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Shruti Pande

Showing results (1-10 of 18) with videos related to

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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 27, 2023
Nuclear proteostasis imbalance in laminopathy-associated premature aging diseasesShruti Pande, Debasish Kumar Ghosh
Genes|August 28, 2025
Structural Variants: Mechanisms, Mapping, and Interpretation in Human GeneticsShruti Pande, Moez Dawood, Christopher M Grochowski
American Journal of Medical Genetics. Part A|October 12, 2020
Trichothiodystrophy type 4 in an Indian familyShruti Pande, Anju Shukla, Katta Mohan Girisha
American Journal of Medical Genetics. Part A|September 11, 2020
Untapped opportunities for rare disease gene discovery in IndiaKatta Mohan Girisha, Shruti Pande, Ashwin Dalal, et al.
American Journal of Medical Genetics. Part A|March 22, 2021
Hedgehog acyl-transferase-related multiple congenital anomalies: Report of an additional family and delineation of the syndromeShruti Pande, Periyasamy Radhakrishnan, Naveenchandra M Shetty, et al.
Plants (Basel, Switzerland)|April 30, 2021
Transcriptome Sequence Reveals Candidate Genes Involving in the Post-Harvest Hardening of Trifoliate Yam <i>Dioscorea dumetorum</i>Christian Siadjeu, Eike Mayland-Quellhorst, Shruti Pande, et al.
Journal of Pediatric Genetics|January 23, 2023
Knobloch Syndrome in Siblings with Posterior Fossa Malformations Along with Cerebellar Midline Cleft Abnormality Caused by Biallelic <i>COL18A1</i> Mutation: Case-Based ReviewSiddaramappa J Patil, Shruti Pande, Jyoti Matalia, et al.
American Journal of Medical Genetics. Part A|April 17, 2026
Biallelic Splicing Variant c.12479+3A>G in FAT4 Causes Hennekam Lymphangiectasia-Lymphedema Syndrome 2Selinda Mascarenhas, Yashavi Gupta, Akhil K A, et al.
American Journal of Medical Genetics. Part A|June 20, 2023
Further validation of craniosynostosis as a part of phenotypic spectrum of BCL11B-related BAFopathyShruti Pande, Selinda Mascarenhas, Aishwarya Venkatraman, et al.
Aging Cell|October 13, 2022
The E262K mutation in Lamin A links nuclear proteostasis imbalance to laminopathy-associated premature agingDebasish Kumar Ghosh, Shruti Pande, Jeevan Kumar, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 27, 2023
Nuclear proteostasis imbalance in laminopathy-associated premature aging diseasesShruti Pande, Debasish Kumar Ghosh
Genes|August 28, 2025
Structural Variants: Mechanisms, Mapping, and Interpretation in Human GeneticsShruti Pande, Moez Dawood, Christopher M Grochowski
American Journal of Medical Genetics. Part A|October 12, 2020
Trichothiodystrophy type 4 in an Indian familyShruti Pande, Anju Shukla, Katta Mohan Girisha
American Journal of Medical Genetics. Part A|September 11, 2020
Untapped opportunities for rare disease gene discovery in IndiaKatta Mohan Girisha, Shruti Pande, Ashwin Dalal, et al.
American Journal of Medical Genetics. Part A|March 22, 2021
Hedgehog acyl-transferase-related multiple congenital anomalies: Report of an additional family and delineation of the syndromeShruti Pande, Periyasamy Radhakrishnan, Naveenchandra M Shetty, et al.
Plants (Basel, Switzerland)|April 30, 2021
Transcriptome Sequence Reveals Candidate Genes Involving in the Post-Harvest Hardening of Trifoliate Yam <i>Dioscorea dumetorum</i>Christian Siadjeu, Eike Mayland-Quellhorst, Shruti Pande, et al.
Journal of Pediatric Genetics|January 23, 2023
Knobloch Syndrome in Siblings with Posterior Fossa Malformations Along with Cerebellar Midline Cleft Abnormality Caused by Biallelic <i>COL18A1</i> Mutation: Case-Based ReviewSiddaramappa J Patil, Shruti Pande, Jyoti Matalia, et al.
American Journal of Medical Genetics. Part A|April 17, 2026
Biallelic Splicing Variant c.12479+3A>G in FAT4 Causes Hennekam Lymphangiectasia-Lymphedema Syndrome 2Selinda Mascarenhas, Yashavi Gupta, Akhil K A, et al.
American Journal of Medical Genetics. Part A|June 20, 2023
Further validation of craniosynostosis as a part of phenotypic spectrum of BCL11B-related BAFopathyShruti Pande, Selinda Mascarenhas, Aishwarya Venkatraman, et al.
Aging Cell|October 13, 2022
The E262K mutation in Lamin A links nuclear proteostasis imbalance to laminopathy-associated premature agingDebasish Kumar Ghosh, Shruti Pande, Jeevan Kumar, et al.
Pageof 2