Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Olivia Grischow"'
Autor:
Kathleen Schieffer, Mariam Mathew, Kristy Lee, Samantha Choi, Elizabeth Varga, Emma Garval, Olivia Grischow, Aimee Jalkanen, Vijayakumar Jayaraman, Don Corsmeier, Ben Kelly, Peter Chang, James Fitch, Katherine Miller, Daniel Koboldt, Peter White, Vincent Magrini, Richard Wilson, Elaine Mardis, Catherine Cottrell
Publikováno v:
Cancer Genetics. :37-38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7df5d4aa647a1db68fef62ff375f1dd
https://doi.org/10.1016/j.cancergen.2022.10.120
https://doi.org/10.1016/j.cancergen.2022.10.120
Autor:
Matthew Cannon, James Stevenson, Kori Kuzma, Colin O'Sullivan, Katherine Miller, Olivia Grischow, Adam Coffman, Susanna Kiwala, Joshua McMichael, Dorian Morrissey, Kelsy Cotto, Obi L. Griffith, Malachi Griffith, Alex Wagner
Publikováno v:
Cancer Genetics. :16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87d5c5f85a1efce9a5305533f8f90fbc
https://doi.org/10.1016/j.cancergen.2022.10.051
https://doi.org/10.1016/j.cancergen.2022.10.051
Autor:
Mohammad, Marhabaie, Scott E, Hickey, Katherine, Miller, Olivia, Grischow, Kathleen M, Schieffer, Samuel J, Franklin, David M, Gordon, Samantha, Choi, Theresa, Mihalic Mosher, Peter, White, Daniel C, Koboldt, Richard K, Wilson
Publikováno v:
Cold Spring Harbor Molecular Case Studies
There is increasing recognition for the contribution of genetic mosaicism to human disease, particularly as high-throughput sequencing has enabled detection of sequence variants at very low allele frequencies. Here, we describe an infant male who pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9730cca7b180db210ee1c48e83ecb519
https://pubmed.ncbi.nlm.nih.gov/34667072
https://pubmed.ncbi.nlm.nih.gov/34667072
Autor:
Matthew Cannon, James Stevenson, Kori Kuzma, Colin O'Sullivan, Katherine Miller, Olivia Grischow, Adam Coffman, Susanna Kiwala, Joshua F. McMichael, Dorian Morrissey, Kelsy Cotto, Obi Griffith, Malachi Griffith, Alex Wagner
Publikováno v:
Cancer Research. 82:1197-1197
The Drug-Gene Interaction Database (DGIdb, www.dgidb.org) is a publicly accessible resource that aggregates 102,426 gene records and 57,498 drug records from 40 drug-gene interaction data sources to aid both researchers and clinicians in identifying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a350786e4f81c13c0b81cd489bf3fbd
https://doi.org/10.1158/1538-7445.am2022-1197
https://doi.org/10.1158/1538-7445.am2022-1197
Autor:
Girish Dhall, Joseph Stanek, Megan Blue, Parth Patel, Diana Thomas, Christopher Pierson, Benita Tamrazi, Kris M Mahadeo, Jessica Fleming, Erica Bell, Katherine Miller, Olivia Grischow, Thomas Liszkay, Scott Coven, Caroline Hastings, Karen Tsui, Claire Mazewski, Gregory Friedman, Christopher Moertel, Derek Hanson, Carl Koschmann, Guy Brock, Kenneth Wong, Arnab Chakravarti, Shahab Asgharzadeh, Marvin N Nelson, Daniel Boue, Jaclyn Biegel, Elaine Mardis, Jonathan Finlay
Publikováno v:
Neuro-Oncology. 24:i192-i192
Advances in RNA and DNA profiling have identified four core molecular subgroups of medulloblastoma of prognostic significance: Sonic Hedgehog (SHH) subtype, WNT subtype, Group 3, and Group 4. Infants and young children with SHH medulloblastoma have d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::498701386341567654bb8216cd3c909c
https://doi.org/10.1093/neuonc/noac079.717
https://doi.org/10.1093/neuonc/noac079.717
Autor:
Catherine E. Cottrell, Jeffrey R. Leonard, Kathleen M. Schieffer, Diana P Rodriguez, Jonathan L. Finlay, Katherine E. Miller, Elaine R. Mardis, Olivia Grischow
Publikováno v:
Cold Spring Harbor Molecular Case Studies
In this follow-up report, we present updated information regarding a previously reported pediatric patient with a World Health Organization grade I ganglioglioma harboring a BRAF p.T599dup mutation (Cold Spring Harb Mol Case Stud 4: a002618). This pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bc57d714b57e81a77039254fcdcba31
http://europepmc.org/articles/PMC8040738
http://europepmc.org/articles/PMC8040738
Autor:
Peter White, Daniel C. Koboldt, Theresa Mihalic Mosher, Scott E. Hickey, Mohammad Marhabaie, Samuel J Franklin, Samantha Choi, Kathleen M. Schieffer, Olivia Grischow, David M Gordon, Katherine E. Miller, Richard K. Wilson
Publikováno v:
Molecular Case Studies. 7:a006122
There is increasing recognition for the contribution of genetic mosaicism to human disease, particularly as high-throughput sequencing has enabled detection of sequence variants at very low allele frequencies. Here, we describe an infant male who pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b62a9ae8e61993d4a5988651d122be7e
https://doi.org/10.1101/mcs.a006122
https://doi.org/10.1101/mcs.a006122