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Induced Muscle and Liver Absence of Gne in Postnatal Mice Does Not Result in Structural or Functional Muscle Impairment Harazi, Avi; Yakovlev, Lena; Ilouz, Nili; Selke, Philipp; Horstkorte, Rudiger; Fellig, Yakov; Lahat, Olga; Lifschytz, Tzuri; Abudi, Nathalie; Abramovitch, Rinat; Argov, Zohar; Mitrani-Rosenbaum, Stella Share Save
Complement-membrane regulatory proteins are absent from the nodes of Ranvier in the peripheral nervous system Karbian, Netanel; Eshed-Eisenbach, Yael; Zeibak, Marian; Tabib, Adi; Sukhanov, Natasha; Vainshtein, Anya; Morgan, B. Paul; Fellig, Yakov; Peles, Elior; Mevorach, Dror Share Save
Biallelic Variants in the Ectonucleotidase ENTPD1 Cause a Complex Neurodevelopmental Disorder with Intellectual Disability, Distinct White Matter Abnormalities, and Spastic Paraplegia Calame, Daniel G.; Herman, Isabella; Maroofian, Reza; Marshall, Aren E.; Donis, Karina Carvalho; Fatih, Jawid M.; Mitani, Tadahiro; Du, Haowei; Grochowski, Christopher M.; Sousa, Sergio B.; Gijavanekar, Charul; Bakhtiari, Somayeh; Ito, Yoko A.; Rocca, Clarissa; Hunter, Jill, V; Sutton, V. Reid; Emrick, Lisa T.; Boycott, Kym M.; Lossos, Alexander; Fellig, Yakov; Prus, Eugenia; Kalish, Yosef; Meiner, Vardiella; Suerink, Manon; Ruivenkamp, Claudia; Muirhead, Kayla; Saadi, Nebal W.; Zaki, Maha S.; Bouman, Arjan; Barakat, Tahsin Stefan; Skidmore, David L.; Osmond, Matthew; Silva, Thiago Oliveira; Murphy, David; Karimiani, Ehsan Ghayoor; Jamshidi, Yalda; Jaddoa, Asaad Ghanim; Tajsharghi, Homa; Jin, Sheng Chih; Abbaszadegan, Mohammad Reza; Ebrahimzadeh-Vesal, Reza; Hosseini, Susan; Alavi, Shahryar; Bahreini, Amir; Zarean, Elahe; Salehi, Mohammad Mehdi; Al-Sannaa, Nouriya Abbas; Zifarelli, Giovanni; Bauer, Peter; Robson, Simon C.; Coban-Akdemir, Zeynep; Travaglini, Lorena; Nicita, Francesco; Jhangiani, Shalini N.; Gibbs, Richard A.; Posey, Jennifer E.; Kruer, Michael C.; Kernohan, Kristin D.; Morales Saute, Jonas A.; Houlden, Henry; Vanderver, Adeline; Elsea, Sarah H.; Pehlivan, Davut; Marafi, Dana; Lupski, James R. Share Save
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BRAF V600E mutation in Juvenile Xanthogranuloma family neoplasms of the central nervous system (CNS-JXG): a revised diagnostic algorithm to include pediatric Erdheim-Chester disease Picarsic, J.; Pysher, T.; Zhou, H.; Fluchel, M.; Pettit, T.; Whitehead, M.; Surrey, L. F.; Harding, B.; Goldstein, G.; Fellig, Y.; Weintraub, M.; Mobley, B. C.; Sharples, P. M.; Sulis, M. L.; Diamond, E. L.; Jaffe, R.; Shekdar, K.; Santi, M. Share Save
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Pax7, Pax3 and Mamstr genes are involved in skeletal muscle impaired regeneration of dy2J/dy2J mouse model of Lama2-CMD Yanay, Nurit; Elbaz, Moran; Konikov-Rozenman, Jenya; Elgavish, Sharona; Nevo, Yuval; Fellig, Yakov; Rabie, Malcolm; Mitrani-Rosenbaum, Stella; Nevo, Yoram Share Save
Radiation-Induced Vascular Malformations Mimicking Tumor in MRI-Based Treatment Response Assessment Maps (TRAMs) Mardor, Y.; Spiegelmann, R.; Guez, D.; Last, D.; Daniels, D.; Sharabi, S.; Nass, D.; Nissim, O.; Tsarfaty, G.; Hoffmann, C.; Talianski, A.; Fellig, Y.; Harnof, S.; Cohen, Z.; Shoshan, Y.; Zach, L. Share Save
NMO-IgG and AQP4 Peptide Can Induce Aggravation of EAMG and Immune-Mediated Muscle Weakness Mizrachi, Tehila; Brill, Livnat; Rabie, Malcolm; Nevo, Yoram; Fellig, Yakov; Zur, Mayan; Karussis, Dimitrios; Abramsky, Oded; Brenner, Talma; Vaknin-Dembinsky, Adi Share Save
Identification of the functional significance of mutations using the novel precision cancer analysis system Tarcic, Gabi; Peled, Nir; Barbash, Zohar; Barabash-Katzir, Naama; Yaakobi, Shlomo; Barabash-Katzir, Naama; Nevo, Hani; Vidne, Michael; Adamek, Mariusz; Kramer, Mordechai R.; Goncharenko, Nikolai; Fellig, Yakov; Meir, Karen; Mostov, Keith; Altschuler, Yoram Share Save
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Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder Lossos, Alexander; Elazar, Nimrod; Lerer, Israela; Schueler-Furman, Ora; Fellig, Yakov; Glick, Benjamin; Zimmerman, Bat-El; Azulay, Haim; Dotan, Shlomo; Goldberg, Sharon; Gomori, John M.; Ponger, Penina; Newman, J. P.; Marreed, Hodaifah; Steck, Andreas J.; Schaeren-Wiemers, Nicole; Mor, Nofar; Harel, Michal; Geiger, Tamar; Eshed-Eisenbach, Yael; Meiner, Vardiella; Peles, Elior Share Save
Nonsyndromic Early-Onset Cone-Rod Dystrophy and Limb-Girdle Muscular Dystrophy in a Consanguineous Israeli Family are Caused by Two Independent yet Linked Mutations in ALMS1 and DYSF Lazar, Csilla H.; Kimchi, Adva; Namburi, Prasanthi; Mutsuddi, Mousumi; Zelinger, Lina; Beryozkin, Avigail; Ben-Simhon, Shiran; Obolensky, Alexey; Ben-Neriah, Ziva; Argov, Zohar; Pikarsky, Eli; Fellig, Yakov; Marks-Ohana, Devorah; Ratnapriya, Rinki; Banin, Eyal; Sharon, Dror; Swaroop, Anand Share Save
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Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5 (vol 134, pg 305, 2015) Magen, Daniella; Ofir, Ayala; Berger, Liron; Goldsher, Dorit; Eran, Ayelet; Katib, Nasser; Nijem, Yousif; Vlodavsky, Euvgeni; Tzur, Shay; Behar, Doron M.; Fellig, Yakov; Mandel, Hanna Share Save
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