Publications by authors named "Alexander Abrams"

Claim this Profile
N
NMR assignment of the conserved bacterial DNA replication protein DnaA domain IV.
Alexander Nguyen Abrams, Geoff Kelly, Julia Hubbard

Biomol NMR Assign· December 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Environmental impacts and daily voluntary movement of horses housed in pasture tracks as compared to conventional pasture housing.
Jenna Farmer Long, Jamie Duberstein, Kayla Costin, Todd Callaway, Alexander Abrams

J Equine Vet Sci· December 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Molecular topography of an entire nervous system.
Seth R Taylor, Gabriel Santpere, Alexis Weinreb, Alec Barrett, Molly B Reilly, Alexander Abrams

Cell· August 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease.
Elena Buglo, Evan Sarmiento, Nicole Belliard Martuscelli, David W Sant, Matt C Danzi, Alexander J Abrams

PLoS One· June 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The stress-responsive gene GDPGP1/mcp-1 regulates neuronal glycogen metabolism and survival.
Alexander Schulz, Yuichi Sekine, Motunrayo J Oyeyemi, Alexander J Abrams, Manasa Basavaraju

J Cell Biol· February 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Insights into the genotype-phenotype correlation and molecular function of SLC25A46.
Alexander J Abrams, Flavia Fontanesi, Natalie B L Tan, Elena Buglo, Ion J Campeanu

Hum Mutat· December 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Cryptic amyloidogenic elements in mutant NEFH causing Charcot-Marie-Tooth 2 trigger aggresome formation and neuronal death.
Arnaud Jacquier, Cécile Delorme, Edwige Belotti, Raoul Juntas-Morales, Guilhem Solé, Alexander Abrams

Acta Neuropathol Commun· July 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish.
Robert A Kozol, Alexander J Abrams, David M James, Elena Buglo, Qing Yan

Front Mol Neurosci· July 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Cryptic Amyloidogenic Elements in the 3' UTRs of Neurofilament Genes Trigger Axonal Neuropathy.
Adriana P Rebelo, Alexander J Abrams, Ellen Cottenie, Alejandro Horga, Michael Gonzalez

Am J Hum Genet· April 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder.
Alexander J Abrams, Robert B Hufnagel, Adriana Rebelo, Claudia Zanna, Neville Patel

Nat Genet· August 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndrome.
Vladimir Camarena, Lei Cao, Clemer Abad, Alexander Abrams, Yaima Toledo

EMBO Mol Med· August 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2.
A Reghan Foley, Manoj P Menezes, Amelie Pandraud, Michael A Gonzalez, Ahmad Al-Odaib, Alexander J Abrams

Brain· January 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1.
Holly N Cukier, Joycelyn M Lee, Deqiong Ma, Juan I Young, Vera Mayo, Alexander J Abrams, Ruth K Abramson

Autism Res· December 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Transgenic complementation of MeCP2 deficiency: phenotypic rescue of Mecp2-null mice by isoform-specific transgenes.
Bredford Kerr, Jessica Soto C, Mauricio Saez, Alexander Abrams, Katherina Walz

Eur J Hum Genet· January 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
S-nitrosylation of ApoE in Alzheimer's disease.
Alexander J Abrams, Amjad Farooq, Gaofeng Wang

Biochemistry· May 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis