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Research 691–720 of 1000+
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Keratin gene mutations in disorders of human skin and its appendages
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Hair Keratin: Composition, Structure and Biogenesis
- Restoration of skin pigmentation after deep partial or full-thickness burn injury
- Turner's syndrome associated with psoriasis and alopecia areata
- Pathogenesis of pili annulati
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Ceramic flat irons: Improper use leading to acquired trichorrhexis nodosa
- Potassium Channel Openers Increase Aortic Elastic Fiber Formation and Reverse the Genetically Determined Elastin Deficit in the BN Rat
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Black Hair Follicular Dysplasia in Black and White Saluki Dogs: Differentiation from Color Mutant Alopecia in the Doberman Pinscher by Microscopic Examination of Hairs
- Genetic Hair Disorders: A Review
- Overexpression of human keratin 16 produces a distinct skin phenotype in transgenic mouse skin
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Hard Keratin IF and Associated Proteins
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Correlation of Hair Mineral Concentrations with Insulin Resistance in Korean Males
- Disorders of hair in infants and children other than alopecia
- Analytical method for the biomonitoring of bisphenols and parabens by liquid chromatography coupled to tandem mass spectrometry in human hair
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Premature androgenic alopecia and insulin resistance. Male equivalent of polycystic ovary syndrome?
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Therapeutic effect of mesenchymal stem cells on histopathological, immunohistochemical, and molecular analysis in second-grade burn model
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Safety of Common Medications for Treating Dermatology Disorders in Pregnant Women
- Exploring the Complexities of Atopic Dermatitis: Pathophysiological Mechanisms and Therapeutic Approaches