Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Robert J. Barndt"'
Autor:
Robert J. Barndt, Qing Liu, Ying Tang, Michael P. Haugh, Jeffery Cui, Stephen Y. Chan, Haodi Wu
Publikováno v:
Biomolecules, Vol 13, Iss 1, p 69 (2022)
Danon disease (DD) is caused by mutations of the gene encoding lysosomal-associated membrane protein type 2 (LAMP2), which lead to impaired autophagy, glycogen accumulation, and cardiac hypertrophy. However, it is not well understood why a large port
Externí odkaz:
https://doaj.org/article/a7d9957abf8345c1a353f6cb845a9281
Autor:
Robert J. Barndt, Ning Ma, Ying Tang, Michael P. Haugh, Laila S. Alamri, Stephen Y. Chan, Haodi Wu
Publikováno v:
Stem Cell Research, Vol 56, Iss , Pp 102544- (2021)
As the most common cause of heart failure, dilated cardiomyopathy (DCM) is characterized by dilated ventricles and weakened contractile force. Mutations in the calcium handling protein phospholamban (PLN) are known to cause inherited DCM. Here, we in
Externí odkaz:
https://doaj.org/article/6b6df6792fc84b2092294be7951a28e6
Autor:
Frank Shiao, Li-Ching O Liu, Nanxi Huang, Ying-Jung J Lai, Robert J Barndt, Chun-Che Tseng, Jehng-Kang Wang, Bailing Jia, Michael D Johnson, Chen-Yong Lin
Publikováno v:
PLoS ONE, Vol 12, Iss 1, p e0170944 (2017)
Mutations of hepatocyte growth factor activator inhibitor (HAI)-2 in humans cause sodium loss in the gastrointestinal (GI) tract in patients with syndromic congenital sodium diarrhea (SCSD). Aberrant regulation of HAI-2 target protease(s) was propose
Externí odkaz:
https://doaj.org/article/bda3179e2def4e39af01ef62acb3ce4b
Autor:
Jehng-Kang Wang, Chen-Yong Lin, Robert J. Barndt, Shih-Ming Huang, Sheng-Wen A Li, Michael D. Johnson, Yayun Gu, Dajun D. Lu, Hui Chen Su
Publikováno v:
Human Cell. 34:771-784
Epidermal differentiation and barrier function require well-controlled matriptase and prostasin proteolysis, in which the Kunitz-type serine protease inhibitor HAI-1 represents the primary enzymatic inhibitor for both proteases. HAI-1, however, also
Autor:
Haodi Wu, Robert J. Barndt, Ning Ma, Stephen Y. Chan, Michael P. Haugh, Ying Tang, Laila S. Alamri
Publikováno v:
Stem Cell Research, Vol 56, Iss, Pp 102544-(2021)
As the most common cause of heart failure, dilated cardiomyopathy (DCM) is characterized by dilated ventricles and weakened contractile force. Mutations in the calcium handling protein phospholamban (PLN) are known to cause inherited DCM. Here, we in
Autor:
Dajun D, Lu, Yayun, Gu, Sheng-Wen A, Li, Robert J, Barndt, Shih-Ming, Huang, Jehng-Kang, Wang, Hui Chen, Su, Michael D, Johnson, Chen-Yong, Lin
Publikováno v:
Human cell. 34(3)
Epidermal differentiation and barrier function require well-controlled matriptase and prostasin proteolysis, in which the Kunitz-type serine protease inhibitor HAI-1 represents the primary enzymatic inhibitor for both proteases. HAI-1, however, also
Autor:
Jehng-Kang Wang, Frank Shiao, Chen-Yong Lin, Robert J. Barndt, Li-Ching O. Liu, Nanxi Huang, Michael D. Johnson, Bailing Jia, Ying-Jung J. Lai, Chun-Che Tseng
Publikováno v:
PLoS ONE, Vol 12, Iss 1, p e0170944 (2017)
PLoS ONE
PLoS ONE
Mutations of hepatocyte growth factor activator inhibitor (HAI)-2 in humans cause sodium loss in the gastrointestinal (GI) tract in patients with syndromic congenital sodium diarrhea (SCSD). Aberrant regulation of HAI-2 target protease(s) was propose
Autor:
Victoria K. Shanmugam, Robert J. Barndt, Chen-Yong Lin, Jehng-Kang Wang, Bai-Yao Wu, Han Chiu, Malvika Kaul, Adrienne N. H. Baksh, Fen-Pai Chou, Zhonghong Xu, Galen Shi, Michael D. Johnson, Hui-Chung Hsiao, Ya-Wen Chen
Publikováno v:
The Journal of investigative dermatology
Genetic defects in matriptase are linked to two congenital ichthyoses: autosomal recessive ichthyosis with hypotrichosis (ARIH, OMIM 610765) and ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis (IFAH, OMIM 602400). Mouse models wi
Autor:
Michael D. Johnson, Ya-Wen Chen, Zijun Y. Xu-Monette, Robert J. Barndt, Jehng-Kang Wang, Chen-Yong Lin, Annie H. Zuo, Feng-Pai Chou, Ronald B. Gartenhaus, Hiroaki Kataoka, Ken H. Young, Xianfeng F. Zhao
Publikováno v:
The American Journal of Pathology. 183(4):1306-1317
Membrane-associated serine protease matriptase is widely expressed by epithelial/carcinoma cells in which its proteolytic activity is tightly controlled by the Kunitz-type protease inhibitor, hepatocyte growth factor activator inhibitor (HAI-1). We d
Autor:
Annie H. Zuo, Amrita K. Cheema, Robert J. Barndt, Surojeet Sengupta, Youhong Wang, Michael D. Johnson, Christine M. Coticchia, Tushar B. Deb
Publikováno v:
American Journal of Physiology-Cell Physiology. 300:C1139-C1154
We have recently described a novel role for pregnancy-upregulated nonubiquitous calmodulin kinase (Pnck) in the induction of ligand-independent epidermal growth factor receptor (EGFR) degradation (Deb TB, Coticchia CM, Barndt R, Zuo H, Dickson RB, an