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

J. H. Pate Skene, Richard D. Jacobson, G. Jackson Snipes, +3

Science

Protein SecretionBrain DevelopmentSynaptic TransmissionPeripheral NerveCell Growth +19

Trembler mouse carries a point mutation in a myelin gene

Ueli Suter, Andrew A. Welcher, Tayfun Özçelık, +6

Nature

Knockout MouseGenetic DisorderNeuroanatomyGeneticsMyelin Gene +7

Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13)

G. Jackson Snipes, Ueli Suter, A.A. Welcher, +1

The Journal of Cell Biology

Peripheral Nerve InjuryOther Myelin ProteinsCytoskeletonPeripheral NervePeripheral Nerves +19

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

Benjamin B. Roa, Carlos A. Garcia, Ueli Suter, +8

New England Journal of Medicine

A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse.

Ueli Suter, John J. Moskow, Andrew A. Welcher, +5

Proceedings of the National Academy of Sciences

Knockout MouseCompact Peripheral MyelinSignal TransductionDevelopmental BiologyMolecular Physiology +13

Nerve injury stimulates the secretion of apolipoprotein E by nonneuronal cells.

G. Jackson Snipes, C. Brian McGuire, J. J. Norden, +1

Proceedings of the National Academy of Sciences

Peripheral Nerve InjuryCell DeathCellular PhysiologySocial SciencesNeuroinflammation +20

A myelin protein is encoded by the homologue of a growth arrest-specific gene.

Andrew A. Welcher, Ueli Suter, Marino De León, +2

Proceedings of the National Academy of Sciences

Peripheral Nerve InjuryPathologyCytoskeletonPeripheral NerveCell Growth +14

Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters.

Ueli Suter, G. Jackson Snipes, R Schoener-Scott, +6

Journal of Biological Chemistry

Expanded CTG repeats within the <i>DMPK</i> 3′ UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy

James P. Orengo, Pierre Chambon, Daniel Metzger, +3

Proceedings of the National Academy of Sciences

Muscle FunctionGeneticsDm1 Skeletal MuscleDisease Gene IdentificationSkeletal Muscle +14

Evidence for a recessive PMP22 point mutation in Charcot–Marie–Tooth disease type 1A

Benjamin B. Roa, Carlos A. Garcia, Pentao Liu, +8

Nature Genetics

Mendelian DisorderGenetic DisorderGeneticsPathogenesisPathology +4