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Subfractionation, characterization, and in-depth proteomic analysis of glomerular membrane vesicles in human urine.
Published in:
Kidney International, 2014, v. 85, n. 5, p. 1225, doi. 10.1038/ki.2013.422
By:
- Hogan, Marie C;
- Johnson, Kenneth L;
- Zenka, Roman M;
- Cristine Charlesworth, M;
- Madden, Benjamin J;
- Mahoney, Doug W;
- Oberg, Ann L;
- Huang, Bing Q;
- Leontovich, Alexey A;
- Nesbitt, Lisa L;
- Bakeberg, Jason L;
- McCormick, Daniel J;
- Robert Bergen, H;
- Ward, Christopher J
Publication type:
Article
Copy number variant analysis using genome‐wide mate‐pair sequencing.
Published in:
Genes, Chromosomes & Cancer, 2018, v. 57, n. 9, p. 459, doi. 10.1002/gcc.5
By:
- Smadbeck, James B.;
- Johnson, Sarah H.;
- Smoley, Stephanie A.;
- Gaitatzes, Athanasios;
- Drucker, Travis M.;
- Zenka, Roman M.;
- Kosari, Farhad;
- Murphy, Stephen J.;
- Hoppman, Nicole;
- Aypar, Umut;
- Sukov, William R.;
- Jenkins, Robert B.;
- Kearney, Hutton M.;
- Feldman, Andrew L.;
- Vasmatzis, George
Publication type:
Article
Cover Image.
Published in:
2019
By:
- Aypar, Umut;
- Smoley, Stephanie A.;
- Pitel, Beth A.;
- Pearce, Kathryn E.;
- Zenka, Roman M.;
- Vasmatzis, George;
- Johnson, Sarah H.;
- Smadbeck, James B.;
- Peterson, Jess F.;
- Geiersbach, Katherine B.;
- Van Dyke, Daniel L.;
- Thorland, Erik C.;
- Jenkins, Robert B.;
- Ketterling, Rhett P.;
- Greipp, Patricia T.;
- Kearney, Hutton M.;
- Hoppman, Nicole L.;
- Baughn, Linda B.
Publication type:
Cover Art
Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia.
Published in:
European Journal of Haematology, 2019, v. 102, n. 1, p. 87, doi. 10.1111/ejh.13179
By:
- Aypar, Umut;
- Smoley, Stephanie A.;
- Pitel, Beth A.;
- Pearce, Kathryn E.;
- Zenka, Roman M.;
- Vasmatzis, George;
- Johnson, Sarah H.;
- Smadbeck, James B.;
- Peterson, Jess F.;
- Geiersbach, Katherine B.;
- Van Dyke, Daniel L.;
- Thorland, Erik C.;
- Jenkins, Robert B.;
- Ketterling, Rhett P.;
- Greipp, Patricia T.;
- Kearney, Hutton M.;
- Hoppman, Nicole L.;
- Baughn, Linda B.
Publication type:
Article
Four‐dimensional proteomics analysis of human cerebrospinal fluid with trapped ion mobility spectrometry using PASEF.
Published in:
Proteomics, 2023, v. 23, n. 10, p. 1, doi. 10.1002/pmic.202200507
By:
- Mun, Dong‐Gi;
- Budhraja, Rohit;
- Bhat, Firdous A.;
- Zenka, Roman M.;
- Johnson, Kenneth L.;
- Moghekar, Abhay;
- Pandey, Akhilesh
Publication type:
Article
Diversity of post-translational modifications and cell signaling revealed by single cell and single organelle mass spectrometry.
Published in:
Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-06579-7
By:
- Mun, Dong-Gi;
- Bhat, Firdous A.;
- Joshi, Neha;
- Sandoval, Leticia;
- Ding, Husheng;
- Jain, Anu;
- Peterson, Jane A.;
- Kang, Taewook;
- Pujari, Ganesh P.;
- Tomlinson, Jennifer L.;
- Budhraja, Rohit;
- Zenka, Roman M.;
- Kannan, Nagarajan;
- Kipp, Benjamin R.;
- Dasari, Surendra;
- Gaspar-Maia, Alexandre;
- Smoot, Rory L.;
- Kandasamy, Richard K.;
- Pandey, Akhilesh
Publication type:
Article
TRIT1 defect leads to a recognizable phenotype of myoclonic epilepsy, speech delay, strabismus, progressive spasticity, and normal lactate levels.
Published in:
Journal of Inherited Metabolic Disease, 2022, v. 45, n. 6, p. 1039, doi. 10.1002/jimd.12550
By:
- Muylle, Ewout;
- Jiang, Huafang;
- Johnsen, Christin;
- Byeon, Seul Kee;
- Ranatunga, Wasantha;
- Garapati, Kishore;
- Zenka, Roman M.;
- Preston, Graeme;
- Pandey, Akhilesh;
- Kozicz, Tamas;
- Fang, Fang;
- Morava, Eva
Publication type:
Article

Found: 7

Subfractionation, characterization, and in-depth proteomic analysis of glomerular membrane vesicles in human urine.

Copy number variant analysis using genome‐wide mate‐pair sequencing.

Cover Image.

Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia.

Four‐dimensional proteomics analysis of human cerebrospinal fluid with trapped ion mobility spectrometry using PASEF.

Diversity of post-translational modifications and cell signaling revealed by single cell and single organelle mass spectrometry.

TRIT1 defect leads to a recognizable phenotype of myoclonic epilepsy, speech delay, strabismus, progressive spasticity, and normal lactate levels.