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NPJ Genomic Medicine
|
November 15, 2016
A <i>de novo</i> 2.78-Mb duplication on chromosome 21q22.11 implicates candidate genes in the partial trisomy 21 phenotype
James D Weisfeld-Adams, Amanda K Tkachuk, Kenneth N Maclean, et al.
Experimental Hematology
|
January 30, 2007
Zebularine inhibits human acute myeloid leukemia cell growth in vitro in association with p15INK4B demethylation and reexpression
Stuart A Scott, Ashakumary Lakshimikuttysamma, David P Sheridan, et al.
Nanomaterials (Basel, Switzerland)
|
November 24, 2023
Enhanced Visible Light-Driven Photocatalytic Water-Splitting Reaction of Titanate Nanotubes Sensitised with Ru(II) Bipyridyl Complex
Mauro Malizia, Stuart A Scott, Laura Torrente-Murciano, et al.
Clinical Pharmacology and Therapeutics
|
June 14, 2023
Clinical Pharmacogenomic MT-RNR1 Screening for Aminoglycoside-Induced Ototoxicity and the Post-Test Counseling Conundrum
Robert Rigobello, Jay Shaw, Daniel Ilg, et al.
Journal of Biotechnology
|
July 14, 2012
Treatment of Phaeodactylum tricornutum cells with papain facilitates lipid extraction
Irmtraud Horst, Brenda M Parker, John S Dennis, et al.
Plant Physiology
|
April 25, 2014
Phycobilisome-Deficient Strains of Synechocystis sp. PCC 6803 Have Reduced Size and Require Carbon-Limiting Conditions to Exhibit Enhanced Productivity
David J Lea-Smith, Paolo Bombelli, John S Dennis, et al.
The Journal of Molecular Diagnostics : JMD
|
January 17, 2016
Analytical Validation of a Personalized Medicine APOL1 Genotyping Assay for Nondiabetic Chronic Kidney Disease Risk Assessment
Jinglan Zhang, Anastasia Fedick, Stephanie Wasserman, et al.
Molecular Genetics & Genomic Medicine
|
June 21, 2019
Prenatal cytogenomic identification and molecular refinement of compound heterozygous STRC deletion breakpoints
Lisong Shi, Yan Bai, Yara Kharbutli, et al.
Leukemia Research
|
October 12, 2004
Methylation status of cyclin-dependent kinase inhibitor genes within the transforming growth factor beta pathway in human T-cell lymphoblastic lymphoma/leukemia
Stuart A Scott, Tomofumi Kimura, Wei-Feng Dong, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2026
Transient Neonatal Zinc Deficiency due to Maternal Variants in SLC30A2: An Emerging and Atypical Candidate Gene for Maternal Carrier Screening
Christopher Carter, Danielle Luz, Emma E Smith, et al.
Page
of 15
Search research articles
Search
Showing results (41-50 of 147) with videos related to
Sort By:
Page
of 15
NPJ Genomic Medicine
|
November 15, 2016
A <i>de novo</i> 2.78-Mb duplication on chromosome 21q22.11 implicates candidate genes in the partial trisomy 21 phenotype
James D Weisfeld-Adams, Amanda K Tkachuk, Kenneth N Maclean, et al.
Experimental Hematology
|
January 30, 2007
Zebularine inhibits human acute myeloid leukemia cell growth in vitro in association with p15INK4B demethylation and reexpression
Stuart A Scott, Ashakumary Lakshimikuttysamma, David P Sheridan, et al.
Nanomaterials (Basel, Switzerland)
|
November 24, 2023
Enhanced Visible Light-Driven Photocatalytic Water-Splitting Reaction of Titanate Nanotubes Sensitised with Ru(II) Bipyridyl Complex
Mauro Malizia, Stuart A Scott, Laura Torrente-Murciano, et al.
Clinical Pharmacology and Therapeutics
|
June 14, 2023
Clinical Pharmacogenomic MT-RNR1 Screening for Aminoglycoside-Induced Ototoxicity and the Post-Test Counseling Conundrum
Robert Rigobello, Jay Shaw, Daniel Ilg, et al.
Journal of Biotechnology
|
July 14, 2012
Treatment of Phaeodactylum tricornutum cells with papain facilitates lipid extraction
Irmtraud Horst, Brenda M Parker, John S Dennis, et al.
Plant Physiology
|
April 25, 2014
Phycobilisome-Deficient Strains of Synechocystis sp. PCC 6803 Have Reduced Size and Require Carbon-Limiting Conditions to Exhibit Enhanced Productivity
David J Lea-Smith, Paolo Bombelli, John S Dennis, et al.
The Journal of Molecular Diagnostics : JMD
|
January 17, 2016
Analytical Validation of a Personalized Medicine APOL1 Genotyping Assay for Nondiabetic Chronic Kidney Disease Risk Assessment
Jinglan Zhang, Anastasia Fedick, Stephanie Wasserman, et al.
Molecular Genetics & Genomic Medicine
|
June 21, 2019
Prenatal cytogenomic identification and molecular refinement of compound heterozygous STRC deletion breakpoints
Lisong Shi, Yan Bai, Yara Kharbutli, et al.
Leukemia Research
|
October 12, 2004
Methylation status of cyclin-dependent kinase inhibitor genes within the transforming growth factor beta pathway in human T-cell lymphoblastic lymphoma/leukemia
Stuart A Scott, Tomofumi Kimura, Wei-Feng Dong, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2026
Transient Neonatal Zinc Deficiency due to Maternal Variants in SLC30A2: An Emerging and Atypical Candidate Gene for Maternal Carrier Screening
Christopher Carter, Danielle Luz, Emma E Smith, et al.
Page
of 15