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Research 31–60 of 1000+
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- 307 Phenotypic-genotypic expansion of plectinopathy in a patient with muscular dystrophy and immune-mediated myasthenia gravis
- 494 Epidermolysis bullosa pruriginosa, muscular dystrophy, and immune-mediated myasthenia gravis in a patient with homozygous nonsense PLEC mutation
- 666 Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in follicular dystrophy and primary cicatricial alopecia
- Analysis of Skin, Hair and Nail Diseases in the Adults with Beta Thalassemia Major
- A patient with diffuse hair loss
- Clinical and histopathologic features of hair loss in patients with HIV-1 infection
- A Guide to Assessing Damage Response Pathways of the Hair Follicle: Lessons From Cyclophosphamide-Induced Alopecia in Mice
- Chemotherapy Targets the Hair-Follicle Vascular Network but Not the Stem Cells
- Alopecia Areata in C3H/HeJ Mice Involves Leukocyte-mediated Root Sheath Disruption in Advance of Overt Hair Loss
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Clinical relevance of hair microscopy in alopecia
- Activation of mTORC1 Signaling is Required for Timely Hair Follicle Regeneration from Radiation Injury
- Parathyroid hormone linked to a collagen binding domain promotes hair growth in a mouse model of chemotherapy-induced alopecia in a dose-dependent manner
- FGF signaling for hair cycle resting phase alleviates radiation alopecia
- Mimicking Senescence Factors to Characterize the Mechanisms Responsible for Hair Regression and Hair Loss: An In Vitro Study
- Effect of N-acetylcysteine on hair follicle changes in mouse model of cyclophosphamide-induced alopecia: histological and biochemical study
- LB789 Novel IFNγ aptamer TAGX-0003 protected hair follicles from immune privilege collapse and reversed Alopecia Areata like phenotype in humanized mouse model
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- A rare case of woolly hair with unusual associations
- Skin features in myotonic dystrophy type 1: An observational study
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Disorders of the Hair and Nails
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]