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1
In vivo functions of the proprotein convertase PC5/6 during mouse development: Gdf11 is a likely substrate.
Proc Natl Acad Sci U S A. 2008 Apr 15;105(15):5750-5. doi: 10.1073/pnas.0709428105. Epub 2008 Mar 31.
2
PCSK5 and GDF11 expression in the hindgut region of mouse embryos with anorectal malformations.
Eur J Pediatr Surg. 2011 Aug;21(4):238-41. doi: 10.1055/s-0031-1273691. Epub 2011 Apr 8.
3
Osteopontin as a novel substrate for the proprotein convertase 5/6 (PCSK5) in bone.
Bone. 2018 Feb;107:45-55. doi: 10.1016/j.bone.2017.11.002. Epub 2017 Nov 7.
4
Deletion of the gene encoding proprotein convertase 5/6 causes early embryonic lethality in the mouse.
Mol Cell Biol. 2006 Jan;26(1):354-61. doi: 10.1128/MCB.26.1.354-361.2006.
7
Thrombin activation of protein C requires prior processing by a liver proprotein convertase.
J Biol Chem. 2017 Jun 23;292(25):10564-10573. doi: 10.1074/jbc.M116.770040. Epub 2017 May 3.
8
Latent transforming growth factor beta-binding proteins-2 and -3 inhibit the proprotein convertase 5/6A.
J Biol Chem. 2011 Aug 19;286(33):29063-29073. doi: 10.1074/jbc.M111.242479. Epub 2011 Jun 23.
9
Proprotein convertase 5/6a is associated with bone morphogenetic protein-2-induced squamous cell differentiation.
Am J Respir Cell Mol Biol. 2015 Jun;52(6):749-61. doi: 10.1165/rcmb.2014-0029OC.

引用本文的文献

1
PCSK5 is a recessive hypomorph exclusive to MCF10DCIS.com cells.
bioRxiv. 2025 Mar 7:2025.03.03.641323. doi: 10.1101/2025.03.03.641323.
4
Proprotein Convertases and the Complement System.
Front Immunol. 2022 Jul 6;13:958121. doi: 10.3389/fimmu.2022.958121. eCollection 2022.
5
Analysis of the Contribution of Proprotein Convertases to the Processing of FGF23.
Front Endocrinol (Lausanne). 2021 Jun 4;12:690681. doi: 10.3389/fendo.2021.690681. eCollection 2021.
6
The Role of Proprotein Convertases in the Regulation of the Function of Immune Cells in the Oncoimmune Response.
Front Immunol. 2021 Apr 29;12:667850. doi: 10.3389/fimmu.2021.667850. eCollection 2021.
7
Growth differentiation factor 11: a "rejuvenation factor" involved in regulation of age-related diseases?
Aging (Albany NY). 2021 Apr 22;13(8):12258-12272. doi: 10.18632/aging.202881.
8
Mouse Models of Human Proprotein Convertase Insufficiency.
Endocr Rev. 2021 May 25;42(3):259-294. doi: 10.1210/endrev/bnaa033.
9
Circulating plasma factors involved in rejuvenation.
Aging (Albany NY). 2020 Nov 16;12(22):23394-23408. doi: 10.18632/aging.103933.
10
Similar sequences but dissimilar biological functions of GDF11 and myostatin.
Exp Mol Med. 2020 Oct;52(10):1673-1693. doi: 10.1038/s12276-020-00516-4. Epub 2020 Oct 19.

本文引用的文献

1
Hepatic proprotein convertases modulate HDL metabolism.
Cell Metab. 2007 Aug;6(2):129-36. doi: 10.1016/j.cmet.2007.07.009.
2
The proprotein convertases are potential targets in the treatment of dyslipidemia.
J Mol Med (Berl). 2007 Jul;85(7):685-96. doi: 10.1007/s00109-007-0172-7. Epub 2007 Mar 10.
3
PDGF signaling specificity is mediated through multiple immediate early genes.
Nat Genet. 2007 Jan;39(1):52-60. doi: 10.1038/ng1922. Epub 2006 Dec 3.
4
Essential pro-Bmp roles of crossveinless 2 in mouse organogenesis.
Development. 2006 Nov;133(22):4463-73. doi: 10.1242/dev.02647. Epub 2006 Oct 11.
5
Proprotein convertases: lessons from knockouts.
FASEB J. 2006 Oct;20(12):1954-63. doi: 10.1096/fj.05-5491rev.
6
Analysis of pancreatic endocrine development in GDF11-deficient mice.
Dev Dyn. 2006 Nov;235(11):3016-25. doi: 10.1002/dvdy.20953.
8
The function of growth/differentiation factor 11 (Gdf11) in rostrocaudal patterning of the developing spinal cord.
Development. 2006 Aug;133(15):2865-74. doi: 10.1242/dev.02478. Epub 2006 Jun 21.
9
Deletion of the gene encoding proprotein convertase 5/6 causes early embryonic lethality in the mouse.
Mol Cell Biol. 2006 Jan;26(1):354-61. doi: 10.1128/MCB.26.1.354-361.2006.

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