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Research 181–210 of 1000+
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- On the effects of testosterone on brain behavioral functions
- Impact of Thyroid Dysfunction on Hair Disorders
- Fever of unknown origin in a male patient with systemic lupus erythematosus.
- A novel human type I hair keratin gene: evidence for two keratin hHa3 isoforms
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- Inducible deletion of epidermal <i>Dicer</i> and <i>Drosha</i> reveals multiple functions for miRNAs in postnatal skin
- Myotonic Dystrophy—A Progeroid Disease?
- Overexpression of hepatoma-derived growth factor in melanocytes does not lead to oncogenic transformation
- Montagna Symposium 2013—Light and Skin: How Light Sustains, Damages, Treats, Images and Modifies Skin Biology
- Applications of Exosomal miRNAs from Mesenchymal Stem Cells as Skin Boosters
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Targeting the Hippo/YAP/TAZ signalling pathway: Novel opportunities for therapeutic interventions into skin cancers
- The potential role of hsa_circ_0001079 in androgenetic alopecia via sponging hsa‐miR‐136‐5p
- Epithelial loss of mitochondrial oxidative phosphorylation leads to disturbed enamel and impaired dentin matrix formation in postnatal developed mouse incisor
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- Seasonal Variability in Transcript Expression of Type I and Type II Keratins in Wool Follicles of Lustrous Fleece-Producing Magra Sheep
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- Unlocking the Power of Light on the Skin: A Comprehensive Review on Photobiomodulation
- CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats
- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- Spatial transcriptomics of a giant pilomatricoma