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Preti Jain

Showing results (11-20 of 19) with videos related to

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Oncotarget|May 21, 2016
Genetic landscape of T- and NK-cell post-transplant lymphoproliferative disordersElizabeth Margolskee, Vaidehi Jobanputra, Preti Jain, et al.
American Journal of Medical Genetics. Part A|October 8, 2021
D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemiaKelly M Werner, Allison J Cox, Emily Qian, et al.
Oncotarget|June 2, 2016
The genetic landscape of dural marginal zone lymphomasKarthik A Ganapathi, Vaidehi Jobanputra, Fabio Iwamoto, et al.
Cell|September 24, 2025
A Validated Regulatory Network for Th17 Cell SpecificationMaria Ciofani, Aviv Madar, Carolina Galan, et al.
Cell|October 2, 2012
A validated regulatory network for Th17 cell specificationMaria Ciofani, Aviv Madar, Carolina Galan, et al.
JAMA Neurology|November 24, 2015
Whole-Exome Sequencing in Familial Parkinson DiseaseJanice L Farlow, Laurie A Robak, Kurt Hetrick, et al.
Nature|September 8, 2012
Architecture of the human regulatory network derived from ENCODE dataMark B Gerstein, Anshul Kundaje, Manoj Hariharan, et al.
Journal of Crohn'S & Colitis|April 23, 2021
Variants in STXBP3 are Associated with Very Early Onset Inflammatory Bowel Disease, Bilateral Sensorineural Hearing Loss and Immune DysregulationJodie Ouahed, Judith R Kelsen, Waldo A Spessott, et al.
Neuron|November 6, 2015
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic DiseaseEnder Karaca, Tamar Harel, Davut Pehlivan, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Oncotarget|May 21, 2016
Genetic landscape of T- and NK-cell post-transplant lymphoproliferative disordersElizabeth Margolskee, Vaidehi Jobanputra, Preti Jain, et al.
American Journal of Medical Genetics. Part A|October 8, 2021
D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemiaKelly M Werner, Allison J Cox, Emily Qian, et al.
Oncotarget|June 2, 2016
The genetic landscape of dural marginal zone lymphomasKarthik A Ganapathi, Vaidehi Jobanputra, Fabio Iwamoto, et al.
Cell|September 24, 2025
A Validated Regulatory Network for Th17 Cell SpecificationMaria Ciofani, Aviv Madar, Carolina Galan, et al.
Cell|October 2, 2012
A validated regulatory network for Th17 cell specificationMaria Ciofani, Aviv Madar, Carolina Galan, et al.
JAMA Neurology|November 24, 2015
Whole-Exome Sequencing in Familial Parkinson DiseaseJanice L Farlow, Laurie A Robak, Kurt Hetrick, et al.
Nature|September 8, 2012
Architecture of the human regulatory network derived from ENCODE dataMark B Gerstein, Anshul Kundaje, Manoj Hariharan, et al.
Journal of Crohn'S & Colitis|April 23, 2021
Variants in STXBP3 are Associated with Very Early Onset Inflammatory Bowel Disease, Bilateral Sensorineural Hearing Loss and Immune DysregulationJodie Ouahed, Judith R Kelsen, Waldo A Spessott, et al.
Neuron|November 6, 2015
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic DiseaseEnder Karaca, Tamar Harel, Davut Pehlivan, et al.
Pageof 2