CFTR polymorphisms of healthy individuals in two Chinese cities--Changchun and Nanjing

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CFTR polymorphisms of healthy individuals in two Chinese cities--Changchun and Nanjing

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2012 nî lūn-bûn

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2012年の論文

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2012年論文

@yue

2012年論文

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2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

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2012年论文

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2012年论文

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CFTR polymorphisms of healthy individuals in two Chinese cities--Changchun and Nanjing

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CFTR polymorphisms of healthy individuals in two Chinese cities--Changchun and Nanjing

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CFTR polymorphisms of healthy individuals in two Chinese cities--Changchun and Nanjing

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P1476

CFTR polymorphisms of healthy individuals in two Chinese cities--Changchun and Nanjing

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P2093

Chun Xiang Jin

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Hiroshi Ishiguro

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Kotoyo Fujiki

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Miyuki Nakakuki

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Mu Xin Wei

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Satoru Naruse

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Su Min Zhang

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Ying Song

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Zhang Ping

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P2860

Identification of the cystic fibrosis gene: chromosome walking and jumping

Connections between genetics and clinical data: Role of MCP-1, CFTR, and SPINK-1 in the setting of acute, acute recurrent, and chronic pancreatitis.

Variation in a repeat sequence determines whether a common variant of the cystic fibrosis transmembrane conductance regulator gene is pathogenic or benign

Corticosteroids correct aberrant CFTR localization in the duct and regenerate acinar cells in autoimmune pancreatitis.

Combined bicarbonate conductance-impairing variants in CFTR and SPINK1 variants are associated with chronic pancreatitis in patients without cystic fibrosis.

Variable deletion of exon 9 coding sequences in cystic fibrosis transmembrane conductance regulator gene mRNA transcripts in normal bronchial epithelium.

Role of genetic disorders in acute recurrent pancreatitis.

Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation.

Mutations of the cystic fibrosis gene in patients with chronic pancreatitis.

Idiopathic chronic pancreatitis in India: phenotypic characterisation and strong genetic susceptibility due to SPINK1 and CFTR gene mutations.

P304

293-301

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P31

scholarly article

P433

3-4

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P478

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P577

2012-08-01T00:00:00Z

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P698

23092102

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P932

4831238

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