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Research 631–660 of 1000+
- Evolution of Trichocyte Keratins
- The Notch Intracellular Domain Has an RBPj-Independent Role during Mouse Hair Follicular Development
- UDP-GlcNAc-1-Phosphotransferase Is a Clinically Important Regulator of Human and Mouse Hair Pigmentation
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Hair follicles modulate skin barrier function
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Stimuli-responsive nanoformulations for CRISPR-Cas9 genome editing
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- The Dark Side of Gefitinib: Reflectance Confocal Microscopy Applied to Hair Hyperpigmentation
- Connexin mutations in human disease
- Skin regional specification and higher-order <i>HoxC</i> regulation
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Dysregulated behaviour of hair follicle stem cells triggers alopecia and provides potential therapeutic targets
- Analogs of human genetic skin disease in domesticated animals
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Apoptosis in Hair and Skin: A Review
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Successful management of Netherton syndrome using IVIG and dupilumab: A case report
- Steatocystoma Multiplex
- Transcriptomes reveal microRNAs and mRNAs in different photoperiods influencing cashmere growth in goat
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Diseases of the Canine Prostate Gland
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Acne Syndromes and Mosaicism
- Antioxidant and Antiproliferative Activity of Finasteride against Glioblastoma Cells
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- Current Genetics in Hair Diseases
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report