E-LIB Suche - Ergebnisse für: Salem, Ikhlass Hadj

1

CAPN3 mRNA processing alteration caused by splicing mutatio..:

Salem, Ikhlass Hadj ; Hsairi, Ines ; Mezghani, Najla...
Journal of Human Genetics. 57 (2011) 2 - p. 92-100 , 2011

2

The First Genome-Wide Scan in a Tunisian Family With Genera..:

Fendri-Kriaa, Nourhene ; Louhichi, Nacim ; Mkaouar-Rebai, Emna...
Journal of Child Neurology. 25 (2010) 11 - p. 1362-1368 , 2010

Link: https://doi.org/10.1177/..

3

Splicing defects in ABCD1 gene leading to both exon skippin..:

Kallabi, Fakhri ; Hadj Salem, Ikhlass ; Ben Chehida, Amel...
Neuroscience Research. 97 (2015) - p. 7-12 , 2015

Link: https://doi.org/10.1016/..

4

Founder effect confirmation of c.241A>G mutation in the L2H..:

Tunisian Network on Mental Retardation study ; Jellouli, Nadege Kammoun ; Hadj Salem, Ikhlass...
Journal of Human Genetics. 59 (2014) 4 - p. 216-222 , 2014

Link: https://doi.org/10.1038/..

5

Molecular confirmation of founder mutation c.-167A>G in Tun..:

Kammoun Jellouli, Nadege ; Hadj Salem, Ikhlass ; Ellouz, Emna...
Gene. 513 (2013) 2 - p. 233-238 , 2013

Link: https://doi.org/10.1016/..

6

A double mutation in AGXT gene in families with primary hyp..:

Kanoun, Houda ; Jarraya, Faiçal ; Hadj Salem, Ikhlass...
Gene. 531 (2013) 2 - p. 451-456 , 2013

Link: https://doi.org/10.1016/..

7

Impact of single-nucleotide polymorphisms at the TP53-bindi..:

Hadj Salem, Ikhlass ; Kamoun, Fatma ; Louhichi, Nacim...
Molecular Biology Reports. 39 (2012) 7 - p. 7479-7486 , 2012

Link: https://doi.org/10.1007/..

8

A whole mitochondrial genome screening in a MELAS patient: ..:

Mezghani, Najla ; Mnif, Mouna ; Kacem, Maha...
Biochemical and Biophysical Research Communications. 407 (2011) 4 - p. 747-752 , 2011

Link: https://doi.org/10.1016/..

9

Co-Culture of Human Bronchial Fibroblasts and CD4+ T Cells ..:

Loubaki, Lionel ; Hadj-Salem, Ikhlass ; Fakhfakh, Raouia...
PLoS ONE. 8 (2013) 12 - p. e81983 , 2013

Link: https://doi.org/10.1371/..

10

Co-culture of human bronchial fibroblasts and CD4+ T cells ..:

Lionel Loubaki ; Ikhlass Hadj-Salem ; Raouia Fakhfakh...
http://europepmc.org/articles/PMC3857794?pdf=render. , 2013

Link: https://doi.org/10.1371/..

11

Novel sequence variations in LAMA2 and SGCG genes modulatin..:

Olfa Siala ; Ikhlass Hadj Salem ; Abdelaziz Tlili...
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000100032. , 2010

Link: https://doaj.org/article..

12

Autosomal Recessive Ataxias:

, In: Essentials of Cerebellum and Cerebellar Disorders,

Beaudin, Marie ; Salem, Ikhlass Haj ; Dupré, Nicolas - p. 547-554 , 2023

Link: https://doi.org/10.1007/..

13

Genetic and epidemiological study of hereditary ataxia and ..:

SALEM, ikhlass HAJ ; Brunet, Francis ; Stumpf, Monica..
Neurology. 94 (2020) 15_supplement - p. , 2020

Link: https://doi.org/10.1212/..

14

A shift in the IL-6/STAT3 signalling pathway imbalance towa..:

Salem, Ikhlass Haj ; Plante, Sophie ; Gounni, Abdelilah S...
Cellular Signalling. 43 (2018) - p. 47-54 , 2018

Link: https://doi.org/10.1016/..

15

The mitochondrial ND1 m.3337G>A mutation associated to mult..:

Mezghani, Najla ; Mnif, Mouna ; Mkaouar-Rebai, Emna...
Biochemical and Biophysical Research Communications. 411 (2011) 2 - p. 247-252 , 2011

Link: https://doi.org/10.1016/..