Characterization of primary cilia features reveal cell-type specific variability in in vitro models of osteogenic and chondrogenic differentiation

por Upadhyai, Priyanka, Guleria, Vishal Singh, Udupa, Prajna
Publicado 2020

Genome sequencing identifies a large non-coding region deletion of SNX10 causing autosomal recessive osteopetrosis

por Udupa, Prajna, Ghosh, Debasish Kumar, Kausthubham, Neethukrishna, Shah, Hitesh, Bartakke, Sandip, Dalal, Ashwin, Girisha, Katta M, Bhavani, Gandham SriLakshmi
Publicado 2022

Exome Sequencing in Monogenic Forms of Rickets

por Jacob, Prince, Bhavani, Gandham SriLakshmi, Udupa, Prajna, Wang, Zheng, Hariharan, Sankar V., Delampady, Kishan, Dalal, Ashwin, Kamath, Nutan, Ikegawa, Shiro, Shenoy, Rathika D., Handattu, Koushik, Shah, Hitesh, Girisha, Katta M.
Publicado 2023

Clinical, genetic and structural delineation of RPL13-related spondyloepimetaphyseal dysplasia suggest extra-ribosomal functions of eL13

por Jacob, Prince, Lindelöf, Hillevi, Rustad, Cecilie F., Sutton, Vernon Reid, Moosa, Shahida, Udupa, Prajna, Hammarsjö, Anna, Bhavani, Gandham SriLakshmi, Batkovskyte, Dominyka, Tveten, Kristian, Dalal, Ashwin, Horemuzova, Eva, Nordgren, Ann, Tham, Emma, Shah, Hitesh, Merckoll, Else, Orellana, Laura, Nishimura, Gen, Girisha, Katta M., Grigelioniene, Giedre
Publicado 2023