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Research 511–540 of 1000+
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- What causes hidradenitis suppurativa ?—15 years after
- The long and the short of it: evidence that <i>FGF5</i> is a major determinant of canine ‘hair’‐itability
- 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.
- The population dynamics of cancer: a Darwinian perspective
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- Skin Keratins
- Animal models of psoriasis—highlights and drawbacks
- Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- What's new in the pathogeneses and triggering factors of bullous pemphigoid
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Practical Guidelines for Evaluation of Loose Anagen Hair Syndrome
- Roles of tumor suppressors in regulating tumor-associated inflammation
- Skin diseases associated with atopic dermatitis
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- Plasticity of differentiated cells in wound repair and tumorigenesis, part II: skin and intestine
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Gene Delivery to the Hair Follicle
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Hair and nail adverse events during treatment with targeted therapies for metastatic melanoma
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*