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Research 121–150 of 1000+
- Non‐endocrine alopecia
- Endocrinopathies, Atypical
- Les hormones sexuelles et la peau : questionnaire à l'attention des vétérinaires praticiens. Mise à jour bibliographique et synthèse
- 42863 The association of milia-like calcinosis cutis, alopecia totalis and hyperthyroidism linked with the novel mutation for RBM28
- Multiorgan Dysfunction in a 7-Month-Old Boy With Developmental Delay and Poor Growth
- Embryonic keratinization in vertebrates in relation to land colonization
- Stromal Vascular Fraction and Platelet-Rich Plasma Upregulate Vascular Endothelial Growth Factor Expression to Promote Hair Growth via the Wnt/β-Catenin Signaling Pathway
- This Month in the Journal
- Dissecting the Molecular Mechanisms Involved in Keloid Pathogenesis and Response to Therapy
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Linking allergy to mercury to HLA and burning mouth syndrome
- Androgenetic alopecia and microinflammation
- Lichen planopilaris and autoimmune thyroiditis
- Finasteride-related Leydig cell tumour: report of a case and literature review
- IN OTHER JOURNALS
- Association of psoriasis and psoriatic arthritis with human leukocyte antigen and killer cell immunoglobulin–like receptor gene frequency: A multiethnic population study
- Vitiligo
- Sunscreen: Cosmetic or medical therapy?
- Keratosis Follicularis Spinulosa Decalvans: Diagnosis and Therapeutic Evaluation.
- Two Cases of Danon Disease – A ‘Cousin’ of Pompe Disease
- Melanocyte Subpopulation Turnover During the Human Hair Cycle: An Immunohistochemical Study
- Lichen planus and other cutaneous manifestations in chronic hepatitis C: pre- and post-interferon-based treatment prevalence vary in a cohort of patients from low hepatitis C virus endemic area
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- Trichothiodystrophy and fragile hair: the distinction between diagnostic signs and diagnostic labels in childhood hair disease
- Generalised cutaneous necrosis: a complication of low-molecular-weight heparin
- Pathological Studies of Cross‐Related Congenital Hypotrichosis in Cattle
- High‐Sulfur Protein Gene Expression in a Transgenic Mouse