Lista de obras - M. Albert Basson - Dominio Público Uruguay

A bi-modal function of Wnt signalling directs an FGF activity gradient to spatially regulate neuronal differentiation in the midbrain

artículo científico publicado en 2013

Advanced paternal age effects in neurodevelopmental disorders-review of potential underlying mechanisms

artículo científico publicado en 2017

Altered Neocortical Gene Expression, Brain Overgrowth and Functional Over-Connectivity in Chd8 Haploinsufficient Mice.

artículo científico publicado en 2018

An FGFR1-SPRY2 Signaling Axis Limits Basal Cell Proliferation in the Steady-State Airway Epithelium

artículo científico publicado en 2016

Autism-linked CHD gene expression patterns during development predict multi-organ disease phenotypes

artículo científico publicado en 2018

Brain mapping across 16 autism mouse models reveals a spectrum of functional connectivity subtypes

artículo científico publicado en 2021

CD3 Ligation on Immature Thymocytes Generates Antagonist-like Signals Appropriate for CD8 Lineage Commitment, Independently of T Cell Receptor Specificity ⬇️

artículo científico publicado el 20 de abril de 1998

CHD7 maintains neural stem cell quiescence and prevents premature stem cell depletion in the adult hippocampus.

artículo científico publicado en 2015

Cell-type-specific synaptic imbalance and disrupted homeostatic plasticity in cortical circuits of ASD-associated Chd8 haploinsufficient mice

scholarly article published 14 May 2020

Cerebellar Vermis and Midbrain Hypoplasia Upon Conditional Deletion of Chd7 from the Embryonic Mid-Hindbrain Region

artículo científico publicado en 2017

Characterization of a Dchs1 mutant mouse reveals requirements for Dchs1-Fat4 signaling during mammalian development

scientific journal article

Congenital hypoplasia of the cerebellum: developmental causes and behavioral consequences

artículo científico publicado en 2013

Convergence of BMI1 and CHD7 on ERK Signaling in Medulloblastoma.

artículo científico publicado en 2017

Coordinated activity of Spry1 and Spry2 is required for normal development of the external genitalia.

artículo científico publicado en 2013

Distinct cerebellar foliation anomalies in a CHD7 haploinsufficient mouse model of CHARGE syndrome.

artículo científico publicado en 2017

Distinct, dosage-sensitive requirements for the autism-associated factor CHD8 during cortical development

artículo científico publicado en 2021

Effects of Low-Dose Gestational TCDD Exposure on Behavior and on Hippocampal Neuron Morphology and Gene Expression in Mice

artículo científico publicado en 2021

Endoderm-specific deletion of Tbx1 reveals an FGF-independent role for Tbx1 in pharyngeal apparatus morphogenesis.

artículo científico publicado en 2014

Engrailed controls epaxial-hypaxial muscle innervation and the establishment of vertebrate three-dimensional mobility.

artículo científico

Epistatic interactions between Chd7 and Fgf8 during cerebellar development: Implications for CHARGE syndrome.

artículo científico publicado en 2014

Expression of fibroblast growth factors (Fgfs) in murine tooth development.

artículo científico

FGF ligands emerge as potential specifiers of synaptic identity ⬇️

artículo científico publicado el 27 de julio de 2010

Functional Insights into Chromatin Remodelling from Studies on CHARGE Syndrome

artículo científico publicado en 2015

Gli3 controls corpus callosum formation by positioning midline guideposts during telencephalic patterning.

artículo científico publicado en 2012

Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice

scientific journal article

Heparan sulfotransferases Hs6st1 and Hs2st keep Erk in check for mouse corpus callosum development

artículo científico publicado en 2014

Infraslow State Fluctuations Govern Spontaneous fMRI Network Dynamics

artículo científico publicado en 2019

Inositol treatment inhibits medulloblastoma through suppression of epigenetic-driven metabolic adaptation

artículo científico publicado en 2021

Insights into T-Cell Development from Studies Using Transgenic and Knockout Mice

article

Itch-/- alphabeta and gammadelta T cells independently contribute to autoimmunity in Itchy mice

artículo científico publicado en 2008

Localised inhibition of FGF signalling in the third pharyngeal pouch is required for normal thymus and parathyroid organogenesis

artículo científico publicado en 2012

Loss of Sprouty1 rescues renal agenesis caused by Ret mutation.

artículo científico publicado en 2008

MicroRNA-21 contributes to myocardial disease by stimulating MAP kinase signalling in fibroblasts

scientific journal article

Periodic stripe formation by a Turing mechanism operating at growth zones in the mammalian palate.

artículo científico publicado en 2012

Regulation of CD4⁺ and CD8⁺ effector responses by Sprouty-1

artículo científico publicado en 2012

Signaling in Cell Differentiation and Morphogenesis ⬇️

artículo científico publicado el 1 de junio de 2012

Specific regions within the embryonic midbrain and cerebellum require different levels of FGF signaling during development.

artículo científico publicado en 2008

Sprouty Is a Negative Regulator of Transforming Growth Factor β-Induced Epithelial-to-Mesenchymal Transition and Cataract ⬇️

artículo científico publicado el 18 de julio de 2012

Sprouty genes are essential for the normal development of epibranchial ganglia in the mouse embryo

artículo científico publicado en 2011

Sprouty genes prevent excessive FGF signalling in multiple cell types throughout development of the cerebellum.

artículo científico publicado en 2011

Sprouty proteins inhibit receptor-mediated activation of phosphatidylinositol-specific phospholipase C.

artículo científico publicado en 2010

Sprouty proteins: multifaceted negative-feedback regulators of receptor tyrosine kinase signaling.

artículo científico publicado en 2005

Sprouty1 Controls Genitourinary Development via its N-Terminal Tyrosine

artículo científico publicado en 2019

Sprouty1 haploinsufficiency prevents renal agenesis in a model of Fraser syndrome.

artículo científico publicado en 2012

Synergistic activity of Sef and Sprouty proteins in regulating the expression of Gbx2 in the mid-hindbrain region.

artículo científico publicado en 2005

Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm

scientific journal article

The AHR pathway represses TGFβ-SMAD3 signalling and has a potent tumour suppressive role in SHH medulloblastoma

scientific article published on 10 January 2020

The aged niche disrupts muscle stem cell quiescence.

artículo científico publicado en 2012

The chromatin remodelling factor Chd7 protects auditory neurons and sensory hair cells from stress-induced degeneration

artículo científico publicado en 2021

The influence of the src-family kinases, Lck and Fyn, on T cell differentiation, survival and activation

artículo científico publicado en 2003

The neuroanatomy of autism - a developmental perspective

artículo científico publicado en 2017

Lista de obras de M. Albert Basson

A bi-modal function of Wnt signalling directs an FGF activity gradient to spatially regulate neuronal differentiation in the midbrain

Advanced paternal age effects in neurodevelopmental disorders-review of potential underlying mechanisms

Altered Neocortical Gene Expression, Brain Overgrowth and Functional Over-Connectivity in Chd8 Haploinsufficient Mice.

An FGFR1-SPRY2 Signaling Axis Limits Basal Cell Proliferation in the Steady-State Airway Epithelium

Autism-linked CHD gene expression patterns during development predict multi-organ disease phenotypes

Brain mapping across 16 autism mouse models reveals a spectrum of functional connectivity subtypes

CD3 Ligation on Immature Thymocytes Generates Antagonist-like Signals Appropriate for CD8 Lineage Commitment, Independently of T Cell Receptor Specificity ⬇️

CHD7 maintains neural stem cell quiescence and prevents premature stem cell depletion in the adult hippocampus.

