Literature DB >> 15060118

A frequent keratin 8 p.L227L polymorphism, but no point mutations in keratin 8 and 18 genes, in patients with various liver disorders.

M Hesse, T Berg, B Wiedenmann, U Spengler, R P Woitas, T M Magin.   

Abstract

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Year:  2004        PMID： 15060118      PMCID： PMC1735733          DOI： 10.1136/jmg.2003.012393

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  3 in total

1.  Keratin 8 sequence variants in patients with pancreatitis and pancreatic cancer.

Authors:  Matthias Treiber; Hans-Ulrich Schulz; Olfert Landt; Joost P H Drenth; Carlo Castellani; Francisco X Real; Nejat Akar; Rudolf W Ammann; Mario Bargetzi; Eesh Bhatia; Andrew Glenn Demaine; Cinzia Battagia; Andrew Kingsnorth; Derek O'Reilly; Kaspar Truninger; Monika Koudova; Julius Spicak; Milos Cerny; Hans-Jürgen Menzel; Pedro Moral; Pier Franco Pignatti; Maria Grazia Romanelli; Olga Rickards; Gian Franco De Stefano; Narcis Octavian Zarnescu; Gourdas Choudhuri; Sadiq S Sikora; Jan B M J Jansen; Frank Ulrich Weiss; Matthias Pietschmann; Niels Teich; Thomas M Gress; Johann Ockenga; Hartmut Schmidt; Andreas Kage; Juliane Halangk; Jonas Rosendahl; David Alexander Groneberg; Renate Nickel; Heiko Witt
Journal:  J Mol Med (Berl)       Date:  2006-10-13       Impact factor: 4.599

Review 2.  The molecular basis of human keratin disorders.

Authors:  Meral Julia Arin
Journal:  Hum Genet       Date:  2009-02-27       Impact factor: 4.132

3.  Non-coding keratin variants associate with liver fibrosis progression in patients with hemochromatosis.

Authors:  Pavel Strnad; Ozlem Kucukoglu; Mariia Lunova; Nurdan Guldiken; Tim C Lienau; Felix Stickel; M Bishr Omary
Journal:  PLoS One       Date:  2012-03-07       Impact factor: 3.240
  3 in total

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