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Research 31–60 of 1000+
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
- [Association of eight single nucleotide polymorphisms of chromosomes 20 and X with androgenetic alopecia among ethnic Han Chinese from Yunnan].
- Severe Variant of X‐linked Dyskeratosis Congenita (Hoyeraal‐Hreidarsson Syndrome) Causes Significant Enterocolitis in Early Infancy
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- 7 Pathogenesis and Classification of Male Pattern Hair Loss (Androgenic Alopecia)
- Non-nutritional rickets: Approach, precision medicine, and outcomes
- Disorders of Keratinization
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Hairless Modulates Ligand-Dependent Activation of the Vitamin D Receptor-Retinoid X Receptor Heterodimer
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- Keratosis follicularis spinulosa decalvans in a female
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- Banding Pattern on Polarized Hair Microscopic Examination and Unilateral Polymicrogyria in a Patient With Steroid Sulfatase Deficiency
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- Roles of steroid sulfatase in brain and other tissues
- Cloning of a Functional Vitamin D Receptor from the Lamprey (Petromyzon marinus), an Ancient Vertebrate Lacking a Calcified Skeleton and Teeth
- Ehlers-Danlos syndrome: From bedside to bench
- Cheveu, vieillissement et environnement : aspects cliniques épidémiologiques
- 42863 The association of milia-like calcinosis cutis, alopecia totalis and hyperthyroidism linked with the novel mutation for RBM28
- Multiorgan Dysfunction in a 7-Month-Old Boy With Developmental Delay and Poor Growth
- British Society for Dermatopathology
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Stromal Vascular Fraction and Platelet-Rich Plasma Upregulate Vascular Endothelial Growth Factor Expression to Promote Hair Growth via the Wnt/β-Catenin Signaling Pathway
- Association of psoriasis and psoriatic arthritis with human leukocyte antigen and killer cell immunoglobulin–like receptor gene frequency: A multiethnic population study
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- High‐Sulfur Protein Gene Expression in a Transgenic Mouse
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- This Month in the Journal
- Generalised cutaneous necrosis: a complication of low-molecular-weight heparin