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Open Forum Infectious Diseases
|
November 17, 2020
A Distinct Phylogenetic Cluster of Indian Severe Acute Respiratory Syndrome Coronavirus 2 Isolates
Sofia Banu, Bani Jolly, Payel Mukherjee, et al.
Journal of Human Genetics
|
June 18, 2024
Whole genome sequencing of families diagnosed with cardiac channelopathies reveals structural variants missed by whole exome sequencing
Vigneshwar Senthivel, Bani Jolly, Arvinden Vr, et al.
Frontiers in Molecular Biosciences
|
December 28, 2023
Scalable noninvasive amplicon-based precision sequencing (SNAPseq) for genetic diagnosis and screening of β-thalassemia and sickle cell disease using a next-generation sequencing platform
Pragya Gupta, V R Arvinden, Priya Thakur, et al.
Plos One
|
September 28, 2018
Large scale changes in the transcriptome of Eisenia fetida during regeneration
Aksheev Bhambri, Neeraj Dhaunta, Surendra Singh Patel, et al.
The Journal of Applied Laboratory Medicine
|
August 14, 2024
A Rapid and Scalable Multiplex PCR-Based Next-Generation Amplicon Sequencing Method for Familial Hypercholesterolemia Genetic Screening
Mohamed Imran, V R Arvinden, Pabithadevi Balaiah Mehanathan, et al.
Plos One
|
July 12, 2021
Whole genome sequencing identifies novel structural variant in a large Indian family affected with X-linked agammaglobulinemia
Abhinav Jain, Geeta Madathil Govindaraj, Athulya Edavazhippurath, et al.
Pharmacogenomics
|
December 15, 2017
Pharmacogenetic landscape of DPYD variants in south Asian populations by integration of genome-scale data
Judith M Hariprakash, Shamsudheen K Vellarikkal, Pavithran Keechilat, et al.
Journal of Medical Virology
|
November 17, 2021
Variants of concern responsible for SARS-CoV-2 vaccine breakthrough infections from India
Urvashi B Singh, Mercy Rophina, Rama Chaudhry, et al.
Plos One
|
September 7, 2013
Systematic pharmacogenomics analysis of a Malay whole genome: proof of concept for personalized medicine
Mohd Zaki Salleh, Lay Kek Teh, Lian Shien Lee, et al.
Nature Communications
|
February 27, 2024
Development of pathophysiologically relevant models of sickle cell disease and β-thalassemia for therapeutic studies
Pragya Gupta, Sangam Giri Goswami, Geeta Kumari, et al.
Page
of 25
Search research articles
Search
Showing results (211-220 of 245) with videos related to
Sort By:
Page
of 25
Open Forum Infectious Diseases
|
November 17, 2020
A Distinct Phylogenetic Cluster of Indian Severe Acute Respiratory Syndrome Coronavirus 2 Isolates
Sofia Banu, Bani Jolly, Payel Mukherjee, et al.
Journal of Human Genetics
|
June 18, 2024
Whole genome sequencing of families diagnosed with cardiac channelopathies reveals structural variants missed by whole exome sequencing
Vigneshwar Senthivel, Bani Jolly, Arvinden Vr, et al.
Frontiers in Molecular Biosciences
|
December 28, 2023
Scalable noninvasive amplicon-based precision sequencing (SNAPseq) for genetic diagnosis and screening of β-thalassemia and sickle cell disease using a next-generation sequencing platform
Pragya Gupta, V R Arvinden, Priya Thakur, et al.
Plos One
|
September 28, 2018
Large scale changes in the transcriptome of Eisenia fetida during regeneration
Aksheev Bhambri, Neeraj Dhaunta, Surendra Singh Patel, et al.
The Journal of Applied Laboratory Medicine
|
August 14, 2024
A Rapid and Scalable Multiplex PCR-Based Next-Generation Amplicon Sequencing Method for Familial Hypercholesterolemia Genetic Screening
Mohamed Imran, V R Arvinden, Pabithadevi Balaiah Mehanathan, et al.
Plos One
|
July 12, 2021
Whole genome sequencing identifies novel structural variant in a large Indian family affected with X-linked agammaglobulinemia
Abhinav Jain, Geeta Madathil Govindaraj, Athulya Edavazhippurath, et al.
Pharmacogenomics
|
December 15, 2017
Pharmacogenetic landscape of DPYD variants in south Asian populations by integration of genome-scale data
Judith M Hariprakash, Shamsudheen K Vellarikkal, Pavithran Keechilat, et al.
Journal of Medical Virology
|
November 17, 2021
Variants of concern responsible for SARS-CoV-2 vaccine breakthrough infections from India
Urvashi B Singh, Mercy Rophina, Rama Chaudhry, et al.
Plos One
|
September 7, 2013
Systematic pharmacogenomics analysis of a Malay whole genome: proof of concept for personalized medicine
Mohd Zaki Salleh, Lay Kek Teh, Lian Shien Lee, et al.
Nature Communications
|
February 27, 2024
Development of pathophysiologically relevant models of sickle cell disease and β-thalassemia for therapeutic studies
Pragya Gupta, Sangam Giri Goswami, Geeta Kumari, et al.
Page
of 25