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Research 661–690 of 1000+
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- British Society for Paediatric Dermatology Annual Meeting, Sheffield, 18-19 November 2016
- Relationships, Intimacy, & Body Image After Breast Cancer
- Androgen Biosynthesis and Gene Defects
- Inflammatory and non-melanocytic tumoral pathology of the nail
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- 9. Immunology and Genetics
- Is knowledge about the genetic and epigenetic alterations in melanoma a basis for targeted therapy?
- Finding models for skin diseases: successes and failures
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- A cross-sectional study of clinical, dermoscopic, histopathological, and molecular patterns of scalp melanoma in patients with or without androgenetic alopecia
- A cross-sectional study of clinical, dermoscopic, histopathological, and molecular patterns of scalp melanoma in patients with or without androgenetic alopecia
- The long and the short of it: evidence that <i>FGF5</i> is a major determinant of canine ‘hair’‐itability
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- Animal models of psoriasis—highlights and drawbacks
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings
- Effectiveness of Anastrozole and Cyproterone Acetate in Two Brothers with Familial Male Precocious Puberty
- Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A<i>LIPH</i>mutation
- Genome‐wide association study identifies variants associated with hair length in Brangus cattle
- Alopecia: Association with Resistance to Thyroid Hormones
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- An adult case of suspected A20 haploinsufficiency mimicking polyarteritis nodosa
- Alopecia in Harlequin mutant mice is associated with reduced AIF protein levels and expression of retroviral elements
- Hox in the Niche Controls Hairy-geneity
- Homologous recombination induced by doxazosin mesylate and saw palmetto in the <i>Drosophila</i> wing‐spot test
- Case of non-Herlitz junctional epidermolysis bullosa with<i>COL17A1</i>mutation