Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 131

1.

Characterization of plasminogen variants in healthy subjects and plasminogen mutants in patients with inherited plasminogen deficiency by isoelectric focusing gel electrophoresis.

Tefs K, Georgieva M, Seregard S, Tait CR, Luchtman-Jones L, Ziegler M, Hügle B, Schuster V.

Thromb Haemost. 2004 Aug;92(2):352-7.

PMID:
15269832
2.

Isoelectric focusing pattern of plasminogen mutants of patients with hypoplasminogenemia: correlation of in-vitro data with computer-predicted isoelectric points (pI).

Tefs K, Ott-Gueorguieva M, Kobelt L, Ziegler M, Hintze C, Hügle B, Schuster V.

Blood Coagul Fibrinolysis. 2011 Sep;22(6):499-505. doi: 10.1097/MBC.0b013e3283472c53.

PMID:
21537161
3.

Plasminogen deficiency.

Schuster V, Hügle B, Tefs K.

J Thromb Haemost. 2007 Dec;5(12):2315-22. Epub 2007 Sep 26. Review.

4.
5.

Plasminogen Tochigi mice exhibit phenotypes similar to wild-type mice under experimental thrombotic conditions.

Tashima Y, Banno F, Kita T, Matsuda Y, Yanamoto H, Miyata T.

PLoS One. 2017 Jul 7;12(7):e0180981. doi: 10.1371/journal.pone.0180981. eCollection 2017.

6.

Molecular and clinical spectrum of type I plasminogen deficiency: A series of 50 patients.

Tefs K, Gueorguieva M, Klammt J, Allen CM, Aktas D, Anlar FY, Aydogdu SD, Brown D, Ciftci E, Contarini P, Dempfle CE, Dostalek M, Eisert S, Gökbuget A, Günhan O, Hidayat AA, Hügle B, Isikoglu M, Irkec M, Joss SK, Klebe S, Kneppo C, Kurtulus I, Mehta RP, Ornek K, Schneppenheim R, Seregard S, Sweeney E, Turtschi S, Veres G, Zeitler P, Ziegler M, Schuster V.

Blood. 2006 Nov 1;108(9):3021-6. Epub 2006 Jul 18.

7.

Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitis.

Schuster V, Zeitler P, Seregard S, Ozcelik U, Anadol D, Luchtman-Jones L, Meire F, Mingers AM, Schambeck C, Kreth HW.

Thromb Haemost. 2001 Jun;85(6):1004-10.

PMID:
11434676
8.

Plasminogen hemizygosity. Detection of a silent allele in 7 members of a family by determination of plasminogen phenotypes, antigenic levels, and functional activity.

Skoda U, Goldmann SF, Händler C, Hummel K, Lechler E, Lübcke I, Mauff G, Meyer-Börnecke D, Pesch S, Pulverer G.

Vox Sang. 1988;54(4):210-4.

PMID:
3388818
9.

Homozygous type I plasminogen deficiency.

Mingers AM, Heimburger N, Zeitler P, Kreth HW, Schuster V.

Semin Thromb Hemost. 1997;23(3):259-69.

PMID:
9255907
10.

Difficulties in mutation screening of the plasminogen (PLG) gene in patients with ligneous conjunctivitis and severe hypoplasminogenemia.

Tefs K, Kobelt L, Ziegler M, Hügle B, Schuster V.

Arch Ophthalmol. 2007 Sep;125(9):1303; author reply 1303. No abstract available.

PMID:
17846386
11.

Identification of three novel plasminogen (PLG) gene mutations in a series of 23 patients with low PLG activity.

Klammt J, Kobelt L, Aktas D, Durak I, Gokbuget A, Hughes Q, Irkec M, Kurtulus I, Lapi E, Mechoulam H, Mendoza-Londono R, Palumbo JS, Steitzer H, Tabbara KF, Ozbek Z, Pucci N, Sotomayor T, Sturm M, Drogies T, Ziegler M, Schuster V.

Thromb Haemost. 2011 Mar;105(3):454-60. doi: 10.1160/TH10-04-0216. Epub 2010 Dec 21.

PMID:
21174000
12.

Polymorphism of plasminogen in healthy individuals and patients with cerebral infarction.

Nishimukai H, Shinmyozu K, Tamaki Y.

Hum Hered. 1986;36(3):137-42.

PMID:
3721516
13.

Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency.

Dönmez-Demir B, Celkan T, Sarper N, Deda G, İnce E, Çalişkan Ü, Öztürk G, Karagün B, Küpesiz A, Tokgöz H, Akar N, Özdağ H.

Blood Coagul Fibrinolysis. 2016 Sep;27(6):637-44. doi: 10.1097/MBC.0000000000000383.

PMID:
26340456
14.

Homozygous mutations in the plasminogen gene of two unrelated girls with ligneous conjunctivitis.

Schuster V, Mingers AM, Seidenspinner S, Nüssgens Z, Pukrop T, Kreth HW.

Blood. 1997 Aug 1;90(3):958-66.

15.

Parentage testing using the serum protein plasminogen (PLG).

Dykes DD, Mount M, Polesky HF.

Am J Clin Pathol. 1984 Dec;82(6):722-5.

PMID:
6507385
16.

The distribution of plasminogen (PLG) polymorphism in the Namibian !Kung San and Kavango populations.

Nabulsi AJ, Christiansen K, Rodewald A.

Anthropol Anz. 1996 Jun;54(2):117-20.

PMID:
8767722
17.

Plasminogen (PLG) polymorphism in northern Japanese: confirmation of PLG*M6 allele.

Sebetan IM, Aoki Y, Funayama M.

Z Rechtsmed. 1989;103(1):43-5.

PMID:
2588818
18.

Three new variants in the plasminogen system.

Nishimukai H, Kera Y, Sakata K, Yamasawa K.

Hum Hered. 1982;32(2):130-2.

PMID:
7095815
19.

Polymorphism of the plasminogen (PLG) system in Cádiz Province, southern Spain.

Gamero JJ, Romero JL, Vizcaya MA, Arufe MI.

J Forensic Sci. 1991 Jan;36(1):226-9.

PMID:
2007871
20.

Genetic polymorphism of human plasminogen (PLG) in a Chinese population.

Yiping H, Qing G, Meiyun W.

Eur J Immunogenet. 1993 Apr;20(2):91-4.

PMID:
8494872

Supplemental Content

Support Center