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Research 871–900 of 1000+
- Receptor tyrosine kinase Kit action in skin melanocytes: is it exclusively cell autonomous?
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- Follicles Twisted During Follicular Unit Excision Could Survive in the Skin of Nude Mice
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Paxbp1 is Indispensable for the Maintenance of Hair Follicle Homeostasis
- Persistent hyperparathyroidism in vitamin D-dependent rickets type 2A does not prevent normalization of hypophosphatemia or healing of the rickets
- UTX (KDM6A) promotes differentiation noncatalytically in somatic self-renewing epithelia
- Fgf21 Deficiency Delays Hair Follicle Cycling and Modulates miRNA–Target Gene Interactions in Mice
- PCSK9: From Nature’s Loss to Patient’s Gain
- Boron deficiency responses in maize (<i>Zea mays</i> L.) roots
- Uncombable hair improved by biotin
- Iron Screening in Alopecia Areata Patients May Catch Hereditary Hemochromatosis Early
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Collodion baby to bathing suit ichthyosis: A 6-year follow-up
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Effects of the bovine slick mutation on heat stress responses and hair growth in mice
- A perspective on predictive markers of alopecia
- Hair Cortisol Is a Potential Indicator of Adrenal Insufficiency in Individuals with Sickle Cell Disease
- P78 Acrodermatitis enteropathica in children: clinical cases
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Skin fragility, diffuse ecchymosis and blisters on a yellowish waxy base
- 441 RPGRIP1L facilitates desmosomal adhesion through suppressing PKCβII-mediated desmoglein endocytosis: Implication in pemphigus
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Trichorrhexis Invaginata and Netherton’s Syndrome
- Metabolic disease with autoimmune phenomena: 2 cases of SLE-like disease in young children diagnosed with lysinuric protein intolerance
- Characterisation, genomic organisation, expression and function of the mEphA1 receptor Tyrosine Kinase
- Does Vitamin D play a role on Msx1 homeoprotein expression involving an endogenous antisense mRNA?*1
- Treatment of Cystathionine β-Synthase Deficiency in Mice Using a Minicircle-Based Naked DNA Vector
- Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak