Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Lindsay R Stolzenburg"'
Autor:
Lindsay R Stolzenburg, Sahar Esmaeeli, Ameya S Kulkarni, Erin Murphy, Taekyung Kwon, Christina Preiss, Lamiaa Bahnassawy, Joshua D Stender, Justine D Manos, Peter Reinhardt, Fedik Rahimov, Jeffrey F Waring, Cyril Y Ramathal
Publikováno v:
PLoS ONE, Vol 18, Iss 9, p e0291029 (2023)
Neurodegenerative diseases encompass a group of debilitating conditions resulting from progressive nerve cell death. Of these, Alzheimer's disease (AD) occurs most frequently, but is currently incurable and has limited treatment success. Late onset A
Externí odkaz:
https://doaj.org/article/395ae1654da24c70810025fdf7471ad2
Autor:
David W Johnson, Jesse R Llop, Sara F Farrell, Jie Yuan, Lindsay R Stolzenburg, Andrew V Samuelson
Publikováno v:
PLoS Genetics, Vol 10, Iss 4, p e1004278 (2014)
The Myc family of transcription factors regulates a variety of biological processes, including the cell cycle, growth, proliferation, metabolism, and apoptosis. In Caenorhabditis elegans, the "Myc interaction network" consists of two opposing heterod
Externí odkaz:
https://doaj.org/article/9744c6b641514d79967098ddb30f86d4
Autor:
Ammar J. Alsheikh, Sabrina Wollenhaupt, Emily A. King, Jonas Reeb, Sujana Ghosh, Lindsay R. Stolzenburg, Saleh Tamim, Jozef Lazar, J. Wade Davis, Howard J. Jacob
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-21 (2022)
Abstract Background The remarkable growth of genome-wide association studies (GWAS) has created a critical need to experimentally validate the disease-associated variants, 90% of which involve non-coding variants. Methods To determine how the field i
Externí odkaz:
https://doaj.org/article/d0874d4b110e421f9c22bf448f29db52
Autor:
Lindsay R. Stolzenburg, Barrett Ainsworth, Bridget Riley-Gillis, Tibor Pakozdi, Areej Ammar, Paul A. Ellis, Julie L. Wilsbacher, Cyril Y. Ramathal
Publikováno v:
Oncotarget. 13:1-12
Autor:
Ammar J. Alsheikh, Sabrina Wollenhaupt, Emily A. King, Jonas Reeb, Sujana Ghosh, Lindsay R. Stolzenburg, Saleh Tamim, Jozef Lazar, J. Wade Davis, Howard J. Jacob
Publikováno v:
BMC medical genomics. 15(1)
Background The remarkable growth of genome-wide association studies (GWAS) has created a critical need to experimentally validate the disease-associated variants, 90% of which involve non-coding variants. Methods To determine how the field is address
Autor:
Lindsay R. Stolzenburg, Ann Harris
Publikováno v:
Cell and Tissue Research. 371:325-338
Tissue fibrosis, the development of fibrous connective tissue as a result of injury or damage, is associated with many common diseases and cannot be treated effectively. The complex biological processes accompanying fibrosis often involve aberrant si
Autor:
Kay-Marie Lamar, Rui Yang, Ann Harris, Andrew D. Hoffmann, Sujana Ghosh, Shih Hsing Leir, Sara L. Fossum, Matthew Xu, Jenny L. Kerschner, Sarah Wachtel, Lindsay R. Stolzenburg
Publikováno v:
Nucleic Acids Research
Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene cause cystic fibrosis (CF), but are not good predictors of lung phenotype. Genome-wide association studies (GWAS) previously identified additional genomic sites associat
Autor:
Lindsay R. Stolzenburg, Ann Harris
Publikováno v:
Biol Chem
Chronic respiratory diseases encompass a group of diverse conditions affecting the airways, which all impair lung function over time. They include cystic fibrosis (CF), idiopathic pulmonary fibrosis (IPF), chronic obstructive pulmonary disease (COPD)
Autor:
Mira Krendel, Sharon E. Chase, Lindsay R. Stolzenburg, Lawrence B. Holzman, Christina V. Encina, Arthur H. Tatum
Publikováno v:
American Journal of Physiology-Renal Physiology. 303:F1099-F1106
Myosin 1e (myo1e) is an actin-dependent molecular motor that plays an important role in kidney functions. Complete knockout of myo1e in mice and Myo1E mutations in humans are associated with nephrotic syndrome and focal segmental glomerulosclerosis.
Autor:
Lindsay R. Stolzenburg, Bertrand Leblond, Sébastien Malinge, Laurent Desire, Thierry Besson, John D. Crispino, Lauren Diebold, Daniel E. Cook, Casagrande Anne-Sophie, Benjamin J. Thompson, Rahul S. Bhansali
Publikováno v:
Journal of Experimental Medicine
Journal of Experimental Medicine, Rockefeller University Press, 2015, 212 (6), pp.723-740. ⟨10.1084/jem.20150002⟩
The Journal of Experimental Medicine
Journal of Experimental Medicine, Rockefeller University Press, 2015, 212 (6), pp.723-740. ⟨10.1084/jem.20150002⟩
The Journal of Experimental Medicine
Thompson et al. identify the dual specificity tyrosine-regulated kinase 1A (DYRK1A) as a new player in the control of lymphopoiesis. Loss of DYRK1A in mice results in Cyclin D3 stabilization and failure to repress E2F target genes, thus impairing cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1059e9ba20e6f80396b909a66ea459f3
https://hal.archives-ouvertes.fr/hal-01160621/file/953.full-1.pdf
https://hal.archives-ouvertes.fr/hal-01160621/file/953.full-1.pdf