Juan Ramon Gonzalez-Garcia
Overview
Explore the profile of Juan Ramon Gonzalez-Garcia including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
17
Citations
15
Followers
0
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Recent Articles
1.
Zepeda-Olmos P, Esparza-Garcia E, Robles-Espinoza K, Gonzalez-Garcia J, Rodriguez Gutierrez P, Magana-Torres M
Genes (Basel)
. 2024 Nov;
15(11).
PMID: 39596579
Noonan syndrome (NS) is a genetic multisystem disease characterized by distinctive facial features, short stature, chest deformity, and congenital heart defects. NS is caused by gene variants of the RAS/MAPK...
2.
Vazquez-Ibarra K, Sanchez Lopez J, Pineda Razo T, Cruz Lozano J, Ortiz-Tamayo B, Palafox-Mariscal L, et al.
Oncol Lett
. 2024 Aug;
28(4):457.
PMID: 39114572
Gastric cancer (GC) is the fourth leading cause of cancer death in the world, and there is a demand for new therapeutic agents to treat GC. Metformin has been demonstrated...
3.
Meza-Espinoza J, Gonzalez-Garcia J, Nieto-Marin N, Patron-Baro L, Gonzalez-Arreola R, Arambula-Meraz E, et al.
Mol Cytogenet
. 2024 Jul;
17(1):17.
PMID: 39020403
Background: Ring chromosome 14 syndrome is a rare disorder primarily marked by early-onset epilepsy, microcephaly, distinctive craniofacial features, hypotonia, intellectual disability, and delay in both development and language acquisition. Case...
4.
Rodriguez-Gutierrez P, Hernandez-Flores T, Zepeda-Olmos P, Reyes-Rodriguez C, Robles-Espinoza K, Solis-Gomez U, et al.
Arch Med Res
. 2024 Mar;
55(3):102971.
PMID: 38513336
Introduction: In Mexico, familial hypercholesterolemia (FH) is underdiagnosed, but population screening in small communities where at least one homozygous patient has already been detected results in a useful and inexpensive...
5.
Gonzalez-Arreola R, Garcia-Romero A, Magana-Torres M, Gonzalez-Garcia J
Mol Cytogenet
. 2023 Aug;
16(1):19.
PMID: 37574565
Background: High expression of the Cytokine Receptor-Like Factor 2 (CRLF2) gene has been observed in patients with acute lymphoblastic leukemia BCR-ABL1-like subtype. Currently, there is no commercial system available for...
6.
Garcia-Romero A, Gonzalez-Arreola R, Borjas-Gutierrez C, Magana-Torres M, Gonzalez-Garcia J
Cytogenet Genome Res
. 2023 Feb;
162(6):306-311.
PMID: 36724749
Acute promyelocytic leukemia (APL) is characterized by the chromosomal translocation t(15;17)(q24;q21), raising two hybrid genes: PML::RARA and RARA::PML. There is a biased clonal evolution in APL since imbalances affecting the...
7.
Rodriguez-Gutierrez P, Colima-Fausto A, Zepeda-Olmos P, Hernandez-Flores T, Gonzalez-Garcia J, Magana-Torres M
Int J Mol Sci
. 2023 Jan;
24(1).
PMID: 36613909
Primary hypertriglyceridemia (PHTG) is characterized by a high concentration of triglycerides (TG); it is divided between familial hyperchylomicronemia syndrome and multifactorial chylomicronemia syndrome. In Mexico, hypertriglyceridemia constitutes a health problem...
8.
Meza-Espinoza J, Contreras-Gutierrez J, Arambula-Meraz E, Gonzalez-Garcia J, Dominguez-Quezada M, Garcia-Magallanes N, et al.
Mol Cytogenet
. 2021 Sep;
14(1):43.
PMID: 34481514
Background: 4q deletion syndrome is a rare chromosomal disorder that mostly arises de novo. The syndrome is characterized by craniofacial dysmorphism, digital abnormalities, skeletal alterations, heart malformations, developmental delay, growth...
9.
Meza-Espinoza J, Vasquez-Jimenez E, Barajas-Torres R, Magana-Torres M, Gonzalez-Garcia J
Ann Clin Lab Sci
. 2019 Dec;
49(6):703-709.
PMID: 31882420
transcripts, the molecular hallmarks of chronic myeloid leukemia (CML), have been detected in peripheral blood from healthy individuals. Although CML is a sporadic disease, familial occurrence has been reported. This...
10.
Cordova-Fletes C, Arambula-Meraz E, Zarazua-Nino A, Maduena-Molina J, Sainz-Barraza M, Gonzalez-Garcia J, et al.
Cytogenet Genome Res
. 2019 Apr;
157(4):231-238.
PMID: 30933949
Constitutional complex chromosomal rearrangements (CCRs) are rare events that typically involve 2 or more chromosomes with at least 3 breakpoints and can result in normal or abnormal phenotypes depending on...