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Research 481–510 of 1000+
- 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
- Organ Specificity in Autoimmune Diseases: Thyroid and Islet Autoimmunity in Alopecia Areata
- <i>WNT10A</i> , dermatology and dentistry
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- What does acne genetics teach us about disease pathogenesis?
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- MicroRNA in skin diseases
- Congenital adrenal hyperplasia
- The Genetics of Human Skin Disease
- Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias
- Primary Scarring Alopecia: Clinical-Pathological Review of 72 Cases and Review of the Literature
- Dermatological Manifestations of Stress in Normal and Psychiatric Populations
- Retinoid Metabolism Is Altered in Human and Mouse Cicatricial Alopecia
- Overexpression of IL-18 in the Proliferative Phase Endometrium of Patients With Polycystic Ovary Syndrome
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Epigenetic regulation in adult stem cells and cancers
- Regulation of pathophysiological and tissue regenerative functions of MSCs mediated via the WNT signaling pathway (Review)
- Genetic basis of polycystic ovary syndrome
- Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor
- Congenital adrenal hyperplasia
- Indian Hedgehog Controls Proliferation and Differentiation in Skin Tumorigenesis and Protects against Malignant Progression
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- Hirsutism in the Adolescent Female
- Polymorphisms in androgen and estrogen receptor genes: effects on male aging
- DMBA/TPA Treatment Is Necessary for BCC Formation from Patched Deficient Epidermal Cells in Ptch flox/flox CD4Cre +/− Mice
- The Biology of Hair Growth
- Vogt-Koyanagi-Harada Disease: A Narrative Review