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Research 241–270 of 1000+
- The Stem Cell Niche in Regenerative Medicine
- Regulation of adult stem cell quiescence and its functions in the maintenance of tissue integrity
- Epigenetic control of adult stem cell function
- Gonadal Function Abnormalities in Sickle Cell Anemia
- 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
- Tracing the developmental origin of tissue stem cells
- 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
- Rehabilitation therapy for a severe case of coronavirus disease 2019: a case report
- Satoyoshi Syndrome: Difficult to find or treat?
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report
- Schimmelpenning Syndrome: A Neuro-Oculo-Cutaneous Disorder
- Effects of Ionizing Radiation on Murine Gene Expression in Skin and Bone
- La confusion des pouvoirs
- Mouse models with a disrupted PTHrP gene or a disrupted PTH gene (PTH−/− mice)
- Vitamin D: More Than a “Bone-a-Fide” Hormone