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Research 871–900 of 1000+
- Biomedical engineering approaches for the delivery of JAGGED1 as a potential tissue regenerative therapy
- An Unusual Case of Diarrhea, Dysgeusia, and Grainy and Nodular Mucosa
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- 1429 Proteomic analysis of cultured dermal papilla, dermal sheath and dermal fibroblast cells from female scalp highlights alterations in the cell populations with increasing age
- Pachyonychia congenita: Sporadic onset with mutation analysis
- 567 Skin aging and carcinogenesis mechanisms by focusing on the stem cell competitive dynamics
- 565 hiPSC-derived skin organoids as tools for disease modelling: characterization of the epidermal-dermal junction
- 569 Hypoxic response of the expression of TGF-β2 and BMP4 in human dermal papilla cells
- LBODP010 A Case of Glucocorticoid Resistance Syndrome
- Multiple follicular abnormalities in a 1‐year old cat consistent with basaloid follicular hamartomas
- Generalized multiple eruptive milia in an infant – An unusual presentation
- Lichen Planopilaris
- Loose anagen syndrome in one identical twin girl
- Spiny Keratoderma
- Clouston’s syndrome: a rare case report
- Hypotrichosis in a child with olmsted syndrome
- SkIndia Quiz 24: Itchy papules over face
- Genetics of Alopecia
- Localized Acquired Hypertrichosis Associated with the Application of a Splint
- TONGUE, RED
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- 50-Year-Old Female with a Burning Scalp and Hair Loss
- Comparative Study of Some Potential Paracrine Factors Produced by Normal and Androgenetic Alopecia Hair Follicles
- A randomized double blind study of the effect of finasteride on hair growth in male patients of androgenetic alopecia
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- FGF5 is a crucial regulator of hair length in humans
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development