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Items: 1 to 20 of 170

1.

Structural stability of wild type and mutated alpha-keratin fragments: molecular dynamics and free energy calculations.

Danciulescu C, Nick B, Wortmann FJ.

Biomacromolecules. 2004 Nov-Dec;5(6):2165-75.

PMID:
15530030
2.

Sequence comparisons of intermediate filament chains: evidence of a unique functional/structural role for coiled-coil segment 1A and linker L1.

Smith TA, Strelkov SV, Burkhard P, Aebi U, Parry DA.

J Struct Biol. 2002 Jan-Feb;137(1-2):128-45.

PMID:
12064940
3.

Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix.

Winter H, Rogers MA, Langbein L, Stevens HP, Leigh IM, Labr├Ęze C, Roul S, Taieb A, Krieg T, Schweizer J.

Nat Genet. 1997 Aug;16(4):372-4.

PMID:
9241275
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6.

De novo mutations in monilethrix.

Horev L, Djabali K, Green J, Sinclair R, Martinez-Mir A, Ingber A, Christiano AM, Zlotogorski A.

Exp Dermatol. 2003 Dec;12(6):882-5.

PMID:
14714571
7.

Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament.

Tanaka S, Miura I, Yoshiki A, Kato Y, Yokoyama H, Shinogi A, Masuya H, Wakana S, Tamura M, Shiroishi T.

Genomics. 2007 Dec;90(6):703-11. Epub 2007 Oct 24.

9.

Dominant and recessive compound heterozygous mutations in epidermolysis bullosa simplex demonstrate the role of the stutter region in keratin intermediate filament assembly.

Yasukawa K, Sawamura D, McMillan JR, Nakamura H, Shimizu H.

J Biol Chem. 2002 Jun 28;277(26):23670-4. Epub 2002 Apr 24.

11.

A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix.

Winter H, Rogers MA, Gebhardt M, Wollina U, Boxall L, Chitayat D, Babul-Hirji R, Stevens HP, Zlotogorski A, Schweizer J.

Hum Genet. 1997 Dec;101(2):165-9.

PMID:
9402962
12.

Coiled-coil trigger motifs in the 1B and 2B rod domain segments are required for the stability of keratin intermediate filaments.

Wu KC, Bryan JT, Morasso MI, Jang SI, Lee JH, Yang JM, Marekov LN, Parry DA, Steinert PM.

Mol Biol Cell. 2000 Oct;11(10):3539-58.

13.

Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype.

Korge BP, Hamm H, Jury CS, Traupe H, Irvine AD, Healy E, Birch-MacHin M, Rees JL, Messenger AG, Holmes SC, Parry DA, Munro CS.

J Invest Dermatol. 1999 Oct;113(4):607-12.

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Conformational changes in the rod domain of human keratin 8 following heterotypic association with keratin 18 and its implication for filament stability.

Waseem A, Karsten U, Leigh IM, Purkis P, Waseem NH, Lane EB.

Biochemistry. 2004 Feb 10;43(5):1283-95.

PMID:
14756564
19.

Hagfish biopolymer: a type I/type II homologue of epidermal keratin intermediate filaments.

Koch EA, Spitzer RH, Pithawalla RB, Castillos FA 3rd, Parry DA.

Int J Biol Macromol. 1995 Oct;17(5):283-92.

PMID:
8580093
20.

Vimentin coil 1A-A molecular switch involved in the initiation of filament elongation.

Meier M, Padilla GP, Herrmann H, Wedig T, Hergt M, Patel TR, Stetefeld J, Aebi U, Burkhard P.

J Mol Biol. 2009 Jul 10;390(2):245-61. doi: 10.1016/j.jmb.2009.04.067. Epub 2009 May 5.

PMID:
19422834

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