Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Lotfi, Cherni"'
Autor:
Kenneth K. Kidd, Baigalmaa Evsanaa, Ariunaa Togtokh, Jane E. Brissenden, Janet M. Roscoe, Mustafa Dogan, Pavlos I. Neophytou, Cemal Gurkan, Ozlem Bulbul, Lotfi Cherni, William C. Speed, Michael Murtha, Judith R. Kidd, Andrew J. Pakstis
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-17 (2022)
Abstract Population genetic studies of North Asian ethnic groups have focused on genetic variation of sex chromosomes and mitochondria. Studies of the extensive variation available from autosomal variation have appeared infrequently. We focus on rela
Externí odkaz:
https://doaj.org/article/864dd4e2964848f28bd1d4e64d090434
Autor:
Sarra Elkamel, Sofia L. Marques, Luis Alvarez, Veronica Gomes, Sami Boussetta, Soufia Mourali-Chebil, Houssein Khodjet-El-Khil, Lotfi Cherni, Amel Benammar-Elgaaied, Maria J. Prata
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract To obtain refreshed insights into the paternal lineages of Tunisian populations, Y-chromosome diversity was assessed in two populations belonging to an Arab genealogical lineage, Kairouan and Wesletia, as well as in four Tunisian Andalusian
Externí odkaz:
https://doaj.org/article/749e912f28314418ba7aa6763a6b8601
Autor:
Souhir Mestiri, Sami Boussetta, Andrew J. Pakstis, Sarra El Kamel, Amel Ben Ammar El Gaaied, Kenneth K. Kidd, Lotfi Cherni
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 3, Pp n/a-n/a (2022)
Abstract Background The single nucleotide polymorphisms (SNPs) of the dopamine D3 receptor (DRD3), the CUB and sushi multiple domains 1 (CSMD1) and the neuregulin 1 (NRG1) genes were used to study the genetic diversity and affinity among North Africa
Externí odkaz:
https://doaj.org/article/907bcba05ac74c1790c6ba8093f328c2
Autor:
Wafa Ziadi, Sami Boussetta, Sarra Elkamel, Andrew J. Pakstis, Kenneth K. Kidd, Imen Medimegh, Amel Ben Ammar Elgaaied, Lotfi Cherni
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 8, Pp n/a-n/a (2021)
Abstract Background Only a few studies have investigated the association of single nucleotide polymorphisms in STAT3 gene with the susceptibility to cancer and response to chemotherapy. Our aim was to determine the allele frequencies of rs3869550, rs
Externí odkaz:
https://doaj.org/article/4cad437252ff41b18ce646658649addf
Autor:
Hocine Badache, Sami Boussetta, Amel Benammar Elgaaeid, Lotfi Cherni, Houssein Khodjet El-khil
Publikováno v:
Annals of Human Biology, Vol 46, Iss 2, Pp 150-159 (2019)
Background: In Algeria, as in all North Africa, Berbers constitute the old background of the population. Today, Berber speakers account for only ∼ 25% of Algerians. This decline is the product of a complex human settlement from pre-history to recen
Externí odkaz:
https://doaj.org/article/1c0a1593336c4bedbc4442bdefad6a93
Publikováno v:
Annals of Human Biology, Vol 44, Iss 4, Pp 366-372 (2017)
Background: The N-acetyltransferase 2 (NAT2) and glutathione transferase enzymes play a crucial role in the metabolism of xenobiotics. Genetic polymorphisms affecting these enzymes can modify their activities with an effect on individual susceptibili
Externí odkaz:
https://doaj.org/article/ed18d912fce04f969ca07a09d6271de2
Autor:
Sarra Elkamel, Lotfi Cherni, Luis Alvarez, Sofia L. Marques, Maria J. Prata, Sami Boussetta, Amel Benammar-Elgaaied, Houssein Khodjet-El-Khil
Publikováno v:
Annals of Human Biology, Vol 44, Iss 2, Pp 180-190 (2017)
Background: Recent genomic analyses suggest that the current North African gene pool was mainly influenced by population flow coming from the East that altered the genetic structure of autochthonous Berber populations. Such genetic flow has not been
Externí odkaz:
https://doaj.org/article/c398e71a26b3469d9ec3c94ad48edace
Autor:
Narjes Mokni, Amel Benammar Elgaaied, Itziar de Rojas, Afef Hammami, Nizar Daouassi, Lotfi Cherni, Agustín Ruiz, Sonia Moreno-Grau, Laura Montrreal, Samia Younes, Imene Mahmoud, Mahbouba Frih-Ayed, Nesrine Ben Salem, Sami Boussetta
Publikováno v:
Molecular Biology Reports. 49:1687-1700
Background Alzheimer's disease (AD) is the most common neurodegenerative disorder in humans and presents a major health problem throughout the world. The etiology of AD is complex, and many factors are implicated, including mitochondria. Mitochondria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba4201a2c54531166c7acd35898143a1
https://doi.org/10.1007/s11033-021-06978-7
https://doi.org/10.1007/s11033-021-06978-7
Autor:
Soufia Mourali-Chebil, Sarra Elkamel, Sami Boussetta, Andrew Pakstis, Kenneth Kidd, Amel Benammar-Elgaaied, Lotfi Cherni
Publikováno v:
Human Biology. 93:163-177
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b25b83669188dbdb28cd708317520dee
https://doi.org/10.1353/hub.2021.0009
https://doi.org/10.1353/hub.2021.0009
Autor:
Nesrine Ben Salem, Sami Boussetta, Itziar de Rojas, Sonia Moreno-Grau, Laura Montrreal, Narjes Mokni, Imene Mahmoud, samia Younes, Nizar Daouassi, Mahbouba Frih-Ayed, Afef Hammami, Amel Ben Ammar Elgaaied, Agustín Ruiz, Lotfi Cherni
Publikováno v:
Molecular biology reports. 49(3)
Background: Alzheimer’s disease (AD) is the most common neurodegenerative disorder in humans and presents a major health problem throughout the world. The etiology of AD is complex, and many factors are implicated, including mitochondria. Mitochond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d589e2fa1f0dfafdbbf1f6811acb59e
https://pubmed.ncbi.nlm.nih.gov/34854014
https://pubmed.ncbi.nlm.nih.gov/34854014