Výsledky vyhledávání - "Jyoti S Shetty"

Characterization of osteoarthritis-derived cartilage and infrapatellar fat pad mesenchymal stromal cells expanded in human platelet lysate

Autor: S. Babu, Arpana Mathur, Siddharth M. Shetty, B Mohana Kumar, Jyoti S Shetty, Narendra Nitilapura, Veena Shetty

Publikováno v: Cytotherapy. 23:S65-S66

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::afc60243d20caa5cddde43b00656fe31
https://doi.org/10.1016/s1465324921003662

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A homozygous mutation in LTBP2 causes isolated microspherophakia

Autor: Jyoti S Shetty, Maheswara R Duvvari, Venkatesh C. Prabhakaran, Gowri J Murthy, Susan H. Blanton, Arun Kumar

Publikováno v: Human Genetics, 128, 4, pp. 365-71
Human Genetics, 128, 365-71

Item does not contain fulltext Microspherophakia is an autosomal-recessive congenital disorder characterized by small spherical lens. It may be isolated or occur as part of a hereditary systemic disorder, such as Marfan syndrome, autosomal dominant a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92534e2be8e4346855b513ff382e473e
https://pubmed.ncbi.nlm.nih.gov/20617341

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Role of CYP1B1, MYOC, OPTN, and OPTC genes in adult-onset primary open-angle glaucoma: predominance of CYP1B1 mutations in Indian patients

Autor: Arun, Kumar, Manjunath G, Basavaraj, Santosh K, Gupta, Imteyaz, Qamar, Abdullah Mahmood, Ali, Vineeta, Bajaj, T K, Ramesh, D Ravi, Prakash, Jyoti S, Shetty, Syril K, Dorairaj

Publikováno v: Molecular Vision

Purpose Mutations in the CYP1B1, MYOC, OPTN, and WDR36 genes result in glaucoma. Given its expression in the optic nerve, it is likely a mutation in the OPTC gene is also involved in initiating glaucoma. This study was designed to evaluate the involv

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::824e8d392d53152c9bbc1c21ae8d0627
https://pubmed.ncbi.nlm.nih.gov/17563717

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Genetic analysis of an Indian family with members affected with juvenile-onset primary open-angle glaucoma

Autor: Ravi Prakash, Selvaraju, Arun Kumar, Syril Dorairaj, Jyoti S Shetty, T. Ramesh, M Markandaya

Publikováno v: Ophthalmic genetics. 25(1)

Purpose: Glaucoma is the second leading cause of blindness. In India, ~1.5 million people are blind due to glaucoma. Mutations in the MYOC gene located at the GLC1A locus on chromosome 1q21–q31 have been found in patients with juvenile-onset primar

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cb6446ecc5ca93dea0b562216f3d1f6
https://pubmed.ncbi.nlm.nih.gov/15255110

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