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Research 31–60 of 1000+
- Epidermal Development in Mammals: Key Regulators, Signals from Beneath, and Stem Cells
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Epidermal Polarity Genes in Health and Disease
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Characterization of Primary Cilia and Intraflagellar Transport 20 in the Epidermis
- 1313 Fzd2 controls multiple aspects of epidermal development through distinct signaling mechanisms
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Hair Shaft Dysplasias
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Long-term complications of Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN): the spectrum of chronic problems in patients who survive an episode of SJS/TEN necessitates multidisciplinary follow-up
- TOXIC EPIDERMAL NECROLYSIS
- Severe Physical Complications among Survivors of Stevens–Johnson Syndrome and Toxic Epidermal Necrolysis
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Clinical report of a Holstein's calf with ichthyosis.
- Dermatopathology and molecular genetics
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Hair and Nail Relationship
- Genetics of Structural Hair Disorders
- Inherited Disorders of the Hair
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- LB1603 Centrosomes are required for the normal development of the skin epithelium
- LB1605 3D imaging of cleared ex vivo normal human skin, skin appendages and psoriasiform skin lesion using light-sheet microscopy
- Molecular biology of hair morphogenesis: Development and cycling
- Expression of Hex during feather bud development
- Scratching the surface of skin development
- Transgenic mice provide new insights into the role of TGF-alpha during epidermal development and differentiation.