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Research 151–180 of 1000+
- Psoriasis y alopecia areata con traquioniquia concurrente en una paciente pediátrica con síndrome de Turner
- Sex-Chromosome-Related Dimorphism in Steroidogenic Enzymes and Androgen Receptor in Response to Testosterone Treatment: An In Vitro Study on Human Primary Skeletal Muscle Cells
- Human Adipose-Derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- THE PATHOGENESIS OF ALOPECIA AREATA
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- Human Adipose-derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Congenital Atrichia: A Case Report
- Monilethrix: Beaded hair and hypotrichosis in a child
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- A Tale of Two Haplotypes: The EDA2R/AR Intergenic Region is the Most Divergent Genomic Segment between Africans and East Asians in the Human Genome
- Do Changes in Chromosomes Cause Aging?
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- Effects of a complex mixture prepared from agrimonia, houttuynia, licorice, peony, and phellodendron on human skin cells
- Role of the Wnt signaling pathway in keratoacanthoma
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Penis Endocrinology
- Human Skin is a Steroidogenic Tissue: Steroidogenic Enzymes and Cofactors Are Expressed in Epidermis, Normal Sebocytes, and an Immortalized Sebocyte Cell Line (SEB-1)
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Differences in Expression of Specific Biomarkers Distinguish Human Beard from Scalp Dermal Papilla Cells
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- The Immunological Impact of IL-1 Family Cytokines on the Epidermal Barrier