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Anh-Thu N Lam

Showing results (1-10 of 15) with videos related to

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Schizophrenia Research|January 26, 2021
Transcriptome analysis of human induced excitatory neurons supports a strong effect of clozapine on cholesterol biosynthesisDebamitra Das, Xi Peng, Anh-Thu N Lam, et al.
Data in Brief|March 8, 2021
Transcriptomic data of Clozapine-treated Ngn2-induced Human Excitatory NeuronsAnh-Thu N Lam, Xi Peng, Debamitra Das, et al.
Neuron|December 6, 2015
Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic MechanismsAlissa M D'Gama, Sirisha Pochareddy, Mingfeng Li, et al.
Scientific Reports|July 13, 2022
CRISPR Del/Rei: a simple, flexible, and efficient pipeline for scarless genome editingKyra L Feuer, Marah H Wahbeh, Christian Yovo, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 6, 2021
SLC26A9 SNP rs7512462 is not associated with lung disease severity or lung function response to ivacaftor in cystic fibrosis patients with G551D-CFTRAlice C Eastman, Rhonda G Pace, Hong Dang, et al.
The Journal of Clinical Investigation|October 4, 2019
Increased expression of anion transporter SLC26A9 delays diabetes onset in cystic fibrosisAnh-Thu N Lam, Melis A Aksit, Briana Vecchio-Pagan, et al.
Scientific Reports|August 22, 2020
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorderKlaus Schmitz-Abe, Guzman Sanchez-Schmitz, Ryan N Doan, et al.
American Journal of Human Genetics|May 6, 2017
Systematic Computational Identification of Variants That Activate Exonic and Intronic Cryptic Splice SitesMelissa Lee, Patrick Roos, Neeraj Sharma, et al.
Neurology|October 1, 2013
Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humansL Benjamin Hills, Amira Masri, Kotaro Konno, et al.
Plos Genetics|November 17, 2018
Capitalizing on the heterogeneous effects of CFTR nonsense and frameshift variants to inform therapeutic strategy for cystic fibrosisNeeraj Sharma, Taylor A Evans, Matthew J Pellicore, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Schizophrenia Research|January 26, 2021
Transcriptome analysis of human induced excitatory neurons supports a strong effect of clozapine on cholesterol biosynthesisDebamitra Das, Xi Peng, Anh-Thu N Lam, et al.
Data in Brief|March 8, 2021
Transcriptomic data of Clozapine-treated Ngn2-induced Human Excitatory NeuronsAnh-Thu N Lam, Xi Peng, Debamitra Das, et al.
Neuron|December 6, 2015
Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic MechanismsAlissa M D'Gama, Sirisha Pochareddy, Mingfeng Li, et al.
Scientific Reports|July 13, 2022
CRISPR Del/Rei: a simple, flexible, and efficient pipeline for scarless genome editingKyra L Feuer, Marah H Wahbeh, Christian Yovo, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 6, 2021
SLC26A9 SNP rs7512462 is not associated with lung disease severity or lung function response to ivacaftor in cystic fibrosis patients with G551D-CFTRAlice C Eastman, Rhonda G Pace, Hong Dang, et al.
The Journal of Clinical Investigation|October 4, 2019
Increased expression of anion transporter SLC26A9 delays diabetes onset in cystic fibrosisAnh-Thu N Lam, Melis A Aksit, Briana Vecchio-Pagan, et al.
Scientific Reports|August 22, 2020
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorderKlaus Schmitz-Abe, Guzman Sanchez-Schmitz, Ryan N Doan, et al.
American Journal of Human Genetics|May 6, 2017
Systematic Computational Identification of Variants That Activate Exonic and Intronic Cryptic Splice SitesMelissa Lee, Patrick Roos, Neeraj Sharma, et al.
Neurology|October 1, 2013
Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humansL Benjamin Hills, Amira Masri, Kotaro Konno, et al.
Plos Genetics|November 17, 2018
Capitalizing on the heterogeneous effects of CFTR nonsense and frameshift variants to inform therapeutic strategy for cystic fibrosisNeeraj Sharma, Taylor A Evans, Matthew J Pellicore, et al.
Pageof 2