Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Sarmad Mehmood"'
Autor:
Sarmad Mehmood, Sajjad Haider, Muhammad Naeem, Raees Khan, Muhammad Faheem, Bushra Bano, Syeda Marriam Bakhtiar, Atif Ali Khan Khalil, Fazli Subhan, Syed Babar Jamal, Adnan Haider
Bone healing and formation are under the control of growth factors. Among these factors, bone morphogenetic proteins (BMPs) have a vital role in bone and cartilage maintenance and formation. BMP itself belongs to the superfamily of transforming growt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0c1eb218443c81a0fac1fe15e533b56
https://doi.org/10.2174/9789815079517122010015
https://doi.org/10.2174/9789815079517122010015
Autor:
Sarmad Mehmood, Faghia Shahid, Sara Khan, Ayesha Siddiqa, Muhammad Rizwan Hafeez, Sibgha Bashir
Publikováno v:
NUST Journal of Natural Sciences. 5:2-8
The goal of this study was to compare the frequency of raised level of anti-thyroid peroxidase antibody in patients of hypothyroidism and the euthyroids. This case-control study was carried out at the department of Pathology, Quaid e Azam Medical Col
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60fa15d2a6277a6f275236f28bd46cbf
https://doi.org/10.53992/njns.v5i1.31
https://doi.org/10.53992/njns.v5i1.31
Autor:
Muhammad Ikram Ullah, Tahir N. Khan, Maimoona Siddiqui, Gaurav V. Harlalka, Erica E. Davis, Talia Akram, Zaineb Akram, Chunyu Liu, Muhammad Jameel, Arsalan Ahmad, Kamal Khan, Sarmad Mehmood, Barry A. Chioza, Muhammad Jawad Hassan, Humayoon Shafique Satti, Raees Khan, Emma A. Baple, Andrew H. Crosby, Shahid Mahmood Baig, Belqees Yawar Faiz, Feng Zhang
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 188(2)
Autosomal recessive limb-girdle muscular dystrophy-1 (LGMDR1) is an autosomal recessive disorder characterized by progressive weakness of the proximal limb and girdle muscles. Biallelic mutations in CAPN3 are reported frequently to cause LGMDR1. Here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8396234000a7691c505bb9260affcc45
https://pubmed.ncbi.nlm.nih.gov/34697879
https://pubmed.ncbi.nlm.nih.gov/34697879
Autor:
Sarmad Mehmood, Sabin Aslam
Publikováno v:
'Essentials of Cancer Genomic, Computational Approaches and Precision Medicine ISBN: 9789811510663
With the advent of genome-editing technologies, targeting genome engineering is no longer a hypothetical abstract. As application area of genome-editing tools is extending beyond the limits of research and biomedical remedies, specific ethical appreh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6f982cc91b423c0754b2552c83749de
https://doi.org/10.1007/978-981-15-1067-0_4
https://doi.org/10.1007/978-981-15-1067-0_4
Autor:
Jay E. Self, Luke O'Gorman, Andrew H. Crosby, Emma L. Baple, Muhammad Jawad Hassan, Siying Lin, Muhammad Ikram Ullah, Shaheer Sabz Ali, Gaurav V. Harlalka, Sarmad Mehmood, Barry A. Chioza, Muhammad Shakil, Muhammad Salman Shabbir, Chelsea S. Norman, Ilaria D'Atri, Sarah Ennis, Haiba Kaul, Muhammad Arshad, Tahir Aman
Publikováno v:
Meta Gene. 17:48-55
Background: Oculocutaneous albinism (OCA) is a genetically heterogeneous disorder of abnormal melanin synthesis, resulting in decreased or absent pigmentation of eyes, skin and hair. OCA has been classified based on genetic findings into seven subtyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be65d1c4ede0c4dcf995ffbcfe7256c8
https://doi.org/10.1016/j.mgene.2018.03.007
https://doi.org/10.1016/j.mgene.2018.03.007
Autor:
Wasim Ahmad, Muhammad Ikram Ullah, Abdul Nasir, Saadullah Khan, Irfan Ullah, Sohail Ahmed, Khadim Shah, Abdul Aziz, Syed Irfan Raza, Muhammad Jawad Hassan, Asmat Ullah, Sarmad Mehmood
Publikováno v:
Volume: 41, Issue: 3 458-468
Turkish Journal of Biology
Turkish Journal of Biology
Genetic deficiency of N-acetylgalactosamine-6-sulfate sulfatase (GALNS) due to mutations in the GALNS gene results in the pathogenesis of Morquio A syndrome. To date, more than 200 mutations have been reported in GALNS, resulting in variable clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bc124ffe07869d5ef5d9ee15407222b
https://doi.org/10.3906/biy-1607-81
https://doi.org/10.3906/biy-1607-81
Objective: The aim of this analysis was to evaluate the frequency of depression, stress and anxiety in dyspeptic symptoms patients admitted for endoscopy. Study design: A cross-sectional study. Place and Duration: In the Medicine Department of Bahawa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d94f09b0764607947518d7d984a3eb7
Autor:
Christian A. Hübner, Muhammad Ikram Ullah, Rubina Dad, Arsalan Ahmad, Muhammad Jawad Hassan, Amjad Ali, Peter John, Sarmad Mehmood, Aisha Mohyuddin
Publikováno v:
Computational biology and chemistry. 89
Congenital insensitivity to pain (CIP), classified as a type of hereditary sensory and autonomic neuropathies, is a rare disease in which the affected individuals fail to perceive sensation of pain. One of the PR/SET Domain Proteins, PRDM12, has been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d83b50564635174ec969c32f4c6cac1
https://pubmed.ncbi.nlm.nih.gov/33010785
https://pubmed.ncbi.nlm.nih.gov/33010785
Autor:
Emma L. Baple, Gaurav V. Harlalka, Jay E. Self, Khadim Shah, Muhammad Jawad Hassan, Sumbul Khalid, Andrew H. Crosby, Siying Lin, Asmat Ullah, Sarmad Mehmood, Shazia Khan, Asma Gul, Wasim Ahmad
Publikováno v:
Annals of human geneticsREFERENCES. 83(6)
Ciliopathies are a clinically and genetically heterogeneous group of disorders often exhibiting phenotypic overlap and caused by abnormalities in the structure or function of cellular cilia. As such, a precise molecular diagnosis is important for gui
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a11156227a3b03f74dcea3ce8532117
https://pubmed.ncbi.nlm.nih.gov/31173343
https://pubmed.ncbi.nlm.nih.gov/31173343
Autor:
Andrew H. Crosby, Emma L. Baple, Rubina Dad, Sarmad Mehmood, Muhammad Ikram Ullah, Barry A. Chioza, Gaurav V. Harlalka, Arsalan Ahmad, Muhammad Jawad Hassan
Publikováno v:
Gene Reports. 16:100445
Distal hereditary motor neuropathy (dHMN), also known as distal spinal muscular atrophy (distal SMA), comprises of a group of progressive neurological diseases resulting in degeneration of lower motor neurons with weakness and atrophy in distal muscl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a2bd475c3ba6c7ae1f3a507daff08e8
https://doi.org/10.1016/j.genrep.2019.100445
https://doi.org/10.1016/j.genrep.2019.100445