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Year Number of Results
1978 1
1980 1
1982 1
1985 1
1989 1
1990 2
1991 2
1992 1
1993 1
1994 1
1995 2
1996 4
1997 1
1998 3
2000 1
2001 2
2002 1
2003 1
2004 1
2005 2
2006 1
2007 4
2008 4
2009 4
2010 8
2011 3
2012 5
2013 4
2014 7
2015 6
2016 7
2017 4
2018 8
2019 8
2020 10
2021 6
2022 10
2023 7
2024 4

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128 results

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Page 1
Decreased expression of serine protease inhibitor family G1 (SERPING1) in prostate cancer can help distinguish high-risk prostate cancer and predicts malignant progression.
Peng S, Du T, Wu W, Chen X, Lai Y, Zhu D, Wang Q, Ma X, Lin C, Li Z, Guo Z, Huang H. Peng S, et al. Urol Oncol. 2018 Aug;36(8):366.e1-366.e9. doi: 10.1016/j.urolonc.2018.05.021. Epub 2018 Jun 19. Urol Oncol. 2018. PMID: 29903461
PURPOSE: The aim of this study was to investigate the associations of serine proteinase inhibitor family G1 (SERPING1) down-regulation with poor prognosis in patients with prostate cancer (PCa). ...Moreover, we used The Cancer Genome Atlas (TCGA) Datab …
PURPOSE: The aim of this study was to investigate the associations of serine proteinase inhibitor family G1 (SERPING1) down-re …
36th International Symposium on Intensive Care and Emergency Medicine : Brussels, Belgium. 15-18 March 2016.
Bateman RM, Sharpe MD, Jagger JE, Ellis CG, Solé-Violán J, López-Rodríguez M, Herrera-Ramos E, Ruíz-Hernández J, Borderías L, Horcajada J, González-Quevedo N, Rajas O, Briones M, Rodríguez de Castro F, Rodríguez Gallego C, Esen F, Orhun G, Ergin Ozcan P, Senturk E, Ugur Yilmaz C, Orhan N, Arican N, Kaya M, Kucukerden M, Giris M, Akcan U, Bilgic Gazioglu S, Tuzun E, Riff R, Naamani O, Douvdevani A, Takegawa R, Yoshida H, Hirose T, Yamamoto N, Hagiya H, Ojima M, Akeda Y, Tasaki O, Tomono K, Shimazu T, Ono S, Kubo T, Suda S, Ueno T, Ikeda T, Hirose T, Ogura H, Takahashi H, Ojima M, Kang J, Nakamura Y, Kojima T, Shimazu T, Ikeda T, Suda S, Izutani Y, Ueno T, Ono S, Taniguchi T, O M, Dinter C, Lotz J, Eilers B, Wissmann C, Lott R, Meili MM, Schuetz PS, Hawa H, Sharshir M, Aburageila M, Salahuddin N, Chantziara V, Georgiou S, Tsimogianni A, Alexandropoulos P, Vassi A, Lagiou F, Valta M, Micha G, Chinou E, Michaloudis G, Kodaira A, Ikeda T, Ono S, Ueno T, Suda S, Izutani Y, Imaizumi H, De la Torre-Prados MV, Garcia-De la Torre A, Enguix-Armada A, Puerto-Morlan A, Perez-Valero V, Garcia-Alcantara A, Bolton N, Dudziak J, Bonney S, Tridente A, Nee P, Nicolaes G, Wiewel M, Schultz M, Wildhag… See abstract for full author list ➔ Bateman RM, et al. Crit Care. 2016 Apr 20;20(Suppl 2):94. doi: 10.1186/s13054-016-1208-6. Crit Care. 2016. PMID: 27885969 Free PMC article.
Ono, T. Kubo, S. Suda, T. Ueno, T. Ikeda P007 - Serial change of c1 inhibitor in patients with sepsis - A prospective observational study T. ...Mebazaa P020 - Impact of disease severity assessment on performance of heparin-binding protein for the prediction o …
Ono, T. Kubo, S. Suda, T. Ueno, T. Ikeda P007 - Serial change of c1 inhibitor in patients with sepsis - A prospective observat …
Restriction of C1-inhibitor activity in hereditary angioedema by dominant-negative effects of disease-associated SERPING1 gene variants.
Ryø LB, Haslund D, Rovsing AB, Pihl R, Sanrattana W, de Maat S, Palarasah Y, Maas C, Thiel S, Mikkelsen JG. Ryø LB, et al. J Allergy Clin Immunol. 2023 Nov;152(5):1218-1236.e9. doi: 10.1016/j.jaci.2023.04.023. Epub 2023 Jun 9. J Allergy Clin Immunol. 2023. PMID: 37301409 Free article.
It is a rare genetic disorder characterized by genetic and clinical heterogenicity. Most cases are caused by genetic variants in the SERPING1 gene leading to plasma deficiency of the encoded protein C1 inhibitor (C1INH). ...OBJECTIVES: The aim was to d …
It is a rare genetic disorder characterized by genetic and clinical heterogenicity. Most cases are caused by genetic variants in the SERP …
Exogenous hormones and hereditary angioedema.
