Luis A Williams
Overview
Explore the profile of Luis A Williams including associated specialties, affiliations and a list of published articles.
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25
Citations
1897
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Recent Articles
1.
Fink J, Delaney-Busch N, Dawes R, Nanou E, Folts C, Harikrishnan K, et al.
Commun Biol
. 2024 Nov;
7(1):1447.
PMID: 39506078
Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by hypermethylation of expanded CGG repeats (>200) in the FMR1 gene leading to gene silencing and loss of Fragile X Messenger...
2.
Nalbach K, Schifferer M, Bhattacharya D, Ho-Xuan H, Tseng W, Williams L, et al.
Nat Commun
. 2023 Dec;
14(1):8322.
PMID: 38097576
No abstract available.
3.
Liu P, Zhang H, Werley C, Pichler M, Ryan S, Lewarch C, et al.
Pain
. 2023 Nov;
165(4):922-940.
PMID: 37963235
Chronic pain associated with osteoarthritis (OA) remains an intractable problem with few effective treatment options. New approaches are needed to model the disease biology and to drive discovery of therapeutics....
4.
Nalbach K, Schifferer M, Bhattacharya D, Ho-Xuan H, Tseng W, Williams L, et al.
Nat Commun
. 2023 Feb;
14(1):870.
PMID: 36797266
Hereditary sensory and autonomic neuropathy 9 (HSAN9) is a rare fatal neurological disease caused by mis- and nonsense mutations in the gene encoding for Tectonin β-propeller repeat containing protein 2...
5.
Williams L, Gerber D, Elder A, Tseng W, Baru V, Delaney-Busch N, et al.
Mol Ther Nucleic Acids
. 2022 Jul;
29:189-203.
PMID: 35860385
Mutations in the gene are the cause of an ultra-rare neurological disorder characterized by intellectual disability, impaired speech, motor delay, and hypotonia evolving to spasticity, central sleep apnea, and premature...
6.
Simkin D, Ambrosi C, Marshall K, Williams L, Eisenberg J, Gharib M, et al.
Trends Pharmacol Sci
. 2022 Apr;
43(5):392-405.
PMID: 35427475
Induced pluripotent stem cell (iPSC) and gene editing technologies have revolutionized the field of in vitro disease modeling, granting us access to disease-pertinent human cells of the central nervous system....
7.
Simkin D, Papakis V, Bustos B, Ambrosi C, Ryan S, Baru V, et al.
Stem Cell Reports
. 2022 Mar;
17(4):993-1008.
PMID: 35276091
The ability to precisely edit the genome of human induced pluripotent stem cell (iPSC) lines using CRISPR/Cas9 has enabled the development of cellular models that can address genotype to phenotype...
8.
Zhang Y, Quraishi I, McClure H, Williams L, Cheng Y, Kale S, et al.
FASEB J
. 2021 Nov;
35(12):e22053.
PMID: 34820911
Mutations in KCNC3, the gene that encodes the Kv3.3 voltage dependent potassium channel, cause Spinocerebellar Ataxia type 13 (SCA13), a disease associated with disrupted motor behaviors, progressive cerebellar degeneration, and...
9.
Borja G, Shroff H, Upadhyay H, Liu P, Baru V, Cheng Y, et al.
Methods Mol Biol
. 2020 Sep;
2191:109-134.
PMID: 32865742
Optogenetics provides a powerful approach for investigating neuronal electrophysiology at the scale required for drug discovery applications. Probing synaptic function with high throughput using optogenetics requires robust tools that enable...
10.
ALS-implicated protein TDP-43 sustains levels of STMN2, a mediator of motor neuron growth and repair
Klim J, Williams L, Limone F, Guerra San Juan I, Davis-Dusenbery B, Mordes D, et al.
Nat Neurosci
. 2019 Jan;
22(2):167-179.
PMID: 30643292
The findings that amyotrophic lateral sclerosis (ALS) patients almost universally display pathological mislocalization of the RNA-binding protein TDP-43 and that mutations in its gene cause familial ALS have nominated altered...