X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
pmp22-deficient mice (8) 8
neurosciences (7) 7
animals (5) 5
index medicus (5) 5
mice (5) 5
hereditary neuropathy (4) 4
marie-tooth-disease (4) 4
myelin (4) 4
pressure palsies (4) 4
basal lamina (3) 3
myelin proteins - genetics (3) 3
pmp22 (3) 3
protein 22-deficient mice (3) 3
schwann cells (3) 3
transgenic mice (3) 3
article (2) 2
biomechanics (2) 2
gene expression regulation - genetics (2) 2
mice, knockout (2) 2
mice, transgenic (2) 2
myelin proteins - biosynthesis (2) 2
myelin proteins - metabolism (2) 2
myelin sheath - metabolism (2) 2
nerve fibers, myelinated - metabolism (2) 2
nerve fibers, myelinated - ultrastructure (2) 2
nervous-system (2) 2
neuropathy (2) 2
peripheral nerves - metabolism (2) 2
peripheral nervous system diseases - genetics (2) 2
peripheral nervous system diseases - pathology (2) 2
schwann cells - metabolism (2) 2
schwann-cell differentiation (2) 2
schwann-cells (2) 2
tomaculous neuropathy (2) 2
abnormalities (1) 1
absence (1) 1
action potentials - physiology (1) 1
adult (1) 1
age factors (1) 1
animal models (1) 1
animals, newborn (1) 1
anterior root fibers (1) 1
apolipoprotein-e (1) 1
apoptosis (1) 1
arrest-specific gene (1) 1
atomic-force microscopy (1) 1
axonal constriction (1) 1
axons - classification (1) 1
axons - physiology (1) 1
axons - transplantation (1) 1
axons - ultrastructure (1) 1
basement membrane - metabolism (1) 1
basement membrane - physiology (1) 1
beta subunit (1) 1
beta-galactosidase - genetics (1) 1
beta-galactosidase - metabolism (1) 1
biochemistry & molecular biology (1) 1
biophysics (1) 1
case-control studies (1) 1
cell count (1) 1
cell cycle (1) 1
cell differentiation - genetics (1) 1
cell size - physiology (1) 1
charcot-marie-tooth disease (1) 1
charcot-marie-tooth disease - physiopathology (1) 1
cholesterol synthesis (1) 1
clinical neurology (1) 1
cmt1a (1) 1
colon-carcinoma cells (1) 1
compression (1) 1
conduction block (1) 1
confocal microscopy (1) 1
cytoskeleton (1) 1
demyelinating neuropathies (1) 1
demyelinating peripheral neuropathy (1) 1
differentiation (1) 1
disease models, animal (1) 1
disease type 1a (1) 1
distinct functions (1) 1
e2f (1) 1
early myelination (1) 1
electric stimulation - methods (1) 1
expression analysis (1) 1
extracellular-matrix (1) 1
female (1) 1
fetus (1) 1
gene (1) 1
gene dosage (1) 1
gene duplication (1) 1
gene expression regulation, developmental - physiology (1) 1
genes, cdc - physiology (1) 1
genes, regulator - physiology (1) 1
genes, reporter - physiology (1) 1
growth arrest (1) 1
heat shock proteins 1a and 1b (1) 1
hereditary motor (1) 1
hereditary neuropathy with liability to pressure palsies (1) 1
hnpp (1) 1
humans (1) 1
inherited neuropathies (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


JOURNAL OF NEUROCHEMISTRY, ISSN 0022-3042, 05/2018, Volume 145, Issue 3, pp. 245 - 257
Peripheral myelin protein 22 (PMP22) is a component of compact myelin in the peripheral nervous system. The amount of PMP22 in myelin is tightly regulated, and... 
myelin | MYELIN PROTEIN | RANVIER | peripheral nerve | PERIPHERAL NERVOUS-SYSTEM | BIOCHEMISTRY & MOLECULAR BIOLOGY | HNPP | Schwann cells | Pmp22 | TOMACULOUS NEUROPATHY | PMP22-DEFICIENT MICE | PROTEIN 22-DEFICIENT MICE | NEUROSCIENCES | SCIATIC-NERVE | Integrin beta 4 | SCHWANN-CELLS | BETA SUBUNIT | DISEASE TYPE 1A
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 01/2010, Volume 30, Issue 2, pp. 600 - 608
Patients with PMP22 deficiency present with focal sensory and motor deficits when peripheral nerves are stressed by mechanical force. It has been hypothesized... 
