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Research 511–540 of 1000+
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Adipose mesenchymal stem cells combined with platelet-rich plasma accelerate diabetic wound healing by modulating the Notch pathway
- Psychocutaneous disease
- Redefining hormone resistance in prostate cancer
- Ruxolitinib for the treatment of severe alopecia areata
- Dermatological symptoms and sexual abuse: a review and case reports
- Apoptotic cells represent a dynamic stem cell niche governing proliferation and tissue regeneration
- Nuclear Factor I-C Regulates TGF-β-dependent Hair Follicle Cycling*
- Medical Treatment of Hepatocellular Carcinoma: Any Progress?
- Pharmacological Options for Treatment of Hyperandrogenic Disorders
- Structure and Function of the Skin
- ANIFROLUMAB IN THE MANAGEMENT OF LUPUS HEADACHES: A CASE REPORT
- ASSOCIATION OF SYSTEMIC LUPUS ERYTHEMATOSUS AND CHRONIC GRANULOMATOUS DISEASE IN ADULTS: REPORT OF 2 CASES
- MIXED CONNECTIVE TISSUE DISEASE EVOLVING FROM THE SEQUENTIAL OVERLAP OF SYSTEMIC LUPUS ERYTHEMATOSUS, SJÖGREN’S SYNDROME, RHEUMATOID ARTHRITIS AND DERMATOMYOSITIS: A FOLLOW-UP
- Terapia capilar: um novo modelo de formação profissional e negócio no setor de beleza masculino
- 毛乳頭細胞と毛包上皮細胞間の細胞内・細胞外情報伝達
- Developmental Mechanisms Controlling Cell Fate, Evolution of
- Potential genetic associations of acne scar phenotypes: IL1A in fibrotic scarring and CYB5R1 in atrophic scarring
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Drought-induced SlCLE10 coordinates ethylene biosynthesis and root hair development to confer osmotic stress tolerance in tomato
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- miR-370-3p Inhibited the Proliferation of Sheep Dermal Papilla Cells by Inhibiting the Expression of SMAD4
- Characterisation and functional analysis of the WIF1 gene and its role in hair follicle growth and development of the Angora rabbit
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Genetic analysis of the role of androgen metabolism in the pathogenesis of prostate cancer
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases