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Research 901–930 of 1000+
- Innovations in Skin and Soft Tissue Aging—A Systematic Literature Review and Market Analysis of Therapeutics and Associated Outcomes
- Trends in Nanotechnology for Practical Applications
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- Tangled Causes, Targeted Solutions: A Comprehensive Review of Alopecia.
- Effect of inhibiting prolactin secretion on secondary hair follicle development in cashmere goats
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- 476 Development of an intrinsic skin sensor for blood glucose level with CRISPR-mediated genome editing in epidermal stem cells
- Hair Growth Defects of Diabetic and Hypercholesterolemic Wistar Albino Rats and Amelioration of Fish Oil-Treatment
- Le gène<i>hairless</i>de la souris
- Sexually dimorphic sail feathers in the Mandarin duck as a model for lifelong developmental modulation
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Modelling androgen synthesis and action during human sexual differentiation
- The in vitro plasticity of hair follicle dermal and mesenchymal stem cells
- An Update of Congenital Adrenal Hyperplasia
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- What causes hidradenitis suppurativa ?—15 years after
- Neuronal plasticity of the “brain–skin connection”: stress-triggered up-regulation of neuropeptides in dorsal root ganglia and skin via nerve growth factor-dependent pathways
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- Alopecia Areata
- The dermatological consequences of obesity
- The developing immune network in human prenatal skin
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Co-opting Developmental Signaling Pathways to Promote Wound Healing
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Inherited Epidermolysis Bullosa: A Clinical Case
- Unravelling the link between insulin resistance and androgen excess
- Australasian Society for Dermatology Research Meeting, May 2006
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?