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Research 451–480 of 1000+
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- E-Poster
- SnapshotDx Quiz: August 2019
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- Analysis of skin mycobiota associated with alopecia in captive cynomolgus macaques (Macaca fascicularis) based on Oxford Nanopore Technologies
- Quoi de neuf en recherche dermatologique ?
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Merkel cell carcinoma: updates in tumor biology, emerging therapies, and preclinical models
- Improving the treatment of bacterial infections caused by multidrug-resistant bacteria through drug repositioning
- The immune response to COVID‐19: Does sex matter?
- UDP-GlcNAc-1-Phosphotransferase Is a Clinically Important Regulator of Human and Mouse Hair Pigmentation
- Recent advances in exosomal non‐coding RNA‐based therapeutic approaches for photoaging
- Volatile organic compounds: A proinflammatory activator in autoimmune diseases
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- 476 Development of an intrinsic skin sensor for blood glucose level with CRISPR-mediated genome editing in epidermal stem cells
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Primary cicatricial alopecia and inflammatory bowel disease – is there a link?
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Wnt Signaling in Skin Development, Homeostasis, and Disease