Updates on Genes and Genetic Mechanisms Implicated in Primary Angle-Closure Glaucoma

gan Kondkar, Altaf A
Cyhoeddwyd yn Appl Clin Genet (2021)

Utility of Circulating MicroRNAs as Clinical Biomarkers for Cardiovascular Diseases

gan Kondkar, Altaf A., Abu-Amero, Khaled K.
Cyhoeddwyd yn Biomed Res Int (2015)

An Updated Review on the Genetics of Primary Open Angle Glaucoma

gan Abu-Amero, Khaled, Kondkar, Altaf A., Chalam, Kakarla V.
Cyhoeddwyd yn Int J Mol Sci (2015)

Genetic analysis of Indian subjects with clinical features of possible type IIa hypercholesterolemia

gan Kondkar, Altaf A., Nair, Kappiareth G., Ashavaid, Tester F.
Cyhoeddwyd yn J Clin Lab Anal (2007)

Editorial: Molecular Mechanisms of Retinal Cell Degeneration and Regeneration

gan Lobo, Glenn P., Biswal, Manas R., Kondkar, Altaf A.
Cyhoeddwyd yn Front Cell Dev Biol (2021)

Resveratrol and Ophthalmic Diseases

gan Abu-Amero, Khaled K., Kondkar, Altaf A., Chalam, Kakarla V.
Cyhoeddwyd yn Nutrients (2016)

A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles

gan Abu-Amero, Khaled K., Kondkar, Altaf A., Khan, Arif O.
Cyhoeddwyd yn BMC Res Notes (2017)

Genetics of Keratoconus: Where Do We Stand?

gan Abu-Amero, Khaled K., Al-Muammar, Abdulrahman M., Kondkar, Altaf A.
Cyhoeddwyd 2014

A novel mutation in ornithine transcarbamylase gene causing mild intermittent hyperammonemia

gan Mohamed, Sarar, Hamad, Muddathir H., Kondkar, Altaf A., Abu-Amero, Khaled K.
Cyhoeddwyd yn Saudi Med J (2015)

Sirtuins Expression and Their Role in Retinal Diseases

gan Balaiya, Sankarathi, Abu-Amero, Khaled K., Kondkar, Altaf A., Chalam, Kakarla V.
Cyhoeddwyd yn Oxid Med Cell Longev (2017)

Analysis of CYP1B1 sequence alterations in patients with primary open-angle glaucoma of Saudi origin

gan Abu-Amero, Khaled K, Sultan, Tahira, Al-Obeidan, Saleh A, Kondkar, Altaf A
Cyhoeddwyd yn Clin Ophthalmol (2018)

Decreased total antioxidants status in the plasma of patients with pseudoexfoliation glaucoma

gan Abu-Amero, Khaled K., Kondkar, Altaf A., Mousa, Ahmed, Osman, Essam A., Al-Obeidan, Saleh A.
Cyhoeddwyd 2011

Lack of association of SNP rs4236601 near CAV1 and CAV2 with POAG in a Saudi cohort

gan Abu-Amero, Khaled K., Kondkar, Altaf A., Mousa, Ahmed, Osman, Essam A., Al-Obeidan, Saleh A.
Cyhoeddwyd 2012

Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder

gan Abu-Amero, Khaled K., Kondkar, Altaf A., Hellani, Ali M., Bosley, Thomas M., Khan, Arif O.
Cyhoeddwyd yn Neurosciences (Riyadh) (2016)

Transfection of Human Platelets with Short Interfering RNA

gan Hong, Wei, Kondkar, Altaf A., Nagalla, Srikanth, Bergmeier, Wolfgang, Jin, Ying, Herman, Jay H., Bray, Paul F.
Cyhoeddwyd 2011

Increased Plasma Levels of 8-Hydroxy-2′-deoxyguanosine (8-OHdG) in Patients with Pseudoexfoliation Glaucoma

gan Kondkar, Altaf A., Sultan, Tahira, Azad, Taif A., Tabussum, Lubna, Osman, Essam A., Al-Obeidan, Saleh A.
Cyhoeddwyd yn J Ophthalmol (2019)

Keratoconus is associated with increased copy number of mitochondrial DNA

gan Abu-Amero, Khaled. K., Kondkar, Altaf A., Azad, Taif Anwar, Sultan, Tahira, Kalantan, Hatem, Al-Muammar, Abdulrahman M.
Cyhoeddwyd 2014

Assessment of the Knowledge and Attitudes of Saudi Mothers towards Newborn Screening

gan Al-Sulaiman, Ayman, Kondkar, Altaf A., Saeedi, Mohammad Y., Saadallah, Amal, Al-Odaib, Ali, Abu-Amero, Khaled K.
Cyhoeddwyd yn Biomed Res Int (2015)

Association of increased levels of plasma tumor necrosis factor alpha with primary open-angle glaucoma

gan Kondkar, Altaf A, Sultan, Tahira, Almobarak, Faisal A, Kalantan, Hatem, Al-Obeidan, Saleh A, Abu-Amero, Khaled K
Cyhoeddwyd yn Clin Ophthalmol (2018)

Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort

gan Kondkar, Altaf A., Sultan, Tahira, Almobarak, Faisal A., Kalantan, Hatem, Abu-Amero, Khaled K., Al-Obeidan, Saleh A.
Cyhoeddwyd yn BMC Res Notes (2018)