Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Muhammad, Kohailan"'
Autor:
Waleed Aamer, Aljazi Al-Maraghi, Najeeb Syed, Geethanjali Devadoss Gandhi, Elbay Aliyev, Alya A. Al-Kurbi, Omayma Al-Saei, Muhammad Kohailan, Navaneethakrishnan Krishnamoorthy, Sasirekha Palaniswamy, Khulod Al-Malki, Saleha Abbasi, Nourhen Agrebi, Fatemeh Abbaszadeh, Ammira S. Al-Shabeeb Akil, Ramin Badii, Tawfeg Ben-Omran, Bernice Lo, The Qatar Genome Program Research Consortium, Younes Mokrab, Khalid A. Fakhro
Publikováno v:
Genome Medicine, Vol 16, Iss 1, Pp 1-17 (2024)
Abstract Background Genome sequencing of large biobanks from under-represented ancestries provides a valuable resource for the interrogation of Mendelian disease burden at world population level, complementing small-scale familial studies. Methods He
Externí odkaz:
https://doaj.org/article/b4266c219952427a95b95677aa94733a
Publikováno v:
Antibiotics, Vol 13, Iss 10, p 958 (2024)
Background: The resurgence of colistin has become critical in combating multidrug-resistant Gram-negative bacteria. However, the emergence of mobilized colistin resistance (mcr) genes presents a crucial global challenge, particularly in the Arab worl
Externí odkaz:
https://doaj.org/article/d4c7c708934d4328baee55e88d2bef76
Autor:
Mona Abdi, Elbay Aliyev, Brett Trost, Muhammad Kohailan, Waleed Aamer, Najeeb Syed, Rulan Shaath, Geethanjali Devadoss Gandhi, Worrawat Engchuan, Jennifer Howe, Bhooma Thiruvahindrapuram, Melissa Geng, Joe Whitney, Amira Syed, Jyothi Lakshmi, Sura Hussein, Najwa Albashir, Amal Hussein, Ilaria Poggiolini, Saba F. Elhag, Sasirekha Palaniswamy, Marios Kambouris, Maria de Fatima Janjua, Mohamed O. El Tahir, Ahsan Nazeer, Durre Shahwar, Muhammad Waqar Azeem, Younes Mokrab, Nazim Abdel Aati, Ammira Akil, Stephen W. Scherer, Madeeha Kamal, Khalid A. Fakhro
Publikováno v:
Genome Medicine, Vol 15, Iss 1, Pp 1-16 (2023)
Abstract Background Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by impaired social and communication skills, restricted interests, and repetitive behaviors. The prevalence of ASD among children in Qatar was recently
Externí odkaz:
https://doaj.org/article/05529e45040b4a24a408cfbaedbd8c6f
Autor:
Geethanjali Devadoss Gandhi, Waleed Aamer, Navaneethakrishnan Krishnamoorthy, Najeeb Syed, Elbay Aliyev, Aljazi Al-Maraghi, Muhammad Kohailan, Jamil Alenbawi, Mohammed Elanbari, Qatar Genome Program Research Consortium (QGPRC), Borbala Mifsud, Younes Mokrab, Charbel Abi Khalil, Khalid A. Fakhro
Publikováno v:
Journal of Translational Medicine, Vol 20, Iss 1, Pp 1-14 (2022)
Abstract Background The genetic architecture underlying Familial Hypercholesterolemia (FH) in Middle Eastern Arabs is yet to be fully described, and approaches to assess this from population-wide biobanks are important for public health planning and
Externí odkaz:
https://doaj.org/article/1923a649220c42af804d280b274f71d7
Autor:
Muhammad Kohailan, Waleed Aamer, Najeeb Syed, Sujitha Padmajeya, Sura Hussein, Amira Sayed, Jyothi Janardhanan, Sasirekha Palaniswamy, Nady El hajj, Ammira Al-Shabeeb Akil, Khalid A. Fakhro
Publikováno v:
Journal of Human Genetics. 67:579-588
While de novo mutations (DNMs) are key to genetic diversity, they are also responsible for a high number of rare disorders. To date, no study has systematically examined the rate and distribution of DNMs in multiplex families in highly consanguineous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e94a01d1823cc3312dc08add306ae4f5
