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Olfa Messaoud

Showing results (1-10 of 46) with videos related to

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Biomed Research International|October 24, 2013
Polymorphisms in the human cytochrome P450 and arylamine N-acetyltransferase: susceptibility to head and neck cancersRim Khlifi, Olfa Messaoud, Ahmed Rebai, et al.
Frontiers in Genetics|December 30, 2021
Editorial: Monogenic vs. Oligogenic ReclassificationOlfa Messaoud, Atanu Kumar Dutta, Mario Reynaldo Cornejo-Olivas, et al.
Gene|October 19, 2013
Mutational spectrum of Xeroderma pigmentosum group A in Egyptian patientsKhalda Amr, Olfa Messaoud, Mohamad El Darouti, et al.
International Journal of Dermatology|April 11, 2019
Congenital lamellar ichthyosis in Tunisia associated with vitamin D rickets caused by a founder nonsense mutation in the TGM1 geneAnissa Zaouak, Ghaith Abdessalem, Rahma Mkaouar, et al.
Molecules (Basel, Switzerland)|June 27, 2024
Novel and Extremely Sensitive NiAl<sub>2</sub>O<sub>4</sub>-NiO Nanostructures on an ITO Sensing Electrode for Enhanced Detection of Ascorbic AcidAsma Hammami, Afrah Bardaoui, Shimaa Eissa, et al.
Skinmed|August 17, 2022
When to Recommend a Peripheral Blood Smear to Patients with Congenital Ichthyosiform ErythrodermaAnissa Zaouak, Ghaith Abdessalem, Olfa Messaoud, et al.
NPJ Genomic Medicine|January 9, 2021
A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North AfricaLilia Romdhane, Nessrine Mezzi, Hamza Dallali, et al.
International Journal of Dermatology|June 11, 2010
Genetic homogeneity of mutational spectrum of group-A xeroderma pigmentosum in Tunisian patientsOlfa Messaoud, Mariem Ben Rekaya, Wafa Cherif, et al.
Molecular Genetics & Genomic Medicine|February 22, 2023
First genetic characterization of Xeroderma pigmentosum in Libya: High frequency of XP-C founder mutationNajlaa Khalat, Olfa Messaoud, Mariem Ben Rekaya, et al.
Archives of Dermatological Research|November 13, 2012
c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosumMohamed Amine Senhaji, Omar Abidi, Sellama Nadifi, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
Biomed Research International|October 24, 2013
Polymorphisms in the human cytochrome P450 and arylamine N-acetyltransferase: susceptibility to head and neck cancersRim Khlifi, Olfa Messaoud, Ahmed Rebai, et al.
Frontiers in Genetics|December 30, 2021
Editorial: Monogenic vs. Oligogenic ReclassificationOlfa Messaoud, Atanu Kumar Dutta, Mario Reynaldo Cornejo-Olivas, et al.
Gene|October 19, 2013
Mutational spectrum of Xeroderma pigmentosum group A in Egyptian patientsKhalda Amr, Olfa Messaoud, Mohamad El Darouti, et al.
International Journal of Dermatology|April 11, 2019
Congenital lamellar ichthyosis in Tunisia associated with vitamin D rickets caused by a founder nonsense mutation in the TGM1 geneAnissa Zaouak, Ghaith Abdessalem, Rahma Mkaouar, et al.
Molecules (Basel, Switzerland)|June 27, 2024
Novel and Extremely Sensitive NiAl<sub>2</sub>O<sub>4</sub>-NiO Nanostructures on an ITO Sensing Electrode for Enhanced Detection of Ascorbic AcidAsma Hammami, Afrah Bardaoui, Shimaa Eissa, et al.
Skinmed|August 17, 2022
When to Recommend a Peripheral Blood Smear to Patients with Congenital Ichthyosiform ErythrodermaAnissa Zaouak, Ghaith Abdessalem, Olfa Messaoud, et al.
NPJ Genomic Medicine|January 9, 2021
A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North AfricaLilia Romdhane, Nessrine Mezzi, Hamza Dallali, et al.
International Journal of Dermatology|June 11, 2010
Genetic homogeneity of mutational spectrum of group-A xeroderma pigmentosum in Tunisian patientsOlfa Messaoud, Mariem Ben Rekaya, Wafa Cherif, et al.
Molecular Genetics & Genomic Medicine|February 22, 2023
First genetic characterization of Xeroderma pigmentosum in Libya: High frequency of XP-C founder mutationNajlaa Khalat, Olfa Messaoud, Mariem Ben Rekaya, et al.
Archives of Dermatological Research|November 13, 2012
c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosumMohamed Amine Senhaji, Omar Abidi, Sellama Nadifi, et al.
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