Cell-type-specific synaptic imbalance and disrupted homeostatic plasticity in cortical circuits of ASD-associated Chd8 haploinsufficient mice

Cerebellar Vermis and Midbrain Hypoplasia Upon Conditional Deletion of Chd7 from the Embryonic Mid-Hindbrain Region

Characterization of a Dchs1 mutant mouse reveals requirements for Dchs1-Fat4 signaling during mammalian development

Congenital hypoplasia of the cerebellum: developmental causes and behavioral consequences

Convergence of BMI1 and CHD7 on ERK Signaling in Medulloblastoma.

Coordinated activity of Spry1 and Spry2 is required for normal development of the external genitalia.

Distinct cerebellar foliation anomalies in a CHD7 haploinsufficient mouse model of CHARGE syndrome.

Distinct, dosage-sensitive requirements for the autism-associated factor CHD8 during cortical development

Effects of Low-Dose Gestational TCDD Exposure on Behavior and on Hippocampal Neuron Morphology and Gene Expression in Mice

Endoderm-specific deletion of Tbx1 reveals an FGF-independent role for Tbx1 in pharyngeal apparatus morphogenesis.

Engrailed controls epaxial-hypaxial muscle innervation and the establishment of vertebrate three-dimensional mobility.

Epistatic interactions between Chd7 and Fgf8 during cerebellar development: Implications for CHARGE syndrome.

Expression of fibroblast growth factors (Fgfs) in murine tooth development.

FGF ligands emerge as potential specifiers of synaptic identity ⬇️

Functional Insights into Chromatin Remodelling from Studies on CHARGE Syndrome

Gli3 controls corpus callosum formation by positioning midline guideposts during telencephalic patterning.

Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice

Heparan sulfotransferases Hs6st1 and Hs2st keep Erk in check for mouse corpus callosum development

Infraslow State Fluctuations Govern Spontaneous fMRI Network Dynamics

Inositol treatment inhibits medulloblastoma through suppression of epigenetic-driven metabolic adaptation

Insights into T-Cell Development from Studies Using Transgenic and Knockout Mice

Itch-/- alphabeta and gammadelta T cells independently contribute to autoimmunity in Itchy mice

Localised inhibition of FGF signalling in the third pharyngeal pouch is required for normal thymus and parathyroid organogenesis

Loss of Sprouty1 rescues renal agenesis caused by Ret mutation.

MicroRNA-21 contributes to myocardial disease by stimulating MAP kinase signalling in fibroblasts

Periodic stripe formation by a Turing mechanism operating at growth zones in the mammalian palate.

Regulation of CD4⁺ and CD8⁺ effector responses by Sprouty-1

Signaling in Cell Differentiation and Morphogenesis ⬇️

Specific regions within the embryonic midbrain and cerebellum require different levels of FGF signaling during development.

Sprouty Is a Negative Regulator of Transforming Growth Factor β-Induced Epithelial-to-Mesenchymal Transition and Cataract ⬇️

Sprouty genes are essential for the normal development of epibranchial ganglia in the mouse embryo

Sprouty genes prevent excessive FGF signalling in multiple cell types throughout development of the cerebellum.

Sprouty proteins inhibit receptor-mediated activation of phosphatidylinositol-specific phospholipase C.

Sprouty proteins: multifaceted negative-feedback regulators of receptor tyrosine kinase signaling.

Sprouty1 Controls Genitourinary Development via its N-Terminal Tyrosine

Sprouty1 haploinsufficiency prevents renal agenesis in a model of Fraser syndrome.

Synergistic activity of Sef and Sprouty proteins in regulating the expression of Gbx2 in the mid-hindbrain region.

Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm

The AHR pathway represses TGFβ-SMAD3 signalling and has a potent tumour suppressive role in SHH medulloblastoma

The aged niche disrupts muscle stem cell quiescence.

The chromatin remodelling factor Chd7 protects auditory neurons and sensory hair cells from stress-induced degeneration

The influence of the src-family kinases, Lck and Fyn, on T cell differentiation, survival and activation

The neuroanatomy of autism - a developmental perspective