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Research 181–210 of 1000+
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Skin Development and Disease: A Molecular Perspective
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Hyperplasia of the Subcutaneous Adipose Tissue Is the Primary Histopathologic Abnormality in Lipedematous Scalp
- A Narrative Review of Advances in Skin Tissue Engineering: From Physiological Architecture to 3D Bioprinting
- Telogen Effluvium
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Telogen Effluvium: A Review
- A case of familial trichomegaly with synophrys in association with loose anagen syndrome
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Short anagen syndrome: Case series and literature review
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- A guide to diagnosis and management of hypertrichosis
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Non-Neoplastic Disorders of Hair
- Assessment of Hair and Scalp Disorders
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Evaluation of hair loss