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GRACE ASHTON, PH.D.
PH.D.
Psychologist
NPI: 1568614139Individual
Specialties, Licenses & Credentials
PsychologistPrimary
Psychologist
Code: 103T00000X
PS016021(PA)
Research & Publications (20)
Mitochondrial DNA reveals multiple Northern Hemisphere introductions of Caprella mutica (Crustacea, Amphipoda).
PMID 18302689·Mol Ecol·2008
7-preclinical
Environmental tolerance of Caprella mutica: implications for its distribution as a marine non-native species.
PMID 17383720·Mar Environ Res·2007
7-preclinical
Alpha 6 beta 4 integrin abnormalities in junctional epidermolysis bullosa with pyloric atresia.
PMID 11251584·Br J Dermatol·2001
5-case
A novel Src kinase inhibitor reduces tumour formation in a skin carcinogenesis model.
PMID 19060248·Carcinogenesis·2009
7-preclinical
Eradication of established B-cell lymphoma by CD19-specific murine T cells is dependent on host lymphopenic environment and can be mediated by CD4+ and CD8+ T cells.
PMID 19242379·J Immunother·2009
7-preclinical
Feedback regulation of p38 activity via ATF2 is essential for survival of embryonic liver cells.
PMID 17699753·Genes Dev·2007
7-preclinical
Eotaxin-2 and colorectal cancer: a potential target for immune therapy.
PMID 17908961·Clin Cancer Res·2007
8-other
Retrospective diagnosis of Kindler syndrome in a 37-year-old man.
PMID 16309479·Clin Exp Dermatol·2006
5-case
Identification of potential biomarkers for measuring inhibition of Src kinase activity in colon cancer cells following treatment with dasatinib.
PMID 17148760·Mol Cancer Ther·2006
7-preclinical
Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene.
PMID 16675959·J Invest Dermatol·2006
8-other
Prenatal diagnosis for severe inherited skin disorders: 25 years' experience.
PMID 16403102·Br J Dermatol·2006
8-other
Loss of Apc allows phenotypic manifestation of the transforming properties of an endogenous K-ras oncogene in vivo.
PMID 16959882·Proc Natl Acad Sci U S A·2006
7-preclinical
Complete paternal uniparental isodisomy of chromosome 1 resulting in Herlitz junctional epidermolysis bullosa.
PMID 15663509·Clin Exp Dermatol·2005
5-case
An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 gene.
PMID 15807691·Clin Exp Dermatol·2005
5-case
Prenatal diagnosis of Herlitz junctional epidermolysis bullosa in nonidentical twins.
PMID 15725250·Clin Exp Dermatol·2005
5-case
Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome.
PMID 14962093·J Invest Dermatol·2004
8-other
Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation.
PMID 12603844·J Invest Dermatol·2003
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 169 CONARROE ST
PHILADELPHIA, PA 19127 - Phone
- (215) 483-2461
Quick Facts
- NPI
- 1568614139
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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