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Select item 103747741.

An atypical expression of core α-Dystroglycan and Laminin-α2 in skin fibroblasts of patients with congenital muscular dystrophies

Sahar Sabry, Mahmoud Y Issa, Mohamed S Abdel-Hamid, Noura R Eissa, Sherif F Abdel-Ghafar, Mona M Ibrahim, Maha S Zaki

Mol Biol Rep. 2023; 50(8): 6373–6379. Published online 2023 Jun 15. doi: 10.1007/s11033-023-08500-7

PMCID:: PMC10374774

Abstract Article PDF–1.0M

Select item 103571502.

Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy – a Genotype/Phenotype Correlation

Clara Gontijo Camelo, Mariana Cunha Artilheiro, Cristiane Araújo Martins Moreno, Suely Fazio Ferraciolli, André Macedo Serafim Silva, Tatiana Ribeiro Fernandes, Leandro Tavares Lucato, Antônio José Rocha, Umbertina Conti Reed, Edmar Zanoteli

J Neuromuscul Dis. 2023; 10(4): 483–492. Prepublished online 2023 May 9. Published online 2023 Jul 4. doi: 10.3233/JND-221638

PMCID:: PMC10357150

Abstract Article PDF–852K

Select item 101905953.

Unique genotype-phenotype correlations within LAMA2-related limb girdle muscular dystrophy in Chinese patients

Xiuli Huang, Dandan Tan, Zaiqiang Zhang, Lin Ge, Jieyu Liu, Juan Ding, Haipo Yang, Cuijie Wei, Xingzhi Chang, Yun Yuan, Chuanzhu Yan, Hui Xiong

Front Neurol. 2023; 14: 1158094. Published online 2023 May 3. doi: 10.3389/fneur.2023.1158094

PMCID:: PMC10190595

Abstract Article PDF–1.2M

Select item 76673174.

Novel mutation identification and copy number variant detection via exome sequencing in congenital muscular dystrophy

Edmund S. Cauley, Alan Pittman, Swati Mummidivarpu, Ehsan G. Karimiani, Samantha Martinez, Isabella Moroni, Reza Boostani, Daniele Podini, Marina Mora, Yalda Jamshidi, Eric P. Hoffman, M. Chiara Manzini

Mol Genet Genomic Med. 2020 Nov; 8(11): e1387. Published online 2020 Sep 16. doi: 10.1002/mgg3.1387

PMCID:: PMC7667317

Abstract Article PDF–676K

Select item 75456095.

Alberto A. Zambon, Deborah Ridout, Marion Main, Rachael Mein, Rahul Phadke, Francesco Muntoni, Anna Sarkozy

Ann Clin Transl Neurol. 2020 Oct; 7(10): 1870–1882. Published online 2020 Sep 10. doi: 10.1002/acn3.51172

Correction in:: Ann Clin Transl Neurol. 2021 Jul; 8(7): 1571.

PMCID:: PMC7545609

Abstract Article PDF–1.3M

Select item 74607306.

Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis

Francesca Magri, Roberta Brusa, Luca Bello, Lorenzo Peverelli, Roberto Del Bo, Alessandra Govoni, Claudia Cinnante, Irene Colombo, Francesco Fortunato, Roberto Tironi, Stefania Corti, Nadia Grimoldi, Monica Sciacco, Nereo Bresolin, Elena Pegoraro, Maurizio Moggio, Giacomo Pietro Comi

Acta Myol. 2020 Jun; 39(2): 67–82. Published online 2020 Jun 1. doi: 10.36185/2532-1900-009

PMCID:: PMC7460730

Abstract Article PDF–313K

Select item 70939657.

LAMA2 regulates the fate commitment of mesenchymal stem cells via hedgehog signaling

Yuan Zhu, Xiao Zhang, Ranli Gu, Xuenan Liu, Siyi Wang, Dandan Xia, Zheng Li, Xiaomin Lian, Ping Zhang, Yunsong Liu, Yongsheng Zhou

Stem Cell Res Ther. 2020; 11: 135. Published online 2020 Mar 25. doi: 10.1186/s13287-020-01631-9

PMCID:: PMC7093965

Abstract Article PDF–9.7M

Select item 63058158.

Novel LAMA2 Gene Mutations Associated with Merosin-Deficient Congenital Muscular Dystrophy

Feyzollah Hashemi-Gorji, Vahid Reza Yassaee, Parisa Dashti, Mohammad Miryounesi

Iran Biomed J. 2018 Nov; 22(6): 408–414. doi: 10.29252/.22.6.408

PMCID:: PMC6305815

Abstract Article PDF–783K

Select item 61774449.

Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy

Lin Ge, Aijie Liu, Kai Gao, Renqian Du, Juan Ding, Bing Mao, Ying Hua, Xiaoli Zhang, Dandan Tan, Haipo Yang, Xiaona Fu, Yanbin Fan, Ling Zhang, Shujuan Song, Jian Wu, Feng Zhang, Yuwu Jiang, Xiru Wu, Hui Xiong

Sci Rep. 2018; 8: 14989. Published online 2018 Oct 9. doi: 10.1038/s41598-018-33098-3

PMCID:: PMC6177444

Abstract Article PDF–2.4M

Select item 597113110.

