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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 Oils
Max 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 Irradiation
Thomas 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 hybridization
Jm 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 phenotype
Sharri 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 Study
Yen-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 Moiety
Shuwen 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 Moiety
Shuwen 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 retardation
J 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 Genes
Sanaa 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 study
Alison M Elliott, Shelin Adam, Christèle du Souich, et al.
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of 64
Search research articles
Search
Showing results (621-630 of 636) with videos related to
Sort By:
Page
of 64
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
August 2, 2017
Laying Waste to Mercury: Inexpensive Sorbents Made from Sulfur and Recycled Cooking Oils
Max 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 Irradiation
Thomas 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 hybridization
Jm 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 phenotype
Sharri 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 Study
Yen-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 Moiety
Shuwen 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 Moiety
Shuwen 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 retardation
J 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 Genes
Sanaa 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 study
Alison M Elliott, Shelin Adam, Christèle du Souich, et al.
Page
of 64