| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Yuko Nitahara-Kasahara, Mutsuki Kuraoka, Yuki Oda, Hiromi Hayashita-Kinoh, Shin'ichi Takeda, Takashi Okad. Enhanced cell survival and therapeutic benefits of IL-10-expressing multipotent mesenchymal stromal cells for muscular dystrophy. Stem cell research & therapy. vol 12. issue 1. 2021-07-05. PMID:33541428. |
mscs are attractive candidates for cell-based strategies that target diseases with chronic inflammation, such as duchenne muscular disease (dmd). |
2021-07-05 |
2023-08-13 |
Not clear |
| K R Valetdinova, M A Maretina, Y V Vyatkin, M P Perepelkina, A A Egorova, V S Baranov, A V Kiselev, P M Gershovich, S M Zakia. Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C. Stem cell research. vol 48. 2021-06-21. PMID:32777771. |
generation of three duchenne muscular dystrophy patient-derived induced pluripotent stem cell (ipsc) lines icgi002-a, icgi002-b and icgi002-c. duchenne muscular dystrophy (dmd) is a severe and rapidly progressive hereditary muscular disease with x-linked recessive inheritance, occurring mainly in males. |
2021-06-21 |
2023-08-13 |
Not clear |
| Elisabetta Catalani, Silvia Bongiorni, Anna Rita Taddei, Marta Mezzetti, Federica Silvestri, Marco Coazzoli, Silvia Zecchini, Matteo Giovarelli, Cristiana Perrotta, Clara De Palma, Emilio Clementi, Marcello Ceci, Giorgio Prantera, Davide Cervi. Defects of full-length dystrophin trigger retinal neuron damage and synapse alterations by disrupting functional autophagy. Cellular and molecular life sciences : CMLS. vol 78. issue 4. 2021-03-03. PMID:32749504. |
dystrophin (dys) mutations predispose duchenne muscular disease (dmd) patients to brain and retinal complications. |
2021-03-03 |
2023-08-13 |
mouse |
| Wen-Chin Weng, Jung-Chih Chen, Chia-Yen Lee, Chia-Wei Lin, Wang-Tso Lee, Jeng-Yi Shieh, Chia-Chen Wang, Ching-Cheng Chuan. Cross-section and feasibility study on the non-invasive evaluation of muscle hemodynamic responses in Duchenne muscular dystrophy by using a near-infrared diffuse optical technique. Biomedical optics express. vol 9. issue 10. 2020-10-01. PMID:30319901. |
duchenne muscular dystrophy (dmd) is an x-linked debilitating muscular disease that may decrease nitric oxide (no) production and lead to functional muscular ischemia. |
2020-10-01 |
2023-08-13 |
human |
| Irene Persiconi, Francesca Cosmi, Noemi Antonella Guadagno, Giuseppe Lupo, Maria Egle De Stefan. Dystrophin Is Required for the Proper Timing in Retinal Histogenesis: A Thorough Investigation on the Frontiers in neuroscience. vol 14. 2020-10-01. PMID:32982660. |
dystrophin is required for the proper timing in retinal histogenesis: a thorough investigation on the duchenne muscular dystrophy (dmd) is a lethal x-linked muscular disease caused by defective expression of the cytoskeletal protein dystrophin (dp427). |
2020-10-01 |
2023-08-13 |
Not clear |
| Dimitrios Tsika. Urinary Dimethylamine (DMA) and Its Precursor Asymmetric Dimethylarginine (ADMA) in Clinical Medicine, in the Context of Nitric Oxide (NO) and Beyond. Journal of clinical medicine. vol 9. issue 6. 2020-09-28. PMID:32545708. |
discussed diseases mainly include those relating to the renal and cardiovascular systems such as peripheral arterial occlusive disease, coronary artery disease, chronic kidney disease, rheumatoid arthritis, becker muscular disease, duchenne muscular disease (dmd), attention deficit hyperactivity disorder (adhd), and type i diabetes. |
2020-09-28 |
2023-08-13 |
human |
