Zobrazeno 101 - 108
of 108
pro vyhledávání: '"Barel, Ortal"'
Autor:
Faraci, Simona, Vardi, Ido, Rea, Francesca, Konnikova, Liza, Romeo, Erminia, Barel, Ortal, De Angelis, Paola, Dall'Oglio, Luigi, Rechavi, Gideon, Snapper, Scott, Somech, Raz, Weiss, Batia, Cancrini, Caterina, Shouval, Dror
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition; 2017 Supplement, Vol. 65, pS11-S12, 2p
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Niceta, Marcello, Lin, Yuh-Charn, Muto, Valentina, Vona, Barbara, Pagnamenta, Alistair T., Maroofian, Reza, Beetz, Christian, Duyvenvoorde, Hermine, Dentici, Maria Lisa, Lauffer, Peter, Vallian, Sadeq, Ciolfi, Andrea, Pizzi, Simone, Bauer, Peter, Gruning, Nana-Maria, Bellacchio, Emanuele, Del Fattore, Andrea, Stefania Petrini, Shaheen, Ranad, Tiosano, Dov, Halloun, Rana, Pode-Shakked, Ben, Albayrak, Hatice Mutlu, Isik, Emregul, Wit, Jan M., Dittrich, Marcus, Freire, Bruna L., Bertola, Debora R., Jorge, Alexander A. L., Barel, Ortal, Sabir, Ataf H., Al Teneiji, Amal M., Taji, Sulaima M., Al-Sannaa, Nouriya, Al-Abdulwahed, Hind, Digilio, Maria Cristina, Irving, Melita, Anikster, Yair, Bhavani, Gandham S. L., Girisha, Katta M., Haaf, Thomas, Taylor, Jenny C., Dallapiccola, Bruno, Alkuraya, Fowzan S., Yang, Ruey-Bing, Tartaglia, Marco
Publikováno v:
Web of Science
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8a717f5c3b3d0d420c8e4c693345393c
https://publons.com/wos-op/publon/53147512/
https://publons.com/wos-op/publon/53147512/
Autor:
Ben-Zeev, Bruria, Barel, Ortal, Malicdan, May Christine, Atawa, Osama, Cohen Ganelin, Et, Heimer, Gali, Nissenkorn, Andreea, Hoffman, Chen, Kandel, Judith, Schrader, Michael, Eckmann, David M., Anikster, Yair
Publikováno v:
European Journal of Paediatric Neurology; Jun2017 Supplement 1, Vol. 21, pe49-e49, 1p
Autor:
Maimuna S. Paul, Anna R. Duncan, Casie A. Genetti, Hongling Pan, Adam Jackson, Patricia E. Grant, Jiahai Shi, Michele Pinelli, Nicola Brunetti-Pierri, Alexandra Garza-Flores, Dave Shahani, Russell P. Saneto, Giuseppe Zampino, Chiara Leoni, Emanuele Agolini, Antonio Novelli, Ulrike Blümlein, Tobias B. Haack, Wolfram Heinritz, Eva Matzker, Bader Alhaddad, Rami Abou Jamra, Tobias Bartolomaeus, Saber AlHamdan, Raphael Carapito, Bertrand Isidor, Seiamak Bahram, Alyssa Ritter, Kosuke Izumi, Ben Pode Shakked, Ortal Barel, Bruria Ben Zeev, Amber Begtrup, Deanna Alexis Carere, Sureni V. Mullegama, Timothy Blake Palculict, Daniel G. Calame, Katharina Schwan, Alicia R.P. Aycinena, Rasa Traberg, Sofia Douzgou, Harrison Pirt, Naila Ismayilova, Siddharth Banka, Hsiao-Tuan Chao, Pankaj B. Agrawal
Publikováno v:
Am J Hum Genet
Eukaryotic initiation factor-4A2 (EIF4A2) is an ATP-dependent RNA helicase and a member of the DEAD-box protein family that recognizes the 5' cap structure of mRNAs, allows mRNA to bind to the ribosome, and plays an important role in microRNA-regulat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbcbe96535e30d1bd009e97bf4064b59
https://hdl.handle.net/11588/907834
https://hdl.handle.net/11588/907834
Autor:
Huang Y; Department of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA., Jay KL; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston TX 77030., Huang AY; Department of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA., Wan J; Department of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA., Jangam SV; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston TX 77030., Chorin O; Institute for Rare Diseases, Sheba Medical Center, Tel HaShomer, Ramat Gan, Israel., Rothschild A; Institute for Rare Diseases, Sheba Medical Center, Tel HaShomer, Ramat Gan, Israel., Barel O; Genomics Unit, The Center for Cancer Research, Sheba Medical Center, Tel Hashomer, Israel; Sheba Medical Center, Wohl Institute of Translational Medicine, Ramat Gan, Israel., Mariani M; Pediatric Department, ASST Lariana, Santa Anna General Hospital, Italy., Iascone M; Laboratorio di Genetica Medica, ASST Papa Giovanni XXIII, Bergamo, Italy., Xue H; Shanghai Institute of Precision Medicine at Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China., Huang J; Shanghai Institute of Precision Medicine at Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China., Mignot C; AP-HP Sorbonne Université, Département de Génétique, France; Centre de Référence Déficiences Intellectuelles de Causes Rares, France., Keren B; Genetic Department, GCS SeqOIA, Pitié-Salpêtrière Hospital, AP-HP, Sorbonne University, Paris, France., Saillour V; Laboratoire de biologie médicale multisites Seqoia - FMG2025, Paris, France., Mah-Som AY; Harvard Medical School Genetics Training Program, Boston, USA., Sacharow S; Division of Genetics and Genomics, Boston Children's Hospital, Boston, USA., Rajabi F; Section of Clinical Genetics and Metabolism, Department of Pediatrics, Children's Hospital Colorado and University of Colorado School of Medicine, Aurora, USA., Costin C; Division of Medical Genetics, Akron Children's Hospital, Akron, USA., Yamamoto S; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston TX 77030., Kanca O; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston TX 77030., Bellen HJ; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston TX 77030., Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Baylor Genetics Laboratories, Houston, USA., Palmer CGS; Department of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA; Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine at UCLA, Los Angeles, USA., Nelson SF; Department of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA., Wangler MF; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston TX 77030. Electronic address: Michael.Wangler@bcm.edu., Martinez-Agosto JA; Department of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA; Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine at UCLA, Los Angeles, USA. Electronic address: Julianmartinez@mednet.ucla.edu.
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2024 Jul 18, pp. 101218. Date of Electronic Publication: 2024 Jul 18.
Autor:
Reynhout S, Jansen S, Haesen D, van Belle S, de Munnik SA, Bongers EMHF, Schieving JH, Marcelis C, Amiel J, Rio M, Mclaughlin H, Ladda R, Sell S, Kriek M, Peeters-Scholte CMPCD, Terhal PA, van Gassen KL, Verbeek N, Henry S, Schwoerer JS, Malik S, Revencu N, Ferreira CR, Macnamara E, Braakman HMH, Brimble E, Ruzhnikov MRZ, Wagner M, Harrer P, Wieczorek D, Kuechler A, Tziperman B, Barel O, de Vries BBA, Gordon CT, Janssens V, Vissers LELM
Publikováno v:
American journal of human genetics [Am J Hum Genet] 2019 Feb 07; Vol. 104 (2), pp. 357.