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1 . Academic Journal
Antibody-mediated neutralization of galectin-3 as a strategy for the treatment of systemic sclerosis
저자
by
Céline Ortega-Ferreira
;
Perrine Soret
;
Gautier Robin
;
Silvia Speca
;
Sandra Hubert
, et al.
소스
Nature Communications, Vol 14, Iss 1, Pp 1-20 (2023)
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7 . Academic Journal
Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case–control study in the Tunisian population and a meta-analysis
저자
by
Hamza Dallali
;
Meriem Hechmi
;
Imane Morjane
;
Sahar Elouej
;
Haifa Jmel
, et al.
소스
Diabetology & Metabolic Syndrome, Vol 14, Iss 1, Pp 1-11 (2022)
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7 . Academic Journal
Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology
저자
by
Sahar Elouej
;
Karim Harhouri
;
Morgane Le Mao
;
Genevieve Baujat
;
Sheela Nampoothiri
, et al.
소스
Nature Communications, Vol 11, Iss 1, Pp 1-15 (2020)
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7 . Academic Journal
Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism
저자
by
Rahma Mkaouar
;
Lamia Cherif Ben Abdallah
;
Chokri Naouali
;
Saida Lahbib
;
Zinet Turki
, et al.
소스
Frontiers in Genetics, Vol 12 (2021)
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7 . Academic Journal
A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrome II Screening in Tunisia: A Case of Diffuse Gastric Carcinoma
저자
by
Maria Kabbage
;
Jihenne Ben Aissa-Haj
;
Houcemeddine Othman
;
Amira Jaballah-Gabteni
;
Sarra Laarayedh
, et al.
소스
Genes, Vol 13, Iss 8, p 1355 (2022)
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7 . Academic Journal
Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype
저자
by
Imen Nabouli
;
Asma Chikhaoui
;
Houcemeddine Othman
;
Sahar Elouej
;
Meriem Jones
, et al.
소스
Frontiers in Genetics, Vol 12 (2021)
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7 . Academic Journal
The Potential of Induced Pluripotent Stem Cells to Test Gene Therapy Approaches for Neuromuscular and Motor Neuron Disorders
저자
by
Marisa Cappella
;
Sahar Elouej
;
Maria Grazia Biferi
.
소스
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
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5 . Academic Journal
Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins
저자
by
Amira Jaballah-Gabteni
;
Haifa Tounsi
;
Maria Kabbage
;
Yosr Hamdi
;
Sahar Elouej
, et al.
소스
Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-13 (2019)
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7 . Academic Journal
FANCA Gene Mutations in North African Fanconi Anemia Patients
저자
by
Abir Ben Haj Ali
;
Olfa Messaoud
;
Sahar Elouej
;
Faten Talmoudi
;
Wiem Ayed
, et al.
소스
Frontiers in Genetics, Vol 12 (2021)
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7 . Academic Journal
Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome
저자
by
Nehla Ghedira
;
Arnaud Lagarde
;
Karim Ben Ameur
;
Sahar Elouej
;
Rania Sakka
, et al.
소스
BMC Pediatrics, Vol 18, Iss 1, Pp 1-7 (2018)
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