Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Satta, Dalila"'
Autor:
Horchi-Mekkaoui Meroua, Achou Rayene, Djoudi Brahim, Laouar Rania, Gharzouli Razika, Taghane Naima, Abadi Noureddine, Satta Dalila
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-6 (2024)
Abstract Background This study aimed to explore the relationship between Parkinson’s disease and insertion/deletion polymorphism (I/D) of the angiotensin-converting enzyme gene (ACE) and to highlight the related risk factors within Eastern Algerian
Externí odkaz:
https://doaj.org/article/6923f4e2c2634464a1a30e61e67f84cb
Autor:
Rezgoune, Mohamed Larbi MLR, Chellat, Djalila DC, Abadi, Noureddine NA, Slama, Abdelhamid AS, Satta, Dalila DS
Publikováno v:
African Journal of Reproductive Health / La Revue Africaine de la Santé Reproductive, 2021 Feb 01. 25(1), 67-75.
Externí odkaz:
https://www.jstor.org/stable/27086588
Publikováno v:
BioMedica, Vol 37, Iss 2, Pp 100-104 (2021)
Background and Objective: Ongoing research suggests that cytochrome P4501A1 (CYP1A1) 3801T > C polymorphism may be correlated with human male infertility but the reported results are conflicting. Hence, this case-control study was conducted in Algeri
Externí odkaz:
https://doaj.org/article/56ce7d258a7f4307b7462cbe2557d644
Publikováno v:
The Pan African Medical Journal, Vol 29, Iss 45 (2018)
INTRODUCTION: triple-negative breast cancer (TNBC) is characterized by the lack of estrogen receptor, progesterone receptor and human epidermal growth factor receptor-2 (HER-2) expression. It is aggressive and most common in African women. In this st
Externí odkaz:
https://doaj.org/article/06fb58e2f3614993908c6126a43fa5b3
Autor:
Touati , Sabrina, Djekkoun , Rachid, Vallières , Luc, Raymond , Vincent, Chabi , Adel, Abadi , Nouredine, Satta , Dalila
Publikováno v:
African Journal of Neurological Sciences; Vol. 40 No. 1 (2021); 49-57
Background:Genome-wide association studies (GWASs) have provided evidence for a polygenic basis of susceptibility to gliomas. The knowledge about these tumors remain very limited in Algeria. We aimed to investigate whether risk alleles identified by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=78975075580c::0456413952e4b1059ad50264e3bff83e
https://www.ajol.info/index.php/ajns/article/view/231892
https://www.ajol.info/index.php/ajns/article/view/231892
Publikováno v:
BioMedica. 37:100-104
Background and Objective: Ongoing research suggests that cytochrome P4501A1 (CYP1A1) 3801T > C polymorphism may be correlated with human male infertility but the reported results are conflicting. Hence, this case-control study was conducted in Algeri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60c8e5dfaab48a2412b75df420a44e56
https://doi.org/10.51441/biomedica/5-281
https://doi.org/10.51441/biomedica/5-281
Autor:
Zidoune, Housna, Ladjouze, Asmahane, Chellat-Rezgoune, Djalila, Boukri, Asma, Dib, Scheher Aman, Nouri, Nassim, Tebibel, Meryem, Sifi, Karima, Abadi, Noureddine, Satta, Dalila, Benelmadani, Yasmina, Bignon-Topalovic, Joelle, El-Zaiat-Munsch, Maëva, Bashamboo, Anu, Mcelreavey, Ken
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, 2022, 13, pp.900574. ⟨10.3389/fgene.2022.900574⟩
Frontiers in Genetics, 2022, 13, pp.900574. ⟨10.3389/fgene.2022.900574⟩
In a majority of individuals with disorders/differences of sex development (DSD) a genetic etiology is often elusive. However, new genes causing DSD are routinely reported and using the unbiased genomic approaches, such as whole exome sequencing (WES
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c147c0962685a11baadd778541cfb128
https://doi.org/10.3389/fgene.2022.900574
https://doi.org/10.3389/fgene.2022.900574
Publikováno v:
Current Trends in Natural Sciences, Vol 9, Iss 18, Pp 218-225 (2020)
CYP1A1 polymorphisms are known to play a crucial role in the development and metastasis of malignant diseases including nasopharyngeal cancer (NPC). Individual susceptibility to cancer from environmental agents may be influenced by polymorphic metabo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c44641e233a41608b7b309cea4684f29
https://natsci.upit.ro/media/2081/030ghania-et-al_final.pdf
https://natsci.upit.ro/media/2081/030ghania-et-al_final.pdf
Autor:
Abadi Noureddine, Hamdouche Nadira, Mahdi Djahida, Satta Dalila, Sifi Karima, Sifi Yamina, Dalichaouche Imen, M’ Zahem Abderrahim
Publikováno v:
South Asian Journal of Experimental Biology. 10:176-182
Duchenne and Becker muscular dystrophy (DMD/BMD) are the most com-mon neuromuscular diseases caused by mutations in the dystrophin gene also called (DMD gene), located at Xp21. We report the clinical and genetic analysis of 74Algerian DMD/BMD patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e82fc2231274354bcbc872955aaf4a9c
https://doi.org/10.38150/sajeb.10(3).p176-182
https://doi.org/10.38150/sajeb.10(3).p176-182
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