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The Journal of Biological Chemistry
|
February 21, 2021
Glycosyltransferase POMGNT1 deficiency strengthens N-cadherin-mediated cell-cell adhesion
Sina Ibne Noor, Marcus Hoffmann, Natalie Rinis, et al.
Journal of Translational Genetics and Genomics
|
February 23, 2023
Epigenetic effects of high-fat diet on intestinal tumorigenesis in C57BL/6J-<i>Apc</i> <sup></sup> mice
Dan C Qu, Devin Neu, Zain Q Khawaja, et al.
Genome Research
|
March 3, 2009
Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns
Michael P Schnetz, Cynthia F Bartels, Kuntal Shastri, et al.
American Journal of Human Genetics
|
October 1, 1992
Identification of two different point mutations associated with the fluoride-resistant phenotype for human butyrylcholinesterase
C P Nogueira, C F Bartels, M C McGuire, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 13, 2020
E.U. paediatric MOG consortium consensus: Part 4 - Outcome of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders
Arlette L Bruijstens, Markus Breu, Eva-Maria Wendel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 9, 2020
E.U. paediatric MOG consortium consensus: Part 1 - Classification of clinical phenotypes of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders
Arlette L Bruijstens, Christian Lechner, Lorraine Flet-Berliac, et al.
Nature Communications
|
November 8, 2023
Temporal chromatin accessibility changes define transcriptional states essential for osteosarcoma metastasis
W Dean Pontius, Ellen S Hong, Zachary J Faber, et al.
BMC Medical Genetics
|
April 11, 2012
Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity
Johanna Korvala, Harald Jüppner, Outi Mäkitie, et al.
JCI Insight
|
February 23, 2018
CHD7 represses the retinoic acid synthesis enzyme ALDH1A3 during inner ear development
Hui Yao, Sophie F Hill, Jennifer M Skidmore, et al.
Environmental Science & Technology
|
October 15, 2025
Greenhills Dunite Subsurface Reaction Kinetics in a Global Mafic-Ultramafic Context
C Heath Stanfield, Quin R S Miller, Ruoshi Cao, et al.
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Search research articles
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Showing results (71-80 of 146) with videos related to
Sort By:
Page
of 15
The Journal of Biological Chemistry
|
February 21, 2021
Glycosyltransferase POMGNT1 deficiency strengthens N-cadherin-mediated cell-cell adhesion
Sina Ibne Noor, Marcus Hoffmann, Natalie Rinis, et al.
Journal of Translational Genetics and Genomics
|
February 23, 2023
Epigenetic effects of high-fat diet on intestinal tumorigenesis in C57BL/6J-<i>Apc</i> <sup></sup> mice
Dan C Qu, Devin Neu, Zain Q Khawaja, et al.
Genome Research
|
March 3, 2009
Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns
Michael P Schnetz, Cynthia F Bartels, Kuntal Shastri, et al.
American Journal of Human Genetics
|
October 1, 1992
Identification of two different point mutations associated with the fluoride-resistant phenotype for human butyrylcholinesterase
C P Nogueira, C F Bartels, M C McGuire, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 13, 2020
E.U. paediatric MOG consortium consensus: Part 4 - Outcome of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders
Arlette L Bruijstens, Markus Breu, Eva-Maria Wendel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 9, 2020
E.U. paediatric MOG consortium consensus: Part 1 - Classification of clinical phenotypes of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders
Arlette L Bruijstens, Christian Lechner, Lorraine Flet-Berliac, et al.
Nature Communications
|
November 8, 2023
Temporal chromatin accessibility changes define transcriptional states essential for osteosarcoma metastasis
W Dean Pontius, Ellen S Hong, Zachary J Faber, et al.
BMC Medical Genetics
|
April 11, 2012
Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity
Johanna Korvala, Harald Jüppner, Outi Mäkitie, et al.
JCI Insight
|
February 23, 2018
CHD7 represses the retinoic acid synthesis enzyme ALDH1A3 during inner ear development
Hui Yao, Sophie F Hill, Jennifer M Skidmore, et al.
Environmental Science & Technology
|
October 15, 2025
Greenhills Dunite Subsurface Reaction Kinetics in a Global Mafic-Ultramafic Context
C Heath Stanfield, Quin R S Miller, Ruoshi Cao, et al.
Page
of 15