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Research 241–270 of 1000+
- Disease causing homozygous variants in the human hairless gene
- 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
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Virilism and Ectopic Expression of HSD17B5 in Mature Cystic Teratoma
- Role of the Wnt signaling pathway in keratoacanthoma
- Human Adipose-derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Psoriasis y alopecia areata con traquioniquia concurrente en una paciente pediátrica con síndrome de Turner
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Dendrobium officinale polysaccharide improves hair regrowth in androgenetic alopecia mice and is associated with coordinated changes in local steroid metabolism, ESR1 activation, and keratin-related follicular responses
- Olink proteomics analysis of scalp psoriasis reveals a cytokine storm inflammatory mainly related to bacterial-derived antigens
- Study on Changes of 19 Steroids in Plasma From 9 Diagnosed Patients With P450 Oxidoreductase Deficiency
- Acne-Associated Syndromes
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development
- Congenital Adrenal Hyperplasia
- Toxic shock syndrome: Recent developments in pathogenesis
- Protective cardiovascular and renal actions of vitamin D and estrogen
- The hair shaft: normality, abnormality, and genetics
- Skin transcriptome reveals the Periodic changes in genes underlying hair follicle cycling in Cashmere goats
- Treatment-resistant Schizophrenia and Global Cortical Atrophy in a Patient with Turner Syndrome
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- What causes hidradenitis suppurativa ?—15 years after