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Pyk2 modulates hippocampal excitatory synapses and contributes to cognitive deficits in a Huntington's disease model

Nature communications, 2017-05, Vol.8 (1), p.15592-15592, Article 15592

2017

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PTK2B/Pyk2 overexpression improves a mouse model of Alzheimer's disease

Experimental neurology, 2018-09, Vol.307, p.62-73

2018

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Separate fusion of outer and inner mitochondrial membranes

EMBO reports, 2005-09, Vol.6 (9), p.853-859

2005

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Conditional BDNF Delivery from Astrocytes Rescues Memory Deficits, Spine Density, and Synaptic Properties in the 5xFAD Mouse Model of Alzheimer Disease

The Journal of neuroscience, 2019-03, Vol.39 (13), p.2441-2458

2019

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Pyk2 Regulates MAMs and Mitochondrial Dynamics in Hippocampal Neurons

Cells (Basel, Switzerland), 2022-03, Vol.11 (5), p.842

2022

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Connexin43 and connexin47 alterations after neural precursor cells transplantation in experimental autoimmune encephalomyelitis

Glia, 2015-10, Vol.63 (10), p.1772-1783

2015

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ALK (Anaplastic Lymphoma Kinase) expression in DRG neurons and its involvement in neuron-Schwann cells interaction

The European journal of neuroscience, 2009-01, Vol.29 (2), p.275-286

2009

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Microtubule-dependent transport and organization of sarcomeric myosin during skeletal muscle differentiation

The EMBO journal, 2005-11, Vol.24 (21), p.3781-3792

2005

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A human dynein heavy chain mutation impacts cortical progenitor cells causing developmental defects, reduced brain size and altered brain architecture

Neurobiology of disease, 2023-05, Vol.180, p.106085-106085, Article 106085

2023

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hVFL3/CCDC61 is a component of mother centriole subdistal appendages required for centrosome cohesion and positioning

Biology of the cell, 2020-01, Vol.112 (1), p.22-37

2020

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Spinal muscular atrophy: Recent advances and future prospects

Muscle & nerve, 2002-07, Vol.26 (1), p.4-13

2002

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Differential impacts of Cntnap2 heterozygosity and Cntnap2 null homozygosity on axon and myelinated fiber development in mouse

Frontiers in neuroscience, 2023-01, Vol.17, p.1100121-1100121

2023

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Protein 4.1B contributes to the organization of peripheral myelinated axons

PloS one, 2011-09, Vol.6 (9), p.e25043-e25043

2011

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Nodes of ranvier and paranodes in chronic acquired neuropathies

PloS one, 2011-01, Vol.6 (1), p.e14533-e14533

2011

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Organelle and cellular abnormalities associated with hippocampal heterotopia in neonatal doublecortin knockout mice

PloS one, 2013-09, Vol.8 (9), p.e72622-e72622

2013

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Riluzole attenuates spinal muscular atrophy disease progression in a mouse model

Muscle & nerve, 2003-10, Vol.28 (4), p.432-437

2003

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Tumor Suppressor Schwannomin/Merlin Is Critical for the Organization of Schwann Cell Contacts in Peripheral Nerves

The Journal of neuroscience, 2008-10, Vol.28 (42), p.10472-10481

2008

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Intact Satellite Cells Lead to Remarkable Protection against Smn Gene Defect in Differentiated Skeletal Muscle

The Journal of cell biology, 2003-05, Vol.161 (3), p.571-582

2003

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Localized deposition of M-cadherin in the glomeruli of the granular layer during the postnatal development of mouse cerebellum

Journal of comparative neurology (1911), 1997-02, Vol.378 (2), p.180-195

1997

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Neurofilament accumulation at the motor endplate and lack of axonal sprouting in a spinal muscular atrophy mouse model

Human molecular genetics, 2002-06, Vol.11 (12), p.1439-1447

2002

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Neuromuscular expression of the BTB/POZ and zinc finger protein myoneurin

Muscle & nerve, 2004-01, Vol.29 (1), p.59-65

2004

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Ultrastructural Evidence for Oxytocin and Oxytocin Receptor at the Spinal Dorsal Horn: Mechanism of Nociception Modulation

Neuroscience, 2021-11, Vol.475, p.117-126

2021

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The molecular bases of spinal muscular atrophy

Current Opinion in Genetics & Development, 2002-06, Vol.12 (3), p.294-298

2002

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Deletion of Murine SMN Exon 7 Directed to Skeletal Muscle Leads to Severe Muscular Dystrophy

The Journal of cell biology, 2001-03, Vol.152 (5), p.1107-1114

2001

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Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophy

Human molecular genetics, 2000-03, Vol.9 (5), p.849-858

2000

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Pyk2 modulates hippocampal excitatory synapses and contributes to cognitive deficits in a Huntington's disease model

PTK2B/Pyk2 overexpression improves a mouse model of Alzheimer's disease

Separate fusion of outer and inner mitochondrial membranes

Conditional BDNF Delivery from Astrocytes Rescues Memory Deficits, Spine Density, and Synaptic Properties in the 5xFAD Mouse Model of Alzheimer Disease

Pyk2 Regulates MAMs and Mitochondrial Dynamics in Hippocampal Neurons

Connexin43 and connexin47 alterations after neural precursor cells transplantation in experimental autoimmune encephalomyelitis

ALK (Anaplastic Lymphoma Kinase) expression in DRG neurons and its involvement in neuron-Schwann cells interaction

Microtubule-dependent transport and organization of sarcomeric myosin during skeletal muscle differentiation

A human dynein heavy chain mutation impacts cortical progenitor cells causing developmental defects, reduced brain size and altered brain architecture

hVFL3/CCDC61 is a component of mother centriole subdistal appendages required for centrosome cohesion and positioning

Spinal muscular atrophy: Recent advances and future prospects

Differential impacts of Cntnap2 heterozygosity and Cntnap2 null homozygosity on axon and myelinated fiber development in mouse

Protein 4.1B contributes to the organization of peripheral myelinated axons

Nodes of ranvier and paranodes in chronic acquired neuropathies

Organelle and cellular abnormalities associated with hippocampal heterotopia in neonatal doublecortin knockout mice

Riluzole attenuates spinal muscular atrophy disease progression in a mouse model

Tumor Suppressor Schwannomin/Merlin Is Critical for the Organization of Schwann Cell Contacts in Peripheral Nerves

Intact Satellite Cells Lead to Remarkable Protection against Smn Gene Defect in Differentiated Skeletal Muscle

Localized deposition of M-cadherin in the glomeruli of the granular layer during the postnatal development of mouse cerebellum

Neurofilament accumulation at the motor endplate and lack of axonal sprouting in a spinal muscular atrophy mouse model

Neuromuscular expression of the BTB/POZ and zinc finger protein myoneurin

Ultrastructural Evidence for Oxytocin and Oxytocin Receptor at the Spinal Dorsal Horn: Mechanism of Nociception Modulation

The molecular bases of spinal muscular atrophy

Deletion of Murine SMN Exon 7 Directed to Skeletal Muscle Leads to Severe Muscular Dystrophy

Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophy

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