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Journal of Clinical Neuromuscular Disease|November 19, 2016
Novel Homozygous Missense Mutation in CAPN3 Gene Detected in a Saudi Arabian Family With Limb-Girdle Muscular Dystrophy Type 2ATalal M Al-Harbi, Sameeh O Abdulmanaʼ, Walid DridiCancer Genetics and Cytogenetics|May 14, 2003
The dominant-negative effect of p53 mutants and p21 induction in tetraploid G1 arrest depends on the type of p53 mutation and the nature of the stimulusWalid Dridi, Raouf Fetni, Josée Lavoie, et al.Journal of Clinical Neuromuscular Disease|August 28, 2019
Novel MFN2 Missense Mutation Induces Hereditary Axonal Motor and Sensory Neuropathy in a Saudi Arabian FamilyTalal M Al-Harbi, Sameeh O Abdulmana, Shahid Bashir, et al.Parasite (Paris, France)|April 4, 2013
Hyalomma scupense (Acari, Ixodidae) in northeast Tunisia: seasonal population dynamics of nymphs and adults on field cattleMohamed Gharbi, Mohamed Ettaïeb Hayouni, Limam Sassi, et al.Medecine Sciences : M/S|March 11, 2006
[Dominant negative activity of mutated p53 proteins]Walid Dridi, Kada Krabchi, Macoura Gadji, et al.Molecular Genetics & Genomic Medicine|May 11, 2022
Saudi Arabian CML patient with a novel four-way translocation at t(9;22;5;2)(q34;q11.2;p13;q44)Walid Dridi, Solaf Kanfar, Patrick M A Sleiman, et al.Parasite (Paris, France)|February 6, 2015
First report of surra (Trypanosoma evansi infection) in a Tunisian dogMohamed Ridha Rjeibi, Taoufik Ben Hamida, Zara Dalgatova, et al.American Journal of Medical Genetics. Part A|October 12, 2021
Rare neurological manifestations in a Saudi Arabian patient with Ehlers-Danlos syndrome and a novel homozygous variant in the TNXB geneTalal M Al-Harbi, Haya Al-Rammah, Naif Al-Zahrani, et al.Human Mutation|February 3, 2017
Loss-of-Function Mutations in KIF15 Underlying a Braddock-Carey GenocopyPatrick M A Sleiman, Michael March, Kenny Nguyen, et al.Pageof 1