Lista de obras - Rudolf Martini - Dominio Público Uruguay

5th Workshop of the European CMT Consortium, 69th ENMC International Workshop: therapeutic approaches in CMT neuropathies and related disorders 23-25 April 1999, Soestduinen, The Netherlands.

artículo científico publicado en 2000

A key role for gp130 expressed on peripheral sensory nerves in pathological pain.

artículo científico publicado en 2009

Absence of the myelin-associated glycoprotein (MAG) and the neural cell adhesion molecule (N-CAM) interferes with the maintenance, but not with the formation of peripheral myelin

scientific article published on 01 January 1997

Accelerated course of experimental autoimmune encephalomyelitis in PD-1-deficient central nervous system myelin mutants

artículo científico publicado en 2009

Accelerated demyelination of peripheral nerves in mice deficient in connexin 32 and protein zero

artículo científico publicado en 1998

Aging-associated changes in motor axon voltage-gated Na(+) channel function in mice

artículo científico publicado en 2015

Altered expression of ion channel isoforms at the node of Ranvier in P0-deficient myelin mutants

artículo científico publicado en 2004

Animal models for inherited peripheral neuropathies.

artículo científico publicado en 1997

Antibodies to the mammalian adhesion molecule J1/tenascin and its carbohydrate epitope L2/HNK-1 label the receptor lymph cavities of insect sensilla

artículo científico publicado en 1989

Attenuated demyelination in the absence of the macrophage-restricted adhesion molecule sialoadhesin (Siglec-1) in mice heterozygously deficient in P0.

artículo científico publicado en 2006

Attenuation of MCP-1/CCL2 expression ameliorates neuropathy in a mouse model for Charcot-Marie-Tooth 1X

artículo científico publicado en 2010

Bone marrow transfer from wild-type mice reverts the beneficial effect of genetically mediated immune deficiency in myelin mutants.

artículo científico publicado en 2001

CNTF is a major protective factor in demyelinating CNS disease: A neurotrophic cytokine as modulator in neuroinflammation

artículo científico publicado en 2002

CSF-1-activated macrophages are target-directed and essential mediators of Schwann cell dedifferentiation and dysfunction in Cx32-deficient mice

artículo científico publicado en 2015

Caspr1/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies.

artículo científico publicado en 2001

Cell degeneration during early development of hymenopteran olfactory sensilla

artículo científico publicado en 1983

Cell-Surface and Secreted Isoforms of CSF-1 Exert Opposing Roles in Macrophage-Mediated Neural Damage in Cx32-Deficient Mice.

artículo científico publicado en 2016

Changes in expression of mRNA specific for cell adhesion molecules (L1 and NCAM) in the transected peripheral nerve of the adult rat

artículo científico publicado en 1990

Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1)

scientific journal article

Clonal expansions of pathogenic CD8+ effector cells in the CNS of myelin mutant mice

artículo científico publicado en 2007

Colony-stimulating factor-1 mediates macrophage-related neural damage in a model for Charcot–Marie–Tooth disease type 1X ⬇️

artículo científico publicado el 16 de noviembre de 2011

Complex expression pattern of tenascin during innervation of the posterior limb buds of the developing chicken

artículo científico publicado en 1991

Crucial role for the myelin-associated glycoprotein in the maintenance of axon-myelin integrity

scientific article published on 01 March 1995

Cytochalasin D disrupts the restricted localization of N-CAM, but not of L1, at sites of Schwann cell-neurite and Schwann cell-Schwann cell contact in culture

artículo científico publicado en 1998

Disruption of the gene for the myelin-associated glycoprotein improves axonal regrowth along myelin in C57BL/Wlds mice.

artículo científico publicado en 1996

Disruption of the mouse L1 gene leads to malformations of the nervous system ⬇️

artículo científico publicado el 1 de noviembre de 1997

Ectopic T-cell specificity and absence of perforin and granzyme B alleviate neural damage in oligodendrocyte mutant mice

artículo científico publicado en 2009

Effective gene transfer of lacZ and P0 into Schwann cells of P0-deficient mice

article

Endogenous antibodies contribute to macrophage-mediated demyelination in a mouse model for CMT1B.