Laminin-deficient Muscular Dystrophy: Molecular Pathogenesis and Structural Repair Strategies

Peter D. Yurchenco, Karen K. McKee, Judith R. Reinhard, Markus A. Rüegg

Matrix Biol. Author manuscript; available in PMC 2019 Oct 1.

Published in final edited form as: Matrix Biol. 2018 Oct; 71-72: 174–187. Published online 2017 Nov 27. doi: 10.1016/j.matbio.2017.11.009

PMCID:: PMC5971131

Abstract Article PDF–1.6M

Select item 442590411.

microRNA network analysis identifies miR-29 cluster as key regulator of LAMA2 in ependymoma

Anbarasu Lourdusamy, Ruman Rahman, Stuart Smith, Richard Grundy

Acta Neuropathol Commun. 2015; 3: 26. Published online 2015 May 10. doi: 10.1186/s40478-015-0206-2

PMCID:: PMC4425904

Article PDF–771K

Select item 418959212.

Diverse modes of genomic alteration in hepatocellular carcinoma

Suchit Jhunjhunwala, Zhaoshi Jiang, Eric W Stawiski, Florian Gnad, Jinfeng Liu, Oleg Mayba, Pan Du, Jingyu Diao, Stephanie Johnson, Kwong-Fai Wong, Zhibo Gao, Yingrui Li, Thomas D Wu, Sharookh B Kapadia, Zora Modrusan, Dorothy M French, John M Luk, Somasekar Seshagiri, Zemin Zhang

Genome Biol. 2014; 15(8): 436. Published online 2014 Aug 26. doi: 10.1186/s13059-014-0436-9

PMCID:: PMC4189592

Abstract Article PDF–2.0M

Select item 275568613.

Crystal Structure of the LG1-3 Region of the Laminin α2 Chain

Federico Carafoli, Naomi J. Clout, Erhard Hohenester

J Biol Chem. 2009 Aug 21; 284(34): 22786–22792. Published online 2009 Jun 24. doi: 10.1074/jbc.M109.026658

PMCID:: PMC2755686

Abstract Article PDF–1.9M

Select item 173473514.

The expanding phenotype of laminin α2 chain (merosin) abnormalities: case series and review

K. Jones, G. Morgan, H. Johnston, V. Tobias, R. Ouvrier, I. Wilkinson, K. North

J Med Genet. 2001 Oct; 38(10): 649–657. doi: 10.1136/jmg.38.10.649

PMCID:: PMC1734735

Summary PDF–214K

Select item 965730915.

Alu Deletions in LAMA2 and CDH4 Genes Are Key Components of Polygenic Predictors of Longevity

Vera V. Erdman, Denis D. Karimov, Ilsia A. Tuktarova, Yanina R. Timasheva, Timur R. Nasibullin, Gulnaz F. Korytina

Int J Mol Sci. 2022 Nov; 23(21): 13492. Published online 2022 Nov 4. doi: 10.3390/ijms232113492

PMCID:: PMC9657309

Abstract Article PDF–330K

Select item 847470916.

LAMA2 and LOXL4 are candidate FSGS genes

Poornima Vijayan, Saidah Hack, Tony Yao, Mohammad Azfar Qureshi, Andrew D. Paterson, Rohan John, Bernard Davenport, Rachel Lennon, York Pei, Moumita Barua

BMC Nephrol. 2021; 22: 320. Published online 2021 Sep 26. doi: 10.1186/s12882-021-02524-6

PMCID:: PMC8474709

Abstract Article PDF–1.1M

Select item 742710017.

Mex3a interacts with LAMA2 to promote lung adenocarcinoma metastasis via PI3K/AKT pathway

Jinghui Liang, Haixia Li, Jingyi Han, Jin Jiang, Jiang Wang, Yongmeng Li, Zitong Feng, Renchang Zhao, Zhenguo Sun, Bin Lv, Hui Tian

Cell Death Dis. 2020 Aug; 11(8): 614. Published online 2020 Aug 13. doi: 10.1038/s41419-020-02858-3

PMCID:: PMC7427100

Abstract Article PDF–4.5M

Select item 479451418.

Controversial opinion: evaluation of EGR1 and LAMA2 loci for high myopia in Chinese populations

Fang-yu Lin, Zhu Huang, Ning Lu, Wei Chen, Hui Fang, Wei Han

J Zhejiang Univ Sci B. 2016 Mar; 17(3): 225–235. doi: 10.1631/jzus.B1500233

PMCID:: PMC4794514

Abstract Article PDF–1.0M

Select item 211993419.

Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues

Reetta Vuolteenaho, Maria Nissinen, Kirsi Sairdo, Mary Byers, Roger Eddy, Harri Hirvonen, Thomas B. Shows, Hannu Sariola, Eva Engvall, Karl Tryggvason

J Cell Biol. 1994 Feb 1; 124(3): 381–394. doi: 10.1083/jcb.124.3.381