Detalhe da pesquisa
1.
Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation.
Cell
; 167(1): 187-202.e17, 2016 Sep 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-27662089
2.
Macrozoospermia: screening for the homozygous c.144delC mutation in AURKC gene in infertile men and estimation of its heterozygosity frequency in the Tunisian population.
J Assist Reprod Genet
; 32(11): 1651-8, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26341096
3.
Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III.
J Hum Genet
; 57(3): 170-5, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22089644
4.
Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11ß hydroxylase deficiency in a Tunisian family.
Gen Comp Endocrinol
; 175(3): 514-8, 2012 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22210247
5.
TGFß: Signaling Blockade for Cancer Immunotherapy.
Annu Rev Cancer Biol
; 6(1): 123-146, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36382146
6.
Enhanced TGF-ß Signaling Contributes to the Insulin-Induced Angiogenic Responses of Endothelial Cells.
iScience
; 11: 474-491, 2019 Jan 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-30684493
7.
ENPP1 Mutation Causes Recessive Cole Disease by Altering Melanogenesis.
J Invest Dermatol
; 138(2): 291-300, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28964717
8.
Frequency of HNF4A-P.I463V Variant in the Tunisian North-African Population and Its Relation with Diabetes Mellitus.
Iran J Public Health
; 44(3): 396-403, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25905084
9.
Genetic study in a tunisian family revealed IVS1+1G>A mutation in the CHM gene.
Ann Biol Clin (Paris)
; 73(4): 469-73, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26411914
10.
From prevention to cure, repurposing anti-viral vaccines for cancer immunotherapy.
Biotarget
; 22018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30906919
11.
Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients.
Eur J Paediatr Neurol
; 16(2): 167-74, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21821450
12.
Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma.
Nat Genet
; 44(11): 1272-6, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23064416
13.
Multiple self-healing palmoplantar carcinoma: a familial predisposition to skin cancer with primary palmoplantar and conjunctival lesions.
J Invest Dermatol
; 135(1): 304-308, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25050600