Search
for
Sort by
Research 601–630 of 1000+
- A systematic summary of survival and death signalling during the life of hair follicle stem cells
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Making the head: Caspases in life and death
- JAK inhibition decreases the autoimmune burden in Down syndrome
- Update on Polycystic Ovary Syndrome
- Cataracts and strabismus associated with hand rearing using artificial milk formulas in Bengal tiger (<i>Panthera tigris spp tigris</i>) cubs
- AcD : A Novel Bioactive Polymer Scaffold of Adipose‐Derived Stem Cells Combining With Decellularized Extracellular Matrix in Tissue Engineering
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Ichthyosis with confetti: clinics, molecular genetics and management
- Serially expanded flap use to treat large hairless scalp lesions
- Delicious Dermatology: Baked-Up Eponyms
- 6 Current concepts of polycystic ovary syndrome
- Incidence, complications and therapeutic evaluation of clinical hypothyroidism in different breeds of dogs
- A guide to diagnosis and management of hypertrichosis
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Acne Vulgaris
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- A study on efficacy of oral zinc therapy for treatment of acrodermatitis enteropathica
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- New developments in the molecular treatment of ichthyosis: review of the literature
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- The developmental basis of fingerprint pattern formation and variation
- Celsr1 and Celsr2 exhibit distinct adhesive interactions and contributions to planar cell polarity
- Regenerative medicine in aesthetics
- Bilateral nevus comedonicus of the eyelids: An unusual cause of ptosis and ectropion
- A Clinical Review of Trichorrhexis Nodosa
- Mesotherapy vs PRP: Hair loss
- The dermatoscope in the hair clinic: Trichoscopy of scarring and nonscarring alopecia