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Research 571–600 of 684
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Mammary Cells with Active Wnt Signaling Resist ErbB2-Induced Tumorigenesis
- An overview of current strategies and future prospects in drug repurposing in tuberculosis
- Celsr1 and Celsr2 exhibit distinct adhesive interactions and contributions to planar cell polarity
- Overactive Wnt5a signaling disrupts hair follicle polarity during mouse skin development
- α-parvin is required for epidermal morphogenesis, hair follicle development and basal keratinocyte polarity
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Structural Abnormalities in the Hair of a Patient with a Novel Ribosomopathy
- Prediction of the Mechanism of Shaoyao Gancao Decoction in the Treatment of Alopecia Areata by Network Pharmacology and Its Preliminary Verification Study
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Engineering a New Mouse Model for Vitiligo
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Molecular Regulatory Mechanisms in Chicken Feather Follicle Morphogenesis
- Immunohistochemical, pharmacovigilance, and omics analyses reveal the involvement of ATP-sensitive K+ channel subunits in cancers: role in drug–disease interactions
- Analogs of human genetic skin disease in domesticated animals
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- Ear pinna growth and differentiation is conserved in murids and requires BMP signaling for chondrocyte proliferation
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Polycystic ovary syndrome and iron overload: biochemical link and underlying mechanisms with potential novel therapeutic avenues
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- A Comprehensive Review of GWASs of Human Hair Traits
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog