Literature DB >> 10586255

Characterization of targeted connexin32-deficient mice: a model for the human Charcot-Marie-Tooth (X-type) inherited disease.

K Willecke1, A Temme, B Teubner, T Ott.   

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Year:  1999        PMID： 10586255

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN： 0077-8923            Impact factor:   5.691


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  4 in total

1.  Gene therapy, CMT1X, and the inherited neuropathies.

Authors:  Michael E Shy
Journal:  Proc Natl Acad Sci U S A       Date:  2016-04-14       Impact factor: 11.205

Review 2.  Connexin mutant embryonic stem cells and human diseases.

Authors:  Kiyomasa Nishii; Yosaburo Shibata; Yasushi Kobayashi
Journal:  World J Stem Cells       Date:  2014-11-26       Impact factor: 5.326

3.  Connexins and apoptotic transformation.

Authors:  Audrone Kalvelyte; Ausra Imbrasaite; Angele Bukauskiene; Vytas K Verselis; Feliksas F Bukauskas
Journal:  Biochem Pharmacol       Date:  2003-10-15       Impact factor: 5.858

4.  Connexins: a myriad of functions extending beyond assembly of gap junction channels.

Authors:  Hashem A Dbouk; Rana M Mroue; Marwan E El-Sabban; Rabih S Talhouk
Journal:  Cell Commun Signal       Date:  2009-03-12       Impact factor: 5.712
  4 in total

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