Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Lamiae Elkhattabi"'
Autor:
Imane Morjane, Hicham Charoute, Sanaa Ouatou, Lamiae Elkhattabi, Houda Benrahma, Rachid Saile, Hassan Rouba, Abdelhamid Barakat
Publikováno v:
Cardiology Research and Practice, Vol 2020 (2020)
Purpose. Coronary artery diseases (CAD) are clinical cardiovascular events associated with dyslipidemia in common. The interaction between environmental and genetic factors can be responsible for CAD. The present paper aimed to examine the associatio
Externí odkaz:
https://doaj.org/article/4ae80b7ce2d74100ad093ab5b8f8a891
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:
Lamiae Elkhattabi, Imane Morjane, Hicham Charoute, Soumaya Amghar, Hind Bouafi, Zouhair Elkarhat, Rachid Saile, Hassan Rouba, Abdelhamid Barakat
Publikováno v:
Journal of Diabetes Research, Vol 2019 (2019)
Resistin (RETN) is a gene coding for proinflammatory adipokine called resistin secreted by macrophages in humans. Single nucleotide polymorphisms (SNPs) in RETN are linked to obesity and insulin resistance in various populations. Using dbSNP, 78 nons
Externí odkaz:
https://doaj.org/article/41e98608f08d48dd86d2f849c1857432
Publikováno v:
Journal of Biomolecular Structure and Dynamics
The SARS-cov-2 RNA dependent RNA polymerase (nsp12) is a crucial viral enzyme that catalyzes the replication of RNA from RNA templates. The fixation of some ligands in the active site may alter the viral life cycle. The aim of the present study is to
Autor:
Zied Riahi, Redouane Boulouiz, Crystel Bonnet, Hicham Charoute, Soukaina Elrharchi, Lamiae Elkhattabi, Sara Salime, Christine Petit, Abdelhamid Barakat, Mostafa Kabine
Publikováno v:
Human Heredity. 85:35-39
Introduction: Auditory neuropathy is a hearing disorder where outer hair cell function within the cochlea is normal, but inner hair cell and/or the auditory nerve function is disrupted. It is a heterogeneous disorder, which can have either congenital
Autor:
Amina Bakhchane, Khalid Snoussi, Crystel Bonnet, Christine Petit, Amale Bousfiha, Hicham Charoute, Zied Riahi, Abdelhamid Barakat, Lamiae Elkhattabi
Publikováno v:
Human Heredity. 84:109-116
Mutations in the mesenchymal epithelial transition factor (MET) gene are frequently associated with multiple human cancers but can also lead to human non-syndromic autosomal recessive deafness (DFNB97). In the present study, we identified a novel hom
The novel COVID-19 pandemic is now a health threat, with a deep-felt impact worldwide. The new coronavirus 2019 (2019 n-Cov) binds to host human receptors through Receptor Binding Domain RBD of Spike glycoprotein (S), making it a prominent drug targe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44684c4437f7f6e68bcb2597988a59f9
https://doi.org/10.26434/chemrxiv.12115638.v1
https://doi.org/10.26434/chemrxiv.12115638.v1
Autor:
Amale, Bousfiha, Zied, Riahi, Lamiae, Elkhattabi, Amina, Bakhchane, Hicham, Charoute, Khalid, Snoussi, Crystel, Bonnet, Christine, Petit, Abdelhamid, Barakat
Publikováno v:
Human Heredity
Human Heredity, 2020, 84 (3), pp.109-116. ⟨10.1159/000503450⟩
Human Heredity, Karger, 2020, 84 (3), pp.109-116. ⟨10.1159/000503450⟩
Human Heredity, 2020, 84 (3), pp.109-116. ⟨10.1159/000503450⟩
Human Heredity, Karger, 2020, 84 (3), pp.109-116. ⟨10.1159/000503450⟩
International audience; Mutations in the mesenchymal epithelial transition factor (MET) gene are frequently associated with multiple human cancers but can also lead to human non-syndromic autosomal recessive deafness (DFNB97). In the present study, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e9640f2dacedd7ba42d79ba0a238b941
https://hal-pasteur.archives-ouvertes.fr/pasteur-03219615
https://hal-pasteur.archives-ouvertes.fr/pasteur-03219615
Autor:
Sanaa Nassereddine, Boutaina Belkady, Lamiae Elkhattabi, Zouhair Elkarhat, Abdelhamid Barakat, Latifa Zarouf, Lunda Razoki, Rachida Cadi, Hassan Rouba, Jamila Aboulfaraj
Publikováno v:
Human Heredity. 83:274-282
Background: Intellectual disability (ID) has been defined as a considerably reduced ability to understand new or complex information and to learn new skills. It is associated with life-long intellectual and adaptive functioning impairments that have
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