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Items: 1 to 20 of 51

1.
NanoLuc reporters identify COL4A5 nonsense mutations susceptible to drug-induced stop codon readthrough
Kohei Omachi, Hirofumi Kai, Michel Roberge, Jeffrey H. Miner
iScience. 2022 Mar 18; 25(3): 103891. Published online 2022 Feb 8. doi: 10.1016/j.isci.2022.103891
PMCID:
PMC8866893
AbstractArticlePDF–5.1M
2.
Intravital imaging reveals glomerular capillary distension and endothelial and immune cell activation early in Alport syndrome
Georgina Gyarmati, Urvi Nikhil Shroff, Audrey Izuhara, Xiaogang Hou, Stefano Da Sacco, Sargis Sedrakyan, Kevin V. Lemley, Kerstin Amann, Laura Perin, János Peti-Peterdi
JCI Insight. 2022 Jan 11; 7(1): e152676. Published online 2022 Jan 11. doi: 10.1172/jci.insight.152676
PMCID:
PMC8765042
AbstractArticlePDF–14M
3.
Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5
Tomohiko Yamamura, Tomoko Horinouchi, Tomomi Adachi, Maki Terakawa, Yutaka Takaoka, Kohei Omachi, Minoru Takasato, Kiyosumi Takaishi, Takao Shoji, Yoshiyuki Onishi, Yoshito Kanazawa, Makoto Koizumi, Yasuko Tomono, Aki Sugano, Akemi Shono, Shogo Minamikawa, China Nagano, Nana Sakakibara, Shinya Ishiko, Yuya Aoto, Misato Kamura, Yutaka Harita, Kenichiro Miura, Shoichiro Kanda, Naoya Morisada, Rini Rossanti, Ming Juan Ye, Yoshimi Nozu, Masafumi Matsuo, Hirofumi Kai, Kazumoto Iijima, Kandai Nozu
Nat Commun. 2020; 11: 2777. Published online 2020 Jun 2. doi: 10.1038/s41467-020-16605-x
PMCID:
PMC7265383
AbstractArticlePDF–3.2M
4.
A step towards clinical application of acellular matrix: a clue from macrophage polarization
Astgik Petrosyan, Stefano Da Sacco, Nikita Tripuraneni, Ursula Kreuser, Maria Lavarreda-Pearce, Riccardo Tamburrini, Roger E. De Filippo, Giuseppe Orlando, Paolo Cravedi, Laura Perin
Matrix Biol. Author manuscript; available in PMC 2019 Sep 1.
Published in final edited form as: Matrix Biol. 2017 Jan; 57-58: 334–346. Published online 2016 Aug 26. doi: 10.1016/j.matbio.2016.08.009
PMCID:
PMC6717660
AbstractArticlePDF–2.5M
5.
Establishment of X-linked Alport syndrome model mice with a Col4a5 R471X mutation
Kentarou Hashikami, Makoto Asahina, Kandai Nozu, Kazumoto Iijima, Michio Nagata, Michiyasu Takeyama
Biochem Biophys Rep. 2019 Mar; 17: 81–86. Published online 2018 Dec 12. doi: 10.1016/j.bbrep.2018.12.003
PMCID:
PMC6295608
AbstractArticlePDF–1.5M
6.
A potential target gene for the host-directed therapy of mycobacterial infection in murine macrophages
Zhang Bao, Ran Chen, Pei Zhang, Shan Lu, Xing Chen, Yake Yao, Xiaozheng Jin, Yilan Sun, Jianying Zhou
Int J Mol Med. 2016 Sep; 38(3): 823–833. Published online 2016 Jul 11. doi: 10.3892/ijmm.2016.2675
PMCID:
PMC4990325
AbstractArticlePDF–933K
7.
Bidirectional, non-necrotizing glomerular crescents are the critical pathology in X-linked Alport syndrome mouse model harboring nonsense mutation of human COL4A5
Jiang Ying Song, Nobuyuki Saga, Kunio Kawanishi, Kentaro Hashikami, Michiyasu Takeyama, Michio Nagata
Sci Rep. 2020; 10: 18891. Published online 2020 Nov 3. doi: 10.1038/s41598-020-76068-4
PMCID:
PMC7642296
AbstractArticlePDF–6.7M
8.
Glomerular endothelial cell heterogeneity in Alport syndrome
Hasmik Soloyan, Matthew Thornton, Valentina Villani, Patrick Khatchadourian, Paolo Cravedi, Andrea Angeletti, Brendan Grubbs, Roger De Filippo, Laura Perin, Sargis Sedrakyan
Sci Rep. 2020; 10: 11414. Published online 2020 Jul 10. doi: 10.1038/s41598-020-67588-0
PMCID:
PMC7351764
AbstractArticlePDF–9.0M
9.
Modification of an aggressive model of Alport Syndrome reveals early differences in disease pathogenesis due to genetic background
Sara Falcone, Laura Wisby, Thomas Nicol, Andrew Blease, Becky Starbuck, Andrew Parker, Jeremy Sanderson, Steve D. M. Brown, Cheryl L. Scudamore, Charles D. Pusey, Frederick W. K. Tam, Paul K. Potter
Sci Rep. 2019; 9: 20398. Published online 2019 Dec 31. doi: 10.1038/s41598-019-56837-6
PMCID:
PMC6938516
AbstractArticlePDF–4.4M
10.
Amniotic fluid stem cell-derived vesicles protect from VEGF-induced endothelial damage
S. Sedrakyan, V. Villani, S. Da Sacco, N. Tripuraneni, S. Porta, A. Achena, M. Lavarreda-Pearce, A. Petrosyan, H. Soloyan, R. E. De Filippo, B. Bussolati, L. Perin
Sci Rep. 2017; 7: 16875. Published online 2017 Dec 4. doi: 10.1038/s41598-017-17061-2
PMCID:
PMC5715019
AbstractArticlePDF–5.5M
11.