artículo científico publicado en 2015

Enhanced expression of the extracellular matrix molecule J1/tenascin in the regenerating adult mouse sciatic nerve ⬇️

artículo científico publicado el 1 de agosto de 1990

Evidence for macrophage-mediated myelin disruption in an animal model for Charcot-Marie-Tooth neuropathy type 1A.

artículo científico publicado en 2005

Expression of J1/tenascin in the crypt-villus unit of adult mouse small intestine: implications for its role in epithelial cell shedding ⬇️

artículo científico publicado el 1 de junio de 1990

Expression of carbohydrate epitopes L2/HNK-1 and L3 in the larva and imago of Drosophila melanogaster and Calliphora vicina.

artículo científico publicado en 1991

Expression of the adhesion molecules L1, N-CAM and J1/tenascin during development of the murine small intestine

artículo científico publicado en 1990

Fine structure and development of the large sensilla basiconica on the antennae of sphecid wasps

scientific article published on 01 January 1986

Formation and maintenance of the myelin sheath in the peripheral nerve: roles of cell adhesion molecules and the gap junction protein connexin 32.

artículo científico publicado en 1998

Functional abnormalities in P0-deficient mice resemble human hereditary neuropathies linked to P0 gene mutations

artículo científico publicado en 1996

Functions of the L2/HNK-1 carbohydrate in the nervous system.

artículo científico publicado en 1995

Glycans and the modulation of neural-recognition molecule function.

artículo científico publicado en 1995

Heterozygous P0 deficiency protects mice from vincristine-induced polyneuropathy

scientific article published on 01 July 2006

Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

scientific article published on 01 November 1995

Immune cells contribute to myelin degeneration and axonopathic changes in mice overexpressing proteolipid protein in oligodendrocytes

artículo científico publicado en 2006

Immune cells perturb axons and impair neuronal survival in a mouse model of infantile neuronal ceroid lipofuscinosis.

artículo científico publicado en 2013

Immune deficiency in mouse models for inherited peripheral neuropathies leads to improved myelin maintenance

artículo científico publicado en 2000

Immunocytochemical localization of the L1 and N-CAM cell adhesion molecules and their shared carbohydrate epitope L2/HNK-1 in the developing and differentiated gustatory papillae of the mouse tongue

artículo científico publicado el 1 de enero de 1992

Immunocytochemical localization of the neural cell adhesion molecules L1, N-CAM, and J1 in Pacinian corpuscles of the mouse during development, in the adult and during regeneration

artículo científico publicado en 1989

Immunocytological localization of the major peripheral nervous system glycoprotein P0 and the L2/HNK-1 and L3 carbohydrate structures in developing and adult mouse sciatic nerve

artículo científico publicado en 1988

Immunological evidence that the neural adhesion molecule L1 is expressed in fish brain and optic nerve: possible association with optic nerve regeneration

artículo científico publicado en 1990

Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage

scientific article published on 01 September 1996

Impaired sensory function in heterozygous P0 knockout mice is associated with nodal changes in sensory nerves

artículo científico publicado en 2002

Increase of MCP-1 (CCL2) in myelin mutant Schwann cells is mediated by MEK-ERK signaling pathway.

artículo científico publicado en 2008

Inherited demyelinating neuropathies: from gene to disease

scientific article published on 01 October 1998

Interactions between Schwann cells and macrophages in injury and inherited demyelinating disease

artículo científico publicado en 2008

Introduction to myelin formation and maintenance ⬇️

artículo científico publicado el 1 de junio de 1998

Lack of evidence for a pathogenic role of T-lymphocytes in an animal model for Charcot-Marie-Tooth disease 1A.

