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Research 271–300 of 1000+
- Autoimmune polyendocrine syndrome type 1 a case report from Bangladesh
- The relevance of collagen XVII expression in epidermal differentiation and proliferation
- Nail lichen planus in a patient with alopecia totalis
- A patient with Cronkhite-Canada syndrome whose entire digestive tracts was examined endoscopically
- Geriatric Dermatology: Overview
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- Alopecia Universalis
- Cutaneous toxicities of cancer therapy
- Mechanical forces in skin disorders
- Cutaneous Drug Eruptions Associated with the Use of New Oncological Drugs
- First symposium on natural gene therapy of the skin
- Erworbene Alopezien im Kindesalter
- Mesenchymal Stem Cells for the Treatment of Skin Diseases
- 688 Precise and efficient editing of the COL7A1 gene in RDEB derived iPSCs with CRISPR/Cas9 and prime editing
- TERMIS ‐ AMERICAS Toronto, Ontario, Canada July 10–13, 2022
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- A patient with diffuse hair loss
- Keratin disorders: from gene to therapy
- Clinical and histopathologic features of hair loss in patients with HIV-1 infection
- Alopecia Areata in C3H/HeJ Mice Involves Leukocyte-mediated Root Sheath Disruption in Advance of Overt Hair Loss
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Clinical relevance of hair microscopy in alopecia
- Activation of mTORC1 Signaling is Required for Timely Hair Follicle Regeneration from Radiation Injury
- Dermatopathology and molecular genetics
- Parathyroid hormone linked to a collagen binding domain promotes hair growth in a mouse model of chemotherapy-induced alopecia in a dose-dependent manner
- Apremilast and tofacitinib exert differential effects in the humanized mouse model of alopecia areata
- Mimicking Hair Disorders by Genetic Manipulation of Organ-Cultured Human Hair Follicles
- Skin manifestations of Bardet–Biedl syndrome
- 516 Possible role of ILC1 in the pathogenesis of alopecia areata (AA)