Mild Electrical Stimulation and Heat Shock Ameliorates Progressive Proteinuria and Renal Inflammation in Mouse Model of Alport Syndrome
Tomoaki Koga, Yukari Kai, Ryosuke Fukuda, Saori Morino-Koga, Mary Ann Suico, Kosuke Koyama, Takashi Sato, Tsuyoshi Shuto, Hirofumi Kai
PLoS One. 2012; 7(8): e43852. Published online 2012 Aug 24. doi: 10.1371/journal.pone.0043852
PMCID:
PMC3427222
AbstractArticlePDF–834K
12.
Alport alloantibodies but not Goodpasture autoantibodies induce murine glomerulonephritis: Protection by quinary crosslinks locking cryptic α3(IV) collagen autoepitopes in vivo
Wentian Luo, Xu-Ping Wang, Clifford E. Kashtan, Dorin-Bogdan Borza
J Immunol. Author manuscript; available in PMC 2011 Sep 15.
Published in final edited form as: J Immunol. 2010 Sep 15; 185(6): 3520–3528. Published online 2010 Aug 13. doi: 10.4049/jimmunol.1001152
PMCID:
PMC2951005
AbstractArticlePDF–1.7M
13.
Bifunctional promoter of type IV collagen COL4A5 and COL4A6 genes regulates the expression of α5 and α6 chains in a distinct cell-specific fashion
Malin Sund, Yohei Maeshima, Raghu Kalluri
Biochem J. 2005 May 1; 387(Pt 3): 755–761. Prepublished online 2004 Dec 15. Published online 2005 Apr 26. doi: 10.1042/BJ20041870
PMCID:
PMC1135006
AbstractArticlePDF–191K
14.
Identification of an Altered Matrix Signature in Kidney Aging and Disease
Michael J. Randles, Franziska Lausecker, Qingyang Kong, Hani Suleiman, Graeme Reid, Maria Kolatsi-Joannou, Bernard Davenport, Pinyuan Tian, Sara Falcone, Paul Potter, Tom Van Agtmael, Jill T. Norman, David A. Long, Martin J. Humphries, Jeffrey H. Miner, Rachel Lennon
J Am Soc Nephrol. 2021 Jul; 32(7): 1713–1732. Published online 2021 Jul. doi: 10.1681/ASN.2020101442
PMCID:
PMC8425653
AbstractArticle
15.
A mouse collagen4a4 mutation causing Alport glomerulosclerosis with abnormal collagen a3a4a5(IV) trimers
Ron Korstanje, Christina Caputo, Rosalinda Doty, Susan Cook, Roderick Bronson, Muriel Davisson, Jeffrey H. Miner
Kidney Int. Author manuscript; available in PMC 2014 Dec 1.
Published in final edited form as: Kidney Int. 2014 Jun; 85(6): 1461–1468. Published online 2014 Feb 12. doi: 10.1038/ki.2013.493
PMCID:
PMC4040157
AbstractArticlePDF–1.8M
16.
Pathogenicity of a Human Laminin β2 Mutation Revealed in Models of Alport Syndrome
Steven D. Funk, Raymond H. Bayer, Andrew F. Malone, Karen K. McKee, Peter D. Yurchenco, Jeffrey H. Miner
J Am Soc Nephrol. 2018 Mar; 29(3): 949–960. Published online 2017 Dec 20. doi: 10.1681/ASN.2017090997
PMCID:
PMC5827610
AbstractArticle
17.
COL4A6 is dispensable for autosomal recessive Alport syndrome
Tomohiro Murata, Kan Katayama, Toshitaka Oohashi, Timo Jahnukainen, Tomoko Yonezawa, Yoshikazu Sado, Eiji Ishikawa, Shinsuke Nomura, Karl Tryggvason, Masaaki Ito
Sci Rep. 2016; 6: 29450. Published online 2016 Jul 5. doi: 10.1038/srep29450
PMCID:
PMC4932521
AbstractArticlePDF–2.3M
18.
Minor Type IV Collagen α5 Chain Promotes Cancer Progression through Discoidin Domain Receptor-1
Qian Xiao, Yan Jiang, Qingbo Liu, Jiao Yue, Chunying Liu, Xiaotong Zhao, Yuemei Qiao, Hongbin Ji, Jianfeng Chen, Gaoxiang Ge
PLoS Genet. 2015 May; 11(5): e1005249. Published online 2015 May 19. doi: 10.1371/journal.pgen.1005249
PMCID:
PMC4438069
AbstractArticlePDF–8.1M
19.
Collagen IV alpha 3, alpha 4, and alpha 5 chains in rodent basal laminae: sequence, distribution, association with laminins, and developmental switches
J Cell Biol. 1994 Nov 1; 127(3): 879–891. doi: 10.1083/jcb.127.3.879
PMCID:
PMC2120241
SummaryPDF–4.2M
20.
A Human-Mouse Chimera of the α3α4α5(IV) Collagen Protomer Rescues the Renal Phenotype in Col4a3−/− Alport Mice
Laurence Heidet, Dorin-Bogdan Borza, Mélanie Jouin, Mireille Sich, Marie-Geneviève Mattei, Yoshikazu Sado, Billy G. Hudson, Nicholas Hastie, Corinne Antignac, Marie-Claire Gubler
Am J Pathol. 2003 Oct; 163(4): 1633–1644. doi: 10.1016/s0002-9440(10)63520-1
PMCID:
PMC1868284
AbstractArticlePDF–669K

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