artículo científico publicado en 2010

Localization and functional roles of PMP22 in peripheral nerves of P0-deficient mice

artículo científico publicado en 1999

Long-lasting significant functional improvement in chronic severe spinal cord injury following scar resection and polyethylene glycol implantation

artículo científico publicado en 2014

MAG-deficient Schwann cells myelinate dorsal root ganglion neurons in culture

scientific article published on 01 March 1998

MCP-1/CCL2 modifies axon properties in a PMP22-overexpressing mouse model for Charcot-Marie-tooth 1A neuropathy.

artículo científico publicado en 2010

Macrophage colony stimulating factor is a crucial factor for the intrinsic macrophage response in mice heterozygously deficient for the myelin protein P0.

artículo científico publicado en 2006

Macrophage-related demyelination in peripheral nerves of mice deficient in the gap junction protein connexin 32.

artículo científico publicado en 2002

Mice deficient for the myelin-associated glycoprotein show subtle abnormalities in myelin.

artículo científico publicado en 1994

Mice doubly deficient in the genes for P0 and myelin basic protein show that both proteins contribute to the formation of the major dense line in peripheral nerve myelin

scientific article published on 01 June 1995

Monocyte chemoattractant protein-1 is a pathogenic component in a model for a hereditary peripheral neuropathy.

artículo científico publicado en 2008

Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons

artículo científico publicado en 1992

Mutation of the TBCE gene causes disturbance of microtubules in the auditory nerve and cochlear outer hair cell degeneration accompanied by progressive hearing loss in the pmn/pmn mouse.

artículo científico publicado en 2013

Myelin and macrophages in the PNS: An intimate relationship in trauma and disease.

artículo científico publicado en 2015

Myelin formation by Schwann cells in the absence of beta4 integrin.

artículo científico publicado en 1999

Myelin-associated glycoprotein is not detectable in perikaryal myelin of spiral ganglion neurons of adult mice

artículo científico publicado en 1994

Na(v)1.8 channelopathy in mutant mice deficient for myelin protein zero is detrimental to motor axons

artículo científico publicado en 2010

Neuregulin-1 alleviates Charcot-Marie-Tooth disease in rats

artículo científico publicado en 2014

Neuroinflammation as modifier of genetically caused neurological disorders of the central nervous system: Understanding pathogenesis and chances for treatment.

artículo científico publicado en 2017

Neuroinflammation by cytotoxic T-lymphocytes impairs retrograde axonal transport in an oligodendrocyte mutant mouse

artículo científico publicado en 2012

Neuroinflammation in the peripheral nerve: Cause, modulator, or bystander in peripheral neuropathies?

artículo científico publicado en 2016

Neuromyotonia in mice with hereditary myelinopathies

scientific article published on 01 May 2000

Neuroprotective effect of the immune system in a mouse model of severe dysmyelinating hereditary neuropathy: enhanced axonal degeneration following disruption of the RAG-1 gene

artículo científico publicado en 2005

Non-invasive assessment of retinal alterations in mouse models of infantile and juvenile neuronal ceroid lipofuscinosis by spectral domain optical coherence tomography

artículo científico publicado en 2014

Nonuniform molecular features of myelinating Schwann cells in models for CMT1: distinct disease patterns are associated with NCAM and c-Jun upregulation

artículo científico publicado en 2014

Origin of CD11b+ macrophage-like cells in the CNS of PLP-overexpressing mice: low influx of haematogenous macrophages and unchanged blood-brain-barrier in the optic nerve.

artículo científico publicado en 2008

Origin of pathogenic macrophages and endoneurial fibroblast-like cells in an animal model of inherited neuropathy

artículo científico publicado en 2003

P(0) glycoprotein overexpression causes congenital hypomyelination of peripheral nerves

artículo científico publicado en 2000

P0-deficient knockout mice as tools to understand pathomechanisms in Charcot-Marie-Tooth 1B and P0-related Déjérine-Sottas syndrome.

