Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Limor Ziv"'
Autor:
Avital Baniel, Limor Ziv, Zohar Ben-Moshe, Ofer Sarig, Janan Mohamad, Alon Peled, Gideon Rechavi, Yoav Gothilf, Eli Sprecher
Publikováno v:
Biomedicines, Vol 10, Iss 12, p 3192 (2022)
Background: Gain-of-function mutations in CARD14 have recently been shown to be involved in the pathogenesis of psoriasis and pityriasis rubra pilaris (PRP). Those mutations were found to activate the NF-kB signaling pathway. Objective: Zebrafish is
Externí odkaz:
https://doaj.org/article/ed303753e0f64c718a3a5cbadf779228
Autor:
Alon Peled, Ofer Sarig, Liat Samuelov, Marta Bertolini, Limor Ziv, Daphna Weissglas-Volkov, Marina Eskin-Schwartz, Christopher A Adase, Natalia Malchin, Ron Bochner, Gilad Fainberg, Ilan Goldberg, Koji Sugawara, Avital Baniel, Daisuke Tsuruta, Chen Luxenburg, Noam Adir, Olivier Duverger, Maria Morasso, Stavit Shalev, Richard L Gallo, Noam Shomron, Ralf Paus, Eli Sprecher
Publikováno v:
PLoS Genetics, Vol 12, Iss 10, p e1006369 (2016)
Despite recent advances in our understanding of the pathogenesis of ectodermal dysplasias (EDs), the molecular basis of many of these disorders remains unknown. In the present study, we aimed at elucidating the genetic basis of a new form of ED featu
Externí odkaz:
https://doaj.org/article/2a310f48642d4138a48fbddd5896a7f3
Publikováno v:
Journalism. 22:1983-2000
Social media editors were initially appointed by media organizations which aimed to extend their reach and to establish their presence in social media. These editors were hired to create content on behalf of mass media organizations, but with social
Autor:
Gideon Rechavi, Itai M. Pessach, Shoshana Greenberger, Limor Ziv-Strasser, Eran Eyal, Ninette Amariglio, Uri Rimon, Aviv Barzilai, Inbal Davidi-Avrahami, Karina Yaniv, Eugenia Manevitz-Mendelson, Keren Chechekes, Ortal Barel, Abraham Hirshberg, Gil S. Leichner
Publikováno v:
Angiogenesis. 21:287-298
Generalized lymphatic anomaly (GLA or lymphangiomatosis) is a rare disease characterized by a diffuse proliferation of lymphatic vessels in skin and internal organs. It often leads to progressive respiratory failure and death, but its etiology is unk
Autor:
Fekado Gadamo, Nivi Dayan, Limor Ziv, Gal Yavetz, Seffefe Ayecheh, Nurit Guttman, Eimi Lev, Elad Segev
Publikováno v:
New Media & Society. 20:2272-2295
The Internet is a major source for health information but contributes to the digital divide and health disparities. Minorities with low literacy skills are at a particular disadvantage in obtaining online information. A website was created with healt
Autor:
Eran Eyal, Karen W. Gripp, Angela L. Duker, Marco Tartaglia, Annick Raas-Rothschild, Karen S. Carvalho, Ben Pode-Shakked, Enrico Bertini, Marcello Niceta, Omer Bar-Yosef, Ortal Barel, Nitzan Kol, Elisabetta Flex, Limor Ziv, Giovanni Chillemi, Mena Scavina, Bruria Ben-Zeev, Yair Anikster, Hila Barash, Dina Marek-Yagel
Publikováno v:
Clinical Genetics. 91:725-738
Microtubule dynamics play a crucial role in neuronal development and function, and several neurodevelopmental disorders have been linked to mutations in genes encoding tubulins and functionally related proteins. Most recently, variants in the tubulin
Autor:
