Results 161 to 170 of about 22,553 (288)

Decreased mechanical stiffness in LMNA−/− cells is caused by defective nucleo-cytoskeletal integrity: implications for the development of laminopathies [PDF]

, 2004
Jos L. V. Broers, Emiel A.G. Peeters, Helma J.H. Kuijpers, J. Endert, Carlijn V. C. Bouten, C.W.J. Oomens, Frank Frank Baaijens, Frans C. S. Ramaekers   +7 more
openalex   +1 more source

Reciprocal knock-in mice to investigate the functional redundancy of lamin B1 and lamin B2. [PDF]

, 2014
Lamins B1 and B2 (B-type lamins) have very similar sequences and are expressed ubiquitously. In addition, both Lmnb1- and Lmnb2-deficient mice die soon after birth with neuronal layering abnormalities in the cerebral cortex, a consequence of defective ...
Coffinier, Catherine, de Jong, Pieter J, Fong, Loren G, Jung, Hea-Jin, Lee, John M, Nobumori, Chika, Tatar, Angelica, Tu, Yiping, Wu, Daniel, Yoshinaga, Yuko, Young, Stephen G   +10 more
core  

Familial partial lipodystrophy associated with compound heterozygosity for novel mutations in the LMNA gene [PDF]

, 2004
David B. Savage, Ian G. McFarlane, Inês Barroso, Maria A. Soos, Andrew Powlson, E. Louise Thomas, Jimmy D. Bell, Ian N. Scobie, P E Belchetz, William F. Kelly, David Halsall, Alan J. Schafer, Stephen O’Rahilly   +12 more
openalex   +1 more source

Maternal serum Lamin A is a potential biomarker that can predict adverse pregnancy outcomes

EBioMedicine, 2022
Summary: Background: Maternal serum Lamin A (LMNA) was reported to have potential diagnostic value in the prenatal diagnosis of congenital heart disease (CHD).
Lizhu Chen, Yun Xiu, Qijun Wu, Yu Wang, Yixin Zhang, Jia Xue, Qinbo Wang, Zhengwei Yuan   +7 more
doaj  

Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathy [PDF]

, 2005
Sara Benedetti
openalex   +1 more source

Deletion of entire LMNA gene as a cause of cardiomyopathy [PDF]

HeartRhythm Case Reports, 2020
Allison L. Cirino, Neal K. Lakdawala, Sarah Cuddy   +2 more
openaire   +4 more sources

Characterization of cardiac involvement in patients with LMNA splice-site mutation–related dilated cardiomyopathy and sudden cardiac death

Frontiers in Genetics
Introduction:LMNA splicing mutations occur in 9.1% of cases with cardiac involvement cases, but the phenotype and severity of disease they cause have not yet been systematically studied. The aim of this study was to understand the clinical and pathogenic
Xuebin Ling, Yanjun Hou, Xingyu Jia, Youling Lan, Xiaoping Wu, Julan Wu, Wei Jie, Hui Liu, Shan Huang, Zhenling Wan, Tianfa Li, Junli Guo, Tiebiao Liang   +12 more
doaj   +1 more source

ALMNASplicing Mutation in Two Sisters with Severe Dunnigan-Type Familial Partial Lipodystrophy Type 2 [PDF]

, 2006
Chantal F. Morel, Mary Ann Thomas, Henian Cao, Caroline O’Neil, J. Geoffrey Pickering, William D. Foulkes, Robert A. Hegele   +6 more
openalex   +1 more source

LMNA Variants and Risk of Adult-Onset Cardiac Disease.

Journal of the American College of Cardiology, 2022
J. Lazarte, S. Jurgens, S. Choi, S. Khurshid, Valerie N. Morrill, L. Weng, V. Nauffal, J. Pirruccello, Jennifer L. Halford, R. Hegele, P. Ellinor, K. Lunetta, S. Lubitz   +12 more
semanticscholar   +1 more source

N of 2 Responders With LMNA-NTRK1 [PDF]

JNCI: Journal of the National Cancer Institute, 2015
Chih-Jian Lih, Alice P. Chen
openaire   +3 more sources