artículo científico publicado en 1999

PD-1 regulates neural damage in oligodendroglia-induced inflammation

artículo científico publicado en 2009

Pathology of a mouse mutation in peripheral myelin protein P0 is characteristic of a severe and early onset form of human Charcot-Marie-Tooth type 1B disorder

artículo científico publicado en 2004

Preserved myelin integrity and reduced axonopathy in connexin32-deficient mice lacking the recombination activating gene-1.

artículo científico publicado en 2003

Progression of motor axon dysfunction and ectopic Nav1.8 expression in a mouse model of Charcot-Marie-Tooth disease 1B.

artículo científico publicado en 2016

Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies

artículo científico publicado en 1995

Proteolipid protein modulates preservation of peripheral axons and premature death when myelin protein zero is lacking

artículo científico publicado en 2015

Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies

scientific journal article

Restricted localization of L1 and N-CAM at sites of contact between Schwann cells and neurites in culture

scientific article published on 01 January 1994

Sialoadhesin deficiency ameliorates myelin degeneration and axonopathic changes in the CNS of PLP overexpressing mice

artículo científico publicado en 2006

Sialoadhesin promotes neuroinflammation-related disease progression in two mouse models of CLN disease.

artículo científico publicado en 2016

Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32

artículo científico publicado en 1997

Subtle roles of neural cell adhesion molecule and myelin-associated glycoprotein during Schwann cell spiralling in P0-deficient mice

scientific article published on 01 September 1999

Tacrolimus (FK506) causes disease aggravation in models for inherited peripheral myelinopathies

artículo científico publicado en 2008

Targeting microglia attenuates neuroinflammation-related neural damage in mice carrying human PLP1 mutations

artículo científico publicado en 2018

Targeting the colony stimulating factor 1 receptor alleviates two forms of Charcot-Marie-Tooth disease in mice

artículo científico publicado en 2015

Tenascin-C expression during wallerian degeneration in C57BL/Wlds mice: possible implications for axonal regeneration

artículo científico publicado en 1995

The L2/HNK-1 Carbohydrate Epitope is Involved in the Preferential Outgrowth of Motor Neurons on Ventral Roots and Motor Nerves

artículo científico publicado en 1992

The L2/HNK-1 carbohydrate is carried by the myelin associated glycoprotein and sulphated glucuronyl glycolipids in muscle but not cutaneous nerves of adult mice

scientific article published on 01 December 1994

The L2/HNK-1 carbohydrate is preferentially expressed by previously motor axon-associated Schwann cells in reinnervated peripheral nerves

artículo científico publicado en 1994

The Wlds mutation delays robust loss of motor and sensory axons in a genetic model for myelin-related axonopathy.

artículo científico publicado en 2003

The co-inhibitory molecule PD-1 modulates disease severity in a model for an inherited, demyelinating neuropathy

artículo científico publicado en 2008

The effect of myelinating Schwann cells on axons.

artículo científico publicado en 2001

The extracellular matrix molecule, tenascin is associated with adult rat CNS axons regenerating into peripheral nerve grafts.

artículo científico publicado en 1994

Triple knock-out of CNTF, LIF, and CT-1 defines cooperative and distinct roles of these neurotrophic factors for motoneuron maintenance and function

scientific journal article

Visualization of degenerating axons in a dysmyelinating mouse mutant with axonal loss

artículo científico publicado en 2007

[The role of the immune system in hereditary demyelinating neuropathies]

artículo científico publicado en 2005

Lista de obras de Rudolf Martini

5th Workshop of the European CMT Consortium, 69th ENMC International Workshop: therapeutic approaches in CMT neuropathies and related disorders 23-25 April 1999, Soestduinen, The Netherlands.

A key role for gp130 expressed on peripheral sensory nerves in pathological pain.

Absence of the myelin-associated glycoprotein (MAG) and the neural cell adhesion molecule (N-CAM) interferes with the maintenance, but not with the formation of peripheral myelin

Accelerated course of experimental autoimmune encephalomyelitis in PD-1-deficient central nervous system myelin mutants

Accelerated demyelination of peripheral nerves in mice deficient in connexin 32 and protein zero

Aging-associated changes in motor axon voltage-gated Na(+) channel function in mice

Altered expression of ion channel isoforms at the node of Ranvier in P0-deficient myelin mutants

Animal models for inherited peripheral neuropathies.

