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Research 511–540 of 789
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Subject Index
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- TONGUE, RED
- Matriptase: Potent Proteolysis on the Cell Surface
- Stratum corneum dysfunction in dandruff
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- Hair and Scalp Disorders in a Tuscan Pediatric Dermatological Outpatient Clinic: A Clinical and Epidemiological Evaluation
- Hair Keratin
- Umbilical remnant allograft application in the treatment of erosive pustular dermatosis of the scalp
- Porokeratotic Eccrine Ostial and Dermal Duct Nevus: A Report of Rare Late-Onset Solitary Lesion
- Circle hairs involving the extremities in a young girl
- ST14 interacts with TMEFF1 and is a predictor of poor prognosis in ovarian cancer
- Author response: Hair follicle epidermal stem cells define a niche for tactile sensation
- Decision letter: Hair follicle epidermal stem cells define a niche for tactile sensation
- Subject Index
- Molecular Genetics of Human Hair Diseases
- Suppression of Vitamin D Receptor and Induction of Retinoid X Receptor α Expression During Squamous Differentiation of Cultured Keratinocytes
- Micronutrients in hair loss
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Intracrine androgen biosynthesis, metabolism and action revisited
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty
- Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Microscopic polyangiitis secondary to Mycobacterium abscessus in a patient with bronchiectasis: a case report