TGDS gene

Known as: GROWTH-INHIBITING PROTEIN 21, TDP-GLUCOSE 4,6-DEHYDRATASE, short chain dehydrogenase/reductase family 2E, member 1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2008-2017
01220082017

Papers overview

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2017
2017
Pierre-Robin sequence, radial deviation, and ulnar clinodactyly of the index fingers due to an additional phalangeal bone, as… (More)
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2017
2017
Methods of diagnosing malignant pheochromocytoma (PCC) or paraganglioma (PGL) are needed. However, there are no reliable… (More)
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2015
2015
Catel-Manzke syndrome is a rare autosomal recessive disorder characterized by Pierre Robin sequence with hyperphalangy and… (More)
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2015
2015
OBJECTIVE The objective of this study was to evaluate the relationship between cognitive impairment and depressive mood in Thai… (More)
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2015
2015
Congenital microcoria (MCOR) is a rare autosomal-dominant disorder characterized by inability of the iris to dilate owing to… (More)
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2014
2014
Catel-Manzke syndrome is characterized by Pierre Robin sequence and a unique form of bilateral hyperphalangy causing a… (More)
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2012
2012
BACKGROUND Evolution of medical technologies extent human life expectancy. The United Nations found Thai elderly population were… (More)
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2008
2008
Accumulating evidence indicates that the high blood pressure (BP) is a potent risk factor for dementia in the elderly. In line… (More)
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