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Research 631–660 of 1000+
- EBF1 expressed in the dermal papilla regulates hair type and length
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Spatial Gene Profiling in the Ischemic Heart
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- Receptor tyrosine kinase Kit action in skin melanocytes: is it exclusively cell autonomous?
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- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Follicles Twisted During Follicular Unit Excision Could Survive in the Skin of Nude Mice
- 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
- Fgf21 Deficiency Delays Hair Follicle Cycling and Modulates miRNA–Target Gene Interactions in Mice
- PCSK9: From Nature’s Loss to Patient’s Gain
- 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
- 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
- Cutaneous wound healing: recruiting developmental pathways for regeneration
- Defining the impact of β-catenin/Tcf transactivation on epithelial stem cells