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The conjugacy problem for symmetric Thompson-like groups

Israel journal of mathematics, 2021-09, Vol.244 (1), p.49-73

Aroca, Julio

2021

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Two remarks about multicurve graphs on infinite-type surfaces

Topology and its applications, 2018-11, Vol.249, p.83-94

Aroca, Julio

2018

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Some embeddings between symmetric R. thompson groups

Proceedings of the Edinburgh Mathematical Society, 2022-02, Vol.65 (1), p.1-18

2022

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A new family of infinitely braided Thompson's groups

Journal of algebra, 2022-10, Vol.607, p.5-34

2022

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Null cyp1b1 Activity in Zebrafish Leads to Variable Craniofacial Defects Associated with Altered Expression of Extracellular Matrix and Lipid Metabolism Genes

International journal of molecular sciences, 2021-06, Vol.22 (12), p.6430

2021

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Transgenic Overexpression of Myocilin Leads to Variable Ocular Anterior Segment and Retinal Alterations Associated with Extracellular Matrix Abnormalities in Adult Zebrafish

International journal of molecular sciences, 2022-09, Vol.23 (17), p.9989

2022

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The Increased Burden of Rare Variants in Four Matrix Metalloproteinase-Related Genes in Childhood Glaucoma Suggests a Complex Genetic Inheritance of the Disease

International journal of molecular sciences, 2024-06, Vol.25 (11), p.5757

2024

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Identification of a Lipase-linked Cell Membrane Receptor for Pigment Epithelium-derived Factor

The Journal of biological chemistry, 2006-12, Vol.281 (49), p.38022-38037

2006

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Identification of myocilin as a blood plasma protein and analysis of its role in leukocyte adhesion to endothelial cell monolayers

PloS one, 2018-12, Vol.13 (12), p.e0209364-e0209364

2018

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Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma

PloS one, 2019-01, Vol.14 (1), p.e0211029

2019

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RNA and protein expression analysis of HLA‐DQB103:01:01:21Q allele: A null allele renamed as HLA‐DQB103:01:01:21N

HLA, 2022-03, Vol.99 (3), p.160-166

2022

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Knockout of myoc Provides Evidence for the Role of Myocilin in Zebrafish Sex Determination Associated with Wnt Signalling Downregulation

Biology (Basel, Switzerland), 2021-01, Vol.10 (2), p.98

2021

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Role of GUCA1C in Primary Congenital Glaucoma and in the Retina: Functional Evaluation in Zebrafish

Genes, 2020-05, Vol.11 (5), p.550

2020

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Hypo- and hypermorphic FOXC1 mutations in dominant glaucoma: transactivation and phenotypic variability

PloS one, 2015-03, Vol.10 (3), p.e0119272-e0119272

2015

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Pigment epithelium-derived factor is a niche signal for neural stem cell renewal

Nature neuroscience, 2006-03, Vol.9 (3), p.331-339

2006

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Goniodysgenesis variability and activity of CYP1B1 genotypes in primary congenital glaucoma

PloS one, 2017-04, Vol.12 (4), p.e0176386-e0176386

2017

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Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development

Scientific reports, 2017-04, Vol.7 (1), p.46175-46175, Article 46175

2017

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Efficacy and safety of the CVnCoV SARS-CoV-2 mRNA vaccine candidate in ten countries in Europe and Latin America (HERALD): a randomised, observer-blinded, placebo-controlled, phase 2b/3 trial

The Lancet infectious diseases, 2022-03, Vol.22 (3), p.329-340

2022

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Bicarbonate-dependent secretion and proteolytic processing of recombinant myocilin

PloS one, 2013-01, Vol.8 (1), p.e54385-e54385

2013

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Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences

European journal of human genetics : EJHG, 2016-05, Vol.24 (5), p.672-680

2016

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Seizures regulate the cation-Cl - cotransporter NKCC1 in a hamster model of epilepsy: implications for GABA neurotransmission

Frontiers in neurology, 2023-06, Vol.14, p.1207616-1207616

2023

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Molecular and neurochemical substrates of the audiogenic seizure strains: The GASH:Sal model

Epilepsy & behavior, 2017-06, Vol.71 (Pt B), p.218-225

2017

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Functional characterization of eight rare missense CYP1B1 variants involved in congenital glaucoma and their association with null genotypes

Acta ophthalmologica (Oxford, England), 2016-11, Vol.94 (7), p.e555-e560

2016

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Interaction of recombinant myocilin with the matricellular protein SPARC: functional implications

Investigative ophthalmology & visual science, 2011-01, Vol.52 (1), p.179-189

2011

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Characterization of the Intracellular Proteolytic Cleavage of Myocilin and Identification of Calpain II as a Myocilin-processing Protease

The Journal of biological chemistry, 2007-09, Vol.282 (38), p.27810-27824

2007

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The conjugacy problem for symmetric Thompson-like groups

Two remarks about multicurve graphs on infinite-type surfaces

Some embeddings between symmetric R. thompson groups

A new family of infinitely braided Thompson's groups

Null cyp1b1 Activity in Zebrafish Leads to Variable Craniofacial Defects Associated with Altered Expression of Extracellular Matrix and Lipid Metabolism Genes

Transgenic Overexpression of Myocilin Leads to Variable Ocular Anterior Segment and Retinal Alterations Associated with Extracellular Matrix Abnormalities in Adult Zebrafish

The Increased Burden of Rare Variants in Four Matrix Metalloproteinase-Related Genes in Childhood Glaucoma Suggests a Complex Genetic Inheritance of the Disease

Identification of a Lipase-linked Cell Membrane Receptor for Pigment Epithelium-derived Factor

Identification of myocilin as a blood plasma protein and analysis of its role in leukocyte adhesion to endothelial cell monolayers

Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma

RNA and protein expression analysis of HLA‐DQB103:01:01:21Q allele: A null allele renamed as HLA‐DQB103:01:01:21N

Knockout of myoc Provides Evidence for the Role of Myocilin in Zebrafish Sex Determination Associated with Wnt Signalling Downregulation

Role of GUCA1C in Primary Congenital Glaucoma and in the Retina: Functional Evaluation in Zebrafish

Hypo- and hypermorphic FOXC1 mutations in dominant glaucoma: transactivation and phenotypic variability

Pigment epithelium-derived factor is a niche signal for neural stem cell renewal

Goniodysgenesis variability and activity of CYP1B1 genotypes in primary congenital glaucoma

Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development

Efficacy and safety of the CVnCoV SARS-CoV-2 mRNA vaccine candidate in ten countries in Europe and Latin America (HERALD): a randomised, observer-blinded, placebo-controlled, phase 2b/3 trial

Bicarbonate-dependent secretion and proteolytic processing of recombinant myocilin

Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences

Seizures regulate the cation-Cl - cotransporter NKCC1 in a hamster model of epilepsy: implications for GABA neurotransmission

Molecular and neurochemical substrates of the audiogenic seizure strains: The GASH:Sal model

Functional characterization of eight rare missense CYP1B1 variants involved in congenital glaucoma and their association with null genotypes

Interaction of recombinant myocilin with the matricellular protein SPARC: functional implications

Characterization of the Intracellular Proteolytic Cleavage of Myocilin and Identification of Calpain II as a Myocilin-processing Protease

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