201 related articles for article (PubMed ID: 7896820)
1. The calcium binding properties and molecular organization of epidermal growth factor-like domains in human fibrillin-1.
Handford P; Downing AK; Rao Z; Hewett DR; Sykes BC; Kielty CM
J Biol Chem; 1995 Mar; 270(12):6751-6. PubMed ID: 7896820
[TBL] [Abstract][Full Text] [Related]
2. Calcium binding properties of an epidermal growth factor-like domain pair from human fibrillin-1.
Knott V; Downing AK; Cardy CM; Handford P
J Mol Biol; 1996 Jan; 255(1):22-7. PubMed ID: 8568869
[TBL] [Abstract][Full Text] [Related]
3. Fibrillin domain folding and calcium binding: significance to Marfan syndrome.
Wu YS; Bevilacqua VL; Berg JM
Chem Biol; 1995 Feb; 2(2):91-7. PubMed ID: 9383409
[TBL] [Abstract][Full Text] [Related]
4. Calcium binding, hydroxylation, and glycosylation of the precursor epidermal growth factor-like domains of fibrillin-1, the Marfan gene protein.
Glanville RW; Qian RQ; McClure DW; Maslen CL
J Biol Chem; 1994 Oct; 269(43):26630-4. PubMed ID: 7929395
[TBL] [Abstract][Full Text] [Related]
5. Solution structure and dynamics of a calcium binding epidermal growth factor-like domain pair from the neonatal region of human fibrillin-1.
Smallridge RS; Whiteman P; Werner JM; Campbell ID; Handford PA; Downing AK
J Biol Chem; 2003 Apr; 278(14):12199-206. PubMed ID: 12511552
[TBL] [Abstract][Full Text] [Related]
6. Metal ion dependency of microfibrils supports a rod-like conformation for fibrillin-1 calcium-binding epidermal growth factor-like domains.
Cardy CM; Handford PA
J Mol Biol; 1998 Mar; 276(5):855-60. PubMed ID: 9566191
[TBL] [Abstract][Full Text] [Related]
7. Fibrillin-1, a calcium binding protein of extracellular matrix.
Handford PA
Biochim Biophys Acta; 2000 Dec; 1498(2-3):84-90. PubMed ID: 11108952
[TBL] [Abstract][Full Text] [Related]
8. EGF-like domain calcium affinity modulated by N-terminal domain linkage in human fibrillin-1.
Smallridge RS; Whiteman P; Doering K; Handford PA; Downing AK
J Mol Biol; 1999 Feb; 286(3):661-8. PubMed ID: 10024441
[TBL] [Abstract][Full Text] [Related]
9. Effects of the N2144S mutation on backbone dynamics of a TB-cbEGF domain pair from human fibrillin-1.
Yuan X; Werner JM; Lack J; Knott V; Handford PA; Campbell ID; Downing AK
J Mol Biol; 2002 Feb; 316(1):113-25. PubMed ID: 11829507
[TBL] [Abstract][Full Text] [Related]
10. A G1127S change in calcium-binding epidermal growth factor-like domain 13 of human fibrillin-1 causes short range conformational effects.
Whiteman P; Smallridge RS; Knott V; Cordle JJ; Downing AK; Handford PA
J Biol Chem; 2001 May; 276(20):17156-62. PubMed ID: 11278305
[TBL] [Abstract][Full Text] [Related]
11. Defective calcium binding to fibrillin-1: consequence of an N2144S change for fibrillin-1 structure and function.
Kettle S; Yuan X; Grundy G; Knott V; Downing AK; Handford PA
J Mol Biol; 1999 Jan; 285(3):1277-87. PubMed ID: 9887276
[TBL] [Abstract][Full Text] [Related]
12. Modification of the structure and function of fibrillin-1 by homocysteine suggests a potential pathogenetic mechanism in homocystinuria.
Hubmacher D; Tiedemann K; Bartels R; Brinckmann J; Vollbrandt T; Bätge B; Notbohm H; Reinhardt DP
J Biol Chem; 2005 Oct; 280(41):34946-55. PubMed ID: 16096271
[TBL] [Abstract][Full Text] [Related]
13. A Gly --> Ser change causes defective folding in vitro of calcium-binding epidermal growth factor-like domains from factor IX and fibrillin-1.
Whiteman P; Downing AK; Smallridge R; Winship PR; Handford PA
J Biol Chem; 1998 Apr; 273(14):7807-13. PubMed ID: 9525872
[TBL] [Abstract][Full Text] [Related]
14. Cellular and molecular studies of Marfan syndrome mutations identify co-operative protein folding in the cbEGF12-13 region of fibrillin-1.
Whiteman P; Willis AC; Warner A; Brown J; Redfield C; Handford PA
Hum Mol Genet; 2007 Apr; 16(8):907-18. PubMed ID: 17324963
[TBL] [Abstract][Full Text] [Related]
15. Four novel FBN1 mutations: significance for mutant transcript level and EGF-like domain calcium binding in the pathogenesis of Marfan syndrome.
Dietz HC; McIntosh I; Sakai LY; Corson GM; Chalberg SC; Pyeritz RE; Francomano CA
Genomics; 1993 Aug; 17(2):468-75. PubMed ID: 8406497
[TBL] [Abstract][Full Text] [Related]
16. Defective secretion of recombinant fragments of fibrillin-1: implications of protein misfolding for the pathogenesis of Marfan syndrome and related disorders.
Whiteman P; Handford PA
Hum Mol Genet; 2003 Apr; 12(7):727-37. PubMed ID: 12651868
[TBL] [Abstract][Full Text] [Related]
17. Molecular effects of calcium binding mutations in Marfan syndrome depend on domain context.
McGettrick AJ; Knott V; Willis A; Handford PA
Hum Mol Genet; 2000 Aug; 9(13):1987-94. PubMed ID: 10942427
[TBL] [Abstract][Full Text] [Related]
18. The role of calcium in the organization of fibrillin microfibrils.
Kielty CM; Shuttleworth CA
FEBS Lett; 1993 Dec; 336(2):323-6. PubMed ID: 8262254
[TBL] [Abstract][Full Text] [Related]
19. ¹H, ¹³C and ¹⁵N resonance assignments for the fibrillin-1 EGF2-EGF3-hybrid1-cbEGF1 four-domain fragment.
Robertson IB; Osuch I; Yadin DA; Handford PA; Jensen SA; Redfield C
Biomol NMR Assign; 2014 Apr; 8(1):189-94. PubMed ID: 23649688
[TBL] [Abstract][Full Text] [Related]
20. 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
Protein Eng; 1998 Nov; 11(11):957-9. PubMed ID: 9876915
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