Gompel A, Fain O, Boccon-Gibod I, Gobert D, Bouillet L. Gompel A, et al. Int Immunopharmacol. 2020 Jan;78:106080. doi: 10.1016/j.intimp.2019.106080. Epub 2019 Dec 16. Int Immunopharmacol. 2020. PMID: 31855692 Review.
Then we will review the different hormone treatments and their implication on the course of HAE in women and men: contraception, Assisted Reproductive Technology (ART), menopause, hormone dependent cancers in women and men, treatment of hyperandrogenism in women....
Then we will review the different hormone treatments and their implication on the course of HAE in women and men: contraception, Assisted Re …
Upregulation of C1-inhibitor in pancreatic cancer.
Osther K, Förnvik K, Liljedahl E, Salford LG, Redebrandt HN. Osther K, et al. Oncotarget. 2019 Oct 1;10(55):5703-5712. doi: 10.18632/oncotarget.27191. eCollection 2019 Oct 1. Oncotarget. 2019. PMID: 31620245 Free PMC article.
C1-INH was significantly upregulated in the pancreatic cancer tissue. ...This could suggest that C1-INH plays a role also in pancreatic cancer....
C1-INH was significantly upregulated in the pancreatic cancer tissue. ...This could suggest that C1-INH plays a role al …
Genetic secrets of long-term glioblastoma survivors.
Jovčevska I. Jovčevska I. Bosn J Basic Med Sci. 2019 May 20;19(2):116-124. doi: 10.17305/bjbms.2018.3717. Bosn J Basic Med Sci. 2019. PMID: 30114377 Free PMC article. Review.
Moreover, a decreased expression of the CHI3L1, FBLN4, EMP3, IGFBP2, IGFBP3, LGALS3, MAOB, PDPN, SERPING1 and TIMP1 genes has been associated with prolonged survival. ...
Moreover, a decreased expression of the CHI3L1, FBLN4, EMP3, IGFBP2, IGFBP3, LGALS3, MAOB, PDPN, SERPING1 and TIMP1 genes has been as …
Dominant-negative SERPING1 variants cause intracellular retention of C1 inhibitor in hereditary angioedema.
Haslund D, Ryø LB, Seidelin Majidi S, Rose I, Skipper KA, Fryland T, Bohn AB, Koch C, Thomsen MK, Palarasah Y, Corydon TJ, Bygum A, Nejsum LN, Mikkelsen JG. Haslund D, et al. J Clin Invest. 2019 Jan 2;129(1):388-405. doi: 10.1172/JCI98869. Epub 2018 Dec 10. J Clin Invest. 2019. PMID: 30398465 Free PMC article.
Hereditary angioedema (HAE) is an autosomal dominant disease characterized by recurrent edema attacks associated with morbidity and mortality. HAE results from variations in the SERPING1 gene that encodes the C1 inhibitor (C1INH), a serine protease inhibit …
Hereditary angioedema (HAE) is an autosomal dominant disease characterized by recurrent edema attacks associated with morbidity and mortalit …
Identification of hub genes for early detection of bone metastasis in breast cancer.
Zhao Z, Yang H, Ji G, Su S, Fan Y, Wang M, Gu S. Zhao Z, et al. Front Endocrinol (Lausanne). 2022 Sep 29;13:1018639. doi: 10.3389/fendo.2022.1018639. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36246872 Free PMC article.
BACKGROUND: Globally, among all women, the most frequently detected and diagnosed and the most lethal type of cancer is breast cancer (BC). In particular, bone is one of the most frequent distant metastases 24in breast cancer patients and bone metastasis aris …
BACKGROUND: Globally, among all women, the most frequently detected and diagnosed and the most lethal type of cancer is breast can …
C1 inhibitor deficiency enhances contact pathway-mediated activation of coagulation and venous thrombosis.
Grover SP, Kawano T, Wan J, Tanratana P, Polai Z, Shim YJ, Snir O, Brækkan S, Dhrolia S, Kasthuri RR, Bendapudi PK, McCrae KR, Wolberg AS, Hansen JB, Farkas H, Mackman N. Grover SP, et al. Blood. 2023 May 11;141(19):2390-2401. doi: 10.1182/blood.2022018849. Blood. 2023. PMID: 36701760 Free PMC article.
C1 inhibitor (C1INH) is a multifunctional serine protease inhibitor that functions as a major negative regulator of several biological pathways, including the contact pathway of blood coagulation. ...
C1 inhibitor (C1INH) is a multifunctional serine protease inhibitor that functions as a major negative regulator of sev …
Hereditary angioedema.
Bracho FA. Bracho FA. Curr Opin Hematol. 2005 Nov;12(6):493-8. doi: 10.1097/01.moo.0000179805.57486.4e. Curr Opin Hematol. 2005. PMID: 16217168 Review.
PURPOSE OF REVIEW: Hereditary angioedema is an autosomal-dominant deficiency of C1 inhibitor--a serpin inhibitor of kallikrein, C1r, C1s, factor XII, and plasmin. ...C1 inhibitor concentrates and fresh frozen plasma are available for acute inter …
PURPOSE OF REVIEW: Hereditary angioedema is an autosomal-dominant deficiency of C1 inhibitor--a serpin inhibitor of kal …
128 results