Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Hassen, HadjKacem"'
Autor:
Alice Pavlowsky, Jean Luc Dupont, Henriette Skala, Robert Gardette, Aurélie Béglé, Hassen Hadjkacem, Nicolas Vitale, Jamel Chelly, Raphael Jean Courjaret, Frédéric Gambino, Bernard Poulain, Yann Humeau, Nadia Bahi
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2007, 104 (21), pp.9063-9068. ⟨10.1073/pnas.0701133104⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2007, 104 (21), pp.9063-9068. ⟨10.1073/pnas.0701133104⟩
Null mutations in the IL1-receptor accessory protein-like 1 gene ( IL1RAPL1 ) are responsible for an inherited X-linked form of cognitive impairment. IL1RAPL1 protein physically interacts with neuronal calcium sensor-1 (NCS-1), but the functional imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64dbf145fa54ecddac0f1ad1177f8e55
https://doi.org/10.1073/pnas.0701133104
https://doi.org/10.1073/pnas.0701133104
Autor:
Ayda, Khalfallah, Isabelle, Schrauwen, Malek, Mnejja, Hassen, HadjKacem, Leila, Dhouib, Mohamed Ali, Mosrati, Bochra, Hakim, Imed, Lahmar, Ilhem, Charfeddine, Nabil, Driss, Hammadi, Ayadi, Abdelmonem, Ghorbel, Guy, Van Camp, Saber, Masmoudi
Publikováno v:
Annals of human genetics. 75(5)
Otosclerosis is a condition characterized by an abnormal bone metabolism in the otic capsule, resulting in conductive and/or sensorineural hearing loss. Otosclerosis is a common disorder in which genes play an important role. Case-control association
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9f80b8c13c3e01526a9420077e510307
https://pubmed.ncbi.nlm.nih.gov/21777208
https://pubmed.ncbi.nlm.nih.gov/21777208