Shay Botchan, Mingyan Fang, Oren Pleniceanu, Benjamin Dekel, Le Cheng, Einat Lahav, Nir Pillar, Noam Shomron, Limor Ziv
Publikováno v:
Human Genetics
Isolated familial hypoparathyroidism is an extremely rare disorder, which to date has been linked to several loci including mutations in CASR, GCM2, and PTH, as well as a rare condition defined as X-linked recessive hypoparathyroidism, previously ass
Autor:
N. Malchin, Noam Shomron, Limor Ziv, Avital Baniel, Daphna Weissglas-Volkov, Maria I. Morasso, Ofer Sarig, Christopher A. Adase, Daisuke Tsuruta, Gilad Fainberg, Liat Samuelov, Stavit A. Shalev, Alon Peled, Eli Sprecher, Koji Sugawara, Olivier Duverger, R. Bochner, Chen Luxenburg, Ilan Goldberg, Ralf Paus, Richard L. Gallo, Marta Bertolini, Noam Adir, M. Eskin-Schwartz
Publikováno v:
Peled, A, Sarig, O, Samuelov, L, Bertolini, M, Ziv, L, Weissglas-Volkov, D, Eskin-Schwartz, M, Adase, C A, Malchin, N, Bochner, R, Fainberg, G, Goldberg, I, Sugawara, K, Baniel, A, Tsuruta, D, Luxenburg, C, Adir, N, Duverger, O, Morasso, M, Shalev, S, Gallo, R L, Shomron, N, Paus, R & Sprecher, E 2016, ' Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis ', PL o S Genetics, vol. 12, no. 10, pp. e1006369 . https://doi.org/10.1371/journal.pgen.1006369
PLoS Genetics
PLoS Genetics, Vol 12, Iss 10, p e1006369 (2016)
PLoS genetics, vol 12, iss 10
PLoS Genetics
PLoS Genetics, Vol 12, Iss 10, p e1006369 (2016)
PLoS genetics, vol 12, iss 10
Despite recent advances in our understanding of the pathogenesis of ectodermal dysplasias (EDs), the molecular basis of many of these disorders remains unknown. In the present study, we aimed at elucidating the genetic basis of a new form of ED featu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a95bbd24fca0fe1dce891229e09d4900
https://doi.org/10.1371/journal.pgen.1006369
https://doi.org/10.1371/journal.pgen.1006369
Autor:
J. Wade Harper, Ben Pode-Shakked, Riccardo Berutti, Tobias B. Haack, Imen Dorboz, Edward L. Huttlin, Georg F. Hoffmann, Thomas Meissner, David Meili, Gerard Schwartz, Manuel Schiff, Limor Ziv-Strasser, Gali Heimer, May Christine V. Malicdan, Corinne Gemperle-Britschgi, Virginia Guarani, Jean-François Benoist, Aurora Martinez, William A. Gahl, Irene Keller, Thomas Meitinger, Yair Anikster, Nan Shen, Kirsten Cremer, Yuval Landau, Holger Prokisch, Ertan Mayatepek, Apolline Imbard, Tim M. Strom, Beat Thöny, Thierry Vilboux, James C. Mullikin, Bruria Ben-Zeev, Friedrich K. Trefz, Dina Marek-Yagel, Joao A. Paulo, Nenad Blau, Hartmut Engels, Thomas Opladen, Rémy Bruggmann
Publikováno v:
Am. J. Hum. Genet. 100, 257-266 (2017)
Phenylketonuria (PKU, phenylalanine hydroxylase deficiency), an inborn error of metabolism, can be detected through newborn screening for hyperphenylalaninemia (HPA). Most individuals with HPA harbor mutations in the gene encoding phenylalanine hydro
Autor:
Herwig Baier, Marcel J. M. Schaaf, Sebastiaan H. Meijsing, Limor Ziv, Peter J. Schoonheim, Keith R. Yamamoto, Akira Muto, Daniel Strasser, Holly A. Ingraham
Publikováno v:
Molecular Psychiatry
Molecular psychiatry
Molecular psychiatry
Upon binding of cortisol, the glucocorticoid receptor (GR) regulates the transcription of specific target genes, including those that encode the stress hormones corticotropin-releasing hormone (CRH) and adrenocorticotropic hormone (ACTH). Dysregulati