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skin development

Known as: animal skin development 
The process whose specific outcome is the progression of the skin over time, from its formation to the mature structure. The skin is the external… 
National Institutes of Health

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establishment of skin barrierkeratinocyte differentiationsebaceous gland developmentskin epidermis development

Papers overview

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2009
2009
Overexpression of connexin26 in the basal keratinocytes reduces sensitivity to tumor promoter TPA
Please cite this paper as: Overexpression of connexin26 in the basal keratinocytes reduces sensitivity to tumor promoter TPA… 
2002
2002
Expression of Hex homeobox gene during skin development: Increase in epidermal cell proliferation by transfecting the Hex to the dermis
A number of homeobox genes have been found to be expressed in skin and its appendages, such as scale and feather, and appear to… 
Review
2001
Review
2001
Peroxisome Proliferator-Activated Receptors and Skin Development
PPARs are nuclear hormone receptors. PPAR subtypes (α, γ, δ, the latter a xPPARβ homologue) were initially investigated in skin… 
Highly Cited
1998
Highly Cited
1998
Bone Morphogenetic Protein‐2 Induces Scar Formation and Skin Maturation in the Second Trimester Fetus
&NA; Fetal mammals heal skin wounds through the second trimester of development without evidence of scar. We have investigated… 
1997
1997
Changing pattern of desmocollin 3 expression accompanies epidermal organisation during skin development
The adhesive core of the desmosome is composed of cadherin‐like glycoproteins of 2 families, desmocollins and desmogleins. The… 
1997
1997
Class IV alcohol/retinol dehydrogenase localization in epidermal basal layer: Potential site of retinoic acid synthesis during skin development
Vitamin A (retinol) plays a signaling role in the development of skin and other epithelial tissues. This is accomplished by a two… 
1997
1997
Apoptosis and Proliferation of Fibroblasts During Postnatal Skin Development and Scleroderma in the Tight-skin Mouse
Tight-skin (Tsk) is a dominant gene mutation that causes a fibrotic skin disease in mice, similar to human scleroderma. Both… 
Highly Cited
1997
Highly Cited
1997
The human homeobox genes MSX-1, MSX-2, and MOX-1 are differentially expressed in the dermis and epidermis in fetal and adult skin.
In order to identify homeobox genes which may regulate skin development and possibly mediate scarless fetal wound healing we have… 
1995
1995
Transforming growth factor-beta 1 and collagen gene expression during postnatal skin development and fibrosis in the tight-skin mouse.
BACKGROUND The tight-skin (Tsk) mutation in the mouse leads to widespread connective tissue abnormalities characterized by… 
1986
1986
Cell surface carbohydrate changes during embryonic and fetal skin development.
Monoclonal antibodies to four type 2 chain carbohydrate antigens were used for immunohistochemical studies of embryonic and fetal… 
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