Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Ayyasamy, Vanniarajan"'
Autor:
Sriee Viswarubhiny, Rupa Anjanamurthy, Ayyasamy Vanniarajan, Devarajan Bharanidharan, Vijayalakshmi Perumalsamy, Periasamy Sundaresan
Publikováno v:
Eye and Vision, Vol 8, Iss 1, Pp 1-11 (2021)
Abstract Background Leber congenital amaurosis (LCA), primarily characterized by retinal degeneration is the most severe form of inherited retinal dystrophy (IRD) responsible for congenital blindness. The presence of phenotypic heterogeneity makes th
Externí odkaz:
https://doaj.org/article/25f9a15be55f4885afed5e711f44e48f
Autor:
Kumar Jeyaprakash, Thennarasu Shanthini, Usha Kim, Veerappan Muthukkaruppan, Ayyasamy Vanniarajan
Publikováno v:
Indian Journal of Ophthalmology, Vol 69, Iss 8, Pp 2111-2115 (2021)
Purpose: This study is aimed to investigate the presence of Human papillomavirus (HPV) DNA in tumors obtained from sporadic retinoblastoma patients. Methods: One hundred six tumor tissues obtained from sporadic RB patients were analyzed for HPV infec
Externí odkaz:
https://doaj.org/article/40940e7b8b984b1f8ff6acdc00643b23
Autor:
Aloysius Abraham, Kannan Thirumalairaj, Namrata Gaikwad, Veerappan Muthukkaruppan, Alla G Reddy, Kumarasamy Thangaraj, Usha Kim, Ayyasamy Vanniarajan
Publikováno v:
Indian Journal of Ophthalmology, Vol 67, Iss 3, Pp 436-439 (2019)
Retinoblastoma has an increased inheritance risk of germline RB1 mutations in offspring and siblings, especially twins. Three families, each having one retinoblastoma-affected twin, were selected for genetic analysis and DNA profiling. Germline RB1 m
Externí odkaz:
https://doaj.org/article/c549d15e887b4d51a2dbc791cfb98584
Autor:
Kumar Jeyaprakash, Kannan Thirumalairaj, Usha Kim, Veerappan Muthukkaruppan, Ayyasamy Vanniarajan
Publikováno v:
Pediatric Blood & Cancer. 70
Akademický článek
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Akademický článek
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Publikováno v:
Eye (Lond)
Upon completion of this activity, participants will be able to: In support of improving patient care, this activity has been planned and implemented by Medscape, LLC and Springer Nature. Medscape, LLC is jointly accredited by the Accreditation Counci
Autor:
Vijayalakshmi Perumalsamy, Rupa Anjanamurthy, Periasamy Sundaresan, Devarajan Bharanidharan, Ayyasamy Vanniarajan, Sriee Viswarubhiny
Publikováno v:
Eye and Vision, Vol 8, Iss 1, Pp 1-11 (2021)
Eye and Vision
Eye and Vision
Background Leber congenital amaurosis (LCA), primarily characterized by retinal degeneration is the most severe form of inherited retinal dystrophy (IRD) responsible for congenital blindness. The presence of phenotypic heterogeneity makes the diagnos
Autor:
Saraswathi Karuvel Kannan, Ulaganathan Shanmugam, Renu P Rajan, Naresh Babu, Ayyasamy Vanniarajan, Sagnik Sen
Publikováno v:
Ophthalmic Genetics. 42:300-303
Background: Gyrate Atrophy (GA) is a rare autosomal recessive disorder characterized by progressive chorioretinal degeneration. It is caused due to mutations in OAT gene that encodes a defective or...
Autor:
Andiappan Rathinavel, Perundurai S. Dhandapany, Madhu Khullar, Kumarasamy Thangaraj, Bindu Rani, Deepa Selvi Rani, Nahid Akthar Khan, Dharma Rakshak, Kumpati Premkumar, Ayyasamy Vanniarajan, Ajay Bahl, K.P. Indumathi, Pandarisamy Sundaravadivel, Calambur Narasimhan, Periyasamy Govindaraj, Rakesh Tamang
Publikováno v:
Mitochondrion. 48:51-59
Idiopathic dilated cardiomyopathy (DCM) is a structural heart disease with strong genetic background. The aim of this study was to assess the role of mitochondrial DNA (mtDNA) variations and haplogroups in Indian DCM patients. Whole mtDNA analysis of