Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Dhandayuthapani Sudha"'
Autor:
Rahini Rajendran, Dhandayuthapani Sudha, Subbulakshmi Chidambaram, Hemavathy Nagarajan, Umashankar Vetrivel, Jayamuruga Pandian Arunachalam
Publikováno v:
BMC Research Notes, Vol 14, Iss 1, Pp 1-7 (2021)
Abstract Objective Retinoschisis and Norrie disease are X-linked recessive retinal disorders caused by mutations in RS1 and NDP genes respectively. Both are likely to be monogenic and no locus heterogeneity has been reported. However, there are repor
Externí odkaz:
https://doaj.org/article/3aa8cae132ad4238822d3b956746910b
Autor:
Dhandayuthapani Sudha, Mahdokht Kohansal-Nodehi, Purnima Kovuri, Srikanth Srinivas Manda, Srividya Neriyanuri, Lingam Gopal, Pramod Bhende, Subbulakshmi Chidambaram, Jayamuruga Pandian Arunachalam
Publikováno v:
Clinical Proteomics, Vol 14, Iss 1, Pp 1-12 (2017)
Abstract Background X-linked retinoschisis (XLRS) is a vitreoretinal degenerative disorder causing vision deterioration, due to structural defects in retina. The hallmark of this disease includes radial streaks arising from the fovea and splitting of
Externí odkaz:
https://doaj.org/article/b8226eddeff041159d5d16642d81724b
Autor:
Dhandayuthapani Sudha, Srividya Neriyanuri, Ramya Sachidanandam, Srikrupa N Natarajan, Mamatha Gandra, Arokiasamy Tharigopala, Muthukumaran Sivashanmugam, Mohammed Alameen, Umashankar Vetrivel, Lingam Gopal, Vikas Khetan, Rajiv Raman, Parveen Sen, Subbulakshmi Chidambaram, Jayamuruga Pandian Arunachalam
Publikováno v:
PLoS ONE, Vol 13, Iss 5, p e0198086 (2018)
X-linked retinoschisis (XLRS) is a retinal degenerative disorder caused by mutations in RS1 gene leading to splitting of retinal layers (schisis) which impairs visual signal processing. Retinoschisin (RS1) is an adhesive protein which is secreted pre
Externí odkaz:
https://doaj.org/article/8d9a99cf407c4c54b57681d629ae9366
Autor:
Subbulakshmi Chidambaram, Jayamuruga Pandian Arunachalam, Dhandayuthapani Sudha, Umashankar Vetrivel, Hemavathy Nagarajan, Rahini Rajendran
Publikováno v:
BMC Research Notes, Vol 14, Iss 1, Pp 1-7 (2021)
BMC Research Notes
BMC Research Notes
Objective Retinoschisis and Norrie disease are X-linked recessive retinal disorders caused by mutations in RS1 and NDP genes respectively. Both are likely to be monogenic and no locus heterogeneity has been reported. However, there are reports showin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::365e1e4c99cf5755fa6f414d14075203
https://doaj.org/article/3aa8cae132ad4238822d3b956746910b
https://doaj.org/article/3aa8cae132ad4238822d3b956746910b
Autor:
Rahini Rajendran, Dhandayuthapani Sudha, Subbulakshmi Chidambaram, Hemavathy Nagarajan, Vetrivel, Umashankar, Arunachalam, Jayamuruga Pandian
Additional file 1: Detailed methodology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29e78c46c561779c1231fac0bbcebc46
Autor:
Neriyanuri, Srividya1, Dhandayuthapani, Sudha2, Arunachalam, Jayamuruga Pandian2, Raman, Rajiv3 rajivpgraman@gmail.com
Publikováno v:
Indian Journal of Ophthalmology. Jul2016, Vol. 64 Issue 7, p513-517. 5p.
Autor:
Shuba Krishna, Srividya Neriyanuri, Dhandayuthapani Sudha, Jayamuruga Pandian Arunachalam, Aparna Ganapathy, Smitha Agarwal, Subbulakshmi Chidambaram, S. Sripriya, Irene Rosita Pia Patric, Parveen Sen
Publikováno v:
Ophthalmic Genetics. 38:260-266
Background: In this study, we present a juvenile retinoschisis patient with developmental delay, sensorineural hearing loss, and reduced axial tone. X-linked juvenile retinoschisis (XLRS) is a retinal dystrophy, most often not associated with systemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9f0503ba37aba325b3a6b17c57e4c53
https://doi.org/10.1080/13816810.2016.1214972
https://doi.org/10.1080/13816810.2016.1214972
BackgroundRetinoschisis and Norrie disease are X-linked recessive retinal disorders caused by mutations in RS1 and NDP genes respectively. Both are likely to be monogenic and no locus heterogeneity has been reported. However, there are reports showin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e7d18b58b528c540136dcf4d2eb52d2
Autor:
Srividya Neriyanuri, Mamatha Gandra, Arokiasamy Tharigopala, Lingam Gopal, Jayamuruga Pandian Arunachalam, Vikas Khetan, Srikrupa N. Natarajan, Mohammed Alameen, Muthukumaran Sivashanmugam, Parveen Sen, Ramya Sachidanandam, Rajiv Raman, Dhandayuthapani Sudha, Umashankar Vetrivel, Subbulakshmi Chidambaram
Publikováno v:
PLoS ONE, Vol 13, Iss 5, p e0198086 (2018)
PLoS ONE
PLoS ONE
X-linked retinoschisis (XLRS) is a retinal degenerative disorder caused by mutations in RS1 gene leading to splitting of retinal layers (schisis) which impairs visual signal processing. Retinoschisin (RS1) is an adhesive protein which is secreted pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d14de034c1294b47c0debe05252605a6
http://europepmc.org/articles/PMC5978886?pdf=render
http://europepmc.org/articles/PMC5978886?pdf=render
Autor:
Shuba Krishna, Srividya Neriyanuri, Subbulakshmi Chidambaram, Jayamuruga Pandian Arunachalam, P. S. Mohan, Pukhraj Rishi, Ashraf U Mannan, Dhandayuthapani Sudha, Aparna Ganapathy, Meenakshi Swaminathan
Publikováno v:
International ophthalmology. 38(3)
NDP-related retinopathies are a group of X-linked disorders characterized by degenerative and proliferative changes of the neuroretina, occasionally accompanied with varying degrees of mental retardation and sensorineural hearing loss. NDP is the pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ca563b38712d15a0f1cd859f21526d1
https://pubmed.ncbi.nlm.nih.gov/28602015
https://pubmed.ncbi.nlm.nih.gov/28602015