| Salvo Danilo Lombardo, Emanuela Mazzon, Katia Mangano, Maria Sofia Basile, Eugenio Cavalli, Santa Mammana, Paolo Fagone, Ferdinando Nicoletti, Maria Cristina Petrali. Transcriptomic Analysis Reveals Involvement of the Macrophage Migration Inhibitory Factor Gene Network in Duchenne Muscular Dystrophy. Genes. vol 10. issue 11. 2020-05-05. PMID:31752120. |
duchenne muscular dystrophy (dmd) is a progressive hereditary muscular disease with x-linked recessive inheritance, that leads patients to premature death. |
2020-05-05 |
2023-08-13 |
Not clear |
| Takuya Hiraide, Tsutomu Ogata, Seiji Watanabe, Mitsuko Nakashima, Tokiko Fukuda, Hirotomo Saits. Coexistence of a CAV3 mutation and a DMD deletion in a family with complex muscular diseases. Brain & development. vol 41. issue 5. 2019-07-26. PMID:30723005. |
coexistence of a cav3 mutation and a dmd deletion in a family with complex muscular diseases. |
2019-07-26 |
2023-08-13 |
Not clear |
| Takuya Hiraide, Tsutomu Ogata, Seiji Watanabe, Mitsuko Nakashima, Tokiko Fukuda, Hirotomo Saits. Coexistence of a CAV3 mutation and a DMD deletion in a family with complex muscular diseases. Brain & development. vol 41. issue 5. 2019-07-26. PMID:30723005. |
we revealed the coexistence of the cav3 mutation and the dmd deletion in a family with complex muscular diseases and confirmed the usefulness of wes for elucidating such etiology. |
2019-07-26 |
2023-08-13 |
Not clear |
| Tetsushi Yamamoto, Hiroyuki Awano, Zhujun Zhang, Mio Sakuma, Shoko Kitaaki, Masaaki Matsumoto, Masashi Nagai, Itsuko Sato, Takamitsu Imanishi, Nobuhide Hayashi, Masafumi Matsuo, Kazumoto Iijima, Jun Saegus. Cardiac Dysfunction in Duchenne Muscular Dystrophy Is Less Frequent in Patients With Mutations in the Dystrophin Dp116 Coding Region Than in Other Regions. Circulation. Genomic and precision medicine. vol 11. issue 1. 2019-03-07. PMID:29874176. |
duchenne muscular dystrophy (dmd), the most common inherited muscular disease in childhood, is caused by dystrophin deficiency because of mutations in the |
2019-03-07 |
2023-08-13 |
Not clear |
| Dilayla K DE Abreu, Janaina M Monteiro, Carolina C Souza, Rafael G Karam, Renata A Fernandes, Thais B Lessa, José J Fagliari, Maria Angelica Miglino, Carlos Eduardo Ambrosi. Immunophenotyping lymphocyte and acute phase proteins in canine X-linked muscular dystrophy. Anais da Academia Brasileira de Ciencias. vol 90. issue 3. 2019-01-08. PMID:30304229. |
duchenne muscular dystrophy (dmd) is the most common x-linked muscular disease affecting humans. |
2019-01-08 |
2023-08-13 |
Not clear |
| Carola Saure, Carolina Caminiti, Julieta Weglinski, Fernanda de Castro Perez, Soledad Monge. Energy expenditure, body composition, and prevalence of metabolic disorders in patients with Duchenne muscular dystrophy. Diabetes & metabolic syndrome. vol 12. issue 2. 2018-09-24. PMID:28869151. |
duchenne muscular dystrophy (dmd) is a severe muscular disease characterized by progressive loss of functional muscle mass followed by changes in body composition. |
2018-09-24 |
2023-08-13 |
Not clear |
| Jillian Davis, Emily Samuels, Lucille Mullin. Nutrition Considerations in Duchenne Muscular Dystrophy. Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition. vol 30. issue 4. 2016-05-04. PMID:25977513. |
duchenne muscular dystrophy (dmd) is a serious degenerative muscular disease affecting males. |
2016-05-04 |
2023-08-13 |
Not clear |
| François-Xavier Goudot, Karim Wahbi, Linda Aïssou, Emmanuel Sorbets, Valérie Siam-Tsieu, Bruno Eymard, Christine Themar Noel, Jean-Yves Devaux, Odile Dessault, Denis Duboc, Christophe Meun. Reduced inotropic reserve is predictive of further degradation in left ventricular ejection fraction in patients with Duchenne muscular dystrophy. European journal of heart failure. vol 17. issue 2. 2015-12-15. PMID:25823361. |
