Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Misbahuddin M Rafeeq"'
Autor:
Mohammed Ali Alshehri, Saeed A Asiri, Nawal Helmi, Hanadi M Baeissa, Abdullah Hamadi, Abdulrahman Alzahrani, Rashed Mohammed Alghamdi, Misbahuddin M Rafeeq, Zeyad M Alharbi, Mohammad Azhar Kamal
Publikováno v:
PLoS ONE, Vol 19, Iss 6, p e0303784 (2024)
Lung cancer, a relentless and challenging disease, demands unwavering attention in drug design research. Single-target drugs have yielded limited success, unable to effectively address this malignancy's profound heterogeneity and often developed resi
Externí odkaz:
https://doaj.org/article/d07255bdbea9442ba6611913ead38986
Autor:
Misbahuddin M Rafeeq, Alaa Hamed Habib, Alaa F. Nahhas, Najat Binothman, Majidah Aljadani, Jawaher Almulhim, Ziaullah M Sain, Mohammad Zubair Alam, Norah A Alturki, Qamre Alam, Manish Manish, Rajnish Kumar Singh
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 11 (2023)
Kaposi’s sarcoma associated herpesvirus (KSHV) is causative agent of Kaposi’s sarcoma, Multicentric Castleman Disease and Pleural effusion lymphoma. KSHV-encoded ORF17 encodes a protease which cleaves -Ala-Ala-, -Ala-Ser- or -Ala-Thr-bonds. The p
Externí odkaz:
https://doaj.org/article/713c3756c12c4c7f97de7867b3dd812d
Autor:
Alrayan Abass Albaz, Misbahuddin M Rafeeq, Ziaullah M Sain, Wael Abdullah Almutairi, Ali Saeed Alamri, Ahmed Hamdan Aloufi, Waleed Hassan Almalki, Mohammed Tarique
Publikováno v:
AIMS Microbiology, Vol 7, Iss 4, Pp 368-398 (2021)
The COVID-19 pandemic caused by highly-infectious virus namely severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in infection of millions of individuals and deaths across the world. The need of an hour is to find the innovativ
Externí odkaz:
https://doaj.org/article/0201d2cf62bf4680ae54615127052df5
Autor:
Mohib Ullah Kakar, Muhammad Akram, Muhammad Zubair Mehboob, Muhammad Younus, Muhammad Bilal, Ahmed Waqas, Amina Nazir, Muhammad Shafi, Muhammad Umair, Sajjad Ahmad, Misbahuddin M Rafeeq
Publikováno v:
PLoS ONE, Vol 17, Iss 6, p e0268078 (2022)
Hearing impairment (HI) is a heterogeneous condition that affects many individuals globally with different age groups. HI is a genetically and phenotypically heterogeneous disorder. Over the last several years, many genes/loci causing rare autosomal
Externí odkaz:
https://doaj.org/article/01b8967f764044289e60be4d605f18f2
Autor:
Muhammad Umair, Farooq Ahmad, Saeed Ahmad, Qamre Alam, Mohd Rehan, Amany I. Alqosaibi, Mashael M. Alnamshan, Misbahuddin M Rafeeq, Shahnaz Haque, Ziaullah M Sain, Muhammad Ismail, Majid Alfadhel
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Background: Polydactyly is a prevalent digit abnormality characterized by having extra digits/toes. Mutations in eleven known genes have been associated to cause nonsyndromic polydactyly: GLI3, GLI1, ZRS regulating LMBR1, IQCE, ZNF141, PITX1, MIPOL1,
Externí odkaz:
https://doaj.org/article/50e4cacf0c6b48ad8a1c76a766459a82
Autor:
Misbahuddin M. Rafeeq, Alaa F. Nahhas, Najat Binothman, Alaa Hamed Habib, Majidah Aljadani, Ziaullah M. Sain, Abeer Al Tuwaijri, Mohammed Ali Alshehri, Othman R. Alzahrani
Publikováno v:
Journal of Biomolecular Structure and Dynamics. :1-13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49053b8f562c26af1faa5055ca2a5aaf
https://doi.org/10.1080/07391102.2022.2140202
https://doi.org/10.1080/07391102.2022.2140202
Autor:
Misbahuddin M. Rafeeq, Muhammad Umair, Muhammad Bilal, Alaa Hamed Habib, Ahmed Waqas, Ziaullah M. Sain, Mohammad Zubair Alam, Raja Hussain Ali
Publikováno v:
neurogenetics. 24:55-60
Cerebellar ataxias (CAs) comprise a rare group of neurological disorders characterized by extensive phenotypic and genetic heterogeneity. In the last several years, our understanding of the CA etiology has increased significantly and resulted in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a71da57b5b4cfa5c16c0987d73b023ab
https://doi.org/10.1007/s10048-022-00701-9
https://doi.org/10.1007/s10048-022-00701-9
Publikováno v:
Journal of Translational Medicine, Vol 15, Iss 1, Pp 1-9 (2017)
Abstract Objectives Study of currently approved drugs and exploration of future clinical development pipeline therapeutics for cystic fibrosis, and possible limitations in their use. Methods Extensive literature search using individual and a combinat
Externí odkaz:
https://doaj.org/article/0758fa136cef4a89ac1004dffa7b6f31
Autor:
Hamed Nawaz, null Mujahid, Sher Alam Khan, Farhana Bibi, Ahmed Waqas, Abdul Bari, null Fardous, Niamatullah Khan, Nazif Muhammad, Amjad Khan, Sohail Aziz Paracha, Qamre Alam, Mohammad Azhar Kamal, Misbahuddin M. Rafeeq, Noor Muhammad, Fayaz Ul Haq, Shazia Khan, Arif Mahmood, Saadullah Khan, Muhammad Umair
Publikováno v:
Genes; Volume 14; Issue 5; Pages: 1113
Bardet–Biedl syndrome (BBS) is a rare clinically and genetically heterogeneous autosomal recessive multi-systemic disorder with 22 known genes. The primary clinical and diagnostic features include six different hallmarks, such as rod–cone dystrop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24fab58cf50e453290c330cabee942e3
Autor:
Alaa Hamed Habib, Ahmed Hamdan Aloufi, Rashed Ahmed Alniwaider, Abdulrahman Almutairi, Norah A. Alturki, Ahmad Alzamami, Majidah Aljadani, Najat Binothman, Khwaja Mohd Amir, Ziaullah M. Sain, Misbahuddin M. Rafeeq
Publikováno v:
Journal of Pharmaceutical Research International. :6-13
The negative effects of leishmanicidal medications are numerous, and drug resistance to all of them has been observed. As a result, new medication development and the identification of novel therapeutic targets are critical. Leishmania major trypanot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57f39c895ed7d7bf50ad1c30a4f42c58
https://doi.org/10.9734/jpri/2022/v34i16b35736
https://doi.org/10.9734/jpri/2022/v34i16b35736