Literature DB >> 28724583

Anoctamins (TMEM16 proteins): Functions and involvement in neurologic disease.

Eduardo E Benarroch1.   

Abstract

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Year:  2017        PMID： 28724583     DOI： 10.1212/WNL.0000000000004246

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  11 in total

Review 1.  ANO10 Function in Health and Disease.

Authors:  Androniki Chrysanthou; Antonis Ververis; Kyproula Christodoulou
Journal:  Cerebellum       Date:  2022-06-01       Impact factor: 3.847

2.  Autosomal recessive adult onset ataxia.

Authors:  Nataša Dragašević-Mišković; Iva Stanković; Andona Milovanović; Vladimir S Kostić
Journal:  J Neurol       Date:  2021-09-09       Impact factor: 4.849

3.  Pangenomics enables genotyping of known structural variants in 5202 diverse genomes.

Authors:  Jouni Sirén; Jean Monlong; Xian Chang; Adam M Novak; Jordan M Eizenga; Charles Markello; Jonas A Sibbesen; Glenn Hickey; Pi-Chuan Chang; Andrew Carroll; Namrata Gupta; Stacey Gabriel; Thomas W Blackwell; Aakrosh Ratan; Kent D Taylor; Stephen S Rich; Jerome I Rotter; David Haussler; Erik Garrison; Benedict Paten
Journal:  Science       Date:  2021-12-17       Impact factor: 63.714

4.  Membrane lipids are both the substrates and a mechanistically responsive environment of TMEM16 scramblase proteins.

Authors:  George Khelashvili; Xiaolu Cheng; Maria E Falzone; Milka Doktorova; Alessio Accardi; Harel Weinstein
Journal:  J Comput Chem       Date:  2019-11-21       Impact factor: 3.376

5.  Role of Dysregulated Ion Channels in Sensory Neurons in Chronic Kidney Disease-Associated Pruritus.

Authors:  Akishi Momose; Micihihiro Yabe; Shigetoshi Chiba; Kenjirou Kumakawa; Yasuo Shiraiwa; Hiroki Mizukami
Journal:  Medicines (Basel)       Date:  2019-11-13

Review 6.  Polymodal Control of TMEM16x Channels and Scramblases.

Authors:  Emilio Agostinelli; Paolo Tammaro
Journal:  Int J Mol Sci       Date:  2022-01-29       Impact factor: 5.923

Review 7.  Lipid Dyshomeostasis and Inherited Cerebellar Ataxia.

Authors:  Jin Zhao; Huan Zhang; Xueyu Fan; Xue Yu; Jisen Huai
Journal:  Mol Neurobiol       Date:  2022-04-14       Impact factor: 5.682

8.  TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia.

Authors:  Luis Carlos Tábara; Fatema Al-Salmi; Reza Maroofian; Amna Mohammed Al-Futaisi; Fathiya Al-Murshedi; Joanna Kennedy; Jacob O Day; Thomas Courtin; Aisha Al-Khayat; Hamid Galedari; Neda Mazaheri; Margherita Protasoni; Mark Johnson; Joseph S Leslie; Claire G Salter; Lettie E Rawlins; James Fasham; Almundher Al-Maawali; Nikol Voutsina; Perrine Charles; Laura Harrold; Boris Keren; Edmund R S Kunji; Barbara Vona; Gholamreza Jelodar; Alireza Sedaghat; Gholamreza Shariati; Henry Houlden; Andrew H Crosby; Julien Prudent; Emma L Baple
Journal:  Brain       Date:  2022-09-14       Impact factor: 15.255

Review 9.  ANO5-related muscle diseases: From clinics and genetics to pathology and research strategies.

Authors:  Jon Christiansen; Anne-Katrin Güttsches; Ulrike Schara-Schmidt; Matthias Vorgerd; Christoph Heute; Corinna Preusse; Werner Stenzel; Andreas Roos
Journal:  Genes Dis       Date:  2022-02-14

10.  Autosomal Recessive Spinocerebellar Ataxia Type 10: A Report of a New Case in Japan.

Authors:  Izumi Aida; Tetsuo Ozawa; Kentaro Ohta; Hidehiko Fujinaka; Kiyoe Goto; Takashi Nakajima
Journal:  Intern Med       Date:  2022-02-01       Impact factor: 1.282
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