Association of intronic repetition of SLC26A4 gene with Hashimoto thyroiditis disease.
SALIMA BELGUITH-MAALEJ , RIHAB KALLEL , MOUNA MNIF , MOHAMED ABID
Genetics Research 95 ( 1) 38 -44
3
2013
Association of COL1A1 and TGFB1 polymorphisms with otosclerosis in a Tunisian population.
Ayda Khalfallah , Isabelle Schrauwen , Malek Mnejja , Hassen HadjKacem
Annals of Human Genetics 75 ( 5) 598 -604
15
2011
Thyroglobulin polymorphisms in Tunisian patients with autoimmune thyroid diseases (AITD).
S BELGUITHMAALEJ , H HADJKACEM , A REBAI , M MNIF
Immunobiology 213 ( 7) 577 -583
7
2008
IL-1 receptor accessory protein like, a protein required for the development of cognitive functions, inhibits calcium current and growth hormone secretion in IL1RAPL-transfected PC12 cells.
D Feng , H Hadjkacem , N Vital , S Peineau
Association of specific ACE2 and TMPRSS2 variants with circulatory cytokines of COVID-19 Emirati patients
Noha M Elemam , Amal Bouzid , Habiba Alsafar , Samrein Ahmed
Frontiers in Immunology 15 1348229 -1348229
2024
Two missense mutations in SLC26A4 gene: a molecular and functional study
I Ben Rebeh , N Yoshimi , H Hadj‐Kacem , S Yanohco
Clinical genetics 78 ( 1) 74 -80
19
2010
Retracted: Genotyping of Tunisian azoospermic men with Sertoli cell‐only and maturation arrest
Lobna Hadjkacem‐Loukil , Hassen Hadj‐kacem , Ikhlass Hadj Salem , Ali Bahloul
Andrologia 50 ( 4) e1088 -e1088
7
2018
PCR–RFLP and species-specific PCR efficiency for the identification of adulteries in meat and meat products
Hassen Hadj Kacem , Héla Gargouri , Nizar Moalla
European Food Research and Technology 1 -10
2021
Nonstop Mutation in the Kisspeptin 1 Receptor (KISS1R) Gene Causes Normosmic Congenital Hypogonadotropic Hypogonadism
Mariam Moalla , Faten Hadj Kacem , Abdullah Fahad Al-Mutery , Mona Mahfood
Journal of Assisted Reproduction and Genetics 36 ( 6) 1273 -1280
4
2019
Evaluation of alternative DNA extraction protocols for the species determination in turkey salami authentication tests
Héla Gargouri , Hassen Hadj Kacem
International Journal of Food Properties 21 ( 1) 733 -745
2
2018
Polymorphisms of HLA DQB1 CAR1/CAR2 and TNFα IR2/IR4 Microsatellite Markers in Patients Affected with Graves Disease
Abdellatif Maalej , Hassen Hadj Kacem , Mohamed Bellassoued , Mohamed Abid
Clinical Immunology 96 ( 2) 91 -93
6
2000
CTLA-4 Gene Polymorphisms in Tunisian Patients with Graves' Disease
Hassen Hadj Kacem , Mohamed Bellassoued , Noura Bougacha-Elleuch , Mohamed Abid
Clinical Immunology 101 ( 3) 361 -365
59
2001
The A/T mutation in exon 2 of the DNASE1 gene is not present in Tunisian patients with systemic lupus erythematosus or in healthy subjects.
Pampa Chakraborty , Hassen Hadj Kacem , Kauothar Makni-Karray , Fai�al Jarraya
Arthritis & Rheumatism 48 ( 11) 3297 -3298
12
2003
Significant transcriptomic changes are associated with differentiation of bone marrow-derived mesenchymal stem cells into neural progenitor-like cells in the presence of bFGF and EGF
Amir Ali Khan , Tee Jong Huat , Abdullah Al Mutery , Ahmed Taher El-Serafi
Cell & Bioscience 10 ( 1) 126 -126
2
2020
Polymorphisms in the MUC16 Gene: Potential Implication in Epithelial Ovarian Cancer
Houda Bouanene , Hassen Hadj Kacem , Leila Ben Fatma , Halima Ben Limem
Pathology & Oncology Research 17 ( 2) 295 -299
3
2011
Intronic variants of SLC26A4 gene enhance splicing efficiency in hybrid minigene assay.
Rihab Kallel-Bouattour , Salima Belguith-Maalej , Emna Zouari-Bradai , Mouna Mnif
Gene 620 10 -14
6
2017
PDS is a new susceptibility gene to autoimmune thyroid diseases: association and linkage study.
Hassen Hadj Kacem , Ahmed Rebai , Noureddine Kaffel , Saber Masmoudi
The Journal of Clinical Endocrinology and Metabolism 88 ( 5) 2274 -2280
33
2003
The genetics of autoimmune thyroid disease
Hammadi Ayadi , Hassen Hadj Kacem , Ahmed Rebai , Nadir R. Farid
Trends in Endocrinology and Metabolism 15 ( 5) 234 -239
26
2004
Genetic investigation of FOXE1 polyalanine tract in thyroid diseases: new insight on the role of FOXE1 in thyroid carcinoma.
Rihab Kallel , Salima Belguith-Maalej , Abdelmounaim Akdi , Mouna Mnif
Cancer Biomarkers 8 ( 1) 43 -51
26
2011
Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss.
Abdelaziz Tlili , Abdullah Al Mutery , Walaa Kamal Eddine Ahmad Mohamed , Mona Mahfood
Genetic Testing and Molecular Biomarkers 21 ( 11) 686 -691
10
2017