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Expanded CTG repeats within the DMPK 3' UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy

Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (7), p.2646-2651

2008

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Oral Curcumin Mitigates the Clinical and Neuropathologic Phenotype of the Trembler-J Mouse: A Potential Therapy for Inherited Neuropathy

American journal of human genetics, 2007-09, Vol.81 (3), p.438-453

2007

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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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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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The Texas Immuno-Oncology Biorepository, a statewide biospecimen collection and clinical informatics system to enable longitudinal tumor and immune profiling

Proceedings - Baylor University. Medical Center, 2023, Vol.36 (1), p.1-7

2023

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Molecular Mechanisms, Diagnosis, and Rational Approaches to Management of and Therapy for Charcot-Marie-Tooth Disease and Related Peripheral Neuropathies

Journal of Investigative Medicine, 2003-09, Vol.51 (5), p.261-283

2003

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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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Reprogramming tumor-infiltrating dendritic cells for CD103+ CD8+ mucosal T-cell differentiation and breast cancer rejection

Cancer immunology research, 2014-05, Vol.2 (5), p.487-500

2014

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Characterization of Chronic Bronchopulmonary Pseudomonas aeruginosa Infection in Resistant and Susceptible Inbred Mouse Strains

American journal of respiratory cell and molecular biology, 1999-04, Vol.20 (4), p.710-719

1999

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Progressive Limb Weakness and Sensory Loss in a Young Woman

McGill journal of medicine, 2020-12, Vol.5 (2)

2020

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Upregulation of Hypoxia-Inducible Factor (HIF)-1α and HIF-2α in Leptomeningeal Vascular Malformations of Sturge-Weber Syndrome

Journal of neuropathology and experimental neurology, 2007-01, Vol.66 (1), p.86-97

2007

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A Protein Induced during Nerve Growth (GAP-43) Is a Major Component of Growth-Cone Membranes

Science (American Association for the Advancement of Science), 1986-08, Vol.233 (4765), p.783-786

1986

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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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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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Upregulation of the Endosomal-Lysosomal Pathway in the Trembler-J Neuropathy

The Journal of neuroscience, 1997-06, Vol.17 (11), p.4190-4200

1997

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Signaling pathways mediating axon-Schwann cell interactions

Trends in neurosciences (Regular ed.), 1994-10, Vol.17 (10), p.399-401

1994

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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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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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The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

Nature genetics, 1992-06, Vol.1 (3), p.159-165

1992

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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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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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Rapid Communication: 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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A Myelin Protein is Encoded by the Homologue of a Growth Arrest-Specific Gene

Proceedings of the National Academy of Sciences - PNAS, 1991-08, Vol.88 (16), p.7195-7199

1991

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An 8.5-kb segment of the PMP22 promoter responds to loss of axon signals during Wallerian degeneration, but does not respond to specific axonal signals during nerve regeneration

Journal of neuroscience research, 2005-04, Vol.80 (1), p.37-46

2005

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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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Expanded CTG repeats within the DMPK 3' UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy

Oral Curcumin Mitigates the Clinical and Neuropathologic Phenotype of the Trembler-J Mouse: A Potential Therapy for Inherited Neuropathy

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

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

The Texas Immuno-Oncology Biorepository, a statewide biospecimen collection and clinical informatics system to enable longitudinal tumor and immune profiling

Molecular Mechanisms, Diagnosis, and Rational Approaches to Management of and Therapy for Charcot-Marie-Tooth Disease and Related Peripheral Neuropathies

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

Reprogramming tumor-infiltrating dendritic cells for CD103+ CD8+ mucosal T-cell differentiation and breast cancer rejection

Characterization of Chronic Bronchopulmonary Pseudomonas aeruginosa Infection in Resistant and Susceptible Inbred Mouse Strains

Progressive Limb Weakness and Sensory Loss in a Young Woman

Upregulation of Hypoxia-Inducible Factor (HIF)-1α and HIF-2α in Leptomeningeal Vascular Malformations of Sturge-Weber Syndrome

A Protein Induced during Nerve Growth (GAP-43) Is a Major Component of Growth-Cone Membranes

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

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

Upregulation of the Endosomal-Lysosomal Pathway in the Trembler-J Neuropathy

Signaling pathways mediating axon-Schwann cell interactions

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

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

The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

Trembler mouse carries a point mutation in a myelin gene

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

Rapid Communication: Human Peripheral Myelin Protein‐22 Carries the L2/HNK‐1 Carbohydrate Adhesion Epitope

A Myelin Protein is Encoded by the Homologue of a Growth Arrest-Specific Gene

An 8.5-kb segment of the PMP22 promoter responds to loss of axon signals during Wallerian degeneration, but does not respond to specific axonal signals during nerve regeneration

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

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