Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Houria Abdelghaffar"'
Autor:
Soukaina Essadssi, Al Mehdi Krami, Lamiae Elkhattabi, Zouhair Elkarhat, Ghita Amalou, Houria Abdelghaffar, Hassan Rouba, Abdelhamid Barakat
Publikováno v:
Journal of Immunology Research, Vol 2019 (2019)
Severe combined immunodeficiency (SCID) is the most severe form of primary immunodeficiency (PID), characterized by fatal opportunistic infections. The ADA gene encodes adenosine deaminase, an enzyme that catalyzes the irreversible deamination of ade
Externí odkaz:
https://doaj.org/article/e85042a2409444ac95a68039de425c73
Autor:
Imane AitRaise, Ghita Amalou, Amale Bousfiha, Hicham Charoute, Hassan Rouba, Houria Abdelghaffar, Crystel Bonnet, Christine Petit, Adbelhamid Barakat
Publikováno v:
Molecular Biology Reports
Molecular Biology Reports, 2022, 49 (5), pp.3949-3954. ⟨10.1007/s11033-022-07245-z⟩
Molecular Biology Reports, 2022, 49 (5), pp.3949-3954. ⟨10.1007/s11033-022-07245-z⟩
International audience; Background: Deafness is the most prevalent human sensorineural defect. It may occur as a result of an external auditory canal involvement, or a deficiency in the sound conduction mechanism, or an impairment of the cochlea, the
Autor:
Ahmed Aziz Bousfiha, Houria Abdelghaffar, Hicham Charoute, Amina Bakhchane, Soukaina Essadssi, Ibtihal Benhsaien, Abdelhamid Barakat
Publikováno v:
Human heredity. 84(6)
Background: The recombination-activating gene 1 and 2 (RAG1/RAG2) proteins are essential to initiate the V(D)J recombination process, the result is a diverse repertoire of antigen receptor genes and the establishment of the adaptive immunity. RAG1 mu
Autor:
Amina Bakhchane, Ahmed Aziz Bousfiha, Houria Abdelghaffar, Abdallah Badou, Ibtihal Benhsaien, Abdelhamid Barakat, Lamiae Elkhattabi, Soukaina Essadssi
Publikováno v:
Immunobiology. 226:152090
Omenn syndrome (OS) is a type of severe combined immunodeficiency (SCID) that is distinguished by, lymphadenopathy, hepatosplenomegaly, erythroderma, alopecia with normal to elevated T-cell counts, eosinophilia, and elevated serum IgE levels. Recombi
Autor:
Christoph Klein, Ayoub Aglaguel, Houria Abdelghaffar, Ahmed Aziz Bousfiha, Sebastian Hesse, Naschla Kohistani, Fatima Ailal, Norddine Habti
Publikováno v:
Journal of Clinical Immunology. 37:357-362
Poikiloderma with Neutropenia (PN) is inherited genodermatosis which results from a biallelic mutation in the USB1 gene (U Six Biogenesis 1). PN, first described in Navajo Native Americans, is characterized by early onset poikiloderma, pachyonychia,