检索结果 - Das, Parimal

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  1. 1
    Novel splicing in IGFN1 intron 15 and role of stable G-quadruplex in the regulation of splicing in renal cell carcinoma

    Novel splicing in IGFN1 intron 15 and role of stable G-quadruplex in the regulation of splicing in renal cell carcinoma 由 Verma, Shiv Prakash, Das, Parimal

    出版 2018
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  2. 2
    Association of PKD1 sequence variants with pathophysiology of ADPKD in Indian patients

    Association of PKD1 sequence variants with pathophysiology of ADPKD in Indian patients 由 Raj, Sonam, Singh, RG, Das, Parimal

    出版 2014
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  3. 3
    Identification and characterization of disease causing genetic variant by conventional genotyping and whole genome sequencing in familial tooth agenesis

    Identification and characterization of disease causing genetic variant by conventional genotyping and whole genome sequencing in familial tooth agenesis 由 Sarkar, Tanmoy, Bansal, Rajesh, Das, Parimal

    出版 2014
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  4. 4
    Whole Genome Sequencing Reveals Novel Non-Synonymous Mutation in Ectodysplasin A (EDA) Associated with Non-Syndromic X-Linked Dominant Congenital Tooth Agenesis

    Whole Genome Sequencing Reveals Novel Non-Synonymous Mutation in Ectodysplasin A (EDA) Associated with Non-Syndromic X-Linked Dominant Congenital Tooth Agenesis 由 Sarkar, Tanmoy, Bansal, Rajesh, Das, Parimal

    出版 2014
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  5. 5
    The influence of new SARS-CoV-2 variant Omicron (B.1.1.529) on vaccine efficacy, its correlation to Delta variants: A computational approach

    The influence of new SARS-CoV-2 variant Omicron (B.1.1.529) on vaccine efficacy, its correlation to Delta variants: A computational approach 由 Ranjan, Prashant, Neha, Devi, Chandra, Devar, Kaaviyapriya Arulmozhi, Das, Parimal

    出版 2022
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  6. 6
    Impact of B.1.617 and RBD SARS-CoV-2 variants on vaccine efficacy: An in-silico approach

    Impact of B.1.617 and RBD SARS-CoV-2 variants on vaccine efficacy: An in-silico approach 由 Ranjan, Prashant, Neha, Devi, Chandra, Jain, Garima, Mallick, Chandana Basu, Das, Parimal

    出版 2022
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  7. 7
    Novel Missense Mutations and a 288-bp Exonic Insertion in PAX9 in Families With Autosomal Dominant Hypodontia

    Novel Missense Mutations and a 288-bp Exonic Insertion in PAX9 in Families With Autosomal Dominant Hypodontia 由 Das, Parimal, Hai, Mehreen, Elcock, Claire, Leal, Suzanne M., Brown, Donald T., Brook, Alan H., Patel, Pragna I.

    出版 2003
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  8. 8
    Identification & characterization of leucine-rich repeat kinase 2 & parkin RBR E3 ubiquitin protein ligase variants in patients with Parkinson's disease

    Identification & characterization of leucine-rich repeat kinase 2 & parkin RBR E3 ubiquitin protein ligase variants in patients with Parkinson's disease 由 Halder, Tamali, Verma, Shiv Prakash, Raj, Janak, Pandey, Sharad, Singh, Ranjeet Kumar, Sharma, Vivek, Joshi, Deepika, Das, Parimal

    出版 2020
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  9. 9
    Low Levels of Genetic Divergence across Geographically and Linguistically Diverse Populations from India

    Low Levels of Genetic Divergence across Geographically and Linguistically Diverse Populations from India 由 Rosenberg, Noah A, Mahajan, Saurabh, Gonzalez-Quevedo, Catalina, Blum, Michael G. B, Nino-Rosales, Laura, Ninis, Vasiliki, Das, Parimal, Hegde, Madhuri, Molinari, Laura, Zapata, Gladys, Weber, James L, Belmont, John W, Patel, Pragna I

    出版 2006
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