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Research 481–510 of 1000+
- Epidermolysis Bullosa Simplex Keratinocytes Show Disturbed Mitochondrial Positioning and Activity
- 509 Using the human iPSCs-derived sensory neurons re-innervated skin ex vivo model to investigate mast cell-nerve fiber cross-talk in solar elastosis
- Keloid pathogenesis and fibroproliferative properties are dependent on stem cells regulated by the HEDGEHOG-GLI1 pathway
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- Mucinosis folicular. Reporte de un caso pediátrico
- 정상 및 배양 피부 , 수종 각화이상성 피부질환에서의 Skin Sulfhydryl Oxidase 발현에 관한 연구
- Gonadal Function Abnormalities in Sickle Cell Anemia
- Hypertrichosis
- Pulmonary Edema in COVID-19 Patients: Mechanisms and Treatment Potential
- How to diagnose a lipodystrophy syndrome
- Scalp whorls
- Alopecia in women.
- Cross-linked features of mouse pelage hair resistant to detergent extraction
- Acquired Localized Hypertrichosis Following Pressure Garment and/or Silicone Therapy in Burn Patients
- Pitfalls of Midface Surgery
- Hypertrichosis lanuginosa acquisita following cytotoxic chemotherapy
- Impact of Laboratory Work Up and Supplementation on Alopecia Patients: A Single-Center Retrospective Chart Review.
- 第34回学校法人日本医科大学外国人留学者研究会抄録
- Research progress on drug-induced gynecomastia
- Review of Hair Removal in Traditional Medicine and Its Clinical Application
- Polycystic ovary syndrome
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- Towards a molecular understanding of hair loss and its treatment
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Activating Wnt/β-catenin signaling pathway for disease therapy: Challenges and opportunities
- Deregulated expression of E2F1 induces hyperplasia and cooperates with ras in skin tumor development
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Phospholipase C 1 is required for skin stem cell lineage commitment
- Planar Cell Polarity Cadherin Celsr1 Regulates Skin Hair Patterning in the Mouse
- Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument