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Research 151–180 of 1000+
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Safety of dermatologic medications in pregnancy and lactation
- Nonclassic adrenal hyperplasia
- Generalized trichoepitheliomas with alopecia and myasthenia gravis: Clinicopathologic and immunohistochemical study and comparison with classic and desmoplastic trichoepithelioma
- Concerted gene duplications in the two keratin gene families
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Gene therapy to enhance angiogenesis in chronic wounds
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep
- Diagnostic approach to low‐renin hypertension
- Interaction between stem cell factor and endothelin-1: effects on melanogenesis in human skin xenografts
- The Genetics of Human Skin Disease
- Transcriptome-based selection and validation of optimal house-keeping genes for skin research in goats (Capra hircus)
- Topical Gene Electrotransfer to the Epidermis of Hairless Guinea Pig by Non-Invasive Multielectrode Array
- The dermatological consequences of obesity
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Advances in the Study of Stem-Cell-Enriched Hair Follicle Bulge Cells: A Review Featuring Characterization and Isolation of Human Bulge Cells
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- The developing immune network in human prenatal skin
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- The relationship among androgens, insulin resistanceand ghrelin polymorphisms in post-adolescent malepatients with severe acne vulgaris
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- A polymorphism in the matrix metalloproteinase-1 gene promoter is associated with the presence of polycystic ovary syndrome in Caucasian women
- A Case of Familial Male-limited Precocious Puberty with a Novel Mutation