Lista de obras - Nael Nadif Kasri - Dominio Público Uruguay

Basal ryanodine receptor activity suppresses autophagic flux

artículo científico publicado en 2017

Binding of IRBIT to the IP3 receptor: determinants and functional effects.

artículo científico publicado en 2006

Choices for Induction of Pluripotency: Recent Developments in Human Induced Pluripotent Stem Cell Reprogramming Strategies

artículo científico publicado en 2016

EHMT1 regulates Parvalbumin-positive interneuron development and GABAergic input in sensory cortical areas

scientific article published on 25 September 2020

Endogenously bound calmodulin is essential for the function of the inositol 1,4,5-trisphosphate receptor

artículo científico publicado en 2006

Epigenetic Etiology of Intellectual Disability

artículo científico publicado en 2017

Euchromatin histone methyltransferase 1 regulates cortical neuronal network development

artículo científico publicado en 2016

Extraction, Identification, and Quantification of Histones from Small Quantities of Specific Brain Tissue

artículo científico publicado en 2016

Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release

Histone Methylation by the Kleefstra Syndrome Protein EHMT1 Mediates Homeostatic Synaptic Scaling

artículo científico publicado en 2016

Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems

scientific journal article

IP(3)-mediated Ca(2+) signals in human neuroblastoma SH-SY5Y cells with exogenous overexpression of type 3 IP(3) receptor.

artículo científico publicado en 2002

Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders

artículo científico publicado en 2021

Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome

artículo científico publicado en 2018

Inhibitory control of the excitatory/inhibitory balance in psychiatric disorders

artículo científico publicado en 2018

Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function.

artículo científico publicado en 2014

Localization and function of a calmodulin-apocalmodulin-binding domain in the N-terminal part of the type 1 inositol 1,4,5-trisphosphate receptor.

artículo científico publicado en 2002

MicroRNA networks direct neuronal development and plasticity.

artículo científico publicado en 2011

MicroRNA-137 Controls AMPA-Receptor-Mediated Transmission and mGluR-Dependent LTD.

artículo científico publicado en 2015

Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition.

artículo científico publicado en 2017

Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling

artículo científico publicado en 2019

Protein tyrosine phosphatase receptor type R is required for Purkinje cell responsiveness in cerebellar long-term depression

artículo científico publicado en 2015

Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse

artículo científico publicado en 2017

PtdIns(4,5)P(2) and phospholipase C-independent Ins(1,4,5)P(3) signals induced by a nitrogen source in nitrogen-starved yeast cells

artículo científico publicado en 2001

Rapid Neuronal Differentiation of Induced Pluripotent Stem Cells for Measuring Network Activity on Micro-electrode Arrays

artículo científico publicado en 2017

Rapid synthesis of the X-linked mental retardation protein OPHN1 mediates mGluR-dependent LTD through interaction with the endocytic machinery.

artículo científico publicado en 2011

Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice

artículo científico publicado en 2013

Reduced Inhibition within Layer IV of Sert Knockout Rat Barrel Cortex is Associated with Faster Sensory Integration.

artículo científico publicado en 2017

Regulation of the phosphorylation of the inositol 1,4,5-trisphosphate receptor by protein kinase C.

artículo científico publicado en 2004

Rho GTPase signaling at the synapse: implications for intellectual disability.

artículo científico

Ryanodine receptors are targeted by anti-apoptotic Bcl-XL involving its BH4 domain and Lys87 from its BH3 domain

artículo científico publicado en 2015

Suramin and disulfonated stilbene derivatives stimulate the Ca2+-induced Ca2+ -release mechanism in A7r5 cells.

artículo científico publicado en 2005

TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function

artículo científico publicado en 2015

The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant.

artículo científico publicado en 2015

The Multifarious Hippocampal Functions of MicroRNA-137.

