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El santuario y las “bajadas” de la Virgen de los Remedios en la configuración de un territorio devocional, en Cholula, Puebla, México

Antípoda : revista de antropología y arqueología, 2023-04 (51), p.103

Alejandra Gámez Espinosa

2023

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New and potential strategies for the treatment of PMM2-CDG

Biochimica et biophysica acta. General subjects, 2020-11, Vol.1864 (11), p.129686-129686, Article 129686

2020

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La construcción discursiva del espacio y tiempo en Cómo me hice monja de César Aira

EN-CLAVES del pensamiento, 2020-01 (27), p.39-58

Gámez Reza, Ilse Alejandra

2020

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Obesity measured as percent body fat, relationship with body mass index, and percentile curves for Mexican pediatric population

PloS one, 2019-02, Vol.14 (2), p.e0212792

2019

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Actitud y consumo de sustancias psicoactivas en adolescentes: correlatos sociodemográficos

Religación. Revista de Ciencias Sociales y Humanidades, 2023-11, Vol.8 (38), p.e2301115

2023

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Transcriptomic analysis identifies dysregulated pathways and therapeutic targets in PMM2-CDG

Biochimica et biophysica acta. Molecular basis of disease, 2024-06, Vol.1870 (5), p.167163, Article 167163

2024

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Genomic profiling in GIST: Implications in clinical outcome and future challenges

Neoplasia (New York, N.Y.), 2024-02, Vol.48, p.100959-100959, Article 100959

2024

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HepG2 PMM2-CDG knockout model: A versatile platform for variant and therapeutic evaluation

Molecular genetics and metabolism, 2024-09, Vol.143 (1-2), p.108538, Article 108538

2024

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DPAGT1-CDG: Functional analysis of disease-causing pathogenic mutations and role of endoplasmic reticulum stress

PloS one, 2017-06, Vol.12 (6), p.e0179456-e0179456

2017

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Impacto de afectividad y habilidades resilientes en la salud mental de adolescentes: fin del confinamiento

Religación. Revista de Ciencias Sociales y Humanidades, 2023-04, Vol.8 (36), p.e2301042

2023

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Pharmacological Chaperoning: A Potential Treatment for PMM2‐CDG

Human mutation, 2017-02, Vol.38 (2), p.160-168

2017

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A functional platform for the selection of pathogenic variants of PMM2 amenable to rescue via the use of pharmacological chaperones

Human mutation, 2022-10, Vol.43 (10), p.1430-1442

2022

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The Effects of PMM2-CDG-Causing Mutations on the Folding, Activity, and Stability of the PMM2 Protein

Human mutation, 2015-09, Vol.36 (9), p.851-860

2015

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Preclinical evaluation of multiple species of PEGylated recombinant phenylalanine ammonia lyase for the treatment of phenylketonuria

Proceedings of the National Academy of Sciences - PNAS, 2008-12, Vol.105 (52), p.20894-20899

2008

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Identification of 34 novel mutations in propionic acidemia: Functional characterization of missense variants and phenotype associations

Molecular genetics and metabolism, 2018-11, Vol.125 (3), p.266-275

2018

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Pathogenic variants of DNAJC12 and evaluation of the encoded cochaperone as a genetic modifier of hyperphenylalaninemia

Human mutation, 2020-07, Vol.41 (7), p.1329-1338

2020

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A Novel Approach to Enhancing Upper Extremity Coordination in Children with Autism Spectrum Disorder

Journal of motor behavior, 2020-05, Vol.52 (3), p.311-317

2020

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Correction of Kinetic and Stability Defects by Tetrahydrobiopterin in Phenylketonuria Patients with Certain Phenylalanine Hydroxylase Mutations

Proceedings of the National Academy of Sciences - PNAS, 2004-11, Vol.101 (48), p.16903-16908

2004

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Evaluation of orally administered PEGylated phenylalanine ammonia lyase in mice for the treatment of Phenylketonuria

