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Research 301–330 of 1000+
- Skin Diseases in Pregnancy
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- The structure of the cornified claw sheath in the domesticated cat (<i>Felis catus</i>): implications for the claw‐shedding mechanism and the evolution of cornified digital end organs
- Risk factors for diabetic foot ulcers mortality and novel negative pressure combined with platelet-rich plasma therapy in the treatment of diabetic foot ulcers
- Hair-thread tourniquet syndrome: a case report and review of treatment
- Achieving Sustained Hair Repigmentation in Poliosis Circumscripta: Retreatment Outcomes Using Exosomes and Fractional Picosecond Laser
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Infected intraosseous epidermoid cyst in the right ankle: a case report
- Inhibition of Bmp signaling affects growth and differentiation in the anagen hair follicle
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis
- Dual‐flow‐RootChip reveals local adaptations of roots towards environmental asymmetry at the physiological and genetic levels
- Androgenetic alopecia: new insights into the pathogenesis and mechanism of hair loss
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- Utilities of Botulinum Toxins in Dermatology and Cosmetology
- Congenital insensitivity to pain with anhidrosis and progressing acro-osteolysis: a case report with 7-year follow-up
- Bone infarcts in a woman with systemic lupus erythematosus and antiphospholipid antibody syndrome
- Alopecia Areata and Habit Tic Deformities
- Social rejection in minority groups and its impact on current and future mental health: a study in transgender people
- Cutis Verticis Gyrata Heralding a Diagnosis of Primary Systemic Amyloidosis in a Patient with Cardioembolic Stroke
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Referee report. For: Pathogenesis of Androgenetic alopecia [v1; indexed, http://f1000r.es/5ar]
- Trichothiodystrophy in a child with occult learning disorder
- A phase 2a study investigating the effects of ritlecitinib on brainstem auditory evoked potentials and intraepidermal nerve fiber histology in adults with alopecia areata
- Pioneer factors govern super-enhancer dynamics in stem cell plasticity and lineage choice
- What does the concept of the stem cell niche really mean today?
- Molecular signaling in feather morphogenesis
- Molecular mechanisms of asymmetric divisions in mammary stem cells
- Defining the Cellular Environment in the Organ of Corti following Extensive Hair Cell Loss: A Basis for Future Sensory Cell Replacement in the Cochlea
- Mesenchymal Stem Cell-Derived Extracellular Vesicles for Therapeutic Use and in Bioengineering Applications