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15篇 您的检索式：作者名="South AP"

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		题名	作者	年代	出处	被引量
	1	NOTCH1 mutations occur early during cutaneous squamous cell carcinogenesis 显示文摘	South AP Purdie KJ Watt SA	2014	J Invest Dermatol2014，134，10：	1
	2	EEC (Ectrodactyly,Ectodermal dysplasia,Clefting) syndrome:heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis显示文摘	South AP Ashton GH Willoughby C Ellis IH Bleck O Hamada T	2002	Br J Dermatol2002，146，2：	1
	3	Growth and neurodevelopment at 16 to 24 months of age for infants born with gastroschisis显示文摘	South AP Marshall DD Bose CL		0，，：	1
	4	EEC(Ectrodactyly,Ectodermal dysplasia,Clefting) syndrome: heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis显示文摘	South AP Ashton GHS	2002	British Journal of Dermatology2002，146，：	1
	5	Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis 显示文摘	Arita K South AP Hans-Filho G	2008	Am J Hum Genet2008，82，：	1
	6	Genotype-phenotype correlation in skin fragility-ectodermal dysplasia syndrome resulting from mutations in plakophilin 1显示文摘	Hamada T South AP Mitsuhashi Y	2002	Exp Dermatol2002，11，2：	1
	7	Reduced expression of insulin-like growth factor-binding protein-3(IGFBP-3)in Squamous cell carcinoma complicating recessive dystrophic epidermolysis bullnsa显示文摘	Mallipeddi R Wessagowit V South AP	2004	J Invest Dermatol2004，122，5：	1
	8	The double-edged sword of Notch signaling in cancer显示文摘	South AP Cho RJ Aster JC	2012	Semin Cell Dev Biol2012，23，4：	1
	9	EEC (Ectro- dactyly, Ectodermal dysplasia, Clefting) syndrome: Hetero- zygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis显示文摘	South AP Ashton GH Willoughby C	2002	Br J Dermatol2002，146，2：	1
	10	The double-edged sword of Notch signaling in cancer显示文摘	South AP Cho RJ Aster JC	2012	Semin Cell Dev Biol2012，23，4：	1
	11	Recurrent mutations in kindlin-1,a novel keratinocyte focal contact protein,in the autosoreal recessive skin fragility and photosensitivity disorder,Kindler syndrome显示文摘	Ashton GH McLean WH South AP	2004	J Invest Dermatol2004，122，1：	1
	12	Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation 显示文摘	Hamada T Wessagowit V South AP	2003	J Invest Dermatol2003，120，3：	1
	13	Lack of plakophilin 1 increases keratinocyte migration and reduces desmosome stability显示文摘	South AP Wan H Stone MG	2003	J Cell Sci2003，116，16：	1
	14	Rapid diagnosis of lipoid proteinosis using an anti-extracellular matrix protein 1 (ECM1) antibody显示文摘	Chan I South AP McGrath JA	2004	J Dermatol Sci2004，35，2：	1
	15	Oncostatin M Receptor-b Mutations Underlie Familial Primary Localized Cutaneous Amyloidosis 显示文摘	Ken Arita South AP Hans-filho G	2008	Am J Hum Genet2008，82，1：	1

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