- Novel c.300_301delinsT Mutation in PITX2 in a Korean Family with Axenfeld-Rieger Syndrome
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Yun JW, Cho HK, Oh SY, Ki CS, Kee C
- KMID: 1781343
- Ann Lab Med.
- 2013 Sep;33(5):360-363.
- doi: 10.3343/alm.2013.33.5.360
Axenfeld-Rieger syndrome (ARS) is characterized by anomalies of the anterior segment of the eye and systemic abnormalities. Mutations in the FOXC1 and PITX2 genes are underlying causes of ARS, but... -
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- Overexpression of neurogenin1 induces neurite outgrowth in F11 neuroblastoma cells
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Kim SY, Ghil SH, Kim SS, Myeong HH, Lee YD, Suh-Kim HY
- KMID: 1121101
- Exp Mol Med.
- 2002 Dec;34(6):469-475.
Neurogenin1 (Ngn1) is a basic helix-loop-helix (bHLH) transcription factor expressed in neuronal precursors in the developing nervous system. The function of Ngn1 in neurogenesis has been shown in various... -
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- Human SNF2L Gene Is Regulated Constitutively and Inducibly in Neural Cells via a cAMP-Response Element
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Xia Y, Wang L, Ma C, Gong Y, Zhao Y
- KMID: 1727896
- Yonsei Med J.
- 2013 May;54(3):772-777.
- doi: 10.3349/ymj.2013.54.3.772
PURPOSE: SNF2L belongs to Imitation Switch family and plays an essential role in neural tissues and gonads. In our previous studies, we have demonstrated that the basal transcription of human... -
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