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Aditi Chawla

Showing results (1-10 of 12) with videos related to

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Current Biology : CB|November 24, 2005
The unfolded protein responseAditi Chawla, Maho Niwa
Contraception and Reproductive Medicine|May 7, 2026
A comparative study on the outcomes of post-placental intrauterine contraceptive device insertion between preterm and term deliveries: a hospital-based observational studySoni Kumari, Sarita Singh, Aditi Chawla, et al.
The Journal of Cell Biology|March 30, 2011
Attenuation of yeast UPR is essential for survival and is mediated by IRE1 kinaseAditi Chawla, Sutapa Chakrabarti, Gourisankar Ghosh, et al.
American Journal of Medical Genetics. Part A|March 26, 2018
Congenital sodium diarrhea and chorioretinal coloboma with optic disc coloboma in a patient with biallelic SPINT2 mutations, including p.(Tyr163Cys)Kristin E Hirabayashi, Anthony T Moore, Bryce A Mendelsohn, et al.
Movement Disorders Clinical Practice|March 27, 2024
A Novel Variant in SQSTM1 Gene Causing Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy in a Peruvian FamilyCesar Chacaltana-Vinas, Patricia Ramirez-Pajares, Alid Manrique-Palomino, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 19, 2020
Spinal muscular atrophy diagnosis and carrier screening from genome sequencing dataXiao Chen, Alba Sanchis-Juan, Courtney E French, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed diseaseAndrew M Gross, Subramanian S Ajay, Vani Rajan, et al.
Medrxiv : the Preprint Server for Health Sciences|May 20, 2024
Development of a comprehensive cardiovascular disease genetic risk assessment testLaura M Amendola, Alison J Coffey, Josh Lowry, et al.
Genetics in Medicine Open|January 19, 2026
Development of a comprehensive cardiovascular disease genetic risk assessment testLaura M Amendola, Alison J Coffey, Josh Lowry, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2019
Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomaliesMichael D Fountain, David S Oleson, Megan E Rech, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Current Biology : CB|November 24, 2005
The unfolded protein responseAditi Chawla, Maho Niwa
Contraception and Reproductive Medicine|May 7, 2026
A comparative study on the outcomes of post-placental intrauterine contraceptive device insertion between preterm and term deliveries: a hospital-based observational studySoni Kumari, Sarita Singh, Aditi Chawla, et al.
The Journal of Cell Biology|March 30, 2011
Attenuation of yeast UPR is essential for survival and is mediated by IRE1 kinaseAditi Chawla, Sutapa Chakrabarti, Gourisankar Ghosh, et al.
American Journal of Medical Genetics. Part A|March 26, 2018
Congenital sodium diarrhea and chorioretinal coloboma with optic disc coloboma in a patient with biallelic SPINT2 mutations, including p.(Tyr163Cys)Kristin E Hirabayashi, Anthony T Moore, Bryce A Mendelsohn, et al.
Movement Disorders Clinical Practice|March 27, 2024
A Novel Variant in SQSTM1 Gene Causing Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy in a Peruvian FamilyCesar Chacaltana-Vinas, Patricia Ramirez-Pajares, Alid Manrique-Palomino, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 19, 2020
Spinal muscular atrophy diagnosis and carrier screening from genome sequencing dataXiao Chen, Alba Sanchis-Juan, Courtney E French, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed diseaseAndrew M Gross, Subramanian S Ajay, Vani Rajan, et al.
Medrxiv : the Preprint Server for Health Sciences|May 20, 2024
Development of a comprehensive cardiovascular disease genetic risk assessment testLaura M Amendola, Alison J Coffey, Josh Lowry, et al.
Genetics in Medicine Open|January 19, 2026
Development of a comprehensive cardiovascular disease genetic risk assessment testLaura M Amendola, Alison J Coffey, Josh Lowry, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2019
Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomaliesMichael D Fountain, David S Oleson, Megan E Rech, et al.
Pageof 2