artículo científico publicado en 2015

The Object Space Task reveals increased expression of cumulative memory in a mouse model of Kleefstra Syndrome

artículo científico publicado en 2020

The Rho-linked mental retardation protein oligophrenin-1 controls synapse maturation and plasticity by stabilizing AMPA receptors

scientific journal article

The X-linked mental retardation protein OPHN1 interacts with Homer1b/c to control spine endocytic zone positioning and expression of synaptic potentiation

artículo científico publicado en 2014

The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective

artículo científico publicado en 2020

The promise of induced pluripotent stem cells for neurodevelopmental disorders

artículo científico publicado en 2017

The role of calmodulin for inositol 1,4,5-trisphosphate receptor function

artículo científico publicado en 2002

The schizophrenia risk gene MIR137 acts as a hippocampal gene network node orchestrating the expression of genes relevant to nervous system development and function.

artículo científico

Unexpected Heterodivalent Recruitment of NOS1AP to nNOS Reveals Multiple Sites for Pharmacological Intervention in Neuronal Disease Models.

artículo científico publicado en 2015

Lista de obras de Nael Nadif Kasri

Basal ryanodine receptor activity suppresses autophagic flux

Binding of IRBIT to the IP3 receptor: determinants and functional effects.

Choices for Induction of Pluripotency: Recent Developments in Human Induced Pluripotent Stem Cell Reprogramming Strategies

EHMT1 regulates Parvalbumin-positive interneuron development and GABAergic input in sensory cortical areas

Endogenously bound calmodulin is essential for the function of the inositol 1,4,5-trisphosphate receptor

Epigenetic Etiology of Intellectual Disability

Euchromatin histone methyltransferase 1 regulates cortical neuronal network development

Extraction, Identification, and Quantification of Histones from Small Quantities of Specific Brain Tissue

Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release

Histone Methylation by the Kleefstra Syndrome Protein EHMT1 Mediates Homeostatic Synaptic Scaling

Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems

IP(3)-mediated Ca(2+) signals in human neuroblastoma SH-SY5Y cells with exogenous overexpression of type 3 IP(3) receptor.

Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders

Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome

Inhibitory control of the excitatory/inhibitory balance in psychiatric disorders

Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function.

Localization and function of a calmodulin-apocalmodulin-binding domain in the N-terminal part of the type 1 inositol 1,4,5-trisphosphate receptor.

MicroRNA networks direct neuronal development and plasticity.

MicroRNA-137 Controls AMPA-Receptor-Mediated Transmission and mGluR-Dependent LTD.

Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition.

Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling

Protein tyrosine phosphatase receptor type R is required for Purkinje cell responsiveness in cerebellar long-term depression

Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse

PtdIns(4,5)P(2) and phospholipase C-independent Ins(1,4,5)P(3) signals induced by a nitrogen source in nitrogen-starved yeast cells

Rapid Neuronal Differentiation of Induced Pluripotent Stem Cells for Measuring Network Activity on Micro-electrode Arrays

Rapid synthesis of the X-linked mental retardation protein OPHN1 mediates mGluR-dependent LTD through interaction with the endocytic machinery.

Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice

Reduced Inhibition within Layer IV of Sert Knockout Rat Barrel Cortex is Associated with Faster Sensory Integration.

Regulation of the phosphorylation of the inositol 1,4,5-trisphosphate receptor by protein kinase C.

Rho GTPase signaling at the synapse: implications for intellectual disability.

Ryanodine receptors are targeted by anti-apoptotic Bcl-XL involving its BH4 domain and Lys87 from its BH3 domain

Suramin and disulfonated stilbene derivatives stimulate the Ca2+-induced Ca2+ -release mechanism in A7r5 cells.

TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function

The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant.

The Multifarious Hippocampal Functions of MicroRNA-137.

The Object Space Task reveals increased expression of cumulative memory in a mouse model of Kleefstra Syndrome

The Rho-linked mental retardation protein oligophrenin-1 controls synapse maturation and plasticity by stabilizing AMPA receptors

The X-linked mental retardation protein OPHN1 interacts with Homer1b/c to control spine endocytic zone positioning and expression of synaptic potentiation

The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective

The promise of induced pluripotent stem cells for neurodevelopmental disorders

The role of calmodulin for inositol 1,4,5-trisphosphate receptor function

The schizophrenia risk gene MIR137 acts as a hippocampal gene network node orchestrating the expression of genes relevant to nervous system development and function.

Unexpected Heterodivalent Recruitment of NOS1AP to nNOS Reveals Multiple Sites for Pharmacological Intervention in Neuronal Disease Models.