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Research 151–180 of 1000+
- 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
- Female pattern hair loss possibly caused by tamoxifen: Androgen receptor expression in the outer root sheath in the affected area
- Investigating the relationship between the hair fiber proteome and hair quality
- Alopecia in three women of southeast asian descent with chronic renal failure: Possible association with erythropoietin use
- P‐51 Drug‐induced erythema multiforme or drug‐induced pemphigus foliaceus: a case report
- Alopecia in association with severe seborrhoeic dermatitis following combination antiretroviral therapy for acute retroviral syndrome
- Changes in expression of the neuropeptide Y Y<sub>1</sub> receptor gene in the medial amygdala of transgenic mice during pregnancy and after delivery
- P‐88 Endocrine dermatosis and granulosa cell tumour in a red panda
- Keratosis Follicularis Spinulosa Decalvans Associated with Acne Keloidalis Nuchae and Tufted Hair Folliculitis