Risultati della ricerca - Nechama Shalva
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1
The mammalian Nek1 kinase is involved in primary cilium formation di Ohad Shalom, Nechama Shalva, Yoram Altschuler, Benny Motro
Pubblicazione 2008Artigo -
2
A Dominant Negative Heterozygous G87R Mutation in the Zinc Transporter, ZnT-2 (SLC30A2), Results in Transient Neonatal Zinc Deficiency di Inbal Lasry, Young Ah Seo, Hadas Ityel, Nechama Shalva, Ben Pode‐Shakked, Fabian Glaser, Bluma Berman, Igor N. Berezovsky, Alexander Goncearenco, Aharon Klar, Jacob Levy, Yair Anikster, Shannon L. Kelleher, Yehuda G. Assaraf
Pubblicazione 2012Artigo -
3
Deleterious variants in TRAK1 disrupt mitochondrial movement and cause fatal encephalopathy di Ortal Barel, May Christine V. Malicdan, Bruria Ben‐Zeev, Judith Kandel, Hadass Pri‐Chen, Joshi Stephen, Inês Gomes Castro, Jeremy Metz, Osama Atawa, Sharon Moshkovitz, Esther Ganelin, Iris Barshack, Sylvie Polak‐Charcon, Dvora Nass, Dina Marek‐Yagel, Ninette Amariglio, Nechama Shalva, Thierry Vilboux, Carlos R. Ferreira, Ben Pode‐Shakked, Gali Heimer, Chen Hoffmann, Tal Yardeni, Andreea Nissenkorn, Camila Avivi, Eran Eyal, Nitzan Kol, Efrat G. Saar, Douglas C. Wallace, William A. Gahl, Gideon Rechavi, Michael Schrader, David M. Eckmann, Yair Anikster
Pubblicazione 2017Artigo -
4
MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder di Gali Heimer, Juha M. Kerätär, Lisa G. Riley, Shanti Balasubramaniam, Eran Eyal, Laura P. Pietikäinen, J. Kalervo Hiltunen, Dina Marek‐Yagel, Jeffrey Hamada, Allison Gregory, Caleb Rogers, Penelope Hogarth, Martha Nance, Nechama Shalva, Alvit Veber, Michal Tzadok, Andreea Nissenkorn, Davide Tonduti, Florence Renaldo, Ichraf Kraoua, Celeste Panteghini, Lorella Valletta, Barbara Garavaglia, Mark J. Cowley, Velimir Gayevskiy, Tony Roscioli, Jonathon M. Silberstein, Chen Hoffmann, Annick Raas‐Rothschild, Valeria Tiranti, Yair Anikster, John Christodoulou, Alexander J. Kastaniotis, Bruria Ben‐Zeev, Susan J. Hayflick, Michael J. Bamshad, Suzanne M. Leal, Deborah A. Nickerson, Peter M. Anderson, Marcus Annable, Elizabeth Blue, Kati J. Buckingham, Jennifer Chin, Jessica X. Chong, Rodolfo Cornejo, Colleen Davis, Christopher Frazar, Zongxiao He, Gail P. Jarvik, Guillaume Jimenez, Eric Johanson, Tom Kolar, Stephanie Krauter, Daniel Luksic, Colby T. Marvin, Sean McGee, Daniel McGoldrick, Karynne Patterson, Marcos Perez, Sam W. Phillips, Jessica Pijoan, Peggy D. Robertson, Regie Lyn P. Santos‐Cortez, Aditi Shankar, Krystal Slattery, Kathryn M. Shively, Deborah L. Siegel, Joshua D. Smith, Monica Tackett, Gao Wang, Marc Wegener, Jeffrey M. Weiss, Riana I. Wernick, Marsha M. Wheeler, Yi Qian
Pubblicazione 2016Artigo
Strumenti per la ricerca:
Soggetti correlati
Biology
Gene
Genetics
Cell biology
Mitochondrion
Molecular biology
Mutant
Mutation
Basal body
Biochemistry
Cell
Cell cycle
Chemistry
Ciliogenesis
Cilium
Complementation
Cytoplasm
Endoplasmic reticulum
Flagellum
Golgi apparatus
Kidney
Kinase
Kinesin
Microtubule
Missense mutation
Mitochondrial DNA
Mitochondrial disease
Mitochondrial respiratory chain
Mitosis
Nonsense mutation