Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Quinn Murphy"'
Autor:
Wenfen Zhang, Zhenhua Tian, Shujie Yang, Joseph Rich, Shuaiguo Zhao, Mikael Klingeborn, Po-Hsun Huang, Zhishang Li, Alexander Stout, Quinn Murphy, Edward Patz, Shusheng Zhang, Guozhen Liu, Tony Jun Huang
Publikováno v:
Microsystems & Nanoengineering, Vol 7, Iss 1, Pp 1-8 (2021)
Abstract Exosomes are cell-derived nanovesicles that have recently gained popularity as potential biomarkers in liquid biopsies due to the large amounts of molecular cargo they carry, such as nucleic acids and proteins. However, most existing exosome
Externí odkaz:
https://doaj.org/article/55eee4995b4944d7992d704e418fc17a
Autor:
Chrystal F. Mavros, Catherine A. Brownstein, Roshni Thyagrajan, Casie A. Genetti, Sahil Tembulkar, Kelsey Graber, Quinn Murphy, Kristin Cabral, Grace E. VanNoy, Matthew Bainbridge, Jiahai Shi, Pankaj B. Agrawal, Alan H. Beggs, Eugene D’Angelo, Joseph Gonzalez-Heydrich
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-7 (2018)
Abstract Background TRRAP encodes a multidomain protein kinase that works as a genetic cofactor to influence DNA methylation patterns, DNA damage repair, and chromatin remodeling. TRRAP protein is vital to early neural developmental processes, and va
Externí odkaz:
https://doaj.org/article/4f0c9b8faf604ddfa7af3f90a5944cfe
Autor:
Amy E O'Connell, Maxim V Gerashchenko, Marie-Francoise O'Donohue, Samantha M Rosen, Eric Huntzinger, Diane Gleeson, Antonella Galli, Edward Ryder, Siqi Cao, Quinn Murphy, Shideh Kazerounian, Sarah U Morton, Klaus Schmitz-Abe, Vadim N Gladyshev, Pierre-Emmanuel Gleizes, Bertrand Séraphin, Pankaj B Agrawal
Publikováno v:
PLoS Genetics, Vol 15, Iss 2, p e1007917 (2019)
Hbs1 has been established as a central component of the cell's translational quality control pathways in both yeast and prokaryotic models; however, the functional characteristics of its human ortholog (Hbs1L) have not been well-defined. We recently
Externí odkaz:
https://doaj.org/article/838e030b6548429aa6d8c95b74d43a7e
Autor:
Isabelle Marty, Jasmine Lin, Pankaj B. Agrawal, Yuanfan Zhang, Qifei Li, Shiyu Luo, Shideh Kazerounian, Quinn Murphy
Publikováno v:
Hum Mol Genet
Striated preferentially expressed gene (SPEG), a member of the myosin light chain kinase family, is localized at the level of triad surrounding myofibrils in skeletal muscles. In humans, SPEG mutations are associated with centronuclear myopathy and c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5461b54aee932a29f1b925546deb7c55
https://doi.org/10.1093/hmg/ddaa276
https://doi.org/10.1093/hmg/ddaa276
Autor:
Po-Hsun Huang, Quinn Murphy, Zhishang Li, Edward F. Patz, Guozhen Liu, Zhenhua Tian, Wenfen Zhang, Shuaiguo Zhao, Alexander Stout, Mikael Klingeborn, Tony Jun Huang, Shujie Yang, Shusheng Zhang, Joseph Rich
Publikováno v:
Microsystems & Nanoengineering, Vol 7, Iss 1, Pp 1-8 (2021)
Exosomes are cell-derived nanovesicles that have recently gained popularity as potential biomarkers in liquid biopsies due to the large amounts of molecular cargo they carry, such as nucleic acids and proteins. However, most existing exosome-based an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78fbf9c9e7fa0fce6ac8d93bff632cca
https://pubmed.ncbi.nlm.nih.gov/34567775
https://pubmed.ncbi.nlm.nih.gov/34567775
Autor:
Katlynn Bugda Gwilt, Angela Lek, Jeffrey J. Widrick, Devin E. Gibbs, Anna Pakula, Yuanfan Zhang, Vandana Gupta, Hiroaki Mitsuhashi, Anusha Manglik, June Criscione, Lillian Mead, Fedik Rahimov, Louis M. Kunkel, Quinn Murphy
Publikováno v:
Human Molecular Genetics. 28:320-331
Facioscapulohumeral dystrophy type 1 (FSHD-1) is the most common autosomal dominant form of muscular dystrophy with a prevalence of ∼1 in 8000 individuals. It is considered a late-onset form of muscular dystrophy and leads to asymmetric muscle weak
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6125e0ec79c277d06a285b54dd19e366
https://doi.org/10.1093/hmg/ddy348
https://doi.org/10.1093/hmg/ddy348
Autor:
Samantha M. Rosen, Shideh Kazerounian, Klaus Schmitz-Abe, Marie-Françoise O'Donohue, Pierre-Emmanuel Gleizes, Pankaj B. Agrawal, Eric Huntzinger, Edward Ryder, Maxim V. Gerashchenko, Vadim N. Gladyshev, Diane Gleeson, Quinn Murphy, Sarah U. Morton, Bertrand Séraphin, Antonella Galli, Amy E. O’Connell, Siqi Cao
Publikováno v:
PLoS Genetics
PLoS Genetics, Public Library of Science, 2019, 15 (2), pp.e1007917. ⟨10.1371/journal.pgen.1007917⟩
PLoS Genetics, Vol 15, Iss 2, p e1007917 (2019)
PLoS Genetics, Public Library of Science, 2019, 15 (2), pp.e1007917. ⟨10.1371/journal.pgen.1007917⟩
PLoS Genetics, Vol 15, Iss 2, p e1007917 (2019)
Hbs1 has been established as a central component of the cell’s translational quality control pathways in both yeast and prokaryotic models; however, the functional characteristics of its human ortholog (Hbs1L) have not been well-defined. We recentl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d61982dfd7029af3e1b0f98d91888846
https://hal.archives-ouvertes.fr/hal-02327840/file/islandora_84261.pdf
https://hal.archives-ouvertes.fr/hal-02327840/file/islandora_84261.pdf
Autor:
Judith R. Kelsen, John T. Boyle, Jay R. Thiagarajah, Amy E. O’Connell, Daniel Kamin, Fanny Zhou, Bharti Gangwani, Quinn Murphy, Hannah Rickner, Pankaj B. Agrawal, Jefferson J. Doyle, Jeff Goldsmith, Camilla A. Richmond, Manasvi S. Shah, David T. Breault
Homozygous nonsense mutations in WNT2B were identified in three individuals from two unrelated families with severe, neonatal-onset osmotic diarrhea after whole-exome sequencing was performed on trios from the two families. Intestinal biopsy samples
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9eebb09757237b50e9264794738fc628
https://europepmc.org/articles/PMC6035368/
https://europepmc.org/articles/PMC6035368/