L Notterpek
Overview
Explore the profile of L Notterpek including associated specialties, affiliations and a list of published articles.
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12
Citations
314
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Recent Articles
1.
Johnson J, Roux K, Fletcher B, Fortun J, Notterpek L
J Neurosci Res
. 2005 Nov;
82(6):743-52.
PMID: 16273544
Alterations in peripheral myelin protein 22 (PMP22) expression are associated with a heterogeneous group of hereditary demyelinating peripheral neuropathies. Two mutations at glycine 94, a single guanine insertion or deletion...
2.
Misko A, Ferguson T, Notterpek L
J Neurochem
. 2002 Nov;
83(4):885-94.
PMID: 12421361
A single point mutation in peripheral myelin protein 22 (pmp22) of the Trembler-J (TrJ) mouse models the human peripheral neuropathy, Charcot-Marie-Tooth disease type 1 A (CMT1A). An unexplored aspect of...
3.
Fletcher B, Dragstedt C, Notterpek L, Nolan G
Leukemia
. 2002 Jul;
16(8):1507-18.
PMID: 12145692
The balance between hematopoietic cell viability and apoptosis is regulated by exogenous growth factors, however, the molecular mechanisms by which these trophic factors exert their effects remain obscure. A functional...
4.
Notterpek L, Roux K, Amici S, Yazdanpour A, Rahner C, Fletcher B
Proc Natl Acad Sci U S A
. 2001 Nov;
98(25):14404-9.
PMID: 11717414
Alterations in peripheral myelin protein 22 (PMP22) gene expression are associated with a host of heritable demyelinating peripheral neuropathies, yet the function of the protein remains unknown. PMP22 expression is...
5.
Zhong L, Manzi A, Skowronski E, Notterpek L, Fluharty A, Faull K, et al.
Cancer Res
. 2001 Aug;
61(15):5741-8.
PMID: 11479210
The cell surface molecules controlling apoptosis in cortical neurons are largely unknown. A monoclonal antibody was derived that induces cultured neocortical neurons to undergo apoptosis. A Fab fragment of the...
6.
Ryan M, Notterpek L, Tobler A, Liu N, SHOOTER E
J Neurochem
. 2000 Sep;
75(4):1465-74.
PMID: 10987826
Peripheral myelin protein 22 (PMP22) is a 22-kDa glycoprotein containing a single N-linked carbohydrate moiety. This posttranslational modification is conserved in PMP22 across species and within members of the PMP22...
7.
Notterpek L, Tolwani R
Lab Anim Sci
. 2000 Jan;
49(6):588-99.
PMID: 10638493
Background And Purpose: Peripheral neuropathies, disorders of peripheral nerves, result from genetic alterations or from metabolic, inflammatory, infectious, or chemical insults. Experimental animal models, spontaneous or induced, exist for many...
8.
Notterpek L, Ryan M, Tobler A, SHOOTER E
Neurobiol Dis
. 1999 Oct;
6(5):450-60.
PMID: 10527811
Peripheral myelin protein 22 (PMP22) is a 22-kDa glycoprotein mainly expressed by Schwann cells (SCs). Duplication or deletion of the PMP22 gene locus is associated with heritable peripheral neuropathies suggesting...
9.
Tobler A, Notterpek L, Naef R, Taylor V, Suter U, SHOOTER E
J Neurosci
. 1999 Mar;
19(6):2027-36.
PMID: 10066256
Peripheral myelin protein 22 (PMP22) is an integral membrane protein that is essential for the normal formation and maintenance of peripheral myelin. Duplications, deletions, or mutations in the PMP22 gene...
10.
Notterpek L, Snipes G, SHOOTER E
Glia
. 1999 Feb;
25(4):358-69.
PMID: 10028918
Peripheral myelin protein 22 (PMP22) was initially described as a minor component of peripheral myelin. Mutations affecting the PMP22 gene cause demyelinating neuropathies, supporting a role for the protein in...