Influence of CYP2D6, CYP2C19 and CYP3A5 polymorphisms on plasma levels of tamoxifen metabolites in Algerian women with ER+ breast cancer

Autor: Amira Boucenna, Khadidja Boudaoud, Ahmed Hireche, Mohamed Larbi Rezgoune, Noureddine Abadi, Taha Filali, Dalila Satta

Publikováno v: Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-11 (2022)

Abstract Background Tamoxifen, a selective estrogen receptor modulator, is indicated for breast cancer developed in response to estrogen. Findings In the current study we explored the relationship between the different variants of CYP2D6, CYP2C19, CY

Externí odkaz: https://doaj.org/article/a68d17d794f54cf3a4f07f9ddfc1ac8e

Association of the CAG repeat polymorphism in mitochondrial polymerase gamma (POLG1) with male infertility: a case-control study in an Algerian population

Autor: Mohamed Larbi, Rezgoune, Djalila, Chellat, Noureddine, Abadi, Abdelhamid, Slama, Dalila, Satta

Publikováno v: African journal of reproductive health. 25(1)

Polymorphisms in the have been speculated to be associated with male infertility. The main objective of our study was to CAG repeat polymorphism in POLG1 gene and male mitochondrial DNA polymerase gamma (POLG) assess the possible association of infer

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b8421637858f0f850a05cb107f3a5ec4
https://pubmed.ncbi.nlm.nih.gov/34077112

Contents Vol. 90, 2013

Autor: Raja B. Khauli, Ken McElreavey, Gonzalo García-Fadrique, Tolga Akman, Yutian Dai, Lei Yin, Gaetano Ciancio, Cevper Ersoz, Bingkun Li, Mesrur Selcuk Silay, Muzaffer Akcay, Jinxian Pu, Shaobo Zheng, Aixia Zhang, M.A. Mirjalili, Dongxu Zhang, Yingbo Dai, Akbar Nouralizadeh, John R. Haaga, Daniel Turudić, Serkan Keskin, Shivam Joshi, Amr Kadah, Manuel Esteban Fuertes, Druck Reinhardt Druck Basel, Wei-Jie Zhu, Ahmet Yaser Muslumanoglu, Dalila Satta, Mohammad Masoud Nikkar, Jianming Guo, Chongrui Jin, Kamran Ahmed, Fenglei Zhang, Berkan Resorlu, Hamane Douadi, Ivan Povo-Martin, Cem Kezer, X. Wang, Jin Tang, Omer Faruk Bozkurt, Akif Erbin, J. Lassmann, A. Miernik, Zhibing Xu, Deirdre Anderson, Manuel Salvador-Marin, Matthew J. Maurice, Nashaat Nabil, Li Lu, Seyed Amir Mohsen Ziaee, Mohammad Hossein Soltani, G. Tosev, Sina Kardas, Noureddine Abadi, M. Kardoust Parizi, J. Liu, Yuemin Xu, Juan Carlos Gallego-Gómez, M. Oezsoy, Ekrem Ozyuvali, Huan Jiang, Danko Batinić, Declan Cahill, Murat Binbay, Hossam Hosny, Michael A. Gorin, Seyed Hossein Hosseini Sharifi, Jonathan Watkiss, Naouel Kherouatou, Nuzhath Khan, Danica Batinić, Jingfei Teng, Yongkang Zhang, M. Schoenthaler, Prokar Dasgupta, Daniel Gallego-Vilar, Zhaowei Zhu, Xu Li, Ali Unsal, Yuanfeng Yang, Sezai Vatansever, P. Weibl, Djalila Chellat, Yong Liu, Guomin Wang, Jose Florensa, Yanjun Zhu, C.L. Zhang, F.E. Kuehhas, Benlatrèche Cherifa, Yinglong Sa, Qilai Long, Tianyuan Xu, N.A. Moosa Nejad, Ljiljana Nizic, Xiang Wang, Yong Lu, Marija Topalović-Grković, Feng Pan, Yuxin Tang, Ali Ahanian, I. Schauer, Rany Shamloul, J.Y. Li, Nazih Khater, Chunxiao Liu, Faruk Tas, Ardalan Ojand, José Escribano, Emilio Rubio, Dean A. Nakamoto, Zhoujun Shen, Hang Wang, Abdullah Armagan, Miguel Vírseda Chamorro, S. Sevcenco, Alireza Lashay, Danfeng Xu, Abdulkadir Tepeler, Xiaohua Zhang, Satz Mengensatzproduktion, Xianzhen Jiang, C.M. Sun, Antonio López García-Moreno, Danko Milosevic, Lee Ponsky, Mohamed Larbi Rezgoune, Sebti Benbouhadja, Lianjun Pan, Jesús Salinas Casado, Emrah Yuruk, Liping Li, Mohammed Shamim Khan, Ben Challacombe, Hulin Li, Kristina Vrljicak, A. Basiri

Publikováno v: Urologia Internationalis. 90:I-IV

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d0c31977b9b58241b84f234d98e709f0
https://doi.org/10.1159/000351508

SRY and NR5A1 gene mutation in Algerian children and adolescents with DSD and testicular dysgenesis

Autor: Noreddine Abadi, Djalila Chellat-Rezgoune, Dalila Satta, Ken Mc Elreavey, Naouel Kherouatou-Chaoui, Mohamed Larbi Rezgoune, Laaldja Souhem Touabti

Publikováno v: BASE-Bielefeld Academic Search Engine
African Health Sciences; Vol. 21 No. 3 (2021); 1491-1497

Background: In humans, sex determination and differentiation is genetically controlled. Disorders of sex development (DSD) result in anomalies of the development of the external and internal genitalia. Variants in transcription factors such as SRY, N

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16f88536f7bf1892bbe0d65470fbaea0
https://www.ajol.info/index.php/ahs/article/view/215243

SRY and NR5A1 gene mutation in Algerian children and adolescents with DSD and testicular dysgenesis.

Autor: Kherouatou-Chaoui, Naouel, Chellat-Rezgoune, Djalila, Rezgoune, Mohamed Larbi, Mc Elreavey, Ken, Touabti, Laaldja Souhem, Abadi, Noreddine, Satta, Dalila

Publikováno v: African Health Sciences; Sep2021, Vol. 21 Issue 3, p1491-1497, 7p