Molecular genetics and metabolism, 2011-11, Vol.104 (3), p.249-254

2011

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Converting an injectable protein therapeutic into an oral form: Phenylalanine ammonia lyase for phenylketonuria

Molecular genetics and metabolism, 2010, Vol.99 (1), p.4-9

2010

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Expression analysis revealing destabilizing mutations in phosphomannomutase 2 deficiency (PMM2‐CDG)

Journal of inherited metabolic disease, 2011-08, Vol.34 (4), p.929-939

2011

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Phenylalanine ammonia lyase, enzyme substitution therapy for phenylketonuria, where are we now?

Molecular genetics and metabolism, 2005-12, Vol.86, p.22-26

2005

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Different altered pattern expression of genes related to apoptosis in isolated methylmalonic aciduria cblB type and combined with homocystinuria cblC type

Biochimica et biophysica acta, 2010-11, Vol.1802 (11), p.959-967

2010

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Retornos salariales de los graduados del programa de Administración Pública de la ESAP

Sociedad y Economía, 2024-01 (51), p.e10712777

2024

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Functional and structural analysis of five mutations identified in methylmalonic aciduria cblB type

Human mutation, 2010-09, Vol.31 (9), p.1033-1042

2010

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El santuario y las “bajadas” de la Virgen de los Remedios en la configuración de un territorio devocional, en Cholula, Puebla, México

New and potential strategies for the treatment of PMM2-CDG

La construcción discursiva del espacio y tiempo en Cómo me hice monja de César Aira

Obesity measured as percent body fat, relationship with body mass index, and percentile curves for Mexican pediatric population

Actitud y consumo de sustancias psicoactivas en adolescentes: correlatos sociodemográficos

Transcriptomic analysis identifies dysregulated pathways and therapeutic targets in PMM2-CDG

Genomic profiling in GIST: Implications in clinical outcome and future challenges

HepG2 PMM2-CDG knockout model: A versatile platform for variant and therapeutic evaluation

DPAGT1-CDG: Functional analysis of disease-causing pathogenic mutations and role of endoplasmic reticulum stress

Impacto de afectividad y habilidades resilientes en la salud mental de adolescentes: fin del confinamiento

Pharmacological Chaperoning: A Potential Treatment for PMM2‐CDG

A functional platform for the selection of pathogenic variants of PMM2 amenable to rescue via the use of pharmacological chaperones

The Effects of PMM2-CDG-Causing Mutations on the Folding, Activity, and Stability of the PMM2 Protein

Preclinical evaluation of multiple species of PEGylated recombinant phenylalanine ammonia lyase for the treatment of phenylketonuria

Identification of 34 novel mutations in propionic acidemia: Functional characterization of missense variants and phenotype associations

Pathogenic variants of DNAJC12 and evaluation of the encoded cochaperone as a genetic modifier of hyperphenylalaninemia

A Novel Approach to Enhancing Upper Extremity Coordination in Children with Autism Spectrum Disorder

Correction of Kinetic and Stability Defects by Tetrahydrobiopterin in Phenylketonuria Patients with Certain Phenylalanine Hydroxylase Mutations

Evaluation of orally administered PEGylated phenylalanine ammonia lyase in mice for the treatment of Phenylketonuria

Converting an injectable protein therapeutic into an oral form: Phenylalanine ammonia lyase for phenylketonuria

Expression analysis revealing destabilizing mutations in phosphomannomutase 2 deficiency (PMM2‐CDG)

Phenylalanine ammonia lyase, enzyme substitution therapy for phenylketonuria, where are we now?

Different altered pattern expression of genes related to apoptosis in isolated methylmalonic aciduria cblB type and combined with homocystinuria cblC type

Retornos salariales de los graduados del programa de Administración Pública de la ESAP

Functional and structural analysis of five mutations identified in methylmalonic aciduria cblB type

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