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Items: 1 to 20 of 51

1.
Genetic determinants of micronucleus formation in vivo
D. J. Adams, B. Barlas, R. E. McIntyre, I. Salguero, L. van der Weyden, A. Barros, J. R. Vicente, N. Karimpour, A. Haider, M. Ranzani, G. Turner, N. A. Thompson, V. Harle, R. Olvera-León, C. D. Robles-Espinoza, A. O. Speak, N. Geisler, W. J. Weninger, S. H. Geyer, J. Hewinson, N. A. Karp, The Sanger Mouse Genetics Project, B. Fu, F. Yang, Z. Kozik, J. Choudhary, L. Yu, M. S. van Ruiten, B. D. Rowland, C. J. Lelliott, M. del Castillo Velasco-Herrera, R. Verstraten, L. Bruckner, A. G. Henssen, M. A. Rooimans, J. de Lange, T. J. Mohun, M. J. Arends, K. A. Kentistou, P. A. Coelho, Y. Zhao, H. Zecchini, J. R. B. Perry, S. P. Jackson, G. Balmus
Nature. 2024; 627(8002): 130–136. Published online 2024 Feb 14. doi: 10.1038/s41586-023-07009-0
PMCID:
PMC10917660
AbstractArticlePDF–4.8M
2.
Loss of the collagen IV modifier prolyl 3-hydroxylase 2 causes thin basement membrane nephropathy
Hande Aypek, Christoph Krisp, Shun Lu, Shuya Liu, Dominik Kylies, Oliver Kretz, Guochao Wu, Manuela Moritz, Kerstin Amann, Kerstin Benz, Ping Tong, Zheng-mao Hu, Sulaiman M. Alsulaiman, Arif O. Khan, Maik Grohmann, Timo Wagner, Janina Müller-Deile, Hartmut Schlüter, Victor G. Puelles, Carsten Bergmann, Tobias B. Huber, Florian Grahammer
J Clin Invest. 2022 May 2; 132(9): e147253. Published online 2022 May 2. doi: 10.1172/JCI147253
PMCID:
PMC9057608
AbstractArticlePDF–17M
3.
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
4.
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
5.
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
6.
FGF8 and BMP2 mediated dynamic regulation of dental mesenchyme proliferation and differentiation via Lhx8/Suv39h1 complex
Chen Zhou, Danying Chen, Jianhan Ren, Delan Huang, Runze Li, Haotian Luo, Chenyu Guan, Yang Cao, Weicai Wang
J Cell Mol Med. 2021 Mar; 25(6): 3051–3062. Published online 2021 Feb 13. doi: 10.1111/jcmm.16351
PMCID:
PMC7957265
AbstractArticlePDF–2.4M
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.
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
10.
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
11.
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
12.
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
13.
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
14.
Type IV collagen α6 chain is a regulator of keratin 10 in keratinization of oral mucosal epithelium
Taishi Komori, Mitsuaki Ono, Emilio Satoshi Hara, Junji Ueda, Ha Thi Thu Nguyen, Ha Thi Nguyen, Tomoko Yonezawa, Takahiro Maeba, Aya Kimura-Ono, Takeshi Takarada, Ryusuke Momota, Kenji Maekawa, Takuo Kuboki, Toshitaka Oohashi
Sci Rep. 2018; 8: 2612. Published online 2018 Feb 8. doi: 10.1038/s41598-018-21000-0
PMCID:
PMC5805778
AbstractArticlePDF–2.3M
15.
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
16.
Quantitative proteomic profiling of the extracellular matrix of pancreatic islets during the angiogenic switch and insulinoma progression
Alexandra Naba, Karl R. Clauser, D. R. Mani, Steven A. Carr, Richard O. Hynes
Sci Rep. 2017; 7: 40495. Published online 2017 Jan 10. doi: 10.1038/srep40495
PMCID:
PMC5223159
AbstractArticlePDF–2.3M
17.
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
18.
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
19.
Thyroid follicle development requires Smad1/5- and endothelial cell-dependent basement membrane assembly
Mylah Villacorte, Anne-Sophie Delmarcelle, Manon Lernoux, Mahé Bouquet, Pascale Lemoine, Jennifer Bolsée, Lieve Umans, Susana Chuva de Sousa Lopes, Patrick Van Der Smissen, Takako Sasaki, Guido Bommer, Patrick Henriet, Samuel Refetoff, Frédéric P. Lemaigre, An Zwijsen, Pierre J. Courtoy, Christophe E. Pierreux
Development. 2016 Jun 1; 143(11): 1958–1970. doi: 10.1242/dev.134171
PMCID:
PMC4920163
AbstractArticle
20.
Developmental distribution of collagen IV isoforms and relevance to ocular diseases
Xiaoyang Bai, David J. Dilworth, Yi-Chinn Weng, Douglas B. Gould
Matrix Biol. Author manuscript; available in PMC 2016 Feb 10.
Published in final edited form as: Matrix Biol. 2009 May; 28(4): 194–201. Published online 2009 Mar 9. doi: 10.1016/j.matbio.2009.02.004
PMCID:
PMC4749355
AbstractArticlePDF–899K

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