Antibodies to the mammalian adhesion molecule J1/tenascin and its carbohydrate epitope L2/HNK-1 label the receptor lymph cavities of insect sensilla

Attenuated demyelination in the absence of the macrophage-restricted adhesion molecule sialoadhesin (Siglec-1) in mice heterozygously deficient in P0.

Attenuation of MCP-1/CCL2 expression ameliorates neuropathy in a mouse model for Charcot-Marie-Tooth 1X

Bone marrow transfer from wild-type mice reverts the beneficial effect of genetically mediated immune deficiency in myelin mutants.

CNTF is a major protective factor in demyelinating CNS disease: A neurotrophic cytokine as modulator in neuroinflammation

CSF-1-activated macrophages are target-directed and essential mediators of Schwann cell dedifferentiation and dysfunction in Cx32-deficient mice

Caspr1/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies.

Cell degeneration during early development of hymenopteran olfactory sensilla

Cell-Surface and Secreted Isoforms of CSF-1 Exert Opposing Roles in Macrophage-Mediated Neural Damage in Cx32-Deficient Mice.

Changes in expression of mRNA specific for cell adhesion molecules (L1 and NCAM) in the transected peripheral nerve of the adult rat

Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1)

Clonal expansions of pathogenic CD8+ effector cells in the CNS of myelin mutant mice

Colony-stimulating factor-1 mediates macrophage-related neural damage in a model for Charcot–Marie–Tooth disease type 1X ⬇️

Complex expression pattern of tenascin during innervation of the posterior limb buds of the developing chicken

Crucial role for the myelin-associated glycoprotein in the maintenance of axon-myelin integrity

Cytochalasin D disrupts the restricted localization of N-CAM, but not of L1, at sites of Schwann cell-neurite and Schwann cell-Schwann cell contact in culture

Disruption of the gene for the myelin-associated glycoprotein improves axonal regrowth along myelin in C57BL/Wlds mice.

Disruption of the mouse L1 gene leads to malformations of the nervous system ⬇️

Ectopic T-cell specificity and absence of perforin and granzyme B alleviate neural damage in oligodendrocyte mutant mice

Effective gene transfer of lacZ and P0 into Schwann cells of P0-deficient mice

Endogenous antibodies contribute to macrophage-mediated demyelination in a mouse model for CMT1B.

Enhanced expression of the extracellular matrix molecule J1/tenascin in the regenerating adult mouse sciatic nerve ⬇️

Evidence for macrophage-mediated myelin disruption in an animal model for Charcot-Marie-Tooth neuropathy type 1A.

Expression of J1/tenascin in the crypt-villus unit of adult mouse small intestine: implications for its role in epithelial cell shedding ⬇️

Expression of carbohydrate epitopes L2/HNK-1 and L3 in the larva and imago of Drosophila melanogaster and Calliphora vicina.

Expression of the adhesion molecules L1, N-CAM and J1/tenascin during development of the murine small intestine

Fine structure and development of the large sensilla basiconica on the antennae of sphecid wasps

Formation and maintenance of the myelin sheath in the peripheral nerve: roles of cell adhesion molecules and the gap junction protein connexin 32.

Functional abnormalities in P0-deficient mice resemble human hereditary neuropathies linked to P0 gene mutations

Functions of the L2/HNK-1 carbohydrate in the nervous system.

Glycans and the modulation of neural-recognition molecule function.

Heterozygous P0 deficiency protects mice from vincristine-induced polyneuropathy

Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

Immune cells contribute to myelin degeneration and axonopathic changes in mice overexpressing proteolipid protein in oligodendrocytes

Immune cells perturb axons and impair neuronal survival in a mouse model of infantile neuronal ceroid lipofuscinosis.

