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S Masmoudi

Showing results (41-50 of 52) with videos related to

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Annals of Human Genetics|December 15, 2006
Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4A Tlili, S Masmoudi, H Dhouib, et al.
Journal De Medecine Vasculaire|July 15, 2017
[Surgical and endoluminal management of the inflammatory aortitis: A Tunisian center experience]H Ben Jmaà, R Karray, H Jmal, et al.
Clinical Genetics|February 5, 2010
Two missense mutations in SLC26A4 gene: a molecular and functional studyI Ben Rebeh, N Yoshimi, H Hadj-Kacem, et al.
Journal of Medical Genetics|November 10, 2000
Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGES Masmoudi, A Elgaied-Boulila, I Kassab, et al.
Archives De L'Institut Pasteur De Tunis|April 10, 2004
[Lipoprotein (a) and ischemic heart diseases in patients with type 2 diabetes]K Ben Hamda, A S Masmoudi, O Mandhouj, et al.
Journal De Medecine Vasculaire|December 6, 2017
[Post-traumatic carotido-jugular fistula: Case report and review of the literature]A Dammak, H Ben Jmaà, S Hadhri, et al.
Nature Genetics|November 1, 2001
Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locusE Verpy, S Masmoudi, I Zwaenepoel, et al.
Clinical Genetics|July 6, 2005
Analysis of GJB2 mutation: evidence for a Mediterranean ancestor for the 35delG mutationH Belguith, S Hajji, N Salem, et al.
Human Mutation|July 20, 2001
Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafnessS Masmoudi, S E Antonarakis, T Schwede, et al.
Frontiers in Microbiology|June 20, 2018
Two New Secreted Proteases Generate a Casein-Derived Antimicrobial Peptide in <i>Bacillus cereus</i> Food Born Isolate Leading to Bacterial Competition in MilkAwatef Ouertani, Ines Chaabouni, Amor Mosbah, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Annals of Human Genetics|December 15, 2006
Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4A Tlili, S Masmoudi, H Dhouib, et al.
Journal De Medecine Vasculaire|July 15, 2017
[Surgical and endoluminal management of the inflammatory aortitis: A Tunisian center experience]H Ben Jmaà, R Karray, H Jmal, et al.
Clinical Genetics|February 5, 2010
Two missense mutations in SLC26A4 gene: a molecular and functional studyI Ben Rebeh, N Yoshimi, H Hadj-Kacem, et al.
Journal of Medical Genetics|November 10, 2000
Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGES Masmoudi, A Elgaied-Boulila, I Kassab, et al.
Archives De L'Institut Pasteur De Tunis|April 10, 2004
[Lipoprotein (a) and ischemic heart diseases in patients with type 2 diabetes]K Ben Hamda, A S Masmoudi, O Mandhouj, et al.
Journal De Medecine Vasculaire|December 6, 2017
[Post-traumatic carotido-jugular fistula: Case report and review of the literature]A Dammak, H Ben Jmaà, S Hadhri, et al.
Nature Genetics|November 1, 2001
Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locusE Verpy, S Masmoudi, I Zwaenepoel, et al.
Clinical Genetics|July 6, 2005
Analysis of GJB2 mutation: evidence for a Mediterranean ancestor for the 35delG mutationH Belguith, S Hajji, N Salem, et al.
Human Mutation|July 20, 2001
Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafnessS Masmoudi, S E Antonarakis, T Schwede, et al.
Frontiers in Microbiology|June 20, 2018
Two New Secreted Proteases Generate a Casein-Derived Antimicrobial Peptide in <i>Bacillus cereus</i> Food Born Isolate Leading to Bacterial Competition in MilkAwatef Ouertani, Ines Chaabouni, Amor Mosbah, et al.
Pageof 6