Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Bliss Magella"'
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Identification of genes associated with childhood-onset nephrotic syndrome has significantly advanced our understanding of the pathogenesis of this complex disease over the past two decades, however the precise etiology in many cases remains unclear.
Externí odkaz:
https://doaj.org/article/25c54d03acc1420b8d84180b095b591c
Autor:
Hanieh Razzaghi, Katherine Nowicki, Susan L. Furth, Andrea M. Knight, Amy J.Goodwin Davies, Christopher B. Forrest, Vikas R. Dharnidharka, Michelle R. Denburg, Mark Mitsnefes, Brian R. Stotter, Scott E. Wenderfer, Bliss Magella, Caroline Gluck, Mahmoud Kallash, William E. Smoyer, Megan Kelton, Meredith A. Atkinson, Joseph T. Flynn, Bradley P. Dixon, Sangeeta Sule, Bailey Lc, Joyce C. Chang, Rebecca Scobell, Cora Sears, Ingrid Luna
Publikováno v:
Clin J Am Soc Nephrol
BACKGROUND AND OBJECTIVES: Performing adequately powered clinical trials in pediatric diseases, such as SLE, is challenging. Improved recruitment strategies are needed for identifying patients. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Electroni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a14d1d796555b31f359fc29533a8a7c
https://doi.org/10.2215/cjn.07810621
https://doi.org/10.2215/cjn.07810621
Autor:
Edward Nehus, Alcia Delaney Edwards-Richards, Chunyan Liu, Amy C. Wilson, Margret Kamel, Kera E. Luckritz, Meredith P. Schuh, Donna J. Claes, Bliss Magella, Abdulla M. Ehlayel, Stephanie Jernigan, Stephanie L. Clark, Aftab S. Chishti, Elif Erkan, Asif Mansuri
Publikováno v:
Pediatric Nephrology. 36:3953-3959
There are no multi-center studies examining omentectomy and peritoneal dialysis (PD) catheter revision in the pediatric dialysis population. We performed a retrospective study at eight centers within the Pediatric Nephrology Research Consortium (PNRC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7aca74dce79c870bd765873acc253d03
https://doi.org/10.1007/s00467-021-05150-4
https://doi.org/10.1007/s00467-021-05150-4
Autor:
Meredith P, Schuh, Edward, Nehus, Chunyan, Liu, Abdulla, Ehlayel, Stephanie, Clark, Aftab, Chishti, Alcia Delaney, Edwards-Richards, Elif, Erkan, Stephanie, Jernigan, Margret, Kamel, Kera, Luckritz, Bliss, Magella, Asif, Mansuri, Amy C, Wilson, Donna J, Claes
Publikováno v:
Pediatric nephrology (Berlin, Germany). 36(12)
There are no multi-center studies examining omentectomy and peritoneal dialysis (PD) catheter revision in the pediatric dialysis population.We performed a retrospective study at eight centers within the Pediatric Nephrology Research Consortium (PNRC)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2a41d9a6c80095816f5d2b46aaac4470
https://pubmed.ncbi.nlm.nih.gov/34128096
https://pubmed.ncbi.nlm.nih.gov/34128096
Publikováno v:
Developmental Biology. 438:84-93
Hox genes can function as key drivers of segment identity, with Hox mutations in Drosophila often resulting in dramatic homeotic transformations. In addition, however, they can serve other essential functions. In mammals, the study of Hox gene roles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a37203b6afc69d40e2f634ed496db840
https://doi.org/10.1016/j.ydbio.2018.03.020
https://doi.org/10.1016/j.ydbio.2018.03.020
Autor:
Nathan Salomonis, S. Steven Potter, Bliss Magella, Mike Adam, Kashish Chetal, Stuart Hay, Andrew S. Potter, Meenakshi Venkatasubramanian
Publikováno v:
Developmental Biology. 434:36-47
The developing kidney provides a useful model for study of the principles of organogenesis. In this report we use three independent platforms, Drop-Seq, Chromium 10x Genomics and Fluidigm C1, to carry out single cell RNA-Seq (scRNA-Seq) analysis of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36c24f9d7568b73393f32374f084402e
https://doi.org/10.1016/j.ydbio.2017.11.006
https://doi.org/10.1016/j.ydbio.2017.11.006
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Frontiers in Pediatrics
Frontiers in Pediatrics
Identification of genes associated with childhood-onset nephrotic syndrome has significantly advanced our understanding of the pathogenesis of this complex disease over the past two decades, however the precise etiology in many cases remains unclear.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c70b84cedfa7ab37fcec2af67666c6da
https://www.frontiersin.org/article/10.3389/fped.2019.00404/full
https://www.frontiersin.org/article/10.3389/fped.2019.00404/full
Publikováno v:
BMC Developmental Biology
The 39 mammalian Hox genes show problematic patterns of functional overlap. In order to more fully define the developmental roles of Hox genes it is necessary to remove multiple combinations of paralogous and flanking genes. In addition, the downstre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b62437648f738bcfa0d63a2d2b51ecf9
https://doi.org/10.1186/s12861-015-0078-5
https://doi.org/10.1186/s12861-015-0078-5
Publikováno v:
Development (Cambridge, England). 141(15)
We used a single cell RNA-seq strategy to create an atlas of gene expression patterns in the developing kidney. At several stages of kidney development, histologically uniform populations of cells give rise to multiple distinct lineages. We performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d9d9b175404f87f064afcf1a455fde3
https://pubmed.ncbi.nlm.nih.gov/25053437
https://pubmed.ncbi.nlm.nih.gov/25053437
Autor:
Mike Adam, Anna M. Raines, S. Steven Potter, Sara E. Meyer, Bliss Magella, Sudhansu K. Dey, H. Leighton Grimes
Hox genes are key regulators of development. In mammals, the study of these genes is greatly confounded by their large number, overlapping functions and interspersed shared enhancers. Here, we describe the use of a novel recombineering strategy to in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a52f6f9f1c6d7d0b491fd96588d0155
https://europepmc.org/articles/PMC3699281/
https://europepmc.org/articles/PMC3699281/