Immune deficiency in mouse models for inherited peripheral neuropathies leads to improved myelin maintenance

Immunocytochemical localization of the L1 and N-CAM cell adhesion molecules and their shared carbohydrate epitope L2/HNK-1 in the developing and differentiated gustatory papillae of the mouse tongue

Immunocytochemical localization of the neural cell adhesion molecules L1, N-CAM, and J1 in Pacinian corpuscles of the mouse during development, in the adult and during regeneration

Immunocytological localization of the major peripheral nervous system glycoprotein P0 and the L2/HNK-1 and L3 carbohydrate structures in developing and adult mouse sciatic nerve

Immunological evidence that the neural adhesion molecule L1 is expressed in fish brain and optic nerve: possible association with optic nerve regeneration

Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage

Impaired sensory function in heterozygous P0 knockout mice is associated with nodal changes in sensory nerves

Increase of MCP-1 (CCL2) in myelin mutant Schwann cells is mediated by MEK-ERK signaling pathway.

Inherited demyelinating neuropathies: from gene to disease

Interactions between Schwann cells and macrophages in injury and inherited demyelinating disease

Introduction to myelin formation and maintenance ⬇️

Lack of evidence for a pathogenic role of T-lymphocytes in an animal model for Charcot-Marie-Tooth disease 1A.

Localization and functional roles of PMP22 in peripheral nerves of P0-deficient mice

Long-lasting significant functional improvement in chronic severe spinal cord injury following scar resection and polyethylene glycol implantation

MAG-deficient Schwann cells myelinate dorsal root ganglion neurons in culture

MCP-1/CCL2 modifies axon properties in a PMP22-overexpressing mouse model for Charcot-Marie-tooth 1A neuropathy.

Macrophage colony stimulating factor is a crucial factor for the intrinsic macrophage response in mice heterozygously deficient for the myelin protein P0.

Macrophage-related demyelination in peripheral nerves of mice deficient in the gap junction protein connexin 32.

Mice deficient for the myelin-associated glycoprotein show subtle abnormalities in myelin.

Mice doubly deficient in the genes for P0 and myelin basic protein show that both proteins contribute to the formation of the major dense line in peripheral nerve myelin

Monocyte chemoattractant protein-1 is a pathogenic component in a model for a hereditary peripheral neuropathy.

Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons

Mutation of the TBCE gene causes disturbance of microtubules in the auditory nerve and cochlear outer hair cell degeneration accompanied by progressive hearing loss in the pmn/pmn mouse.

Myelin and macrophages in the PNS: An intimate relationship in trauma and disease.

Myelin formation by Schwann cells in the absence of beta4 integrin.

Myelin-associated glycoprotein is not detectable in perikaryal myelin of spiral ganglion neurons of adult mice

Na(v)1.8 channelopathy in mutant mice deficient for myelin protein zero is detrimental to motor axons

Neuregulin-1 alleviates Charcot-Marie-Tooth disease in rats

Neuroinflammation as modifier of genetically caused neurological disorders of the central nervous system: Understanding pathogenesis and chances for treatment.

Neuroinflammation by cytotoxic T-lymphocytes impairs retrograde axonal transport in an oligodendrocyte mutant mouse

Neuroinflammation in the peripheral nerve: Cause, modulator, or bystander in peripheral neuropathies?

Neuromyotonia in mice with hereditary myelinopathies

Neuroprotective effect of the immune system in a mouse model of severe dysmyelinating hereditary neuropathy: enhanced axonal degeneration following disruption of the RAG-1 gene

Non-invasive assessment of retinal alterations in mouse models of infantile and juvenile neuronal ceroid lipofuscinosis by spectral domain optical coherence tomography

Nonuniform molecular features of myelinating Schwann cells in models for CMT1: distinct disease patterns are associated with NCAM and c-Jun upregulation

Origin of CD11b+ macrophage-like cells in the CNS of PLP-overexpressing mice: low influx of haematogenous macrophages and unchanged blood-brain-barrier in the optic nerve.