Search
for
Sort by
Research 391–420 of 1000+
- A Comprehensive Review of GWASs of Human Hair Traits
- Cushings syndrome complicating pemphigoid gestationis
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Longitudinal Assessment of the Prevalence of Actinic Keratosis and Extensive Risk Factor Evaluation: An Update from the Rotterdam Study
- Dermatological concerns for women and girls with turner syndrome
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Inhibition of JAK-STAT Signaling with Baricitinib Reduces Inflammation and Improves Cellular Homeostasis in Progeria Cells
- Premature aging syndromes: From patients to mechanism
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Congenital atrichia associated with nevus flammeus: A rare association
- Hair That Is Difficult to Manage in a Hispanic Girl
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Cellular plasticity in reprogramming, rejuvenation and tumorigenesis: a pioneer TF perspective
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Parsing patterns: Emerging roles of tissue self-organization in health and disease
- Impact of electrical impedance spectroscopy on dermatologists' number needed to biopsy metric and biopsy decisions for pigmented skin lesions
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Lymphocytic Mural Folliculitis Resembling Epitheliotropic Lymphoma in Tigers (<i>Panthera tigris</i>)
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Involvement of Wnt, Eda and Shh at defined stages of sweat gland development
- Morphea: progress to date and the road ahead