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1 . Academic Journal
Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.
저자
by
AitRaise, Imane
;
Amalou, Ghita
;
Bakhchane, Amina
;
Bousfiha, Amale
;
Abdelghaffar, Houria
, et al.
소스
Biochemical Genetics
. Jun2024, Vol. 62 Issue 3, p1914-1924. 11p.
Web of Science
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7 . Academic Journal
Novel pathogenic WHRN variant causing hearing loss in a moroccan family.
저자
by
AitRaise, Imane
;
Amalou, Ghita
;
Redouane, Salaheddine
;
Charoute, Hicham
;
Snoussi, Khalid
, et al.
소스
Molecular Biology Reports; Dec2023, Vol. 50 Issue 12, p10663-10669, 7p
Web of Science
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7 . Academic Journal
Omenn syndrome caused by a novel homozygous mutation in recombination activating gene 1
저자
by
Benhsaien, Ibtihal
;
Essadssi, Soukaina
;
Elkhattabi, Lamiae
;
Bakhchane, Amina
;
Abdelghaffar, Houria
, et al.
소스
In
Immunobiology
May 2021 226(3)
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7 . Academic Journal
Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco.
저자
by
AitRaise, Imane
;
Amalou, Ghita
;
Bousfiha, Amale
;
Charoute, Hicham
;
Rouba, Hassan
, et al.
소스
Molecular Biology Reports; May2022, Vol. 49 Issue 5, p3949-3954, 6p
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7 . Academic Journal
Computational Analysis of nsSNPs of Gene in Severe Combined Immunodeficiency Using Molecular Modeling and Dynamics Simulation.
저자
by
Essadssi, Soukaina
;
Krami, Al Mehdi
;
Elkhattabi, Lamiae
;
Elkarhat, Zouhair
;
Amalou, Ghita
, et al.
소스
Journal of Immunology Research
. 11/3/2019, p1-14. 14p. 2 Diagrams, 2 Charts, 4 Graphs.
Open Access (Wiley)
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7 . Academic Journal
A Homozygous RAG1 Gene Mutation in a Case of Combined Immunodeficiency: Clinical, Molecular, and Computational Analysis.
저자
by
Essadssi, Soukaina
;
Benhsaien, Ibtihal
;
Bakhchane, Amina
;
Charoute, Hicham
;
Abdelghaffar, Houria
, et al.
소스
Human Heredity; 2019, Vol. 84 Issue 6, p272-278, 7p, 2 Diagrams, 2 Charts, 1 Graph
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7 . Academic Journal
Poikiloderma with Neutropenia in Morocco: a Report of Four Cases.
저자
by
Aglaguel, Ayoub
;
Abdelghaffar, Houria
;
Ailal, Fatima
;
Habti, Norddine
;
Hesse, Sebastian
, et al.
소스
Journal of Clinical Immunology
. May2017, Vol. 37 Issue 4, p357-362. 6p.
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7 . Academic Journal
A Homozygous RAG1 Gene Mutation in a Case of Combined Immunodeficiency: Clinical, Molecular, and Computational Analysis
저자
by
Essadssi, Soukaina
;
Benhsaien, Ibtihal
;
Bakhchane, Amina
;
Charoute, Hicham
;
Abdelghaffar, Houria
, et al.
소스
HUMAN HEREDITY
; NOV 2020, 84 6, p272-p278, 7p.
Scopus
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7 . Periodical
The Macrolide Roxithromycin Impairs NADPH Oxidase Activation and Alters Translocation of Its Cytosolic Components to the Neutrophil Membrane In Vitro
저자
by
Abdelghaffar, Houria
;
Babin-Chevaye, Catherine
;
Labro, Marie-Thérèse
.
소스
Antimicrobial Agents and Chemotherapy; July 2005, Vol. 49 Issue: 7 p2986-2989, 4p
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5 . Periodical
Interaction of the New Ketolide ABT-773 (Cethromycin) with Human Polymorphonuclear Neutrophils and the Phagocytic Cell Line PLB-985 In Vitro
저자
by
Labro, Marie Thérèse
;
Abdelghaffar, Houria
;
Babin-Chevaye, Catherine
.
소스
Antimicrobial Agents and Chemotherapy; April 2004, Vol. 48 Issue: 4 p1096-1104, 9p
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