Suchergebnisse - Jian‐Min Chen

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  1. 1
    Mutational analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene in hereditary and sporadic chronic pancreatitis

    Mutational analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene in hereditary and sporadic chronic pancreatitis von Jian‐Min Chen

    Veröffentlicht 2000
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  2. 2
    Evolution of Trypsinogen Activation Peptides

    Evolution of Trypsinogen Activation Peptides von Jian‐Min Chen

    Veröffentlicht 2003
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  3. 3
    Genome-wide identification, characterization, and expression analysis of m6A readers-YTH domain-containing genes in alfalfa

    Genome-wide identification, characterization, and expression analysis of m6A readers-YTH domain-containing genes in alfalfa von Shugao Fan, Xiao Xu, Jian‐Min Chen, Yanling Yin, Ying Zhao

    Veröffentlicht 2024
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  4. 4
    A Conservative Assessment of the Major Genetic Causes of Idiopathic Chronic Pancreatitis: Data from a Comprehensive Analysis of PRSS1, SPINK1, CTRC and CFTR Genes in 253 Young French Patients

    A Conservative Assessment of the Major Genetic Causes of Idiopathic Chronic Pancreatitis: Data from a Comprehensive Analysis of PRSS1, SPINK1, CTRC and CFTR Genes in 253 Young Fren... von Emmanuelle Masson, Jian‐Min Chen, M.‐P. Audrézet, D.N. Cooper, Claude Férec

    Veröffentlicht 2013
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  5. 5
    Meta‐Analysis of gross insertions causing human genetic disease: Novel mutational mechanisms and the role of replication slippage

    Meta‐Analysis of gross insertions causing human genetic disease: Novel mutational mechanisms and the role of replication slippage von Jian‐Min Chen, Nadia Chuzhanova, Peter D. Stenson, Claude Férec, D.N. Cooper

    Veröffentlicht 2005
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  6. 6
    Complex gene rearrangements caused by serial replication slippage

    Complex gene rearrangements caused by serial replication slippage von Jian‐Min Chen, Nadia Chuzhanova, Peter D. Stenson, Claude Férec, D.N. Cooper

    Veröffentlicht 2005
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  7. 7
    Functional analysis of pancreatitis-associated missense mutations in the pancreatic secretory trypsin inhibitor (SPINK1) gene

    Functional analysis of pancreatitis-associated missense mutations in the pancreatic secretory trypsin inhibitor (SPINK1) gene von Arnaud Boulling, Cédric Le Maréchal, Pascal Trouvé, Odile Raguénès, Jian‐Min Chen, Claude Férec

    Veröffentlicht 2007
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  8. 8
    Mutations of the pancreatic secretory trypsin inhibitor (PSTI) gene in idiopathic chronic pancreatitis

    Mutations of the pancreatic secretory trypsin inhibitor (PSTI) gene in idiopathic chronic pancreatitis von Jian‐Min Chen, Bernard Mercier, Marie‐Pierre Audrézet, Odile Raguénès, I. Quéré, Claude Férec

    Veröffentlicht 2001
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  9. 9
    Genetics and clinical implications of SPINK1 in the pancreatitis continuum and pancreatic cancer

    Genetics and clinical implications of SPINK1 in the pancreatitis continuum and pancreatic cancer von Qiwen Wang, Wen‐Bin Zou, Emmanuelle Masson, Claude Férec, Zhuan Liao, Jian‐Min Chen

    Veröffentlicht 2025
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  10. 10
    Genetics and Pathogenesis of Autosomal Dominant Polycystic Kidney Disease: 20 Years On

    Genetics and Pathogenesis of Autosomal Dominant Polycystic Kidney Disease: 20 Years On von Émilie Cornec-Le Gall, Marie‐Pierre Audrézet, Yannick Le Meur, Jian‐Min Chen, Claude Férec

    Veröffentlicht 2014
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  11. 11
    Effects of Lisdexamfetamine, a Prodrug of D-Amphetamine, on Locomotion, Spatial Cognitive Processing and Neurochemical Profiles in Rats: A Comparison With Immediate-Release Amphetamine

    Effects of Lisdexamfetamine, a Prodrug of D-Amphetamine, on Locomotion, Spatial Cognitive Processing and Neurochemical Profiles in Rats: A Comparison With Immediate-Release Ampheta... von Jian-min, Chen, Zhi-yuan, Wang, Shi-xuan, Wu, Rui, Song, Ning, Wu, Jin, Li

    Veröffentlicht 2022
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  12. 12
    On the sequence-directed nature of human gene mutation: The role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease

    On the sequence-directed nature of human gene mutation: The role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherit... von D.N. Cooper, Albino Bacolla, Claude Férec, Karen M. Vásquez, Hildegard Kehrer‐Sawatzki, Jian‐Min Chen

