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Research 571–600 of 1000+
- Spironolactone‐induced hepatitis
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Fibrotic enzymes modulate wound‐induced skin tumorigenesis
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- The role of cathepsin E in terminal differentiation of keratinocytes
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Early embryonic exposure of freshwater gastropods to pharmaceutical 5-alpha-reductase inhibitors results in a surprising open-coiled “banana-shaped” shell
- Potential Role of the Epidermal Differentiation Complex in the Pathogenesis of Psoriasis
- Loose anagen hair syndrome: Treatment with systemic minoxidil characterised by marked hair colour change
- Uncombable-hair Syndrome
- Successful induction of oral tolerance in Netherton syndrome
- A retrospective study of thyroid structural abnormalities in alopecia patients
- BIOACTIVE AND PERIPHERAL ANDROGENS IN PREPUBERTAL SIMPLE HYPERTRICHOSIS
- Comparison of hair manifestations in cardio‐facio‐cutaneous and Costello syndromes highlights the influence of the RAS pathway on hair growth
- Mesalazine in the treatment of extensive alopecia areata: A new therapeutic option?
- Epidermal growth factor, innovation and safety
- Arginosuccinicaciduria
- The coudability sign of alopecia areata: the real story
- Acquired Hair Fragility in Pili anulati: Causal Relationship with Androgenetic Alopecia
- Pleiotropic effects of the nude mutation.
- Establishment of Tsc2-deficient rat embryonic stem cells
- Current concepts in the pathogenesis and treatment of acne
- Eruptive Vellus Hair Cyst
- Testosterone- and Cortisol-Secreting Adrenocortical Oncocytoma: An Unusual Cause of Hirsutism
- Menstrual Disorders
- Hot Flashes in a Young Girl: A Wake-up Call Concerning Serenoa repens Use in Children
- Disease Prevention and Alleviation by Human Myoblast Transplantation
- Congenital dyserythropoietic anaemia and dyskeratosis in Australian Poll Hereford calves
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Disorders of Sex Development