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author = "Albers, Kathryn M."
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Found 2 documents, displaying page 1 of 1
Transcriptional and Post-Transcriptional Regulation of SPAST, the Gene Most Frequently Mutated in Hereditary Spastic Paraplegia
Author(s) :
Henson, Brian J.
,
Zhu, Wan
,
Hardaway, Kelsey
,
Wetzel, Jaime L.
,
Stefan, Mihaela
,
Albers, Kathryn M.
,
Nicholls, Robert D.
Description :
Hereditary spastic paraplegias (HSPs) comprise a group of neurodegenerative disorders that are characterized by progressive spasticity of the lower extremities, due to axonal degeneration in the corticospinal motor tracts. HSPs are genetically heterogeneous and show autosomal dominant inheritance in...
Repository :
Europe PubMed Central
Language(s) :
English
A New Role for Neurotrophin-3 : Involvement in the Regulation of Hair Follicle Regression (Catagen)
Author(s) :
Botchkarev, Vladimir A.
,
Welker, Pia
,
Albers, Kathryn M.
,
Botchkareva, Natalia V.
,
Metz, Martin
,
Lewin, Gary R.
Description :
Nervous system and hair follicle epithelium share a common ectodermal origin, and some neurotrophins (NTs) can modulate keratinocyte proliferation and apoptosis. Therefore, it is reasonable to ask whether NTs are also involved in hair growth control. Here, we show that the expression of NT-3 and its...
Repository :
Europe PubMed Central
Language(s) :
English
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Found 2 documents, displaying page 1 of 1