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Sinnakaruppan Mathavan

Showing results (1-10 of 52) with videos related to

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Indian Journal of Ophthalmology|March 17, 2021
The yield of diabetic retinopathy screening in patients with long-standing diabetesGeetha Kumar, Saranya Velu, Sinnakaruppan Mathavan, et al.
Differentiation; Research in Biological Diversity|January 27, 2015
Zebrafish Rnf111 is encoded by multiple transcripts and is required for epiboly progression and prechordal plate developmentDmitri A Bessarab, Sinnakaruppan Mathavan, C Michael Jones, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 19, 2021
Exploring Translational Control of Maternal mRNAs in ZebrafishCecilia Lanny Winata, Maciej Łapiński, Hisyam Ismail, et al.
Plos One|December 29, 2010
Tiling histone H3 lysine 4 and 27 methylation in zebrafish using high-density microarraysLeif C Lindeman, Andrew H Reiner, Sinnakaruppan Mathavan, et al.
Human Genome Variation|March 30, 2021
Whole-exome sequencing identifies two novel ALMS1 mutations in Indian patients with Leber congenital amaurosisNatarajan N Srikrupa, Sarangapani Sripriya, Suriyanarayanan Pavithra, et al.
BMC Genomics|November 13, 2015
Genome-wide mapping of Hif-1α binding sites in zebrafishDavid Greenald, Justin Jeyakani, Bernd Pelster, et al.
The International Journal of Developmental Biology|March 26, 2010
Chromatin states of developmentally-regulated genes revealed by DNA and histone methylation patterns in zebrafish embryosLeif C Lindeman, Cecilia L Winata, Hvard Aanes, et al.
Biochemical and Biophysical Research Communications|February 12, 2019
Transcriptomic analyses of oncogenic hepatocytes reveal common and different molecular pathways of hepatocarcinogenesis in different developmental stages and genders in kras<sup>G12V</sup> transgenic zebrafishXiaojing Huo, Hankun Li, Zhen Li, et al.
Development (Cambridge, England)|June 23, 2012
Dorsal activity of maternal squint is mediated by a non-coding function of the RNAShimin Lim, Pooja Kumari, Patrick Gilligan, et al.
Ophthalmic Genetics|September 1, 2020
CERKL mutation causing retinitis pigmentosa(RP) in Indian population - a genotype and phenotype correlation studyParveen Sen, Puja Maitra, Srikrupa Natarajan, et al.
Pageof 6

Showing results (1-10 of 52) with videos related to

Sort By:
Pageof 6
Indian Journal of Ophthalmology|March 17, 2021
The yield of diabetic retinopathy screening in patients with long-standing diabetesGeetha Kumar, Saranya Velu, Sinnakaruppan Mathavan, et al.
Differentiation; Research in Biological Diversity|January 27, 2015
Zebrafish Rnf111 is encoded by multiple transcripts and is required for epiboly progression and prechordal plate developmentDmitri A Bessarab, Sinnakaruppan Mathavan, C Michael Jones, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 19, 2021
Exploring Translational Control of Maternal mRNAs in ZebrafishCecilia Lanny Winata, Maciej Łapiński, Hisyam Ismail, et al.
Plos One|December 29, 2010
Tiling histone H3 lysine 4 and 27 methylation in zebrafish using high-density microarraysLeif C Lindeman, Andrew H Reiner, Sinnakaruppan Mathavan, et al.
Human Genome Variation|March 30, 2021
Whole-exome sequencing identifies two novel ALMS1 mutations in Indian patients with Leber congenital amaurosisNatarajan N Srikrupa, Sarangapani Sripriya, Suriyanarayanan Pavithra, et al.
BMC Genomics|November 13, 2015
Genome-wide mapping of Hif-1α binding sites in zebrafishDavid Greenald, Justin Jeyakani, Bernd Pelster, et al.
The International Journal of Developmental Biology|March 26, 2010
Chromatin states of developmentally-regulated genes revealed by DNA and histone methylation patterns in zebrafish embryosLeif C Lindeman, Cecilia L Winata, Hvard Aanes, et al.
Biochemical and Biophysical Research Communications|February 12, 2019
Transcriptomic analyses of oncogenic hepatocytes reveal common and different molecular pathways of hepatocarcinogenesis in different developmental stages and genders in kras<sup>G12V</sup> transgenic zebrafishXiaojing Huo, Hankun Li, Zhen Li, et al.
Development (Cambridge, England)|June 23, 2012
Dorsal activity of maternal squint is mediated by a non-coding function of the RNAShimin Lim, Pooja Kumari, Patrick Gilligan, et al.
Ophthalmic Genetics|September 1, 2020
CERKL mutation causing retinitis pigmentosa(RP) in Indian population - a genotype and phenotype correlation studyParveen Sen, Puja Maitra, Srikrupa Natarajan, et al.
Pageof 6