https://doi.org/10.1038/s10038-022-01054-9
https://doi.org/10.1038/s10038-022-01054-9
Autor:
Abdelhabib Semlali, Narasimha Reddy Parine, Maha Arafah, Lamjed Mansour, Arezki Azzi, Omair Al Shahrani, Abdullah Al Amri, Jilani P Shaik, Abdulrahman M Aljebreen, Othman Alharbi, Majid A Almadi, Nahla Ali Azzam, Muhammad Kohailan, Mahmoud Rouabhia, Mohammad Saud Alanazi
Publikováno v:
PLoS ONE, Vol 11, Iss 1, p e0146333 (2016)
Our aim was to evaluate the association between the expression and the polymorphism of TLR4/NF-κB pathways and colon cancer. TLR4 (rs4986790, rs10759932, rs10759931 and rs2770150) were genotyped in blood samples from Colorectal patients and healthy
Externí odkaz:
https://doaj.org/article/be0422c73bca403cacc2711dc5be6391
Autor:
Muhammad, Kohailan, Omayma, Al-Saei, Sujitha, Padmajeya, Waleed, Aamer, Najwa, Elbashir, Ammira, Al-Shabeeb Akil, Abdul-Rauf, Kamboh, Khalid, Fakhro
Publikováno v:
Cold Spring Harbor molecular case studies. 8(4)
Mandibulofacial dysostosis with microcephaly (MFDM) is a rare genetic disorder inherited in an autosomal dominant pattern. Major characteristics include developmental delay, craniofacial malformations such as malar and mandibular hypoplasia, and ear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e2b42b181ef081214501ce564de4a536
https://pubmed.ncbi.nlm.nih.gov/35732499
https://pubmed.ncbi.nlm.nih.gov/35732499
Autor:
Abdelhabib Semlali, Abdullah Al Amri, Arezki Azzi, Omair Al Shahrani, Maha Arafah, Muhammad Kohailan, Abdulrahman M Aljebreen, Othman Alharbi, Majid A Almadi, Nahla Ali Azzam, Narasimha Reddy Parine, Mahmoud Rouabhia, Mohammad S Alanazi
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0126868 (2015)
The development of cancer involves genetic predisposition and a variety of environmental exposures. Genome-wide linkage analyses provide evidence for the significant linkage of many diseases to susceptibility loci on chromosome 8p23, the location of
Externí odkaz:
https://doaj.org/article/1bacf5735a0c4c4eb2f5c70b427fa877
Autor:
Abdelhabib Semlali, Muhammad Kohailan, Mohammad Alanazi, Mahmoud Rouabhia, Abdullah Al Amri, Narasimha Reddy Parine
Publikováno v:
OncoTargets and therapy
Muhammad Kohailan,1 Mohammad Alanazi,1 Mahmoud Rouabhia,2 Abdullah Al Amri,1 Narasimha Reddy Parine,1 Abdelhabib Semlali1 1Department of Biochemistry, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia; 2Groupe de Recherche en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddda4c5efc17046993df7b02c67c49d9
http://europepmc.org/articles/PMC5308598
http://europepmc.org/articles/PMC5308598
Autor:
Jilani P. Shaik, Arezki Azzi, Narasimha Reddy Parine, Mohammad Alanazi, Muhammad Kohailan, Mahmoud Rouabhia, Abdulrahman M Aljebreen, Majid A Almadi, Abdelhabib Semlali, Othman Alharbi, Abdullah Al Amri, Maha Arafah, Nahla Azzam
Publikováno v:
OncoTargets and Therapy. 10:1-11
Objective The authors aimed to explore the relationship between the expression/polymorphisms of TLR-9 and susceptibility to colon cancer development in the Saudi Arabian population. Methods In total, blood samples from 115 patients with colon cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d0433c9b236a840a3e371feb240e9ea
https://doi.org/10.2147/ott.s106024
https://doi.org/10.2147/ott.s106024