Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Michael Schlabach"'
Autor:
Karrie Wong, Sharon Lin, Christopher Wrocklage, Katri Sofjan, Leila Williams, Mallory Brady, Nicholas Colletti, Noah Tubo, Hugh Gannon, Robert LaMothe, Tianlei Xu, Tracy VandenBerg, Sol Shenker, Caroline Dugopolski, Frank Stegmeier, Louise Cadzow, Michael Schlabach, Micah Benson
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 9, Iss Suppl 2 (2021)
Externí odkaz:
https://doaj.org/article/490a3e91b10d4fd1b0d7fff1fe4208ff
Autor:
Sharon Lin, Leila Williams, Mitali Ghose, Hugh Gannon, Conor Calnan, Angelina Pizzo, Pei-Lun Kao, Mallory Brady, Katri Sofjan, Anne Dodson, Sol Shenker, Michael Schlabach, Fiona Sharp, Frank Stegmeier, Micah Benson, Karrie Wong
Publikováno v:
Regular and Young Investigator Award Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82c507cbbaec94af8cd61117bc10704a
https://doi.org/10.1136/jitc-2022-sitc2022.0255
https://doi.org/10.1136/jitc-2022-sitc2022.0255
Autor:
Sumeet Nayak, Pamela Sullivan, Yuji Mishina, Anne Dodson, Pei-Lun Kao, Hugh Gannon, Chris Middleton, Sol Shenker, Morgan Murray, Michael Schlabach, Frank Stegmeier, Erica Tobin, Louise Cadzow, Andrew Wylie
Publikováno v:
Cancer Research. 83:2771-2771
Tumors with defects in DNA double strand break (DSB) repair pathways, including those with mutations in BRCA1/2, are often treated with either poly (ADP-ribose) polymerase-1 (PARP1) inhibitors or platinum-based chemotherapy. Despite their clinical be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55ed71f623d3a547b0b49dcefbb20be7
https://doi.org/10.1158/1538-7445.am2023-2771
https://doi.org/10.1158/1538-7445.am2023-2771
Autor:
Christie M. Ballantyne, Danièle Zoch, Dan Bercovich, Olaf Bodamer, Arthur L. Beaudet, Michael Schlabach
Publikováno v:
Clinical Chemistry. 48:1913-1918
Background: Autosomal dominant familial hypercholesterolemia (FH) attributable to mutations in the LDL receptor (LDLR) gene is one of the most common genetic disorders associated with significant morbidity and mortality. Definitive diagnosis would he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5afc9a4bf8c6ef06739704b1d021db12
https://doi.org/10.1093/clinchem/48.11.1913
https://doi.org/10.1093/clinchem/48.11.1913
Autor:
Olaf A, Bodamer, Dan, Bercovich, Michael, Schlabach, Christie, Ballantyne, Danièle, Zoch, Arthur L, Beaudet
Publikováno v:
Clinical chemistry. 48(11)
Autosomal dominant familial hypercholesterolemia (FH) attributable to mutations in the LDL receptor (LDLR) gene is one of the most common genetic disorders associated with significant morbidity and mortality. Definitive diagnosis would help to initia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d47295c634d0c8b24066e0925d721ad3
https://pubmed.ncbi.nlm.nih.gov/12406975
https://pubmed.ncbi.nlm.nih.gov/12406975