijns JH, van Iperen L, de Groot JC, Huisman MA, Chuva de Sousa Lopes SM (October 2013). "Neurosensory development and cell fate determination in the human cochlea". Neural Development. 8 (1) 20. doi:10.1186/1749-8104-8-20. PMC 3854452. PMID 24131517.
Ponnath A, Depreux FF, Jodelka FM, Rigo F, Farris HE, Hastings ML, Lentz JJ (February 2018). "Rescue of Outer Hair Cells with Antisense Oligonucleotides in Usher Mice Is Dependent on Age of Treatment". Journal of the Association for Research in Otolaryngology. 19 (1): 1–16. doi:10.1007/s10162-017-0640-x. PMC 5783922. PMID 29027038.
Shnerson A, Willott JF (February 1980). "Ontogeny of the acoustic startle response in C57BL/6J mouse pups". Journal of Comparative and Physiological Psychology. 94 (1): 36–40. doi:10.1037/h0077648. PMID 7372853.
Pan B, Askew C, Galvin A, Heman-Ackah S, Asai Y, Indzhykulian AA, et al. (March 2017). "Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c". Nature Biotechnology. 35 (3): 264–272. doi:10.1038/nbt.3801. PMC 5340578. PMID 28165476.
Gonçalves GA, Paiva RM (2017). "Gene therapy: advances, challenges and perspectives". Einstein. 15 (3): 369–375. doi:10.1590/S1679-45082017RB4024. PMC 5823056. PMID 29091160.

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: USH1C Usher syndrome 1C (autosomal recessive, severe)".
Gregory FD, Bryan KE, Pangršič T, Calin-Jageman IE, Moser T, Lee A (August 2011). "Harmonin inhibits presynaptic Cav1.3 Ca²⁺ channels in mouse inner hair cells". Nature Neuroscience. 14 (9): 1109–1111. doi:10.1038/nn.2895. PMC 3164920. PMID 21822269.
Gregory FD, Pangrsic T, Calin-Jageman IE, Moser T, Lee A (July 2013). "Harmonin enhances voltage-dependent facilitation of Cav1.3 channels and synchronous exocytosis in mouse inner hair cells". The Journal of Physiology. 591 (13): 3253–3269. doi:10.1113/jphysiol.2013.254367. PMC 3717226. PMID 23613530.
Millán JM, Aller E, Jaijo T, Blanco-Kelly F, Gimenez-Pardo A, Ayuso C (2010-12-23). "An update on the genetics of usher syndrome". Journal of Ophthalmology. 2011 417217. doi:10.1155/2011/417217. PMC 3017948. PMID 21234346.
Grillet N, Xiong W, Reynolds A, Kazmierczak P, Sato T, Lillo C, et al. (May 2009). "Harmonin mutations cause mechanotransduction defects in cochlear hair cells". Neuron. 62 (3): 375–387. doi:10.1016/j.neuron.2009.04.006. PMC 2691393. PMID 19447093.
Boëda B, El-Amraoui A, Bahloul A, Goodyear R, Daviet L, Blanchard S, et al. (December 2002). "Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle". The EMBO Journal. 21 (24): 6689–6699. doi:10.1093/emboj/cdf689. PMC 139109. PMID 12485990.
Siemens J, Kazmierczak P, Reynolds A, Sticker M, Littlewood-Evans A, Müller U (November 2002). "The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions". Proceedings of the National Academy of Sciences of the United States of America. 99 (23): 14946–14951. Bibcode:2002PNAS...9914946S. doi:10.1073/pnas.232579599. PMC 137525. PMID 12407180.
Yu IM, Planelles-Herrero VJ, Sourigues Y, Moussaoui D, Sirkia H, Kikuti C, et al. (June 2017). "Myosin 7 and its adaptors link cadherins to actin". Nature Communications. 8 (1) 15864. Bibcode:2017NatCo...815864Y. doi:10.1038/ncomms15864. PMC 5493754. PMID 28660889.
Wang L, Kempton JB, Jiang H, Jodelka FM, Brigande AM, Dumont RA, et al. (May 2020). "Fetal antisense oligonucleotide therapy for congenital deafness and vestibular dysfunction". Nucleic Acids Research. 48 (9): 5065–5080. doi:10.1093/nar/gkaa194. PMC 7229850. PMID 32249312.
de Joya EM, Colbert BM, Tang PC, Lam BL, Yang J, Blanton SH, et al. (April 2021). "Usher Syndrome in the Inner Ear: Etiologies and Advances in Gene Therapy". International Journal of Molecular Sciences. 22 (8): 3910. doi:10.3390/ijms22083910. PMC 8068832. PMID 33920085.
Locher H, Frijns JH, van Iperen L, de Groot JC, Huisman MA, Chuva de Sousa Lopes SM (October 2013). "Neurosensory development and cell fate determination in the human cochlea". Neural Development. 8 (1) 20. doi:10.1186/1749-8104-8-20. PMC 3854452. PMID 24131517.
Ponnath A, Depreux FF, Jodelka FM, Rigo F, Farris HE, Hastings ML, Lentz JJ (February 2018). "Rescue of Outer Hair Cells with Antisense Oligonucleotides in Usher Mice Is Dependent on Age of Treatment". Journal of the Association for Research in Otolaryngology. 19 (1): 1–16. doi:10.1007/s10162-017-0640-x. PMC 5783922. PMID 29027038.
Pan B, Askew C, Galvin A, Heman-Ackah S, Asai Y, Indzhykulian AA, et al. (March 2017). "Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c". Nature Biotechnology. 35 (3): 264–272. doi:10.1038/nbt.3801. PMC 5340578. PMID 28165476.
Gonçalves GA, Paiva RM (2017). "Gene therapy: advances, challenges and perspectives". Einstein. 15 (3): 369–375. doi:10.1590/S1679-45082017RB4024. PMC 5823056. PMID 29091160.

semanticscholar.org (Global: 11^th place; English: 8^th place)

api.semanticscholar.org

Verpy E, Leibovici M, Zwaenepoel I, Liu XZ, Gal A, Salem N, et al. (September 2000). "A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C". Nature Genetics. 26 (1): 51–55. doi:10.1038/79171. PMID 10973247. S2CID 9383331.
Ahmed ZM, Smith TN, Riazuddin S, Makishima T, Ghosh M, Bokhari S, et al. (June 2002). "Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC". Human Genetics. 110 (6): 527–531. doi:10.1007/s00439-002-0732-4. PMID 12107438. S2CID 24276167.
Bitner-Glindzicz M, Lindley KJ, Rutland P, Blaydon D, Smith VV, Milla PJ, et al. (September 2000). "A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene". Nature Genetics. 26 (1): 56–60. doi:10.1038/79178. PMID 10973248. S2CID 2237489.
Lentz J, Savas S, Ng SS, Athas G, Deininger P, Keats B (February 2005). "The USH1C 216G-->A splice-site mutation results in a 35-base-pair deletion". Human Genetics. 116 (3): 225–227. doi:10.1007/s00439-004-1217-4. PMID 15578223. S2CID 31987210.

zenodo.org (Global: 621^st place; English: 380^th place)

Ahmed ZM, Smith TN, Riazuddin S, Makishima T, Ghosh M, Bokhari S, et al. (June 2002). "Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC". Human Genetics. 110 (6): 527–531. doi:10.1007/s00439-002-0732-4. PMID 12107438. S2CID 24276167.

USH1C (English Wikipedia)

discovermagazine.com (Global: 3,042nd place; English: 2,171st place)

doi.org (Global: 2nd place; English: 2nd place)

ensembl.org (Global: 1,626th place; English: 1,007th place)