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Research 331–360 of 1000+
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Platelet-derived growth factor signaling modulates adult hair follicle dermal stem cell maintenance and self-renewal
- Planar cell polarity-dependent and independent functions in the emergence of tissue-scale hair follicle patterns
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Diagnostic approach to low‐renin hypertension
- Dietary isoflavone increases insulin-like growth factor-I production, thereby promoting hair growth in mice
- Identification and dissection of an enhancer controlling epithelial gene expression in skin
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Field Cancerization: From Molecular Basis to Selective Field-Directed Management of Actinic Keratosis
- Genetically separable determinants of hair keratin gene expression
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Alopecia Areata
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Epigenetic regulation in adult stem cells and cancers
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary cilia
- Genetics of Structural Hair Disorders
- Cutaneous gene therapy
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Comprehensive Transcriptome Profiling of Balding and Non-Balding Scalps in Trichorhinophalangeal Syndrome Type I Patient
- Expression analysis of KAP9.2 and Hoxc13 genes during different cashmere growth stages by qRT-PCR method
- Multiple Roles of Integrin-Linked Kinase in Epidermal Development, Maturation and Pigmentation Revealed by Molecular Profiling