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Research 751–780 of 1000+
- Lambertianic Acid from Platycladus orientalis Inhibits Muscle Atrophy in Dexamethasone-Induced C2C12 Muscle Atrophy Cells
- Ectodysplasin-A (EDA) Signaling Cross-Talk in Skeletogenesis
- Ligand-Independent Actions of Vitamin D Receptor
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency
- Expression of the Scube3 epidermal growth factor-related gene during early embryonic development in the mouse
- Ichthyosis hystrix
- Rickets with Alopecia Signals Vitamin D Dependent Rickets Type II
- Part 1. Genetic pathway of maternal transmission in Topiramate-treated zebrafish modelPart 2.Effects of herbal medicine on zebrafish embryos
- 447 Skin-Associated Cartilage Consists of Lipid-Filled Cells That Modify Hair Growth via BMP and WNT Signaling
- Two Cases of Danon Disease – A ‘Cousin’ of Pompe Disease
- Mitochondrial dysfunction as a cause of ageing
- The Stem Cell Niche in Regenerative Medicine
- Epigenetic control of adult stem cell function
- 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
- The function of TRPS1 in the development and differentiation of bone, kidney, and hair follicles.
- Nevus comedonicus
- Satoyoshi syndrome: A rare multisystemic disorder requiring systemic and symptomatic treatment
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Misdiagnosis as asphyxiating thoracic dystrophy and CMV-associated haemophagocytic lymphohistiocytosis in Shwachman-Diamond syndrome
- A Case of Satoyoshi Syndrome: A Multisystem Disorder
- Satoyoshi Syndrome
- Treatment of Satoyoshi syndrome: a systematic review
- Becker’s Nevus Syndrome in a Pediatric Female Patient
- Becker's Nevus Syndrome
- Ichthyosis linearis circumflexa with bamboo hair: challenges in the diagnosis and management
- Pathophysiology of Insulin Resistance and Related Skin Diseases ( Review Article)
- The Mechanisms of Anabolic Steroids, Selective Androgen Receptor Modulators and Myostatin Inhibitors
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome