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T Gibson

Showing results (621-630 of 636) with videos related to

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Chemistry (Weinheim an Der Bergstrasse, Germany)|August 2, 2017
Laying Waste to Mercury: Inexpensive Sorbents Made from Sulfur and Recycled Cooking OilsMax J H Worthington, Renata L Kucera, Inês S Albuquerque, et al.
Journal of the American Chemical Society|December 3, 2025
Making and Unmaking Poly(trisulfides) with Light: Precise Regulation of Radical Concentrations via Pulsed LED IrradiationThomas P Nicholls, Jasmine M M Pople, Madison R Harvey, et al.
BMC Genomics|November 18, 2009
Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridizationJm Friedman, Shelin Adam, Laura Arbour, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 19, 2019
Rare SUZ12 variants commonly cause an overgrowth phenotypeSharri S Cyrus, Ana S A Cohen, Ruky Agbahovbe, et al.
Medrxiv : the Preprint Server for Health Sciences|May 9, 2025
Identifying Rare Germline Variants Associated with Metastatic Prostate Cancer Through an Extreme Phenotype StudyYen-Yi Lin, Hamideh Sharifi Noghabi, Stanislav Volik, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Potent DGAT1 Inhibitors in the Benzimidazole Class with a Pyridyl-oxy-cyclohexanecarboxylic Acid MoietyShuwen He, Qingmei Hong, Zhong Lai, et al.
ACS Medicinal Chemistry Letters|October 29, 2014
Discovery of a Potent and Selective DGAT1 Inhibitor with a Piperidinyl-oxy-cyclohexanecarboxylic Acid MoietyShuwen He, Qingmei Hong, Zhong Lai, et al.
American Journal of Human Genetics|August 16, 2006
Oligonucleotide microarray analysis of genomic imbalance in children with mental retardationJ M Friedman, Agnes Baross, Allen D Delaney, et al.
American Journal of Human Genetics|April 4, 2020
DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex GenesSanaa Choufani, William T Gibson, Andrei L Turinsky, et al.
HGG Advances|May 23, 2022
Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES studyAlison M Elliott, Shelin Adam, Christèle du Souich, et al.
Pageof 64

Showing results (621-630 of 636) with videos related to

Sort By:
Pageof 64
Chemistry (Weinheim an Der Bergstrasse, Germany)|August 2, 2017
Laying Waste to Mercury: Inexpensive Sorbents Made from Sulfur and Recycled Cooking OilsMax J H Worthington, Renata L Kucera, Inês S Albuquerque, et al.
Journal of the American Chemical Society|December 3, 2025
Making and Unmaking Poly(trisulfides) with Light: Precise Regulation of Radical Concentrations via Pulsed LED IrradiationThomas P Nicholls, Jasmine M M Pople, Madison R Harvey, et al.
BMC Genomics|November 18, 2009
Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridizationJm Friedman, Shelin Adam, Laura Arbour, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 19, 2019
Rare SUZ12 variants commonly cause an overgrowth phenotypeSharri S Cyrus, Ana S A Cohen, Ruky Agbahovbe, et al.
Medrxiv : the Preprint Server for Health Sciences|May 9, 2025
Identifying Rare Germline Variants Associated with Metastatic Prostate Cancer Through an Extreme Phenotype StudyYen-Yi Lin, Hamideh Sharifi Noghabi, Stanislav Volik, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Potent DGAT1 Inhibitors in the Benzimidazole Class with a Pyridyl-oxy-cyclohexanecarboxylic Acid MoietyShuwen He, Qingmei Hong, Zhong Lai, et al.
ACS Medicinal Chemistry Letters|October 29, 2014
Discovery of a Potent and Selective DGAT1 Inhibitor with a Piperidinyl-oxy-cyclohexanecarboxylic Acid MoietyShuwen He, Qingmei Hong, Zhong Lai, et al.
American Journal of Human Genetics|August 16, 2006
Oligonucleotide microarray analysis of genomic imbalance in children with mental retardationJ M Friedman, Agnes Baross, Allen D Delaney, et al.
American Journal of Human Genetics|April 4, 2020
DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex GenesSanaa Choufani, William T Gibson, Andrei L Turinsky, et al.
HGG Advances|May 23, 2022
Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES studyAlison M Elliott, Shelin Adam, Christèle du Souich, et al.
Pageof 64