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Hyperexcitability and translational phenotypes in a preclinical mouse model of SYNGAP1-related intellectual disability

Translational psychiatry, 2024-10, Vol.14 (1), p.405

2024

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Redescription of Apanteles mimoristae (Hymenoptera, Braconidae), a parasitoid of the native pyralid cactus moth Melitara cf. nephelepasa in central Mexico

Journal of Hymenoptera research, 2024-03, Vol.97 (4), p.207-228

2024

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Activity of Bacteriophage D29 Loaded on Nanoliposomes against Macrophages Infected with Mycobacterium tuberculosis

Diseases, 2023-12, Vol.11 (4), p.150

2023

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Activity of Bacteriophage D29 Loaded on Nanoliposomes against Macrophages Infected with IMycobacterium tuberculosis/I

Diseases, 2023-10, Vol.11 (4)

2023

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Parallel functional testing identifies enhancers active in early postnatal mouse brain

eLife, 2021-10, Vol.10

2021

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Deletion of a non-canonical regulatory sequence causes loss of Scn1a expression and epileptic phenotypes in mice

Genome medicine, 2021-04, Vol.13 (1), p.69-22, Article 69

2021

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19.5 ACUTE AND LASTING IMPACTS OF MATERNAL IMMUNE ACTIVATION ON PRENATAL CORTICAL DEVELOPMENT

Journal of the American Academy of Child and Adolescent Psychiatry, 2020-10, Vol.59 (10), p.S295-S295

2020

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CRL5-dependent regulation of the small GTPases ARL4C and ARF6 controls hippocampal morphogenesis

Proceedings of the National Academy of Sciences - PNAS, 2020-09, Vol.117 (37), p.23073-23084

2020

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RUVBL1/RUVBL2 ATPase Activity Drives PAQosome Maturation, DNA Replication and Radioresistance in Lung Cancer

Cell chemical biology, 2020-01, Vol.27 (1), p.105-121.e14

2020

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Abstract 1174: Characterization of the immunologic intra-tumor heterogeneity in early stages of non-small cell lung carcinoma using multiplex immunofluorescence and image analysis approaches

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.1174-1174

2018

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Caracterización socio-demográfica y clínica de pacientes adultos en ventilación mecánica no invasiva domiciliaria. Ministerio de Salud. Chile

Revista chilena de enfermedades respiratorias, 2018, Vol.34 (1), p.10-18

2018

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CUBIC Protocol Visualizes Protein Expression at Single Cell Resolution in Whole Mount Skin Preparations

Journal of visualized experiments, 2016-08 (114)

2016

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CUBIC Protocol Visualizes Protein Expression at Single Cell Resolution in Whole Mount Skin Preparations

Journal of visualized experiments, 2016-08 (114)

2016

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RNA-Seq analysis of Gtf2ird1 knockout epidermal tissue provides potential insights into molecular mechanisms underpinning Williams-Beuren syndrome

BMC genomics, 2016-06, Vol.17 (1), p.450-450, Article 450

2016

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The nuclear localization pattern and interaction partners of GTF2IRD1 demonstrate a role in chromatin regulation

Human genetics, 2015-10, Vol.134 (10), p.1099-1115

2015

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The role of GTF2IRD1 in the auditory pathology of Williams-Beuren Syndrome

European journal of human genetics : EJHG, 2015-06, Vol.23 (6), p.774-780

2015

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Characterization of a Trpc6 Transgenic Mouse Associated with Early Onset FSGS

British journal of medicine and medical research, 2015, Vol.5 (10), p.1198-1212

2015

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RAI1 transcription factor activity is impaired in mutants associated with Smith-Magenis Syndrome

PloS one, 2012-09, Vol.7 (9), p.e45155-e45155

2012

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Definition of a critical genetic interval related to kidney abnormalities in the Potocki-Lupski syndrome

American journal of medical genetics. Part A, 2012-07, Vol.158A (7), p.1579-1588

2012

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Copy number variation and susceptibility to complex traits

EMBO molecular medicine, 2011-01, Vol.3 (1), p.1-4

2011

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La pulsioximetría y su aplicación en pruebas de esfuerzo máximo

Apunts : medicina de l'esport, 2011, Vol.46 (169), p.23-27

2011

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Podocyte-specific overexpression of wild type or mutant trpc6 in mice is sufficient to cause glomerular disease

PloS one, 2010-09, Vol.5 (9), p.e12859-e12859

2010

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Functional and cellular characterization of human Retinoic Acid Induced 1

BMC molecular biology, 2010-08, Vol.11, p.63

2010

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Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome

BMC molecular biology, 2010-08, Vol.11 (1), p.63-63, Article 63

2010

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Hyperexcitability and translational phenotypes in a preclinical mouse model of SYNGAP1-related intellectual disability

Redescription of Apanteles mimoristae (Hymenoptera, Braconidae), a parasitoid of the native pyralid cactus moth Melitara cf. nephelepasa in central Mexico

Activity of Bacteriophage D29 Loaded on Nanoliposomes against Macrophages Infected with Mycobacterium tuberculosis

Activity of Bacteriophage D29 Loaded on Nanoliposomes against Macrophages Infected with IMycobacterium tuberculosis/I

Parallel functional testing identifies enhancers active in early postnatal mouse brain

Deletion of a non-canonical regulatory sequence causes loss of Scn1a expression and epileptic phenotypes in mice

Sequential perturbations to mouse corticogenesis following in utero maternal immune activation

19.5 ACUTE AND LASTING IMPACTS OF MATERNAL IMMUNE ACTIVATION ON PRENATAL CORTICAL DEVELOPMENT

CRL5-dependent regulation of the small GTPases ARL4C and ARF6 controls hippocampal morphogenesis

RUVBL1/RUVBL2 ATPase Activity Drives PAQosome Maturation, DNA Replication and Radioresistance in Lung Cancer

Abstract 1174: Characterization of the immunologic intra-tumor heterogeneity in early stages of non-small cell lung carcinoma using multiplex immunofluorescence and image analysis approaches

Caracterización socio-demográfica y clínica de pacientes adultos en ventilación mecánica no invasiva domiciliaria. Ministerio de Salud. Chile

CUBIC Protocol Visualizes Protein Expression at Single Cell Resolution in Whole Mount Skin Preparations

CUBIC Protocol Visualizes Protein Expression at Single Cell Resolution in Whole Mount Skin Preparations

RNA-Seq analysis of Gtf2ird1 knockout epidermal tissue provides potential insights into molecular mechanisms underpinning Williams-Beuren syndrome

The nuclear localization pattern and interaction partners of GTF2IRD1 demonstrate a role in chromatin regulation

The role of GTF2IRD1 in the auditory pathology of Williams-Beuren Syndrome

Characterization of a Trpc6 Transgenic Mouse Associated with Early Onset FSGS

RAI1 transcription factor activity is impaired in mutants associated with Smith-Magenis Syndrome

Definition of a critical genetic interval related to kidney abnormalities in the Potocki-Lupski syndrome

Copy number variation and susceptibility to complex traits

La pulsioximetría y su aplicación en pruebas de esfuerzo máximo

Podocyte-specific overexpression of wild type or mutant trpc6 in mice is sufficient to cause glomerular disease

Functional and cellular characterization of human Retinoic Acid Induced 1

Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome

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