Literature DB >> 21204801

Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy?

M Krahn, M Goicoechea, F Hanisch, E Groen, M Bartoli, C Pécheux, F Garcia-Bragado, F Leturcq, P-Y Jeannet, J A Lobrinus, S Jacquemont, J Strober, J A Urtizberea, A Saenz, K Bushby, N Lévy, A Lopez de Munain.   

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Year:  2011        PMID： 21204801     DOI： 10.1111/j.1399-0004.2010.01620.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  8 in total

1.  Clinical and Genomic Evaluation of 207 Genetic Myopathies in the Indian Subcontinent.

Authors:  Samya Chakravorty; Babi Ramesh Reddy Nallamilli; Satish Vasant Khadilkar; Madhu Bala Singla; Ashish Bhutada; Rashna Dastur; Pradnya Satish Gaitonde; Laura E Rufibach; Logan Gloster; Madhuri Hegde
Journal:  Front Neurol       Date:  2020-11-05       Impact factor: 4.086

2.  Calpain 3 and CaMKIIβ signaling are required to induce HSP70 necessary for adaptive muscle growth after atrophy.

Authors:  Irina Kramerova; Jorge A Torres; Ascia Eskin; Stanley F Nelson; Melissa J Spencer
Journal:  Hum Mol Genet       Date:  2018-05-01       Impact factor: 6.150

3.  Limb-girdle Muscular Dystrophy Type 2A with Muscular Eosinophilic Infiltration in a Chinese Patient.

Authors:  Yue-Bei Luo; Qiu-Xiang Li; Hui-Qian Duan; Fang-Fang Bi; Huan Yang
Journal:  Chin Med J (Engl)       Date:  2018-09-05       Impact factor: 2.628

4.  Eosinophils in hereditary and inflammatory myopathies.

Authors:  Thomas Schröder; Johann Fuchss; Ilka Schneider; Gisela Stoltenburg-Didinger; Frank Hanisch
Journal:  Acta Myol       Date:  2013-12

5.  Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease.

Authors:  Leah C Kottyan; Benjamin P Davis; Joseph D Sherrill; Kan Liu; Mark Rochman; Kenneth Kaufman; Matthew T Weirauch; Samuel Vaughn; Sara Lazaro; Andrew M Rupert; Mojtaba Kohram; Emily M Stucke; Katherine A Kemme; Albert Magnusen; Hua He; Phillip Dexheimer; Mirna Chehade; Robert A Wood; Robbie D Pesek; Brian P Vickery; David M Fleischer; Robert Lindbad; Hugh A Sampson; Vincent A Mukkada; Phil E Putnam; J Pablo Abonia; Lisa J Martin; John B Harley; Marc E Rothenberg
Journal:  Nat Genet       Date:  2014-07-13       Impact factor: 38.330

Review 6.  Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations.

Authors:  Jaione Lasa-Elgarresta; Laura Mosqueira-Martín; Neia Naldaiz-Gastesi; Amets Sáenz; Adolfo López de Munain; Ainara Vallejo-Illarramendi
Journal:  Int J Mol Sci       Date:  2019-09-13       Impact factor: 5.923

7.  Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia.

Authors:  Stojan Peric; Jelena Stevanovic; Katherine Johnson; Ana Kosac; Marina Peric; Marija Brankovic; Ana Marjanovic; Milena Jankovic; Bojan Banko; Sanja Milenkovic; Milica Durdic; Ivo Bozovic; Jelena Nikodinovic Glumac; Dragana Lavrnic; Ruzica Maksimovic; Vedrana Milic-Rasic; Vidosava Rakocevic-Stojanovic
Journal:  Acta Myol       Date:  2019-09-01

8.  Gene expression profiling identifies molecular pathways associated with collagen VI deficiency and provides novel therapeutic targets.

Authors:  Sonia Paco; Susana G Kalko; Cristina Jou; María A Rodríguez; Joan Corbera; Francesco Muntoni; Lucy Feng; Eloy Rivas; Ferran Torner; Francesca Gualandi; Anna M Gomez-Foix; Anna Ferrer; Carlos Ortez; Andrés Nascimento; Jaume Colomer; Cecilia Jimenez-Mallebrera
Journal:  PLoS One       Date:  2013-10-11       Impact factor: 3.240
  8 in total

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