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Association of Calnexin with Mutant Peripheral Myelin Protein-22 ex vivo: A Basis for "Gain-of-Function" ER Diseases

Proceedings of the National Academy of Sciences - PNAS, 2002-07, Vol.99 (15), p.9852-9857

2002

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Characterization of a Novel Peripheral Nervous System Myelin Protein (PMP-22/SR13)

The Journal of cell biology, 1992-04, Vol.117 (1), p.225-238

1992

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Surgical treatment of epilepsy in tuberous sclerosis: strategies and results in 18 patients

Neurology, 1998-11, Vol.51 (5), p.1263

1998

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Biology and genetics of hereditary motor and sensory neuropathies

Annual review of neuroscience, 1995-01, Vol.18 (1), p.45-75

1995

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A Leucine-to-Proline Mutation in the Putative First Transmembrane Domain of the 22-kDa Peripheral Myelin Protein in the Trembler-J Mouse

Proceedings of the National Academy of Sciences - PNAS, 1992-05, Vol.89 (10), p.4382-4386

1992

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Peripheral myelin protein 22: Facts and hypotheses

Journal of neuroscience research, 1995-02, Vol.40 (2), p.145-151

1995

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Curcumin Treatment Abrogates Endoplasmic Reticulum Retention and Aggregation-Induced Apoptosis Associated with Neuropathy-Causing Myelin Protein Zero–Truncating Mutants

American journal of human genetics, 2005-11, Vol.77 (5), p.841-850

2005

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Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene

The New England journal of medicine, 1993-07, Vol.329 (2), p.96-101

1993

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Trigeminal nerve hypertrophy in chronic inflammatory demyelinating polyradiculoneuropathy

Neurology, 1998-11, Vol.51 (5), p.1459-1462

1998

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Intracerebral Adenovirus-mediated p53 Tumor Suppressor Gene Therapy for Experimental Human Glioma

Clinical cancer research, 1999-03, Vol.5 (3), p.637-642

1999

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Detection and processing of peripheral myelin protein PMP22 in cultured Schwann cells

The Journal of biological chemistry, 1993-05, Vol.268 (14), p.10372-10379

1993

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Molecular anatomy and genetics of myelin proteins in the peripheral nervous system

Journal of anatomy, 1995-06, Vol.186 ( Pt 3) (Pt 3), p.483-494

1995

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Meningeal melanocytoma. Report of a case and a historical comparison

Journal of neurosurgery, 1998-01, Vol.88 (1), p.116-121

1998

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Progress in the molecular understanding of hereditary peripheral neuropathies reveals new insights into the biology of the peripheral nervous system

Trends in neurosciences (Regular ed.), 1993-02, Vol.16 (2), p.50-56

1993

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Human peripheral myelin protein-22 carries the L2/HNK-1 carbohydrate adhesion epitope

Journal of neurochemistry, 1993-11, Vol.61 (5), p.1961-1964

1993

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Nerve Injury Stimulates the Secretion of Apolipoprotein E by Nonneuronal Cells

Proceedings of the National Academy of Sciences - PNAS, 1986-02, Vol.83 (4), p.1130-1134

1986

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Phenotypic Differences between Peripheral Myelin Protein-22 (PMP22) and Myelin Protein Zero (P0) Mutations Associated with Charcot-Marie-Tooth-Related Diseases

Journal of neuropathology and experimental neurology, 2003-07, Vol.62 (7), p.751-764

2003

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Suppression of Rac activity induces apoptosis of human glioma cells but not normal human astrocytes

Cancer research (Chicago, Ill.), 2002-04, Vol.62 (7), p.2131-2140

2002

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Ultrastructural Distribution of PMP22 in Charcot-Marie-Tooth Disease Type 1A

Journal of neuropathology and experimental neurology, 1996-03, Vol.55 (3), p.290-299

1996

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Temporal expression pattern of peripheral myelin protein 22 during in vivo and in vitro myelination

Glia, 1999-02, Vol.25 (4), p.358-369

1999

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PMP22 Carrying the Trembler or Trembler-J Mutation Is Intracellularly Retained in Myelinating Schwann Cells

Neurobiology of disease, 2000-12, Vol.7 (6), p.561-573

2000

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Curcumin facilitates a transitory cellular stress response in Trembler-J mice

Human molecular genetics, 2013-12, Vol.22 (23), p.4698-4705

2013

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Trembler mouse carries a point mutation in a myelin gene

Nature (London), 1992-03, Vol.356 (6366), p.241-244

1992

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Progressive myoclonus epilepsy in young adults with neuropathologic features of Alzheimer's disease

Neurology, 1997-12, Vol.49 (6), p.1732-1733

1997

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Intranidal aneurysms in cerebral arteriovenous malformations: evaluation and endovascular treatment

Radiology, 1992-05, Vol.183 (2), p.355-360

1992

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Association of Calnexin with Mutant Peripheral Myelin Protein-22 ex vivo: A Basis for "Gain-of-Function" ER Diseases

Characterization of a Novel Peripheral Nervous System Myelin Protein (PMP-22/SR13)

Surgical treatment of epilepsy in tuberous sclerosis: strategies and results in 18 patients

Biology and genetics of hereditary motor and sensory neuropathies

A Leucine-to-Proline Mutation in the Putative First Transmembrane Domain of the 22-kDa Peripheral Myelin Protein in the Trembler-J Mouse

Peripheral myelin protein 22: Facts and hypotheses

Curcumin Treatment Abrogates Endoplasmic Reticulum Retention and Aggregation-Induced Apoptosis Associated with Neuropathy-Causing Myelin Protein Zero–Truncating Mutants

Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene

Trigeminal nerve hypertrophy in chronic inflammatory demyelinating polyradiculoneuropathy

Intracerebral Adenovirus-mediated p53 Tumor Suppressor Gene Therapy for Experimental Human Glioma

Detection and processing of peripheral myelin protein PMP22 in cultured Schwann cells

Molecular anatomy and genetics of myelin proteins in the peripheral nervous system

Meningeal melanocytoma. Report of a case and a historical comparison

Progress in the molecular understanding of hereditary peripheral neuropathies reveals new insights into the biology of the peripheral nervous system

Human peripheral myelin protein-22 carries the L2/HNK-1 carbohydrate adhesion epitope

Nerve Injury Stimulates the Secretion of Apolipoprotein E by Nonneuronal Cells

Phenotypic Differences between Peripheral Myelin Protein-22 (PMP22) and Myelin Protein Zero (P0) Mutations Associated with Charcot-Marie-Tooth-Related Diseases

Suppression of Rac activity induces apoptosis of human glioma cells but not normal human astrocytes

Ultrastructural Distribution of PMP22 in Charcot-Marie-Tooth Disease Type 1A

Temporal expression pattern of peripheral myelin protein 22 during in vivo and in vitro myelination

PMP22 Carrying the Trembler or Trembler-J Mutation Is Intracellularly Retained in Myelinating Schwann Cells

Curcumin facilitates a transitory cellular stress response in Trembler-J mice

Trembler mouse carries a point mutation in a myelin gene

Progressive myoclonus epilepsy in young adults with neuropathologic features of Alzheimer's disease

Intranidal aneurysms in cerebral arteriovenous malformations: evaluation and endovascular treatment

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