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Research 511–540 of 1000+
- Genetic Hair Disorders: A Review
- Ichthyosis with confetti: clinics, molecular genetics and management
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Zebrafish Model of Hereditary Pigmentary Disorders
- Correlation Analysis of BLTP1 (KIAA1109) and KIF27 Gene Polymorphisms with Wool Traits in Subo Merino Sheep
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- Skin, Genetic Defects, and Aging
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Frizzled Receptors in Development and Disease
- Skin morphology of the mutant hairless USP mouse
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- WNT Signaling in Disease
- Pathology of Mouse Models of Accelerated Aging
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Targeting integrin pathways: mechanisms and advances in therapy
- Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Skin Development and Disease: A Molecular Perspective
- Proteomic Analysis of Two Stem Cell Secretomes Used in Combination in a Topical Skin Care Product That Has Demonstrated Efficacy in a Double-Blinded, Vehicle-Controlled Clinical Trial
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- E-Poster
- An Infant with Worsening Rash
- Autoimmune Diseases and Acquired Von Willebrand Disease in Two Cases of Progeria
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed