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ALLISON HANAUER, PH.D.
PH.D.
Clinical Psychologist
NPI: 1336296771Individual
Specialties, Licenses & Credentials
Clinical PsychologistPrimary
Psychologist — Clinical
Code: 103TC0700X
1180(AL)2676(TN)
Research & Publications (20)
P90 Ribosomal s6 kinase 2 negatively regulates axon growth in motoneurons.
PMID 19555761·Mol Cell Neurosci·2009
7-preclinical
Fibroblast growth factor receptor 3 associates with and tyrosine phosphorylates p90 RSK2, leading to RSK2 activation that mediates hematopoietic transformation.
PMID 19223461·Mol Cell Biol·2009
7-preclinical
Dopaminergic system dysregulation in the mrsk2_KO mouse, an animal model of the Coffin-Lowry syndrome.
PMID 18823370·J Neurochem·2008
7-preclinical
The Coffin-Lowry syndrome-associated protein RSK2 is implicated in calcium-regulated exocytosis through the regulation of PLD1.
PMID 18550821·Proc Natl Acad Sci U S A·2008
7-preclinical
Inactivation of the CDKL3 gene at 5q31.1 by a balanced t(X;5) translocation associated with nonspecific mild mental retardation.
PMID 18412109·Am J Med Genet A·2008
7-preclinical
Electrocautery versus 23% NaOH infiltration to induce subglottic stenosis in a canine experimental model.
PMID 17899131·Pediatr Surg Int·2007
4-observational
The first large duplication of the RSK2 gene identified in a Coffin-Lowry syndrome patient.
PMID 17717706·Hum Genet·2007
5-case
Deletion of the Coffin-Lowry syndrome gene Rsk2 in mice is associated with impaired spatial learning and reduced control of exploratory behavior.
PMID 17033934·Behav Genet·2007
7-preclinical
Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome.
PMID 16879200·Clin Genet·2006
8-other
Genetic background of HSH in three Polish families and a patient with an X;9 translocation.
PMID 16267500·Eur J Hum Genet·2006
8-other
Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation.
PMID 16249884·Hum Genet·2006
7-preclinical
p90Rsk is not involved in cytostatic factor arrest in mouse oocytes.
PMID 15837801·J Cell Biol·2005
7-preclinical
ATF4 is a substrate of RSK2 and an essential regulator of osteoblast biology; implication for Coffin-Lowry Syndrome.
PMID 15109498·Cell·2004
7-preclinical
Delineation of the mechanisms of aberrant splicing caused by two unusual intronic mutations in the RSK2 gene involved in Coffin-Lowry syndrome.
PMID 14973203·Nucleic Acids Res·2004
8-other
Expression of the RSK2 gene during early human development.
PMID 14678837·Gene Expr Patterns·2004
8-other
Expression analysis of RSK gene family members: the RSK2 gene, mutated in Coffin-Lowry syndrome, is prominently expressed in brain structures essential for cognitive function and learning.
PMID 12393804·Hum Mol Genet·2002
7-preclinical
A syndromic form of X-linked mental retardation: the Coffin-Lowry syndrome.
PMID 12014383·Eur J Pediatr·2002
6-review
Unusual splice-site mutations in the RSK2 gene and suggestion of genetic heterogeneity in Coffin-Lowry syndrome.
PMID 11992250·Am J Hum Genet·2002
8-other
X-linked Coffin-Lowry syndrome (CLS, MIM 303600, RPS6KA3 gene, protein product known under various names: pp90(rsk2), RSK2, ISPK, MAPKAP1).
PMID 11896450·Eur J Hum Genet·2002
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3950 NEW COVINGTON PIKE STE 110
MEMPHIS, TN 38128 - Phone
- (901) 387-2900
Quick Facts
- NPI
- 1336296771
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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