duchenne muscular dystrophy (dmd), an inherited x-linked muscular disease, is associated with dilated cardiomyopathy that is responsible for death in 40% of patients. |
2015-12-15 |
2023-08-13 |
Not clear |
| Emma Tabe Eko Niba, Van Khanh Tran, Le Anh Tuan-Pham, Dung Chi Vu, Ngoc Khanh Nguyen, Van Thanh Ta, Thinh Huy Tran, Tomoko Lee, Yasuhiro Takeshima, Masafumi Matsu. Validation of ambiguous MLPA results by targeted next-generation sequencing discloses a nonsense mutation in the DMD gene. Clinica chimica acta; international journal of clinical chemistry. vol 436. 2015-08-27. PMID:24892813. |
duchenne muscular dystrophy (dmd) is the most common inherited muscular disease and caused by mutations in the dmd gene on the x-chromosome. |
2015-08-27 |
2023-08-13 |
Not clear |
| Valentina Saccone, Silvia Consalvi, Lorenzo Giordani, Chiara Mozzetta, Iros Barozzi, Martina Sandoná, Tammy Ryan, Agustin Rojas-Muñoz, Luca Madaro, Pasquale Fasanaro, Giovanna Borsellino, Marco De Bardi, Gianmaria Frigè, Alberto Termanini, Xin Sun, Janet Rossant, Benoit G Bruneau, Mark Mercola, Saverio Minucci, Pier Lorenzo Pur. HDAC-regulated myomiRs control BAF60 variant exchange and direct the functional phenotype of fibro-adipogenic progenitors in dystrophic muscles. Genes & development. vol 28. issue 8. 2014-05-29. PMID:24682306. |
whether faps support muscle regeneration or promote fibro-adipogenic degeneration is emerging as a key determinant in the pathogenesis of muscular diseases, including duchenne muscular dystrophy (dmd). |
2014-05-29 |
2023-08-12 |
mouse |
| Yoichi Negishi, Nobuhito Hamano, Hitomi Shiono, Saki Akiyama, Yoko Endo-Takahashi, Ryo Suzuki, Kazuo Maruyama, Yukihiko Aramak. [Development of an ultrasound-mediated nucleic acid delivery system for treating muscular dystrophies]. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan. vol 132. issue 12. 2014-04-03. PMID:23208045. |
duchenne muscular dystrophy (dmd) is a fatal, x-linked muscular disease that occurs in 1 out of every 3500 males. |
2014-04-03 |
2023-08-12 |
Not clear |
| Thi Hoai Thu Tran, Zhujun Zhang, Mariko Yagi, Tomoko Lee, Hiroyuki Awano, Atsushi Nishida, Takeshi Okinaga, Yasuhiro Takeshima, Masafumi Matsu. Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq28. Journal of human genetics. vol 58. issue 1. 2013-11-14. PMID:23223008. |
duchenne muscular dystrophy (dmd) is the most common inherited muscular disease and is characterized by progressive muscle wasting. |
2013-11-14 |
2023-08-12 |
Not clear |
| Hideya Mizuno, Akinori Nakamura, Yoshitsugu Aoki, Naoki Ito, Soichiro Kishi, Kazuhiro Yamamoto, Masayuki Sekiguchi, Shin'ichi Takeda, Kazuo Hashid. Identification of muscle-specific microRNAs in serum of muscular dystrophy animal models: promising novel blood-based markers for muscular dystrophy. PloS one. vol 6. issue 3. 2011-07-26. PMID:21479190. |
creatine kinase (ck) is generally used as a blood-based biomarker for muscular disease including dmd, but it is not always reliable since it is easily affected by stress to the body, such as exercise. |
2011-07-26 |
2023-08-12 |
mouse |
| Mirella Meregalli, Andrea Farini, Yvan Torrent. Combining stem cells and exon skipping strategy to treat muscular dystrophy. Expert opinion on biological therapy. vol 8. issue 8. 2008-08-28. PMID:18613758. |
mutations in the dystrophin gene cause hereditary muscular diseases such as becker muscular dystrophy (bmd) and duchenne muscular dystrophy (dmd), the most severe form. |
2008-08-28 |
2023-08-12 |
Not clear |