PERIPHERAL-NERVES | DEMYELINATING NEUROPATHIES | SODIUM-CHANNELS | TOMACULOUS NEUROPATHY | HEREDITARY NEUROPATHY | PNEUMATIC TOURNIQUET | PRESSURE PALSIES | PMP22-DEFICIENT MICE | PROTEIN 22-DEFICIENT MICE | NEUROSCIENCES | MYELIN-ASSOCIATED GLYCOPROTEIN | Peripheral Nerves - ultrastructure | Protein Binding - genetics | Age Factors | Microscopy, Electron, Transmission - methods | Myelin Proteins - deficiency | Myelin-Associated Glycoprotein - metabolism | Peripheral Nervous System Diseases - physiopathology | Nerve Block - methods | Saxitoxin - pharmacokinetics | Sodium Channels - metabolism | Peripheral Nervous System Diseases - pathology | Peripheral Nervous System Diseases - genetics | Electric Stimulation - methods | Disease Models, Animal | Nerve Fibers - pathology | Nerve Fibers - metabolism | Myelin Basic Protein - metabolism | Neural Conduction - genetics | Gene Expression Regulation - genetics | Neural Conduction - physiology | Biophysics | Reaction Time - genetics | Peripheral Nerves - pathology | Mice, Knockout | Peripheral Nerves - physiopathology | Action Potentials - physiology | Animals | Kv1.2 Potassium Channel - metabolism | Muscle, Skeletal - physiopathology | Luminescent Proteins - genetics | Mice | Tritium - pharmacokinetics | Index Medicus | myelin | paranode | axonal constriction | conduction block | Schwann cell | Charcot-Marie-Tooth disease | tomacula | PMP22 | hereditary neuropathy with liability to pressure palsies (HNPP)
Journal Article
JOURNAL OF NEUROSCIENCE, ISSN 0270-6474, 01/2006, Volume 26, Issue 4, pp. 1179 - 1189
Peripheral myelin protein 22 (PMP22) is a tetraspan membrane glycoprotein, the misexpression of which is associated with hereditary demyelinating neuropathies.... 
TREMBLER-J MOUSE | EXPRESSION ANALYSIS | Schwann cells | PMP22-DEFICIENT MICE | NEUROSCIENCES | COLON-CARCINOMA CELLS | integrins | basal lamina | PMP22 GENE | NERVE EXTRACELLULAR-MATRIX | myelination | neuropathy | laminin | HEREDITARY NEUROPATHY | DIFFERENTIATION | PRESSURE PALSIES | TRANSGENIC MICE
Journal Article
Molecular and Cellular Neuroscience, ISSN 1044-7431, 05/2002, Volume 20, Issue 1, pp. 93 - 109
Minor changes in PMP22 gene dosage have profound effects on the development and maintenance of peripheral nerves. This is evident from the genetic disease... 
NERVOUS-SYSTEM | MARIE-TOOTH-DISEASE | GROWTH ARREST | TREMBLER MOUSE | TRANSCRIPTION FACTOR SOX10 | MEMBRANE-PROTEIN | SCHWANN-CELL DIFFERENTIATION | PMP22-DEFICIENT MICE | NEUROSCIENCES | ARREST-SPECIFIC GENE | TRANSGENIC MICE | Wallerian Degeneration - pathology | Viscera - cytology | Peripheral Nerves - embryology | Male | Neurons - cytology | Nerve Fibers, Myelinated - ultrastructure | Lac Operon - physiology | Schwann Cells - cytology | Myelin Sheath - metabolism | Cell Differentiation - genetics | Motor Neurons - cytology | Genes, Regulator - physiology | beta-Galactosidase - metabolism | Female | Fetus | Neurons - metabolism | Peripheral Nerves - metabolism | Gene Expression Regulation, Developmental - physiology | Nerve Fibers, Myelinated - metabolism | Nerve Regeneration - genetics | Neurons, Afferent - cytology | Viscera - metabolism | Wallerian Degeneration - metabolism | Transgenes - genetics | Wallerian Degeneration - physiopathology | Myelin Proteins - biosynthesis | Mice, Transgenic | Up-Regulation - genetics | Schwann Cells - metabolism | Mutation - genetics | Myelin Proteins - genetics | Genes, Reporter - physiology | Motor Neurons - metabolism | Animals | Promoter Regions, Genetic - physiology | Mice | Myelin Sheath - ultrastructure | Neurons, Afferent - metabolism | beta-Galactosidase - genetics | Peripheral Nerves - growth & development | Index Medicus
Journal Article
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.