Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sarmeela, Sharma"'
Autor:
Abhishek Sheemar, Keerthi Bellala, Sumant Vinayak Sharma, Sarmeela Sharma, Inderjeet Kaur, Padmaja Rani, Sobha Sivaprasad, KM Venkat Narayan, Taraprasad Das, Brijesh Takkar
Publikováno v:
Indian Journal of Ophthalmology, Vol 72, Iss 6, Pp 796-808 (2024)
The response of retinal pathology to interventions in diabetic retinopathy (DR) is often independent of the glycated hemoglobin (HbA1c) values at the point of care. This is despite glucose control being one of the strongest risk factors for the devel
Externí odkaz:
https://doaj.org/article/594280c220c1457a9b5f9db54f693e73
Autor:
Prerna Kulshrestha, Sarmeela Sharma, Sushma Vishwakarma, Mohammed J Ali, Tarjani V Dave, Inderjeet Kaur
Publikováno v:
Indian Journal of Ophthalmology, Vol 72, Iss 7, Pp 962-967 (2024)
Purpose: Human ocular tissue banking plays an important part in the advancement of translational research for identifying the molecular processes involved in disease etiology and pathogenesis. Timely obtaining a good-quality ocular tissue from a cada
Externí odkaz:
https://doaj.org/article/ce490c80b18c488ab9e4514cf055be7a
Autor:
Vinod Singh, Ekta Rai, Swarkar Sharma, Shruti Sharma, John Zohmingthanga, Nachimuthu Senthil Kumar, Freda Lalrohlui, Indu Sharma, Tasmeen Javed Parihar, Sarmeela Sharma, Varun Sharma
Publikováno v:
International Journal of Diabetes in Developing Countries. 40:513-517
Uncoupling protein 3 (UCP3) has been identified as a type 2 diabetes (T2D) candidate gene and variant rs1800849 is of potential interest as it is present in the regulatory region of UCP3. The aim of the present candidate gene case-control association
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0afb39bd315449260b3563835affce32
https://doi.org/10.1007/s13410-020-00812-9
https://doi.org/10.1007/s13410-020-00812-9
Autor:
Debasmita, Saha, Sushma, Vishwakarma, Rishikesh Kumar, Gupta, Avnika, Pant, Vaibhav, Dhyani, Sarmeela, Sharma, Saptarshi, Majumdar, Inderjeet, Kaur, Lopamudra, Giri
Publikováno v:
Neurochemistry International. 164:105466
Cellular hypoxia is a major cause of oxidative stress, culminating in neuronal damage in neurodegenerative diseases. Numerous ex vivo studies have implicated hypoxia episodes in the disruption of Ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a06a90c6b61d70a03b5d157c73905cd
https://doi.org/10.1016/j.neuint.2022.105466
https://doi.org/10.1016/j.neuint.2022.105466
Publikováno v:
Ophthalmic genetics. 42(1)
Traboulsi syndrome is a rare autosomal recessive genetic disorder. The present study aimed to identify the pathogenic variants in theDNA was isolated from the blood samples from 3 clinically diagnosed Traboulsi syndrome patients (n = 3) after obtaini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f38da0f3206d3fa3504dc98518b73758
https://pubmed.ncbi.nlm.nih.gov/33251883
https://pubmed.ncbi.nlm.nih.gov/33251883
Publikováno v:
Metagenomics: Techniques, Applications, Challenges and Opportunities ISBN: 9789811565281
Microbes are essential for the smooth functioning of life as every life process in the biosphere involves the contribution of microbes. Previously, the study of the microbes has been primarily centred over laboratory-based pure-culture techniques due
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b3793beca41e020099fc22a3fa35a44
https://doi.org/10.1007/978-981-15-6529-8_2
https://doi.org/10.1007/978-981-15-6529-8_2
Traboulsi syndrome is a rare autosomal recessive genetic disorder. The present study aimed to identify the pathogenic variants in the ASPH gene responsible for a rare and unique presentation of Traboulsi syndrome associated with cardiac disorder. DNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af01e44ac6021936af37e18858d90bb9