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Research 631–660 of 1000+
- Morphological Approach to Hair Disorders
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Female pattern alopecia: current perspectives
- Exploring the effects of Chinese herbal ingredients on the signaling pathway of alopecia and the screening of effective Chinese herbal compounds
- Aberrant inflammasome activation as a driving force of human autoimmune skin disease
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- AIRE Deficiency Leads to the Development of Alopecia Areata‒Like Lesions in Mice
- Farmácia São Lázaro - Porto e nos Serviços Farmacêuticos do Hospital Privado de Vila Real (Grupo Trofa Saúde) - Vila Real
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Androgenetic Alopecia: update on Etiology, Pathophysiology, Diagnosis and Treatment
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- Drug Discovery Today: Therapeutic Strategies - 2006 Editorial
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Parasitic dermatitis in dogs: A literature review of clinical and diagnostic aspects and treatment approaches
- Emerging interactions between skin stem cells and their niches
- COVID-19 and Sex Differences
- Immunohistochemical localization of types 1 and 2 5α-reductase in human scalp
- Cutaneous reactions to chemotherapeutic drugs and targeted therapy for cancer
- Activator Protein-1 Activity Regulates Epithelial Tumor Cell Identity
- Apoptosis and cutaneous biology
- Stress and Psychoneuroimmunologic Factors in Dermatology
- Murine Cytomegalovirus is Not Associated With Alopecia Areata in C3H/HeJ Mice
- Hair and Nail Relationship
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- Glucocorticoid and Sex Hormone Receptors: Clinical Implications and Therapeutic Relevance
- iNOS inhibits hair regeneration in obese diabetic (ob/ob) mice
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene