Detalhe da pesquisa
1.
Mitochondrial dysfunction: The pathological link between psoriasis and insulin resistance?
J Eur Acad Dermatol Venereol
; 37(2): 340-347, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36184894
2.
Diagnosis and treatment of benign adipocytic tumors in children.
Pediatr Surg Int
; 38(12): 2045-2051, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36264345
3.
Characterization of Human Sperm Protamine Proteoforms through a Combination of Top-Down and Bottom-Up Mass Spectrometry Approaches.
J Proteome Res
; 19(1): 221-237, 2020 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31703166
4.
Molecular genetic diagnosis by next-generation sequencing in a cohort of Mexican patients with haemophilia and report of novel variants.
Blood Cells Mol Dis
; 83: 102423, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32224444
5.
Analysis of the pathogenic variants of BRCA1 and BRCA2 using next-generation sequencing in women with familial breast cancer: a case-control study.
BMC Cancer
; 19(1): 722, 2019 Jul 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-31331294
6.
Bioinformatic Analysis of Gene Variants from Gastroschisis Recurrence Identifies Multiple Novel Pathogenetic Pathways: Implication for the Closure of the Ventral Body Wall.
Int J Mol Sci
; 20(9)2019 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31075877
7.
A Consensus Position Paper From REAL-PANLAR Group About the Methodological Approach for the Accreditation Process of Centers of Excellence in Rheumatoid Arthritis in Latin America.
J Clin Rheumatol
; 25(1): 54-58, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29596208
8.
Familial occurrence of gastroschisis: a population-based overview on recurrence risk, sex-dependent influence, and geographical distribution.
Pediatr Surg Int
; 34(3): 277-282, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29335896
9.
Genetic variants conferring susceptibility to gastroschisis: a phenomenon restricted to the interaction with the environment?
Pediatr Surg Int
; 34(5): 505-514, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29550988
10.
A clinical-pathogenetic approach on associated anomalies and chromosomal defects supports novel candidate critical regions and genes for gastroschisis.
Pediatr Surg Int
; 34(9): 931-943, 2018 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-30094464
11.
Emergency arising from patients' fear of taking antimalarials during these COVID-19 times: are antimalarials as unsafe for cardiovascular health as recent reports suggest?
Ann Rheum Dis
; 81(8): e154, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32647029
12.
Vitamin D deficiency in Mexican mothers and their newborns. / Deficiencia de vitamina D en madres y neonatos mexicanos.
Gac Med Mex
; 153(5): 559-565, 2017.
Artigo
em Espanhol
| MEDLINE | ID: mdl-29099117
13.
Experience of telemedicine use in a big cohort of patients with rheumatoid arthritis during COVID-19 pandemic.
Ann Rheum Dis
; 80(5): e65, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32586920
14.
Olfactomedin-like 2 A and B (OLFML2A and OLFML2B) expression profile in primates (human and baboon).
Biol Res
; 49(1): 44, 2016 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27821182
15.
Unconventional secretion is a major contributor of cancer cell line secretomes.
Mol Cell Proteomics
; 12(5): 1046-60, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23268930
16.
Molecular evolution and expression profile of the chemerine encoding gene RARRES2 in baboon and chimpanzee.
Biol Res
; 48: 31, 2015 Jun 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26063455
17.
Enhancing the Biological Relevance of Secretome-Based Proteomics by Linking Tumor Cell Proliferation and Protein Secretion.
J Proteome Res
; 13(8): 3706-3721, 2014 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24897304
18.
A novel EBP c.224T>A mutation supports the existence of a male-specific disorder independent of CDPX2.
Am J Med Genet A
; 164A(7): 1642-7, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24700572
19.
PSMB8 encoding the ß5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy syndrome.
Am J Hum Genet
; 87(6): 866-72, 2010 Dec 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-21129723
20.
A novel phenotype characterized by digital abnormalities, intellectual disability, and short stature in a Mexican family maps to Xp11.4-p11.21.
Am J Med Genet A
; 161A(2): 237-43, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23307567