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Research 331–360 of 1000+
- The senescence-like activity of BMS-470539 is associated with anti-fibrotic actions in models of dermal fibrosis
- British Society for Dermatopathology: Summaries of Papers
- Morphological Approach to Hair Disorders
- Alopecia areata in a rhesus monkey (Macaca mulatta)
- COVID-19 infection leading to acute pustular dermatoses
- Structural optimization of pep7, a small peptide extracted from epimorphin, for effective induction of hair follicle anagen
- ER-located Ca2+ ATPase ACA2 regulates Ca2+ cytoplasmic pool linked to root hair growth in Arabidopsis thaliana
- Follicular Neutrophilic Inflammation (Hidradenitis Suppurativa)
- A novel therapeutic paradigm for patients with extensive alopecia areata
- Extracellular Matrix as a Regulator of Epidermal Stem Cell Fate
- Successful management of Netherton syndrome using IVIG and dupilumab: A case report
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis
- The heme-responsive PrrH sRNA regulates <i>Pseudomonas aeruginosa</i> pyochelin gene expression
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF‐β/Smad signaling pathway in CARASIL model mice
- <i>Pseudomonas aeruginosa</i> heme metabolites biliverdin IXβ and IXδ are integral to lifestyle adaptations associated with chronic infection
- Андрогенетическая алопеция: патогенетические механизмы и подходы к лечению
- Identification and characterization of genes for skin and hair disorders
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Bachmann–Bupp syndrome and treatment
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- FOXN1 deficient nude severe combined immunodeficiency
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- Establishment of Tsc2-deficient rat embryonic stem cells
- Keratins and disease at a glance
- Acne-Associated Syndromes
- Role of FGFR2-signaling in the pathogenesis of acne
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies