Guillermo Rodriguez Bey
Overview
Explore the profile of Guillermo Rodriguez Bey including associated specialties, affiliations and a list of published articles.
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5
Citations
41
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Recent Articles
1.
Vollmer L, Liu F, Nmezi B, Bey G, Herdman N, Shun T, et al.
Sci Rep
. 2025 Mar;
15(1):7314.
PMID: 40025114
Lamin B1 (LMNB1) is an intermediate filament protein that is an integral component of the nuclear lamina, a structure that is critical for nuclear organization and function. Mutations involving the...
2.
Nmezi B, Bey G, Oranburg T, Dudnyk K, Lardo S, Herdman N, et al.
Nat Commun
. 2025 Feb;
16(1):1373.
PMID: 39910058
The role of non-coding regulatory elements and how they might contribute to tissue type specificity of disease phenotypes is poorly understood. Autosomal Dominant Leukodystrophy (ADLD) is a fatal, adult-onset, neurological...
3.
Werren E, Bey G, Majethia P, Kaur P, Patil S, Kekatpure M, et al.
Brain
. 2024 Sep;
147(12):4033-4042.
PMID: 39292993
Erythrocyte membrane protein band 4.1 like 3 (EPB41L3: NM_012307.5), also known as DAL1, encodes the ubiquitously expressed, neuronally enriched 4.1B protein, part of the 4.1 superfamily of membrane-cytoskeleton adaptors. The...
4.
Nmezi B, Bey G, Oranburg T, Dudnyk K, Lardo S, Herdman N, et al.
bioRxiv
. 2023 Aug;
PMID: 37609196
The role of non-coding regulatory elements and how they might contribute to tissue type specificity of disease phenotypes is poorly understood. Autosomal Dominant Leukodystrophy (ADLD) is a fatal, adult-onset, neurological...
5.
Bey G, Padiath Q
BMC Res Notes
. 2023 Aug;
16(1):161.
PMID: 37542275
Objective: Oligodendrocytes (OL) are the glial cell type in the CNS that are responsible for myelin formation. The ability to culture OLs in vitro has provided critical insights into the...
6.
do Rosario M, Bey G, Nmezi B, Liu F, Oranburg T, Cohen A, et al.
Brain
. 2022 Aug;
145(12):4202-4209.
PMID: 35953447
Hypomyelinating leukodystrophies comprise a subclass of genetic disorders with deficient myelination of the CNS white matter. Here we report four unrelated families with a hypomyelinating leukodystrophy phenotype harbouring variants in...
7.
Curiel J, Bey G, Takanohashi A, Bugiani M, Fu X, Wolf N, et al.
Hum Mol Genet
. 2017 Oct;
26(22):4506-4518.
PMID: 28973395
Hypomyelinating leukodystrophies are heritable disorders defined by lack of development of brain myelin, but the cellular mechanisms of hypomyelination are often poorly understood. Mutations in TUBB4A, encoding the tubulin isoform...