    Veröffentlicht 2011
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  13. 13
    Two novel severe mutations in the pancreatic secretory trypsin inhibitor gene ( <i>SPINK1</i> ) cause familial and/or hereditary pancreatitis

    Two novel severe mutations in the pancreatic secretory trypsin inhibitor gene ( <i>SPINK1</i> ) cause familial and/or hereditary pancreatitis von Cédric Le Maréchal, Jian‐Min Chen, C. Gall, Ghislaine Plessis, J Chipponi, Nadia Chuzhanova, Odile Raguénès, Claude Férec

    Veröffentlicht 2004
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  14. 14
    Gene conversion causing human inherited disease: Evidence for involvement of non-B-DNA-forming sequences and recombination-promoting motifs in DNA breakage and repair

    Gene conversion causing human inherited disease: Evidence for involvement of non-B-DNA-forming sequences and recombination-promoting motifs in DNA breakage and repair von Nadia Chuzhanova, Jian‐Min Chen, Albino Bacolla, George P. Patrinos, Claude Férec, Robert D. Wells, D.N. Cooper

    Veröffentlicht 2009
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  15. 15
    miRNA-181b increases the sensitivity of pancreatic ductal adenocarcinoma cells to gemcitabine in vitro and in nude mice by targeting BCL-2

    miRNA-181b increases the sensitivity of pancreatic ductal adenocarcinoma cells to gemcitabine in vitro and in nude mice by targeting BCL-2 von Baobao Cai, Yong An, Nan Lv, Jian‐Min Chen, Min Tu, Jie Sun, Pengfei Wu, Jishu Wei, Kuirong Jiang, Yi Miao

    Veröffentlicht 2013
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  16. 16
    Determination of the relative contribution of three genes–the cystic fibrosis transmembrane conductance regulator gene, the cationic trypsinogen gene, and the pancreatic secretory trypsin inhibitor gene–to the etiology of idiopathic chronic pancreatitis

    Determination of the relative contribution of three genes–the cystic fibrosis transmembrane conductance regulator gene, the cationic trypsinogen gene, and the pancreatic secretory... von Marie‐Pierre Audrézet, Jian‐Min Chen, Cédric Le Maréchal, Philippe Ruszniewski, Michel Robaszkiewicz, Odile Raguénès, I. Quéré, Virginie Scotet, Claude Férec

    Veröffentlicht 2002
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  17. 17
    Signal peptide variants that impair secretion of pancreatic secretory trypsin inhibitor (SPINK1) cause autosomal dominant hereditary pancreatitis

    Signal peptide variants that impair secretion of pancreatic secretory trypsin inhibitor (SPINK1) cause autosomal dominant hereditary pancreatitis von Orsolya Király, Arnaud Boulling, Heiko Witt, Cédric Le Maréchal, Jian‐Min Chen, Jonas Rosendahl, Cinzia Battaggia, Thomas Wartmann, Miklós Sahin‐Tóth, Claude Férec

    Veröffentlicht 2007
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  18. 18
    Persistent activation of pancreatic stellate cells creates a microenvironment favorable for the malignant behavior of pancreatic ductal adenocarcinoma

    Persistent activation of pancreatic stellate cells creates a microenvironment favorable for the malignant behavior of pancreatic ductal adenocarcinoma von Dong Tang, Daorong Wang, Zhongxu Yuan, Xiaofeng Xue, Ye Zhang, Yong An, Jian‐Min Chen, Min Tu, Zipeng Lu, Jishu Wei, Kuirong Jiang, Yi Miao

    Veröffentlicht 2012
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  19. 19
    Autosomal dominant polycystic kidney disease: Comprehensive mutation analysis of PKD1 and PKD2 in 700 unrelated patients

    Autosomal dominant polycystic kidney disease: Comprehensive mutation analysis of PKD1 and PKD2 in 700 unrelated patients von Marie‐Pierre Audrézet, Émilie Cornec-Le Gall, Jian‐Min Chen, Sylvia Redon, I. Quéré, J. Creff, Caroline Bénech, Sandrine Maestri, Yannick Le Meur, Claude Férec

    Veröffentlicht 2012
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  20. 20
    Trypsinogen Copy Number Mutations in Patients With Idiopathic Chronic Pancreatitis

    Trypsinogen Copy Number Mutations in Patients With Idiopathic Chronic Pancreatitis von Emmanuelle Masson, Cédric Le Maréchal, Giriraj R. Chandak, J. Lamoril, Stéphane Bézieau, Swapna Mahurkar‐Joshi, Seema Bhaskar, D. Nageshwar Reddy, Jian‐Min Chen, Claude Férec

    Veröffentlicht 2007
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