Briana E Pinales
Overview
Explore the profile of Briana E Pinales including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
7
Citations
11
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Pinales B, Palomino C, Rosas-Acosta G, Francia G, Quintana A
Differentiation
. 2024 Dec;
142:100831.
PMID: 39676000
Vitamin B, otherwise known as cobalamin, is an essential water-soluble vitamin that is obtained from animal derived dietary sources. Mutations in the genes that encode proteins responsible for cobalamin uptake,...
2.
Reyes-Nava N, Paz D, Pinales B, Perez I, Gil C, Gonzales A, et al.
Differentiation
. 2024 Jun;
138:100790.
PMID: 38908344
Mutation of the GABRA1 gene is associated with neurodevelopmental defects and epilepsy. GABRA1 encodes for the α1 subunit of the γ-aminobutyric acid type A receptor (GABAR), which regulates the fast...
3.
Perez I, Reyes-Nava N, Pinales B, Quintana A
Am J Undergrad Res
. 2024 Apr;
20(1):77-84.
PMID: 38617190
ZNF143 is a sequence-specific DNA binding protein that regulates the expression of protein-coding genes and small RNA molecules. In humans, ZNF143 interacts with HCFC1, a transcriptional cofactor, to regulate the...
4.
Paz D, Pinales B, Castellanos B, Perez I, Gil C, Madrigal L, et al.
Differentiation
. 2023 May;
131:74-81.
PMID: 37167860
Variants in the MMACHC gene cause combined methylmalonic acidemia and homocystinuria cblC type, the most common inborn error of intracellular cobalamin (vitamin B12) metabolism. cblC is associated with neurodevelopmental, hematological,...
5.
Paz D, Reyes-Nava N, Pinales B, Perez I, Gil C, Gonzales A, et al.
bioRxiv
. 2023 Feb;
PMID: 36747751
Mutation of the gene is associated with neurodevelopmental defects and epilepsy. encodes for the α1 subunit of the gamma-aminobutyric acid type A receptor (GABAR), which regulates the fast inhibitory impulses...
6.
Paz D, Pinales B, Castellanos B, Perez I, Gil C, Madrigal L, et al.
bioRxiv
. 2023 Jan;
PMID: 36711998
Variants in the gene cause combined methylmalonic acidemia and homocystinuria type, the most common inborn error of intracellular cobalamin (vitamin B12) metabolism. is associated with neurodevelopmental, hematological, ocular, and biochemical...
7.
Uribe K, Correa V, Pinales B, Flores R, Cruz B, Shan Z, et al.
Neuropsychopharmacology
. 2019 Oct;
45(2):394-403.
PMID: 31614362
This study assessed the role of stress systems in the nucleus accumbens (NAc) in promoting sex differences in the reinforcing effects of nicotine. Intravenous self-administration (IVSA) of various doses of...