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Indrajit Nanda

Showing results (51-60 of 59) with videos related to

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Genomics|October 28, 2006
The DNA sequence of medaka chromosome LG22Takashi Sasaki, Atsushi Shimizu, Sabine K Ishikawa, et al.
Zebrafish|April 2, 2008
Molecular analysis of the sex-determining region of the platyfish Xiphophorus maculatusChristina Schultheis, Qingchun Zhou, Alexander Froschauer, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|February 23, 2017
SLC2A3 single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorderSören Merker, Andreas Reif, Georg C Ziegler, et al.
Genes|November 14, 2020
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani FamiliesJulia Doll, Barbara Vona, Linda Schnapp, et al.
Cell|January 14, 2017
DNA Damage Signaling Instructs Polyploid Macrophage Fate in GranulomasLaura Herrtwich, Indrajit Nanda, Konstantinos Evangelou, et al.
Cell|August 25, 2018
DNA Damage Signaling Instructs Polyploid Macrophage Fate in GranulomasLaura Herrtwich, Indrajit Nanda, Konstantinos Evangelou, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2026
<i>FRMPD4</i> , a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing lossDaniel Liedtke, Kristen Rak, Katrina M Schrode, et al.
American Journal of Human Genetics|April 30, 2013
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticityHiromi Hirata, Indrajit Nanda, Anne van Riesen, et al.
Cytogenetic and Genome Research|August 19, 2015
Third Report on Chicken Genes and Chromosomes 2015Michael Schmid, Jacqueline Smith, David W Burt, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
Genomics|October 28, 2006
The DNA sequence of medaka chromosome LG22Takashi Sasaki, Atsushi Shimizu, Sabine K Ishikawa, et al.
Zebrafish|April 2, 2008
Molecular analysis of the sex-determining region of the platyfish Xiphophorus maculatusChristina Schultheis, Qingchun Zhou, Alexander Froschauer, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|February 23, 2017
SLC2A3 single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorderSören Merker, Andreas Reif, Georg C Ziegler, et al.
Genes|November 14, 2020
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani FamiliesJulia Doll, Barbara Vona, Linda Schnapp, et al.
Cell|January 14, 2017
DNA Damage Signaling Instructs Polyploid Macrophage Fate in GranulomasLaura Herrtwich, Indrajit Nanda, Konstantinos Evangelou, et al.
Cell|August 25, 2018
DNA Damage Signaling Instructs Polyploid Macrophage Fate in GranulomasLaura Herrtwich, Indrajit Nanda, Konstantinos Evangelou, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2026
<i>FRMPD4</i> , a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing lossDaniel Liedtke, Kristen Rak, Katrina M Schrode, et al.
American Journal of Human Genetics|April 30, 2013
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticityHiromi Hirata, Indrajit Nanda, Anne van Riesen, et al.
Cytogenetic and Genome Research|August 19, 2015
Third Report on Chicken Genes and Chromosomes 2015Michael Schmid, Jacqueline Smith, David W Burt, et al.
Pageof 6