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Nature Biotechnology|April 15, 2020
Sci-fate characterizes the dynamics of gene expression in single cellsJunyue Cao, Wei Zhou, Frank Steemers, et al.
Neurobiology of Aging|March 2, 2015
HMSN-P caused by p.Pro285Leu mutation in TFG is not confined to patients with Far East ancestryAfagh Alavi, Hosein Shamshiri, Shahriar Nafissi, et al.
European Journal of Medical Genetics|October 2, 2013
Mutation in CYP27A1 identified in family with coronary artery diseaseKolsoum Inanloorahatloo, Amir Farhang Zand Parsa, Klaus Huse, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 3, 2016
Mutation in ADORA1 identified as likely cause of early-onset parkinsonism and cognitive dysfunctionElham Jaberi, Mohammad Rohani, Gholam Ali Shahidi, et al.
Scientific Reports|January 9, 2014
Mutation in ST6GALNAC5 identified in family with coronary artery diseaseKolsoum InanlooRahatloo, Amir Farhang Zand Parsa, Klaus Huse, et al.
Neurobiology of Aging|December 18, 2015
Identification of mutation in GTPBP2 in patients of a family with neurodegeneration accompanied by iron deposition in the brainElham Jaberi, Mohammad Rohani, Gholam Ali Shahidi, et al.
Science (New York, N.Y.)|December 7, 2019
Massively multiplex chemical transcriptomics at single-cell resolutionSanjay R Srivatsan, José L McFaline-Figueroa, Vijay Ramani, et al.
Mutation Research|April 15, 2005
High-throughput SNP genotyping on universal bead arraysRichard Shen, Jian-Bing Fan, Derek Campbell, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|November 30, 2016
PRODUCTION OF A PRELIMINARY QUALITY CONTROL PIPELINE FOR SINGLE NUCLEI RNA-SEQ AND ITS APPLICATION IN THE ANALYSIS OF CELL TYPE DIVERSITY OF POST-MORTEM HUMAN BRAIN NEOCORTEXBrian Aevermann, Jamison McCorrison, Pratap Venepally, et al.
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