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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.Developmental Cell|April 29, 2022
Functional genetic screen identifies ITPR3/calcium/RELB axis as a driver of colorectal cancer metastatic liver colonizationRyan H Moy, Alexander Nguyen, Jia Min Loo, et al.Genome Research|October 21, 2014
In vitro, long-range sequence information for de novo genome assembly via transposase contiguityAndrew Adey, Jacob O Kitzman, Joshua N Burton, et al.Cell Reports|July 16, 2013
A neurodegeneration-specific gene-expression signature of acutely isolated microglia from an amyotrophic lateral sclerosis mouse modelIsaac M Chiu, Emiko T A Morimoto, Hani Goodarzi, et al.Nature Genetics|October 20, 2014
Haplotype-resolved whole-genome sequencing by contiguity-preserving transposition and combinatorial indexingSasan Amini, Dmitry Pushkarev, Lena Christiansen, 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.Genome Research|June 23, 2019
Genome wide analysis of 3' UTR sequence elements and proteins regulating mRNA stability during maternal-to-zygotic transition in zebrafishCharles E Vejnar, Mario Abdel Messih, Carter M Takacs, et al.Cell|July 8, 2021
Molecular topography of an entire nervous systemSeth R Taylor, Gabriel Santpere, Alexis Weinreb, et al.Communications Biology|January 12, 2023
OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseasesGabriel Sturm, Kalpita R Karan, Anna S Monzel, et al.Pageof 8