Zobrazeno 1 - 10
of 935
pro vyhledávání: '"M Baca"'
Publikováno v:
ZooKeys, Vol 1025, Iss , Pp 177-201 (2021)
The New World species of the minute aquatic beetle genus Notomicrus Sharp compose a much greater diversity than their Old World congeners, with 14 of the 17 known Notomicrus species occurring in the Neotropics. A recent phylogenetic study recovered f
Externí odkaz:
https://doaj.org/article/7de550ce068b4390b2095759c9025223
Publikováno v:
Annals of Hepatology, Vol 27, Iss , Pp 100594- (2022)
Introduction and Objectives: Kidney injury has become one of the main causes of decompensation in cirrhotic patients. There are few studies in our country that compare various methods to assess kidney function in these patients. Objective: To evaluat
Externí odkaz:
https://doaj.org/article/33c41958d0f143778883a1f3512adca8
Publikováno v:
The Journal of Headache and Pain, Vol 19, Iss 1, Pp 1-13 (2018)
Abstract The discovery that intravenous (IV) infusions of the neuropeptide PACAP-38 (pituitary adenylyl cyclase activating peptide-38) induced delayed migraine-like headaches in a large majority of migraine patients has resulted in considerable excit
Externí odkaz:
https://doaj.org/article/825c9e78dded431baae9909062c0f2f5
Autor:
Matthew N. Svalina, Christian A. Cea-Del Rio, J. Keenan Kushner, Abigail Levy, Serapio M. Baca, E. Mae Guthman, Maya Opendak, Regina M. Sullivan, Diego Restrepo, Molly M. Huntsman
Publikováno v:
J Neurosci
Fragile X Syndrome is a neurodevelopmental disorder and the most common monogenic cause of intellectual disability, autism spectrum disorders, and anxiety disorders. Loss of fragile x mental retardation protein results in disruptions of synaptic deve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::787aab9ca946efcfaee80929622f49df
https://doi.org/10.1523/jneurosci.1776-21.2022
https://doi.org/10.1523/jneurosci.1776-21.2022
Autor:
AmirAli Talasaz, Richard B. Lanman, Darya I. Chudova, Helmy Eltoukhy, Arthur M. Baca, Rebecca J. Nagy, Justin I. Odegaard, Philip C. Mack, David R. Gandara, Reza Mokhtari, James V. Vowles, Stefanie A. Mortimer, Stephen R. Fairclough, Kimberly C. Banks, Oliver A. Zill
Supplemental Methods, Supplemental References, Supplemental Figure Legends, Figure S1-13, Table S1-5 and S14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3426a5c012c8b062ed7b409de9e9d680
https://doi.org/10.1158/1078-0432.22470290
https://doi.org/10.1158/1078-0432.22470290
Autor:
AmirAli Talasaz, Richard B. Lanman, Darya I. Chudova, Helmy Eltoukhy, Arthur M. Baca, Rebecca J. Nagy, Justin I. Odegaard, Philip C. Mack, David R. Gandara, Reza Mokhtari, James V. Vowles, Stefanie A. Mortimer, Stephen R. Fairclough, Kimberly C. Banks, Oliver A. Zill
cfDNA variants associated with resistance to on-label targeted therapies across six cancer types
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::501bf51b954f47c255577dd17466678e
https://doi.org/10.1158/1078-0432.22470287
https://doi.org/10.1158/1078-0432.22470287
Autor:
AmirAli Talasaz, Richard B. Lanman, Darya I. Chudova, Helmy Eltoukhy, Arthur M. Baca, Rebecca J. Nagy, Justin I. Odegaard, Philip C. Mack, David R. Gandara, Reza Mokhtari, James V. Vowles, Stefanie A. Mortimer, Stephen R. Fairclough, Kimberly C. Banks, Oliver A. Zill
Purpose: Cell-free DNA (cfDNA) sequencing provides a noninvasive method for obtaining actionable genomic information to guide personalized cancer treatment, but the presence of multiple alterations in circulation related to treatment and tumor hetero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9eb8eb0e52eb86c9f15f9a125774c668
https://doi.org/10.1158/1078-0432.c.6527498.v1
https://doi.org/10.1158/1078-0432.c.6527498.v1
Autor:
AmirAli Talasaz, Richard B. Lanman, Darya I. Chudova, Helmy Eltoukhy, Arthur M. Baca, Rebecca J. Nagy, Justin I. Odegaard, Philip C. Mack, David R. Gandara, Reza Mokhtari, James V. Vowles, Stefanie A. Mortimer, Stephen R. Fairclough, Kimberly C. Banks, Oliver A. Zill
Mutual exclusivity statistics for cfDNA alterations in lung adenocarcinoma, breast cancer, and colorectal cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ea2ab48268a3d1e033a43bffd4a6797
https://doi.org/10.1158/1078-0432.22470281.v1
https://doi.org/10.1158/1078-0432.22470281.v1
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