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AEM Education and Training
|
August 4, 2025
A Novel Model of Patient Handover in Emergency Medicine-Addressing Hidden Tensions in Culture
Stella H Yiu, Marianne Yeung, Warren Cheung, et al.
Plos One
|
January 24, 2008
Gene characterization index: assessing the depth of gene annotation
Danielle Kemmer, Raf M Podowski, Dimas Yusuf, et al.
Human Mutation
|
June 29, 2016
Inborn Error of Cobalamin Metabolism Associated with the Intracellular Accumulation of Transcobalamin-Bound Cobalamin and Mutations in ZNF143, Which Codes for a Transcriptional Activator
Mihaela Pupavac, David Watkins, Francis Petrella, et al.
Research Square
|
April 8, 2025
Evolving epigenomics of immune cells in type 1 diabetes at single nuclei resolution
Tomi Pastinen, Elin Grundberg, Todd Bradley, et al.
Scientific Reports
|
May 9, 2025
CpG methylation changes associated with hyperglycemia in type 1 diabetes occur at angiogenic glomerular and retinal gene loci
Xiaojian Shao, Sophie Le Fur, Warren Cheung, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 23, 2024
Complex trait associations in rare diseases and impacts on Mendelian variant interpretation
Craig Smail, Bing Ge, Marissa R Keever-Keigher, et al.
Human Molecular Genetics
|
April 28, 2017
Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities
Anita M Quintana, Hung-Chun Yu, Alison Brebner, et al.
Cell
|
November 19, 2016
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells
Lu Chen, Bing Ge, Francesco Paolo Casale, et al.
Nature
|
September 15, 2015
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture
Hou-Feng Zheng, Vincenzo Forgetta, Yi-Hsiang Hsu, et al.
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Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
AEM Education and Training
|
August 4, 2025
A Novel Model of Patient Handover in Emergency Medicine-Addressing Hidden Tensions in Culture
Stella H Yiu, Marianne Yeung, Warren Cheung, et al.
Plos One
|
January 24, 2008
Gene characterization index: assessing the depth of gene annotation
Danielle Kemmer, Raf M Podowski, Dimas Yusuf, et al.
Human Mutation
|
June 29, 2016
Inborn Error of Cobalamin Metabolism Associated with the Intracellular Accumulation of Transcobalamin-Bound Cobalamin and Mutations in ZNF143, Which Codes for a Transcriptional Activator
Mihaela Pupavac, David Watkins, Francis Petrella, et al.
Research Square
|
April 8, 2025
Evolving epigenomics of immune cells in type 1 diabetes at single nuclei resolution
Tomi Pastinen, Elin Grundberg, Todd Bradley, et al.
Scientific Reports
|
May 9, 2025
CpG methylation changes associated with hyperglycemia in type 1 diabetes occur at angiogenic glomerular and retinal gene loci
Xiaojian Shao, Sophie Le Fur, Warren Cheung, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 23, 2024
Complex trait associations in rare diseases and impacts on Mendelian variant interpretation
Craig Smail, Bing Ge, Marissa R Keever-Keigher, et al.
Human Molecular Genetics
|
April 28, 2017
Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities
Anita M Quintana, Hung-Chun Yu, Alison Brebner, et al.
Cell
|
November 19, 2016
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells
Lu Chen, Bing Ge, Francesco Paolo Casale, et al.
Nature
|
September 15, 2015
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture
Hou-Feng Zheng, Vincenzo Forgetta, Yi-Hsiang Hsu, et al.
Page
of 2