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Journal of Human Genetics
|
March 5, 2020
A novel biallelic single base insertion in WNK1 in a Pakistani family with congenital insensitivity to pain
Stephen Pastore, Ricardo Harripaul, Matloob Azam, et al.
Current Psychiatry Reports
|
April 11, 2003
Anticipation and CAG*CTG repeat expansion in schizophrenia and bipolar affective disorder
M Teresa Fortune, James L Kennedy, John B Vincent
Journal of Mass Spectrometry : JMS
|
November 30, 2011
Effects of transition metal ion coordination on the collision-induced dissociation of polyalanines
Heather M Watson, John B Vincent, Carolyn J Cassady
Biological Trace Element Research
|
November 9, 2023
Binding Chromium(III) to Form Mixed Cr(III),Fe(III) Serum Transferrins
Dylan R Graham, Eilidh Drummond, Marlena Barrido, et al.
Journal of Inorganic Biochemistry
|
November 19, 2013
Formation of oxo-centered trinuclear chromium carboxylate complexes and hydrolysis of Cr3 as established by paramagnetic (2)H NMR spectroscopy
April C Royer, Kathryn Russell, Ken Belmore, et al.
Current Topics in Medicinal Chemistry
|
April 19, 2016
Histone Variants and Composition in the Developing Brain: Should MeCP2 Care?
Valentina Zago, Cristina Pinar-CabezaDeVaca, John B Vincent, et al.
Human Mutation
|
February 13, 2018
MeCP2 AT-Hook1 mutations in patients with intellectual disability and/or schizophrenia disrupt DNA binding and chromatin compaction in vitro
Taimoor I Sheikh, Ricardo Harripaul, Muhammad Ayub, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire
|
January 6, 2025
Multifaceted roles of MeCP2 in cellular regulation and phase separation: implications for neurodevelopmental disorders, depression, and oxidative stress
Katrina V Good, Ladan Kalani, John B Vincent, et al.
Human Molecular Genetics
|
September 11, 2023
MeCP2 ubiquitination and sumoylation, in search of a function†
Ladan Kalani, Bo-Hyun Kim, John B Vincent, et al.
Orphanet Journal of Rare Diseases
|
July 23, 2013
A synonymous change, p.Gly16Gly in MECP2 Exon 1, causes a cryptic splice event in a Rett syndrome patient
Taimoor I Sheikh, Kirti Mittal, Mary J Willis, et al.
Page
of 24
Search research articles
Search
Showing results (41-50 of 231) with videos related to
Sort By:
Page
of 24
Journal of Human Genetics
|
March 5, 2020
A novel biallelic single base insertion in WNK1 in a Pakistani family with congenital insensitivity to pain
Stephen Pastore, Ricardo Harripaul, Matloob Azam, et al.
Current Psychiatry Reports
|
April 11, 2003
Anticipation and CAG*CTG repeat expansion in schizophrenia and bipolar affective disorder
M Teresa Fortune, James L Kennedy, John B Vincent
Journal of Mass Spectrometry : JMS
|
November 30, 2011
Effects of transition metal ion coordination on the collision-induced dissociation of polyalanines
Heather M Watson, John B Vincent, Carolyn J Cassady
Biological Trace Element Research
|
November 9, 2023
Binding Chromium(III) to Form Mixed Cr(III),Fe(III) Serum Transferrins
Dylan R Graham, Eilidh Drummond, Marlena Barrido, et al.
Journal of Inorganic Biochemistry
|
November 19, 2013
Formation of oxo-centered trinuclear chromium carboxylate complexes and hydrolysis of Cr3 as established by paramagnetic (2)H NMR spectroscopy
April C Royer, Kathryn Russell, Ken Belmore, et al.
Current Topics in Medicinal Chemistry
|
April 19, 2016
Histone Variants and Composition in the Developing Brain: Should MeCP2 Care?
Valentina Zago, Cristina Pinar-CabezaDeVaca, John B Vincent, et al.
Human Mutation
|
February 13, 2018
MeCP2 AT-Hook1 mutations in patients with intellectual disability and/or schizophrenia disrupt DNA binding and chromatin compaction in vitro
Taimoor I Sheikh, Ricardo Harripaul, Muhammad Ayub, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire
|
January 6, 2025
Multifaceted roles of MeCP2 in cellular regulation and phase separation: implications for neurodevelopmental disorders, depression, and oxidative stress
Katrina V Good, Ladan Kalani, John B Vincent, et al.
Human Molecular Genetics
|
September 11, 2023
MeCP2 ubiquitination and sumoylation, in search of a function†
Ladan Kalani, Bo-Hyun Kim, John B Vincent, et al.
Orphanet Journal of Rare Diseases
|
July 23, 2013
A synonymous change, p.Gly16Gly in MECP2 Exon 1, causes a cryptic splice event in a Rett syndrome patient
Taimoor I Sheikh, Kirti Mittal, Mary J Willis, et al.
Page
of 24