Literature DB >> 23196365

Chaperoning the synapse--NMNAT protects Bruchpilot from crashing.

Elsa Lauwers1, Patrik Verstreken.   

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Year:  2012        PMID: 23196365      PMCID: PMC3537146          DOI: 10.1038/embor.2012.193

Source DB:  PubMed          Journal:  EMBO Rep        ISSN: 1469-221X            Impact factor:   8.807


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  12 in total

1.  WldS prevents axon degeneration through increased mitochondrial flux and enhanced mitochondrial Ca2+ buffering.

Authors:  Michelle A Avery; Timothy M Rooney; Jignesh D Pandya; Thomas M Wishart; Thomas H Gillingwater; James W Geddes; Patrick G Sullivan; Marc R Freeman
Journal:  Curr Biol       Date:  2012-03-15       Impact factor: 10.834

2.  Optical quantal analysis of synaptic transmission in wild-type and rab3-mutant Drosophila motor axons.

Authors:  Einat S Peled; Ehud Y Isacoff
Journal:  Nat Neurosci       Date:  2011-03-06       Impact factor: 24.884

3.  ELP3 controls active zone morphology by acetylating the ELKS family member Bruchpilot.

Authors:  Katarzyna Miśkiewicz; Liya E Jose; André Bento-Abreu; Marcus Fislage; Ines Taes; Jarosław Kasprowicz; Jef Swerts; Stephan Sigrist; Wim Versées; Wim Robberecht; Patrik Verstreken
Journal:  Neuron       Date:  2011-12-08       Impact factor: 17.173

4.  Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe macular and optic atrophy.

Authors:  Isabelle Perrault; Sylvain Hanein; Xavier Zanlonghi; Valérie Serre; Michael Nicouleau; Sabine Defoort-Delhemmes; Nathalie Delphin; Lucas Fares-Taie; Sylvie Gerber; Olivia Xerri; Catherine Edelson; Alice Goldenberg; Alice Duncombe; Gylène Le Meur; Christian Hamel; Eduardo Silva; Patrick Nitschke; Patrick Calvas; Arnold Munnich; Olivier Roche; Hélène Dollfus; Josseline Kaplan; Jean-Michel Rozet
Journal:  Nat Genet       Date:  2012-07-29       Impact factor: 38.330

5.  Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis.

Authors:  Pei-Wen Chiang; Juan Wang; Yang Chen; Quan Fu; Jing Zhong; Yanhua Chen; Xin Yi; Renhua Wu; Haixue Gan; Yong Shi; Yanling Chen; Christopher Barnett; Dianna Wheaton; Megan Day; Joanne Sutherland; Elise Heon; Richard G Weleber; Luis Alexandre Rassi Gabriel; Peikuan Cong; KuangHsiang Chuang; Sheng Ye; Juliana Maria Ferraz Sallum; Ming Qi
Journal:  Nat Genet       Date:  2012-07-29       Impact factor: 38.330

6.  Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration.

Authors:  Robert K Koenekoop; Hui Wang; Jacek Majewski; Xia Wang; Irma Lopez; Huanan Ren; Yiyun Chen; Yumei Li; Gerald A Fishman; Mohammed Genead; Jeremy Schwartzentruber; Naimesh Solanki; Elias I Traboulsi; Jingliang Cheng; Clare V Logan; Martin McKibbin; Bruce E Hayward; David A Parry; Colin A Johnson; Mohammed Nageeb; James A Poulter; Moin D Mohamed; Hussain Jafri; Yasmin Rashid; Graham R Taylor; Vafa Keser; Graeme Mardon; Huidan Xu; Chris F Inglehearn; Qing Fu; Carmel Toomes; Rui Chen
Journal:  Nat Genet       Date:  2012-07-29       Impact factor: 38.330

7.  Nicotinamide mononucleotide adenylyltransferase maintains active zone structure by stabilizing Bruchpilot.

Authors:  Shaoyun Zang; Yousuf O Ali; Kai Ruan; R Grace Zhai
Journal:  EMBO Rep       Date:  2012-11-16       Impact factor: 8.807

8.  A novel Drosophila model of nerve injury reveals an essential role of Nmnat in maintaining axonal integrity.

Authors:  Yanshan Fang; Lorena Soares; Xiuyin Teng; Melissa Geary; Nancy M Bonini
Journal:  Curr Biol       Date:  2012-03-15       Impact factor: 10.834

9.  Drosophila NMNAT maintains neural integrity independent of its NAD synthesis activity.

Authors:  R Grace Zhai; Yu Cao; P Robin Hiesinger; Yi Zhou; Sunil Q Mehta; Karen L Schulze; Patrik Verstreken; Hugo J Bellen
Journal:  PLoS Biol       Date:  2006-11       Impact factor: 8.029

10.  NMNAT1 mutations cause Leber congenital amaurosis.

Authors:  Marni J Falk; Qi Zhang; Eiko Nakamaru-Ogiso; Chitra Kannabiran; Zoe Fonseca-Kelly; Christina Chakarova; Isabelle Audo; Donna S Mackay; Christina Zeitz; Arundhati Dev Borman; Magdalena Staniszewska; Rachna Shukla; Lakshmi Palavalli; Saddek Mohand-Said; Naushin H Waseem; Subhadra Jalali; Juan C Perin; Emily Place; Julian Ostrovsky; Rui Xiao; Shomi S Bhattacharya; Mark Consugar; Andrew R Webster; José-Alain Sahel; Anthony T Moore; Eliot L Berson; Qin Liu; Xiaowu Gai; Eric A Pierce
Journal:  Nat Genet       Date:  2012-07-29       Impact factor: 38.330

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  2 in total

Review 1.  New approaches for studying synaptic development, function, and plasticity using Drosophila as a model system.

Authors:  C Andrew Frank; Xinnan Wang; Catherine A Collins; Avital A Rodal; Quan Yuan; Patrik Verstreken; Dion K Dickman
Journal:  J Neurosci       Date:  2013-11-06       Impact factor: 6.167

2.  Alpha-synucleinopathy reduces NMNAT3 protein levels and neurite formation that can be rescued by targeting the NAD+ pathway.

Authors:  Richard B Parsons; Altin Kocinaj; Gustavo Ruiz Pulido; Sarah A Prendergast; Anna E Parsons; Paul D Facey; Frank Hirth
Journal:  Hum Mol Genet       Date:  2022-08-25       Impact factor: 5.121

  2 in total

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