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Research 181–210 of 1000+
- Erythromelanosis follicularis faciei et colli with reticulated hyperpigmentation of the extremities
- Inflammatory auxo-action in the stem cell division theory of cancer
- Male infertility and genitourinary birth defects: there is more than meets the eye
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Skinspan: A Holistic Roadmap for Extending Skin Longevity With Evidence‐Based Interventions
- Genome-Wide Identification and Characterization of the Wnt Gene Family in Donkey (Equus asinus): Phylogenetic Analysis and Expression Profiling
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Detection of the nuclear translocation of androgen receptor using quantitative and automatic cell imaging analysis
- Polycystic ovary syndrome (PCOS), an inflammatory, systemic, lifestyle endocrinopathy
- FOXP3 <sup>+</sup> regulatory T cells and age‐related diseases
- Telomere dysfunction impairs epidermal stem cell specification and differentiation by disrupting BMP/pSmad/P63 signaling
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- A study on efficacy of oral zinc therapy for treatment of acrodermatitis enteropathica
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Testosterone: The Male Sex Hormone
- The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Factors regulating quiescent stem cells: insights from the intestine and other self-renewing tissues
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Survival of patchwork melanoblasts is dependent upon their number in the hair follicle at the end of embryogenesis
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- Limb amputations; etiopathogenesis, diagnosis and the multidisciplinary therapeutic approach
- Cellular senescence and polycystic ovary syndrome: mechanisms and therapeutic strategies from a new perspective
- Challenges, Progress, and Prospects of Developing Therapies to Treat Autoimmune Diseases
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Fertility evaluation of infertile women: a committee opinion