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Research 61–90 of 1000+
- A Case of Hair Structure Abnormality Associated with Iron Deficiency Anaemia
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Keratins: the hair shaft's backbone revealed
- Genetics of Structural Hair Disorders
- Tooth, hair and claw: Comparing epithelial stem cell niches of ectodermal appendages
- Hair loss among a group of Egyptian children
- Inherited Disorders of the Hair
- Lichen Planopilaris with Pili Torti and Ectodermal Dysplasia: a hair curling case report.
- Black Hair Follicular Dysplasia in Black and White Saluki Dogs: Differentiation from Color Mutant Alopecia in the Doberman Pinscher by Microscopic Examination of Hairs
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Disorders of hair
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Current Genetics in Hair Diseases
- Clinical and trichoscopic features of early congenital syphilis: a single-center cross-sectional study
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Epidermal abnormalities and increased malignancy of skin tumors in human epidermal keratin 8‐expressing transgenic mice
- Dynamic expression of Runx1 in skin affects hair structure
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Facial Follicular Spicules: A Rare Cutaneous Presentation of Trichodysplasia Spinulosa
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Follicular Transplantation
- Keratin disorders: from gene to therapy
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report