Analysis of mutations of MDR3 exons 9 and 23 in infants with parenteral nutrition-associated cholestasis.

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Analysis of mutations of MDR3 exons 9 and 23 in infants with parenteral nutrition-associated cholestasis.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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Analysis of mutations of MDR3 ...... rition-associated cholestasis.

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Analysis of mutations of MDR3 ...... rition-associated cholestasis.

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Analysis of mutations of MDR3 ...... rition-associated cholestasis.

@en

P1476

Analysis of mutations of MDR3 ...... rition-associated cholestasis.

@en

P2093

Guo-Sheng Liu

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Min-Xu Li

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Xiu-Fang Yang

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P2860

Structure of the human MDR3 gene and physical mapping of the human MDR locus

Enterohepatic bile salt transporters in normal physiology and liver disease

Parenteral nutrition-associated cholestasis in small for gestational age infants.

A mutation in the canalicular phospholipid transporter gene, ABCB4, is associated with cholestasis, ductopenia, and cirrhosis in adults.

Parenteral nutrition associated liver disease.

Intrahepatic cholestasis of pregnancy: the severe form is associated with common variants of the hepatobiliary phospholipid transporter ABCB4 gene.

First description of ABCB4 gene deletions in familial low phospholipid-associated cholelithiasis and oral contraceptives-induced cholestasis.

Intrauterine growth restriction impacts tolerance to total parenteral nutrition in extremely low birth weight infants.

Hepatocanalicular transport defects: pathophysiologic mechanisms of rare diseases.

Function and pathophysiological importance of ABCB4 (MDR3 P-glycoprotein).

P304

2361-2365

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P31

scholarly article

P356

10.3892/ETM.2015.2800

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P433

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P478

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P577

2015-10-14T00:00:00Z

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P5875

283564736

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P698

26668642

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P932

4665683

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