Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Rubab Raza"'
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 16, p 9336 (2022)
Psoriasis is an immune-mediated chronic and painful disease characterized by red raised patches of inflamed skin that may have desquamation, silvery-white scales, itching and cracks. The susceptibility of developing psoriasis depends on multiple fact
Externí odkaz:
https://doaj.org/article/d2ea17d2f6bb474f8c2c4e1490cae236
Autor:
Wasim Ahmad, Noor Muhammad, Rubab Raza, Wasim Ullah, Sher Alam Khan, Saadullah Khan, Asmat Ullah, Umm e-Kalsoom, Ayesha Rukan, Muhammad Humayun, Nousheen Bibi
Publikováno v:
European Journal of Dermatology. 30:408-416
Hypohidrotic ectodermal dysplasia (HED) is a congenital anomaly characterized by hypohydrosis, hypotrichosis and hypodontia. Mutations in at least four genes (EDAR, EDARADD, WNT10A, TRAF6) have been reported to cause both autosomal recessive and auto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82955c2a11d54ae18062c0242c59afec
https://doi.org/10.1684/ejd.2020.3844
https://doi.org/10.1684/ejd.2020.3844
Autor:
Rubab Raza, Asmat Ullah, Nighat Haider, Jai Krishin, Muqadar Shah, Fati Ullah Khan, null Abdullah, Torben Hansen, Syed Irfan Raza, Wasim Ahmad, Sulman Basit
Publikováno v:
Raza, R, Ullah, A, Haider, N, Krishin, J, Shah, M, Khan, F U, Abdullah,, Hansen, T, Raza, S I, Ahmad, W & Basit, S 2022, ' Exome sequencing reveals the first intragenic deletion in ABCA5 underlying autosomal recessive hypertrichosis ', Clinical and Experimental Dermatology, vol. 47, no. 6, pp. 1137-1143 . https://doi.org/10.1111/ced.15128
Summary Background Hereditary hypertrichosis (HH) is characterized by excessive hair growth on various body areas, which is independent of the individual's age. This rare hair disorder has been classified by its origin (genetic or acquired), age of o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81f9261c31b60b49e0811b3f32fe88a6
https://curis.ku.dk/ws/files/320494471/MJAC_Clin_Experimental_Derm_2022_Raza_Exome_Sequencing_Revealed_the_First_Intragenic_Deletion_in_ABCA5_Underlying.pdf
https://curis.ku.dk/ws/files/320494471/MJAC_Clin_Experimental_Derm_2022_Raza_Exome_Sequencing_Revealed_the_First_Intragenic_Deletion_in_ABCA5_Underlying.pdf
Autor:
Rubab Raza, Gagan Chhabra, Muhammad Bilal, Mary A. Ndiaye, Khurram Liaqat, Shoaib Nawaz, Jean-Yves Sgro, Ivan Rayment, Wasim Ahmad, Nihal Ahmad
Publikováno v:
Journal of Investigative Dermatology. 143:173-176.e3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ff7307256e91dc32f5d713aa16c34ea
https://doi.org/10.1016/j.jid.2022.07.010
https://doi.org/10.1016/j.jid.2022.07.010
Autor:
Rubab Raza, Zara Khalid, Atteaya Zaman, Sadaf Jafar, Muhammad Zeeshan Anwar, Syed Waqas Hassan, Momin Iqbal, Sajid Rashid, Wasim Ahmad, Syed Irfan Raza
Publikováno v:
Gene Reports. 29:101699
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ccf2427f410cc1740660334346d264a
https://doi.org/10.1016/j.genrep.2022.101699
https://doi.org/10.1016/j.genrep.2022.101699
Autor:
Irfan Raza, Sajid Rashid, Ana Krolo, Muhammad Zeeshan Anwar, Raul Jimenez-Heredia, Kaan Boztug, Asmat Ullah, Ayisha Zia, Wasim Ahmad, Rubab Raza
Purpose Systemic auto-inflammatory diseases are a diverse group of heterogeneous disorders resulting in development of the systemic inflammation in absence of the inflammatory induction. Sequence variants in the OTULIN gene, which disrupts its ubiqui
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69313abbeee9652f6ddb4d02e73fb7bb
https://doi.org/10.21203/rs.3.rs-164929/v1
https://doi.org/10.21203/rs.3.rs-164929/v1
Background: The heart breaks in cases of liver cirrhosis when its perceived cardiovascular disease does not occur means Cirrhotic cardiomyopathy (CCM). Methods: From October 2019 to November 2020, our recent research was conducted at Jinnah Hospital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::416ff75cf9907bbb5ea43aa3478ad27a
Aim: Heart protuberance to wants pacemaker foundation as association propose in trauma center. Objective: The target of this examination was to manage threat angles additionally proposals for suffering pacing in patients providing for the single card
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cee95efeefbdd912a0b00ac4eb065ee
Autor:
Wasim Ahmad, Alamgir Khan, Rubab Raza, Muhammad Zeeshan Anwar, Sadaf Jaffar, Syed Irfan Raza, Hamid Nawaz Tipu
Publikováno v:
Immunobiology. 225(3)
Leukocyte adhesion deficiency I (LADI) is an autosomal recessive type of primary immunodeficiency characterized by occurrence of repeated bacterial infections, impaired pus formation and wound healing. Genetic variations in the β-2 integrin subunit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b66f9090caee4f03702744cd718982b4
https://pubmed.ncbi.nlm.nih.gov/32279896
https://pubmed.ncbi.nlm.nih.gov/32279896