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Research 421–450 of 1000+
- Follikelhormone
- Self-Assessment
- Telogen Effluvium
- Hair and Scalp Variation Related to Gender
- A review on Hair Loss & Damage
- Long-term consequences of critical illness
- Long-term consequences of critical illness
- Modelling androgen synthesis and action during human sexual differentiation
- Dermatological manifestations associated with pregnancy
- Abstracts Pt.30
- Syndromes of Severe Insulin Resistance (SSIRs)
- Letters to the Editor
- Oral cyclosporin does not arrest progression of androgenetic alopecia
- 056 IKZF1 and IKAROS overexpression contributes to the pathogenesis of alopecia areata
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
- GLI2 Is Expressed in Normal Human Epidermis and BCC and Induces GLI1 Expression by Binding to its Promoter
- Targeting of CXXC5 by a Competing Peptide Stimulates Hair Regrowth and Wound-Induced Hair Neogenesis
- CXXC5: A novel regulator and coordinator of TGF-β, BMP and Wnt signaling
- Hair follicle epithelial stem cells contribute to interfollicular epidermis during homeostasis
- Variation in Ovine KRTAP13-3 and Its Association with Wool Characteristics in Chinese Tan Sheep
- Molecular mechanism for transcriptional regulation of the parathyroid hormone gene by Epiprofin
- [Molecular cloning of full-long cDNA sequences encoding hairless gene in the Kunming mouse].
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- The Krüppel-like Factor Epiprofin Is Expressed by Epithelium of Developing Teeth, Hair Follicles, and Limb Buds and Promotes Cell Proliferation
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia