about
Profiles of Amino Acids and Acylcarnitines Related with Insecticide Exposure in Culex quinquefasciatus (Say)An autosomal recessive syndrome of joint contractures, muscular atrophy, microcytic anemia, and panniculitis-associated lipodystrophy.PSMB8 encoding the β5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy syndrome.Plasma and urine metabolic profiles are reflective of altered beta-oxidation in non-diabetic obese subjects and patients with type 2 diabetes mellitus.Identification of novel mutations in Mexican patients with Aarskog-Scott syndrome.Molecular evolution and expression profile of the chemerine encoding gene RARRES2 in baboon and chimpanzee.Reference values for amino acids and acylcarnitines in peripheral blood in Quarter horses and American Miniature horses.Impact of an exercise program on acylcarnitines in obesity: a prospective controlled studyCandidate gene polymorphisms and risk of psoriasis: A pilot study.Olfactomedin-like 2 A and B (OLFML2A and OLFML2B) expression profile in primates (human and baboon)Genetic variants in KCNJ11, TCF7L2 and HNF4A are associated with type 2 diabetes, BMI and dyslipidemia in families of Northeastern Mexico: A pilot study.Proteomic profile of serum of pregnant women carring a fetus with Down syndrome using nano uplc Q-tof ms/ms technology.Dosage of Sex Chromosomal Genes in Blood Deposited on Filter Paper for Neonatal Screening of Sex Chromosome Aneuploidy.Association of the polymorphism 12109g>A from the REN gene as a risk factor for preterm birth.Molecular cloning of the myo-inositol oxygenase gene from the kidney of baboons.[Folic acid levels, homocysteine and polymorphism of methylenetetrahydrofolate reductase enzyme (MTHFR) in patients with pre-eclampsia and eclampsia].GJB2 and GJB6 mutations are an infrequent cause of autosomal-recessive nonsyndromic hearing loss in residents of Mexico.[Impact of weekly administration of folic acid on folic acid blood levels]Folate levels and N(5),N(10)-methylenetetrahydrofolate reductase genotype (MTHFR) in mothers of offspring with neural tube defects: a case-control study.Evaluation of familial factors in a Mexican population-based setting with gastroschisis: Further evidence for an underlying genetic susceptibility.Phenotypic Variation in Patients with Homozygous c.1678G>T Mutation in EVC Gene: Report of Two Mexican Families with Ellis-van Creveld Syndrome.Familial occurrence of gastroschisis: a population-based overview on recurrence risk, sex-dependent influence, and geographical distribution.Should the dose of folic acid be adjusted for Mexican population? The pilot prevention program implemented in Nuevo Leon, Mexico.Vitamin D deficiency in Mexican mothers and their newborns.Genetic variants conferring susceptibility to gastroschisis: a phenomenon restricted to the interaction with the environment?Effects of toxin T-544 from the Karwinskia humboldtiana (buckthorn) plant upon mouse embryos explanted at 11 daysCultivation of mouse embryos explanted at 11 daysEffects of hormones on postimplantation mouse embryos in vitro. II. Progesterone and estrogenIn vitro selective toxicity of toxin T-514 from Karwinskia humboldtiana (buckthorn) plant on various human tumor cell linesEffect of toxins 544 and 514 from Karwinskia humboldtiana (buckthorn) plant upon fetal development of the mouseA novel phenotype characterized by digital abnormalities, intellectual disability, and short stature in a Mexican family maps to Xp11.4-p11.21Detection of Turner Syndrome by quantitative PCR of SHOX and VAMP7 genesA novel EBP c.224T>A mutation supports the existence of a male-specific disorder independent of CDPX2An investigation into the MMP1 gene promoter region polymorphism--1607 2G with recessive dystrophic epidermolysis bullosa disease severity in northeastern Mexican patientsPrimary hypertrophic osteoarthropathy: Report of two novel genetic variants in the SLCO2A1 gene in two Mexican patientsA clinical-pathogenetic approach on associated anomalies and chromosomal defects supports novel candidate critical regions and genes for gastroschisisAnalysis of the pathogenic variants of BRCA1 and BRCA2 using next-generation sequencing in women with familial breast cancer: a case-control studyExpanding the phenotype of MTOR-related disorders and the Smith-Kingsmore syndrome
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Laura E Martínez-Garza
@ast
Laura E Martínez-Garza
@en
Laura E Martínez-Garza
@es
Laura E Martínez-Garza
@nl
type
label
Laura E Martínez-Garza
@ast
Laura E Martínez-Garza
@en
Laura E Martínez-Garza
@es
Laura E Martínez-Garza
@nl
prefLabel
Laura E Martínez-Garza
@ast
Laura E Martínez-Garza
@en
Laura E Martínez-Garza
@es
Laura E Martínez-Garza
@nl
P106
P1153
55347113800
6602217087
P21
P31
P496
0000-0003-1442-9089