Zobrazeno 1 - 10
of 118
pro vyhledávání: '"Altaf A Kondkar"'
Autor:
Altaf A Kondkar, Taif A Azad, Tahira Sultan, Essam A Osman, Faisal A Almobarak, Glenn P Lobo, Saleh A Al-Obeidan
Publikováno v:
PLoS ONE, Vol 18, Iss 4, p e0284852 (2023)
AimIn a retrospective and exploratory case-control study, we examined the genetic association of two common polymorphisms in the 3' untranslated region (UTR) of DICER1 (rs3742330) and DROSHA (rs10719) genes in primary open-angle glaucoma (POAG) and p
Externí odkaz:
https://doaj.org/article/cdb0133f63984265887ecac414eacf68
Autor:
Altaf A Kondkar, Taif A Azad, Tahira Sultan, Essam A Osman, Faisal A Almobarak, Saleh A Al-Obeidan
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0227417 (2020)
AIM:To investigate the association of endothelial nitric oxide synthase (NOS3) gene polymorphisms in patients with primary open-angle glaucoma (POAG) of Saudi origin. METHODS:This case-control study included 173 patients with POAG (94 men and 79 wome
Externí odkaz:
https://doaj.org/article/f4f97b053dc74020bfcaf7289feefd11
Autor:
Altaf A. Kondkar, Tahira Sultan, Taif A. Azad, Tanvir Khatlani, Glenn P. Lobo, Hatem Kalantan, Saleh A. Al-Obeidan, Abdulrahman M. Al-Muammar
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
ObjectiveTo investigate the association of specific genetic polymorphisms (rs2371597 in STON2, rs11720822 in PDIA5, rs387907358 in WNT1, and rs77542162 in ABCA6) in a Saudi cohort of keratoconus (KC) patients compared to controls.MethodsA retrospecti
Externí odkaz:
https://doaj.org/article/a1d8a0d5c3574ffc89a6ccdd16b2ed48
Autor:
Deepak P Edward, Hind Alkatan, Qundeel Rafiq, Charles Eberhart, Saleh Al Mesfer, Nicola Ghazi, Leen Al Safieh, Altaf A Kondkar, Khaled K Abu Amero
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0121706 (2015)
To study the differential expression of microRNA (miRNA) profiles between intraocular medulloepithelioma (ME) and normal control tissue (CT).Total RNA was extracted from formalin fixed paraffin embedded (FFPE) intraocular ME (n=7) and from age matche
Externí odkaz:
https://doaj.org/article/1a34181cd3af42e3875fed6be71420ee
Autor:
Altaf A. Kondkar, Taif A. Azad, Tahira Sultan, Faisal A. Al-Mobarak, Hatem Kalantan, Saleh A. Al-Obeidan
Publikováno v:
BMC Research Notes, Vol 12, Iss 1, Pp 1-6 (2019)
Abstract Objective The genetic spectrum of primary open-angle glaucoma (POAG) in middle-eastern Saudi’s is still elusive. To this end, we investigated an association between rs693421, rs2499601 and their haplotypes at chromosome 1q43 locus with POA
Externí odkaz:
https://doaj.org/article/eda68b26a2db470ea08e5e9163c0885c
Autor:
Altaf A. Kondkar, Tahira Sultan, Faisal A. Almobarak, Hatem Kalantan, Khaled K. Abu-Amero, Saleh A. Al-Obeidan
Publikováno v:
BMC Research Notes, Vol 11, Iss 1, Pp 1-5 (2018)
Abstract Objective Plexin domain containing 2 (PLXDC2), a cell surface transmembrane protein receptor for pigment epithelium derived factor, is expressed in many tissues including the eye. Polymorphism rs7081455 flanking PLXDC2 has been associated wi
Externí odkaz:
https://doaj.org/article/2f2b8ed72624411e89063c53d65fcf55
Autor:
Hatem Kalantan, Altaf A. Kondkar, Tahira Sultan, Taif A. Azad, Nasser A. Alsabaani, Masoud Ali AlQahtani, Abdulrahman Almummar, Yuato Liu, Khaled K. Abu-Amero
Publikováno v:
BMC Research Notes, Vol 10, Iss 1, Pp 1-5 (2017)
Abstract Objective Polymorphism rs13334190 in the zinc finger protein 469 gene has been suggested to predispose toward a “thin” cornea, which then becomes keratoconic or is directly pathogenic. Thus, we genotyped polymorphism rs13334190 in 127 un
Externí odkaz:
https://doaj.org/article/ebf438a316274aba9bfbac5d19fb4169
Publikováno v:
BMC Research Notes, Vol 10, Iss 1, Pp 1-5 (2017)
Abstract Objective Congenital fibrosis of the extraocular muscles type 1 (CFEOM1) is known to be caused by mutations in KIF21A or TUBB3 or other known genes (SALL4, CHN1, HOXA1). However, affected children may harbor other genetic defects. Therefore,
Externí odkaz:
https://doaj.org/article/8db5309e3fbc4b679aed28169ceac2ef
Autor:
Altaf A. Kondkar, Tahira Sultan, Taif A. Azad, Lubna Tabussum, Essam A. Osman, Saleh A. Al-Obeidan
Publikováno v:
Journal of Ophthalmology, Vol 2019 (2019)
Purpose. To investigate systemic oxidative stress-induced DNA damage in patients with pseudoexfoliation glaucoma (PXG), we estimated plasma levels of 8-hydroxy-2′-deoxyguanosine (8-OHdG) as a marker for oxidative DNA damage in comparison to control
Externí odkaz:
https://doaj.org/article/a9be27f2b563460790eda44fb5020b0c
Autor:
Rakesh Radhakrishnan, Venkateshwara R. Dronamraju, Matthias Leung, Andrew Gruesen, Ashish K. Solanki, Stephen Walterhouse, Heidi Roehrich, Grace Song, Rafael da Costa Monsanto, Sebahattin Cureoglu, René Martin, Altaf A. Kondkar, Frederik J. van Kuijk, Sandra R. Montezuma, Hans-Joachim Knöelker, Robert B. Hufnagel, Glenn P. Lobo
Publikováno v:
Ophthalmic Genet
Rods and cones are photoreceptor neurons in the retina that are required for visual sensation in vertebrates, wherein the perception of vision is initiated when these neurons respond to photons in the light stimuli. The photoreceptor cell is structur