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Research 421–450 of 703
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- A Clinicopathological and Immunofluorescence study of Lichen Planus
- Role of caffeine in the management of androgenetic alopecia
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- 878 Individual variation in balance between platelet-secreted growth factors causing contradictory effects on hair follicle could potentially impact response to PRP therapy in patients with scalp hair loss
- 876 Imaging nanoscale changes in desmosome protein organization
- 875 A novel animal model of Desmoglein 1 (Dsg1) deficiency reveals an essential role for Dsg1 in epidermal barrier formation
- 879 IL-9 mediated human primary keratinocytes invasion is dependent on MLC controlled contractility and independent of MMP activity
- 874 Elevated expression of osteopontin splice variants in nonmelanoma skin cancer compared to normal skin and adult keratinocytes
- Decades of progressive red and yellow nodules
- Teaching dermatosurgery
- Correspondence
- Hair growth promoting effects of adipose tissue-derived stem cells
- Frontal fibrosing alopecia: treatment with oral dutasteride and topical pimecrolimus
- Dermatopathology and molecular genetics
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- Tendency to underestimate the severity of androgenetic alopecia
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Thyroid Autoimmunity in Patients with Skin Disorders
- Papillon-Lefévre Syndrome: A Rare Case Report and a Brief Review of Literature
- 892 Behavior of the two circulating androgens testosterone and DHEA and their main intracellular metabolites in an androgen-sensitive sebocyte cell line
- 890 Development of pigmented reconstructed human epidermis model containing human melanoblasts from keratinocyte culture
- Therapeutic Evaluvation of Patients with Alopecia Areata.
- Fibroblast heterogeneity: implications for human disease
- Wnt Signaling in Skin Development, Homeostasis, and Disease
- Coordinated Activation of Wnt in Epithelial and Melanocyte Stem Cells Initiates Pigmented Hair Regeneration