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Research 931–960 of 1000+
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Lysophospholipid Mediators in Health and Disease
- Regulation of the Wound Healing Response during Aging
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- The Notch Intracellular Domain Has an RBPj-Independent Role during Mouse Hair Follicular Development
- Fibrotic enzymes modulate wound‐induced skin tumorigenesis
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Hair follicles modulate skin barrier function
- Human melanocyte development and melanoma dedifferentiation at single cell resolution
- Expression profile analysis of microRNAs during hair follicle development in the sheep foetus
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Androgen receptor CAG repeat length is associated with ovarian reserve but not with ovarian response
- A newborn presenting with congenital blistering
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Hedgehog Signaling in Papillary Fibroblasts Is Essential for Hair Follicle Regeneration during Wound Healing
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Alopezien und Hypotrichosen im Kindesalter
- Single-cell analysis of temporal immune cell dynamics in alopecia areata reveals a causal role for clonally expanded CD8+ T cells in disease