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Research 151–180 of 1000+
- Target-Adverse Events and Fear of Cancer Progression, Anxiety, and Depression in Patients with Advanced Non-Small Cell Lung Cancer
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- WNT10B (wingless-type MMTV integration site family)
- Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
- Methylated CpG dinucleotides in 5-α reductase 2 gene might explain the finasteride-resistance in BPE patients
- Bioregenerative Applications of the Human Mesenchymal Stem Cell- Derived Secretome: Part-II
- Criteria for Defining Polycystic Ovary Syndrome as a Predominantly Hyperandrogenic Syndrome: An Androgen Excess Society Guideline
- The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- Control of hair growth and follicle size by VEGF-mediated angiogenesis
- Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition
- Alopecia Areata
- The cutaneous serotoninergic/melatoninergic system: securing a place under the sun
- Leucine-Rich Repeat-Containing G-Protein-Coupled Receptors as Markers of Adult Stem Cells
- Coordinated Activation of Wnt in Epithelial and Melanocyte Stem Cells Initiates Pigmented Hair Regeneration
- Interrelation of immunity and tissue repair or regeneration
- Serotoninergic and melatoninergic systems are fully expressed in human skin
- Cutaneous Androgen Metabolism: Basic Research and Clinical Perspectives
- Tracing the cellular origin of cancer
- Screening for 21-hydroxylase–deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study
- Ultrafast Mid-IR Laser Scalpel: Protein Signals of the Fundamental Limits to Minimally Invasive Surgery
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Vitamin D metabolism and function in the skin
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- The PDGF/PDGFR pathway as a drug target
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Androgenetic alopecia: pathogenesis and potential for therapy
- In vivo transcriptional governance of hair follicle stem cells by canonical Wnt regulators
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development
- An Update of Congenital Adrenal Hyperplasia