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Prajna Udupa

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

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Traffic (Copenhagen, Denmark)|January 25, 2024
The emerging functions of intraflagellar transport 52 in ciliary transport and ciliopathiesPrajna Udupa, Debasish Kumar Ghosh
Methods in Molecular Biology (Clifton, N.J.)|October 6, 2023
Implementation of Exome Sequencing to Identify Rare Genetic DiseasesPrajna Udupa, Debasish Kumar Ghosh
Peerj|September 5, 2020
Characterization of primary cilia features reveal cell-type specific variability in in vitro models of osteogenic and chondrogenic differentiationPriyanka Upadhyai, Vishal Singh Guleria, Prajna Udupa
Metabolism: Clinical and Experimental|October 24, 2022
Acyl-CoA binding protein regulates nutrient-dependent autophagyPrajna Udupa, Abhishek Kumar, Rahul Parit, et al.
Clinical Genetics|November 28, 2023
Assessing type I collagen expression and quality in cellular models of osteogenesis imperfectaPrajna Udupa, Akshaykumar Nanaji Shrikondawar, Akash Ranjan, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|December 16, 2022
Mutant MESD links cellular stress to type I collagen aggregation in osteogenesis imperfecta type XXDebasish Kumar Ghosh, Prajna Udupa, Akshaykumar Nanaji Shrikondawar, et al.
Journal of Human Genetics|December 16, 2022
Genome sequencing identifies a large non-coding region deletion of SNX10 causing autosomal recessive osteopetrosisPrajna Udupa, Debasish Kumar Ghosh, Neethukrishna Kausthubham, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|May 5, 2023
Deep intronic mutation in CRTAP results in unstable isoforms of the protein to induce type I collagen aggregation in a lethal type of osteogenesis imperfecta type VIIPrajna Udupa, Akshaykumar Nanaji Shrikondawar, Shalini S Nayak, et al.
Indian Journal of Pediatrics|January 24, 2023
Exome Sequencing in Monogenic Forms of RicketsPrince Jacob, Gandham SriLakshmi Bhavani, Prajna Udupa, et al.
NPJ Genomic Medicine|November 22, 2023
Clinical, genetic and structural delineation of RPL13-related spondyloepimetaphyseal dysplasia suggest extra-ribosomal functions of eL13Prince Jacob, Hillevi Lindelöf, Cecilie F Rustad, et al.
Pageof 1

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

Sort By:
Pageof 1
Traffic (Copenhagen, Denmark)|January 25, 2024
The emerging functions of intraflagellar transport 52 in ciliary transport and ciliopathiesPrajna Udupa, Debasish Kumar Ghosh
Methods in Molecular Biology (Clifton, N.J.)|October 6, 2023
Implementation of Exome Sequencing to Identify Rare Genetic DiseasesPrajna Udupa, Debasish Kumar Ghosh
Peerj|September 5, 2020
Characterization of primary cilia features reveal cell-type specific variability in in vitro models of osteogenic and chondrogenic differentiationPriyanka Upadhyai, Vishal Singh Guleria, Prajna Udupa
Metabolism: Clinical and Experimental|October 24, 2022
Acyl-CoA binding protein regulates nutrient-dependent autophagyPrajna Udupa, Abhishek Kumar, Rahul Parit, et al.
Clinical Genetics|November 28, 2023
Assessing type I collagen expression and quality in cellular models of osteogenesis imperfectaPrajna Udupa, Akshaykumar Nanaji Shrikondawar, Akash Ranjan, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|December 16, 2022
Mutant MESD links cellular stress to type I collagen aggregation in osteogenesis imperfecta type XXDebasish Kumar Ghosh, Prajna Udupa, Akshaykumar Nanaji Shrikondawar, et al.
Journal of Human Genetics|December 16, 2022
Genome sequencing identifies a large non-coding region deletion of SNX10 causing autosomal recessive osteopetrosisPrajna Udupa, Debasish Kumar Ghosh, Neethukrishna Kausthubham, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|May 5, 2023
Deep intronic mutation in CRTAP results in unstable isoforms of the protein to induce type I collagen aggregation in a lethal type of osteogenesis imperfecta type VIIPrajna Udupa, Akshaykumar Nanaji Shrikondawar, Shalini S Nayak, et al.
Indian Journal of Pediatrics|January 24, 2023
Exome Sequencing in Monogenic Forms of RicketsPrince Jacob, Gandham SriLakshmi Bhavani, Prajna Udupa, et al.
NPJ Genomic Medicine|November 22, 2023
Clinical, genetic and structural delineation of RPL13-related spondyloepimetaphyseal dysplasia suggest extra-ribosomal functions of eL13Prince Jacob, Hillevi Lindelöf, Cecilie F Rustad, et al.
Pageof 1