Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kate Merath"'
Autor:
Prahlad K. Rao, Kate Merath, Eugene Drigalenko, Avinash Y. L. Jadhav, Richard A. Komorowski, Matthew I. Goldblatt, Anand Rohatgi, Mark A. Sarzynski, Samer Gawrieh, Michael Olivier
Publikováno v:
Clinical Proteomics, Vol 15, Iss 1, Pp 1-9 (2018)
Abstract Background Metabolic diseases such as obesity and diabetes are associated with changes in high-density lipoprotein (HDL) particles, including changes in particle size and protein composition, often resulting in abnormal function. Recent stud
Externí odkaz:
https://doaj.org/article/75780205fac44129ae8958577d1a86dd
Autor:
Hyder A. Jinnah, Henrique B. Ferraz, Stephanie Standal, Pooia Fattahi, Aleks Zuzek, Nabilah Alibhai, Kate Merath
Publikováno v:
Toxicon. 214:S28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb2c30689a43621ad65e35c319ec5162
https://doi.org/10.1016/j.toxicon.2021.11.068
https://doi.org/10.1016/j.toxicon.2021.11.068
Autor:
Richard A. Komorowski, Kate Merath, Matthew I. Goldblatt, Michael Olivier, Samer Gawrieh, Anand Rohatgi, Prahlad K. Rao, Avinash Y. L. Jadhav, Eugene Drigalenko, Mark A. Sarzynski
Publikováno v:
Clinical Proteomics
Clinical Proteomics, Vol 15, Iss 1, Pp 1-9 (2018)
Clinical Proteomics, Vol 15, Iss 1, Pp 1-9 (2018)
Background Metabolic diseases such as obesity and diabetes are associated with changes in high-density lipoprotein (HDL) particles, including changes in particle size and protein composition, often resulting in abnormal function. Recent studies sugge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5bde704c61b70b6e0d3b96d6e44c4cb
https://doi.org/10.1186/s12014-018-9186-0
https://doi.org/10.1186/s12014-018-9186-0
Autor:
Christy B. Erbe, Christina L. Runge, Joseph E. Kerschner, Gabor T. Marth, David R. Friedland, Wai-Meng Kwok, Regina Cole, Kate Merath, Roland James, Amit Indap, Ericka King, Harald H H Göring, Jack Littrell, Jack W. Kent, Michael Olivier, Yifan Zhou, Franz Rüschendorf, Norbert Hubner
Publikováno v:
JAMA otolaryngology-- headneck surgery. 142(9)
Importance Sensorineural hearing loss (SNHL) is commonly caused by conditions that affect cochlear structures or the auditory nerve, and the genes identified as causing SNHL to date only explain a fraction of the overall genetic risk for this debilit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bc8f1d0f3f2a92d24a992299f5f3d6c
https://pubmed.ncbi.nlm.nih.gov/27311106
https://pubmed.ncbi.nlm.nih.gov/27311106
The goal of this study was to functionally evaluate three previously uncharacterized heat shock factor protein 4 (HSF4) mutations (c.595_599delGGGCC, c.1213CT, c.1327+4AG) encoding mutant HSF4 proteins (G199EfsX15, R405X, and M419GfsX29) with missing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f42548eb9304d6c7454dae1a51030a5
https://europepmc.org/articles/PMC3796937/
https://europepmc.org/articles/PMC3796937/
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 22(11-12)
Lens opacity 13 (lop13) is a spontaneous, autosomal recessive mouse mutant that exhibits nuclear cataracts. Histological analysis revealed swollen lens fiber cells and the presence of bladder cells within the lens cortex, as well as morgagnian globul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b6d81fda7523250b585279a20a02be4
https://pubmed.ncbi.nlm.nih.gov/21858719
https://pubmed.ncbi.nlm.nih.gov/21858719