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Research 361–390 of 736
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- m6A Methylation Analysis of Differentially Expressed Genes in Skin Tissues of Coarse and Fine Type Liaoning Cashmere Goats
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Bimatoprost in the treatment of eyelash hypotrichosis
- 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.
- Structure and expression of genes for a class of cysteine-rich proteins of the cuticle layers of differentiating wool and hair follicles.
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Role of FGFR2-signaling in the pathogenesis of acne
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- The chemokine SDF-1/CXCL12 regulates the migration of melanocyte progenitors in mouse hair follicles
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Parathyroid Hormone-related Protein in Normal and Neoplastic Canine Tissues: Immunohistochemical Localization and Biochemical Extraction
- SARS-CoV-2 Non-Structural Proteins and Their Roles in Host Immune Evasion
- Epidermal and Hair Follicle Progenitor Cells Express Melanoma-Associated Chondroitin Sulfate Proteoglycan Core Protein
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Newly Developed Targeted Therapies Against the Androgen Receptor in Triple-Negative Breast Cancer: A Review
- Oxidative DNA Damage Accelerates Skin Inflammation in Pristane-Induced Lupus Model
- Progenitor Cell Dysfunctions Underlie Some Diabetic Complications
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Dynamic expression of Runx1 in skin affects hair structure
- Alleviation of Multidrug Resistance by Flavonoid and Non-Flavonoid Compounds in Breast, Lung, Colorectal and Prostate Cancer
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Long and short non-coding RNA and radiation response: a review