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Research 331–360 of 1000+
- Hair follicles modulate skin barrier function
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Engineering a New Mouse Model for Vitiligo
- Differential expression of KRT83 regulated by the transcript factor CAP1 in Chinese Tan sheep
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Polycystic Ovary Syndrome in the Context of Pituitary Adenomas: Prevalence, Pathophysiology and Clinical Management
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Familial Frontal Fibrosing Alopecia
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- A Holistic Approach to Unravel Keloid Pathogenesis and Optimize Therapeutic Outcomes
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Genetics of infertility and “assisted fertilization” in the Bible: The case of Abraham and his family
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- A review of isotretinoin in the treatment of frontal fibrosing alopecia
- A cross-sectional, observational study of the clinico-epidemiological profile of female pattern hair loss in Western India and its association with metabolic syndrome
- TRP Channels in Skin Biology and Pathophysiology
- Frizzled Receptors in Development and Disease
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- B-Raf and C-Raf Are Required for Melanocyte Stem Cell Self-Maintenance
- Co-factors of LIM domains (Clims/Ldb/Nli) regulate corneal homeostasis and maintenance of hair follicle stem cells
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Expression of Signaling Components in Embryonic Eyelid Epithelium
- The Wound Healing: A Mystery Still to Be Solved—What Is the Future?