Search
for
Sort by
Research 151–180 of 1000+
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Nonclassic adrenal hyperplasia
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Evolution of Trichocyte Keratins
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Semidominant Inheritance in Epidermolytic Ichthyosis
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- The efficacy of adipose stem cell‐derived exosomes in hair regeneration based on a preclinical and clinical study
- Etiopathogenesis of Alopecia Areata
- Pharmacogenomic variation and chemotherapy-related toxicity profiles in pediatric patients with cancer in Tanzania: a cross-sectional study
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- Improvement of androgenic alopecia by extracellular vesicles secreted from hyaluronic acid-stimulated induced mesenchymal stem cells
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- A missense mutation in Lama3 causes androgen alopecia
- Molecular Basis of Hereditary Hair Diseases
- Chronic Overlapping Pain Conditions and Nociplastic Pain
- Cepharanthine Inhibits Doxorubicin-Induced Cellular Senescence by Activating Autophagy via the mTOR Signaling Pathway
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- SnapshotDx Quiz: August 2019
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- MON-218 Inflammatory Role of Sex Steroids in Hidradenitis Suppurativa: An Androgenic Phenotype
- 303 The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
- Local Artemis dysfunction may be one molecular mechanism for androgenetic alopecia via telomere shortening
- Severe metabolic disorders coexisting with Werner syndrome: a case report
- Keloid risk in patients with atopic dermatitis: a nationwide retrospective cohort study in Taiwan
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature