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Research 421–450 of 1000+
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- Acute telogen effluvium associated with SARS-CoV-2 infection
- Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary cilia
- [Cutaneous manifestations of malabsorption diseases (author's transl)].
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Diffuse Alopecia and Thyroid Atrophy in Sheep
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- Cutaneous Manifestations of PCOS
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Case for diagnosis. Pregnant woman in the 3rd trimester with pruritic papules and pustules on the trunk. Pruritic folliculitis of pregnancy
- Hypotrichosis in a child with olmsted syndrome
- Lesions in the Axilla After Hair Removal Using Intense Pulsed Light
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Cylindroma as Tumor of Hair Follicle Origin
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Expression of Cyclooxygenase Isozymes During Morphogenesis and Cycling of Pelage Hair Follicles in Mouse Skin: Precocious Onset of the First Catagen Phase and Alopecia upon Cyclooxygenase-2 Overexpression
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Nevus lipomatosus cutaneous superficialis with folliculosebaceous cystic hamartoma
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Targeted inactivation of integrin-linked kinase in hair follicle stem cells reveals an important modulatory role in skin repair after injury
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Murine Epidermal Ceramide Synthase 4 Is a Key Regulator of Skin Barrier Homeostasis
- Use of dermoscopy in the diagnosis of temporal triangular alopecia
- Frontal fibrosing alopecia: a disease that remains enigmatic
- [Translated article] Trichoscopy: An Update
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- T-Cell Reconstitution after Thymus Xenotransplantation Induces Hair Depigmentation and Loss
- Serum anti-Müllerian hormone as a predictor of polycystic ovarian syndrome among women of reproductive age