Related references
Note: Only part of the references are listed.Regional changes in CNS and retinal glycerophospholipid profiles with age: a molecular blueprint
Blake R. Hopiavuori et al.
JOURNAL OF LIPID RESEARCH (2017)
Lipids and Their Trafficking: An Integral Part of Cellular Organization
Catherine L. Jackson et al.
DEVELOPMENTAL CELL (2016)
Functional diversity of astrocytes in neural circuit regulation
Lucile Ben Haim et al.
NATURE REVIEWS NEUROSCIENCE (2016)
A New ELOVL4 Mutation in a Case of Spinocerebellar Ataxia With Erythrokeratodermia
Cynthia V. Bourassa et al.
JAMA NEUROLOGY (2015)
A Novel Mutation in ELOVL4 Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia A Broadened Spectrum of SCA34
Kokoro Ozaki et al.
JAMA NEUROLOGY (2015)
A novel recessive mutation in the gene ELOVL4 causes a neuro-ichthyotic disorder with variable expressivity
Hina Mir et al.
BMC MEDICAL GENETICS (2014)
Endoplasmic reticulum microenvironment and conserved histidines govern ELOVL4 fatty acid elongase activity
Sreemathi Logan et al.
JOURNAL OF LIPID RESEARCH (2014)
Expanding the Clinical Phenotype Associated With ELOVL4 Mutation Study of a Large French-Canadian Family With Autosomal Dominant Spinocerebellar Ataxia and Erythrokeratodermia
Maxime Cadieux-Dion et al.
JAMA NEUROLOGY (2014)
A Role for ELOVL4 in the Mouse Meibomian Gland and Sebocyte Cell Biology
Anne McMahon et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2014)
Effect of Reduced Retinal VLC-PUFA on Rod and Cone Photoreceptors
Lea D. Bennett et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2014)
Allen Brain Atlas: an integrated spatio-temporal portal for exploring the central nervous system
Susan M. Sunkin et al.
NUCLEIC ACIDS RESEARCH (2013)
Deciphering mutant ELOVL4 activity in autosomal-dominant Stargardt macular dystrophy
Sreemathi Logan et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
Impaired neurotransmission in ether lipid-deficient nerve terminals
Alexander Brodde et al.
HUMAN MOLECULAR GENETICS (2012)
Recessive Mutations in ELOVL4 Cause Ichthyosis, Intellectual Disability, and Spastic Quadriplegia
Mohammed A. Aldahmesh et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Retinal very long-chain PUFAs: new insights from studies on ELOVL4 protein
Martin-Paul Agbaga et al.
JOURNAL OF LIPID RESEARCH (2010)
Polyunsaturated fatty acids influence synaptojanin localization to regulate synaptic vesicle recycling
Esther Marza et al.
MOLECULAR BIOLOGY OF THE CELL (2008)
Role of Stargardt-3 macular dystrophy protein (ELOVL4) in the biosynthesis of very long chain fatty acids
Martin-Paul Agbaga et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Loss of functional ELOVL4 depletes very long-chain fatty acids (≥C28) and the unique ω-O-acylceramides in skin leading to neonatal death
Vidyullatha Vasireddy et al.
HUMAN MOLECULAR GENETICS (2007)
Genome-wide atlas of gene expression in the adult mouse brain
Ed S. Lein et al.
NATURE (2007)
Polyunsaturated fatty acids and neurotransmission in Caenorhabditis elegans
E Marza et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2006)
Dominant negative mechanism underlies autosomal dominant Stargardt-like macular dystrophy linked to mutations in ELOVL4
C Grayson et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Characterization of mouse orthologue of ELOVL4:: genomic organization and spatial and temporal expression
MNA Mandal et al.
GENOMICS (2004)
Atrophic macular degeneration mutations in ELOVL4 result in the intracellular misrouting of the protein
R Ambasudhan et al.
GENOMICS (2004)
DSPP mutation in dentinogenesis imperfecta Shields type II
XH Zhang et al.
NATURE GENETICS (2001)
Share Paper
