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Research 121–150 of 1000+
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Gastrointestinal polyposis with protein-losing enteropathy, abnormal skin pigmentation and loss of hair and nails (Cronkhite-Canada syndrome)
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- The Effects of a Powder of the Fruiting Body of Commercial Lingzhi or Reishi Medicinal Mushroom Ganoderma lucidum (W.Curt.:Fr.) P.Karts.,] on Hypercholesterolemic Rat Skin, Applied With a Topical Application of Benzo(a)pyrene
- Obstetric and Gynecologic Dermatology
- Acne
- Postgraduate seminar in pediatric dermatology
- Successful treatment of ulcerated infantile hemangioma associated with PELVIS syndrome using oral propanolol
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- Gene-knockout mice with abnormal epidermal and hair follicular development
- The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control epithelial differentiation
- Histological and dermatoscopic description of sphynx cat skin
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Trichoscopic Findings of Frontal Fibrosing Alopecia
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- The disintegrin/metalloproteinase Adam10 is essential for epidermal integrity and Notch-mediated signaling
- Bloom's syndrome–‐a first report from India
- Description and characterization of a hair coat disorder in schipperkes
- Clouston’s syndrome: a rare case report
- Expression of ΔNLef1 in mouse epidermis results in differentiation of hair follicles into squamous epidermal cysts and formation of skin tumours
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Murine Epidermal Ceramide Synthase 4 Is a Key Regulator of Skin Barrier Homeostasis
- Interactions between epidermal growth factor and the <i>Tabby</i> mutation in skin
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis