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Research 301–330 of 1000+
- Skin diseases associated with atopic dermatitis
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- The Molecular Basis of Androgen Insensitivity
- Histopathology of Hypotrichosis with Juvenile Macular Dystrophy
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Severe metabolic disorders coexisting with Werner syndrome: a case report
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- Attenuation of Autoimmune Phenomena in a Patient with Autoimmune Polyglandular Syndrome Type 1
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Support for dermatological research in Sub‐Saharan Africa: insights from African hair and skin research programs
- 284 Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- Characterization of Human Keratin-Associated Protein 1 Family Members
- Clinical Impact of Molecular Diagnostics in Endocrinology
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Agouti and Agouti-related Protein: Analogies and Contrasts
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- 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.
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Alopezien und Hypotrichosen im Kindesalter
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia