Leikin S - Search Results

1

Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding.

Barnes AM, Carter EM, Cabral WA, Weis M, Chang W, Makareeva E, Leikin S, Rotimi CN, Eyre DR, Raggio CL, Marini JC. Barnes AM, et al. Among authors: leikin s. N Engl J Med. 2010 Feb 11;362(6):521-8. doi: 10.1056/NEJMoa0907705. Epub 2010 Jan 20. N Engl J Med. 2010. PMID: 20089953 Free PMC article.

2

Osteogenesis imperfecta murine: interaction between type I collagen homotrimers.

Kuznetsova N, McBride DJ Jr, Leikin S. Kuznetsova N, et al. Among authors: leikin s. J Mol Biol. 2001 Jun 8;309(3):807-15. doi: 10.1006/jmbi.2001.4682. J Mol Biol. 2001. PMID: 11397098

3

Type I collagen triplet duplication mutation in lethal osteogenesis imperfecta shifts register of alpha chains throughout the helix and disrupts incorporation of mutant helices into fibrils and extracellular matrix.

Cabral WA, Mertts MV, Makareeva E, Colige A, Tekin M, Pandya A, Leikin S, Marini JC. Cabral WA, et al. Among authors: leikin s. J Biol Chem. 2003 Mar 21;278(12):10006-12. doi: 10.1074/jbc.M212523200. Epub 2003 Jan 20. J Biol Chem. 2003. PMID: 12538651 Free article.

4

Changes in thermal stability and microunfolding pattern of collagen helix resulting from the loss of alpha2(I) chain in osteogenesis imperfecta murine.

Kuznetsova NV, McBride DJ, Leikin S. Kuznetsova NV, et al. Among authors: leikin s. J Mol Biol. 2003 Aug 1;331(1):191-200. doi: 10.1016/s0022-2836(03)00715-0. J Mol Biol. 2003. PMID: 12875845

5

Structure, stability and interactions of type I collagen with GLY349-CYS substitution in alpha 1(I) chain in a murine Osteogenesis Imperfecta model.

Kuznetsova NV, Forlino A, Cabral WA, Marini JC, Leikin S. Kuznetsova NV, et al. Among authors: leikin s. Matrix Biol. 2004 May;23(2):101-12. doi: 10.1016/j.matbio.2004.03.002. Matrix Biol. 2004. PMID: 15246109

6

Mutations near amino end of alpha1(I) collagen cause combined osteogenesis imperfecta/Ehlers-Danlos syndrome by interference with N-propeptide processing.

Cabral WA, Makareeva E, Colige A, Letocha AD, Ty JM, Yeowell HN, Pals G, Leikin S, Marini JC. Cabral WA, et al. Among authors: leikin s. J Biol Chem. 2005 May 13;280(19):19259-69. doi: 10.1074/jbc.M414698200. Epub 2005 Feb 22. J Biol Chem. 2005. PMID: 15728585 Free article.

7

Molecular mechanism of alpha 1(I)-osteogenesis imperfecta/Ehlers-Danlos syndrome: unfolding of an N-anchor domain at the N-terminal end of the type I collagen triple helix.

Makareeva E, Cabral WA, Marini JC, Leikin S. Makareeva E, et al. Among authors: leikin s. J Biol Chem. 2006 Mar 10;281(10):6463-70. doi: 10.1074/jbc.M511830200. Epub 2006 Jan 5. J Biol Chem. 2006. PMID: 16407265 Free article.

8

Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta.

Barnes AM, Chang W, Morello R, Cabral WA, Weis M, Eyre DR, Leikin S, Makareeva E, Kuznetsova N, Uveges TE, Ashok A, Flor AW, Mulvihill JJ, Wilson PL, Sundaram UT, Lee B, Marini JC. Barnes AM, et al. Among authors: leikin s. N Engl J Med. 2006 Dec 28;355(26):2757-64. doi: 10.1056/NEJMoa063804. N Engl J Med. 2006. PMID: 17192541 Free PMC article.

9

Y-position cysteine substitution in type I collagen (alpha1(I) R888C/p.R1066C) is associated with osteogenesis imperfecta/Ehlers-Danlos syndrome phenotype.

Cabral WA, Makareeva E, Letocha AD, Scribanu N, Fertala A, Steplewski A, Keene DR, Persikov AV, Leikin S, Marini JC. Cabral WA, et al. Among authors: leikin s. Hum Mutat. 2007 Apr;28(4):396-405. doi: 10.1002/humu.20456. Hum Mutat. 2007. PMID: 17206620

10

Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta.

Cabral WA, Chang W, Barnes AM, Weis M, Scott MA, Leikin S, Makareeva E, Kuznetsova NV, Rosenbaum KN, Tifft CJ, Bulas DI, Kozma C, Smith PA, Eyre DR, Marini JC. Cabral WA, et al. Among authors: leikin s. Nat Genet. 2007 Mar;39(3):359-65. doi: 10.1038/ng1968. Epub 2007 Feb 4. Nat Genet. 2007. PMID: 17277775 Free PMC article.

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