Similar articles for PMID: 1986355

Year	Number of Results
1983	1
1984	1
1987	2
1988	1
1989	3
1990	7
1991	3
1992	7
1993	3
1994	2
1995	7
1996	3
1997	2
1998	3
2006	2
2007	1
2018	1
2024	0

1

Two types of abnormal genes for plasminogen in families with a predisposition for thrombosis.

Ichinose A, Espling ES, Takamatsu J, Saito H, Shinmyozu K, Maruyama I, Petersen TE, Davie EW. Ichinose A, et al. Proc Natl Acad Sci U S A. 1991 Jan 1;88(1):115-9. doi: 10.1073/pnas.88.1.115. Proc Natl Acad Sci U S A. 1991. PMID: 1986355 Free PMC article.

2

Congenital plasminogen deficiency caused by a Ser572 to Pro mutation.

Azuma H, Uno Y, Shigekiyo T, Saito S. Azuma H, et al. Blood. 1993 Jul 15;82(2):475-80. Blood. 1993. PMID: 8392398 Free article.

3

Plasminogen with type-I mutation is polymorphic in the Japanese population.

Kikuchi S, Yamanouchi Y, Li L, Kobayashi K, Ijima H, Miyazaki R, Tsuchiya S, Hamaguchi H. Kikuchi S, et al. Hum Genet. 1992 Sep-Oct;90(1-2):7-11. doi: 10.1007/BF00210737. Hum Genet. 1992. PMID: 1427790

4

A novel missense mutation in two families with congenital plasminogen deficiency: identification of an Ala675 to Thr675 substitution.

Mima N, Azuma H, Shigekiyo T, Saito S. Mima N, et al. Thromb Haemost. 1996 Jan;75(1):96-100. Thromb Haemost. 1996. PMID: 8713786

5

Multiple members of the plasminogen-apolipoprotein(a) gene family associated with thrombosis.

Ichinose A. Ichinose A. Biochemistry. 1992 Mar 31;31(12):3113-8. doi: 10.1021/bi00127a011. Biochemistry. 1992. PMID: 1554698

6

A recombination event in the closely linked plasminogen and apolipoprotein(a) gene loci.

Magnaghi P, Agazzi A, Semino O, Ferrari M, Barbui T, D'Angelo A, Taramelli R. Magnaghi P, et al. Clin Genet. 1995 Jun;47(6):285-9. doi: 10.1111/j.1399-0004.1995.tb03966.x. Clin Genet. 1995. PMID: 7554360

7

Characterization of a splicing mutation in group A xeroderma pigmentosum.

Satokata I, Tanaka K, Miura N, Miyamoto I, Satoh Y, Kondo S, Okada Y. Satokata I, et al. Proc Natl Acad Sci U S A. 1990 Dec;87(24):9908-12. doi: 10.1073/pnas.87.24.9908. Proc Natl Acad Sci U S A. 1990. PMID: 1702221 Free PMC article.

8

Hereditary protein C deficiency associated with mutations in exon IX of the protein C gene.

Doig RG, Begley CG, McGrath KM. Doig RG, et al. Thromb Haemost. 1994 Aug;72(2):203-8. Thromb Haemost. 1994. PMID: 7831652

9

Characterization by yeast artificial chromosome cloning of the linked apolipoprotein(a) and plasminogen genes and identification of the apolipoprotein(a) 5' flanking region.

Malgaretti N, Acquati F, Magnaghi P, Bruno L, Pontoglio M, Rocchi M, Saccone S, Della Valle G, D'Urso M, LePaslier D, et al. Malgaretti N, et al. Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11584-8. doi: 10.1073/pnas.89.23.11584. Proc Natl Acad Sci U S A. 1992. PMID: 1454851 Free PMC article.

10

Presence of two plasminogen alleles in normal populations.

Kida M, H-Kawabata M, Yamazaki T, Ichinose A. Kida M, et al. Thromb Haemost. 1998 Jan;79(1):150-4. Thromb Haemost. 1998. PMID: 9459341 Clinical Trial.

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