Similar articles for PMID: 8988160

Year	Number of Results
1991	2
1992	1
1993	4
1994	10
1995	3
1996	2
1997	9
1998	5
1999	3
2003	1
2006	1
2010	1
2019	1
2020	1
2024	0

1

P1148A in fibrillin-1 is not a mutation anymore.

Wang M, Mathews KR, Imaizumi K, Beiraghi S, Blumberg B, Scheuner M, Graham JM Jr, Godfrey M. Wang M, et al. Nat Genet. 1997 Jan;15(1):12. doi: 10.1038/ng0197-12. Nat Genet. 1997. PMID: 8988160 No abstract available.

2

P1148A in fibrillin-1 is not a mutation leading to Shprintzen-Goldberg syndrome.

Watanabe Y, Yano S, Koga Y, Yukizane S, Nishiyori A, Yoshino M, Kato H, Ogata T, Adachi M. Watanabe Y, et al. Hum Mutat. 1997;10(4):326-7. doi: 10.1002/(SICI)1098-1004(1997)10:4<326::AID-HUMU10>3.0.CO;2-1. Hum Mutat. 1997. PMID: 9338588 No abstract available.

3

NMR analysis of cbEGF domains gives new insights into the structural consequences of a P1148A substitution in fibrillin-1.

Whiteman P, Downing AK, Handford PA. Whiteman P, et al. Protein Eng. 1998 Nov;11(11):957-9. doi: 10.1093/protein/11.11.957. Protein Eng. 1998. PMID: 9876915

4

Identification of a novel nonsense mutation in the fibrillin gene (FBN1) using nonisotopic techniques.

Hayward C, Porteous ME, Brock DJ. Hayward C, et al. Hum Mutat. 1994;3(2):159-62. doi: 10.1002/humu.1380030212. Hum Mutat. 1994. PMID: 7911051 No abstract available.

5

A novel mutation in the fibrillin gene (FBN1) in familial arachnodactyly.

Hayward C, Porteous ME, Brock DJ. Hayward C, et al. Mol Cell Probes. 1994 Aug;8(4):325-7. doi: 10.1006/mcpr.1994.1045. Mol Cell Probes. 1994. PMID: 7870075

6

Fibrillin-1 mutations in Marfan syndrome and other type-1 fibrillinopathies.

Hayward C, Brock DJ. Hayward C, et al. Hum Mutat. 1997;10(6):415-23. doi: 10.1002/(SICI)1098-1004(1997)10:6<415::AID-HUMU1>3.0.CO;2-C. Hum Mutat. 1997. PMID: 9401003 Review.

7

Fibrillin (FBN1) mutations in Marfan syndrome.

Hayward C, Keston M, Brock DJ, Dietz HC. Hayward C, et al. Hum Mutat. 1992;1(1):79. doi: 10.1002/humu.1380010115. Hum Mutat. 1992. PMID: 1301195 No abstract available.

8

An RsaI polymorphism for the fibrillin gene (FBN1).

Black CM, Withers AP, Boxer M. Black CM, et al. Hum Mol Genet. 1994 Aug;3(8):1442. doi: 10.1093/hmg/3.8.1442-a. Hum Mol Genet. 1994. PMID: 7987336 No abstract available.

9

Silent mutation induces exon skipping of fibrillin-1 gene in Marfan syndrome.

Liu W, Qian C, Francke U. Liu W, et al. Nat Genet. 1997 Aug;16(4):328-9. doi: 10.1038/ng0897-328. Nat Genet. 1997. PMID: 9241263 No abstract available.

10

Mutation screening of all 65 exons of the fibrillin-1 gene in 60 patients with Marfan syndrome: report of 12 novel mutations.

Hayward C, Porteous ME, Brock DJ. Hayward C, et al. Hum Mutat. 1997;10(4):280-9. doi: 10.1002/(SICI)1098-1004(1997)10:4<280::AID-HUMU3>3.0.CO;2-L. Hum Mutat. 1997. PMID: 9338581

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