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Research 91–120 of 184
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
- Diagnostic utility of preferentially expressed antigen in melanoma immunohistochemistry in the evaluation of melanomas with a co-existent nevoid melanocytic population: A single-center retrospective cohort study
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Development of Heritable Melanoma in Transgenic Mice
- Pubertal Development
- Correction of ornithine transcarbamylase (OTC) deficiency in spf‐ash mice by introduction of rat OTC gene
- The Study of Growth Factors in Patients with Androgenic Alopecia
- Mechanism of Targeting the Hedgehog Signaling Pathway against Chemotherapeutic Resistance in Multiple Myeloma
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Cutaneous and Oral Mucosal Lesions in Cri-du-chat Syndrome
- Hormonal Organization of Sex Differences in Play Fighting and Spatial Behavior
- The Human Hair Follicle: A Reservoir of CD40+ B7-Deficient Langerhans Cells that Repopulate Epidermis After UVB Exposure
- Characterization of sciellin, a precursor to the cornified envelope of human keratinocytes
- 9-cis-Retinoic Acid Capsules in the Treatment of AIDS-Related Kaposi Sarcoma
- Long and short non-coding RNA and radiation response: a review
- 9 Diagnosis and therapy of hyperandrogenism
- Ex Vivo Organ Culture of Human Hair Follicles: A Model Epithelial–Neuroectodermal–Mesenchymal Interaction System
- Accurate quantification of minimal residual disease at day 15, by real-time quantitative polymerase chain reaction identifies also patients with B-precursor acute lymphoblastic leukemia at high risk for relapse
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Nilontinib induced keratosis pilaris atrophicans
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Overlap Between Ulerythema Ophryogenes and Keratosis Follicularis Spinulosa Decalvans: a Case Report
- 85 Primary cutaneous follicle center lymphoma spans yet unrecognised subtypes including polyclonal reactions
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- Hair Follicle Culture
- The inheritance of common baldness: Two B or not two B ?
- Unravelling a novel role for cannabidivarin in the modulation of subventricular zone postnatal neurogenesis
- Stigmata of Liver Disease in a Cirrhotic Patient
- Human Skin is a Steroidogenic Tissue: Steroidogenic Enzymes and Cofactors Are Expressed in Epidermis, Normal Sebocytes, and an Immortalized Sebocyte Cell Line (SEB-1)