Zobrazeno 1 - 10
of 133
pro vyhledávání: '"Charles D. Boyd"'
Autor:
Matthew B. Heller, Kornelia M. Szauter, Matthias K. Jansen, Michael Loomis, Katalin Csiszar, James H. Kimura, Tercia Ku, Richard A. Girton, Charles D. Boyd, Gordon Okimoto, Maarit Tiirikainen
Publikováno v:
Biochemistry Insights, Vol 2011, Iss 4, Pp 13-27 (2011)
Biochemistry Insights, Vol 4 (2011)
Biochemistry Insights, Vol 4 (2011)
In spite of current standard therapies to target the major pathomechanisms in myocardial infarction (MI), inflammatory gene expression patterns have been consistently revealed in MI patients. In a multiethnic cohort, we aimed to identify MI-associate
Autor:
R. M. Laxer, A. Hinek, Kornelia M. Szauter, Elena Pope, Katalin Csiszar, Anita Ordas, Charles D. Boyd, D. Wherrett, Mátyás Mink, Benjamin A. Alman
Publikováno v:
British Journal of Dermatology. 163:1102-1115
Clinical evaluation of a young woman with subcutaneous fibrotic nodules, progressive distal joint contractures and marfanoid stature revealed a previously unrecognized fibrotic disorder characterized by several unique phenotypic features and some fea
Publikováno v:
Histochemistry and Cell Biology. 123:517-528
To determine the tissue distribution of the ABC transporter ABCC6 in normal human tissues, we analyzed tissue arrays for the presence of ABCC6 mRNA by in situ hybridization and ABCC6 protein by immunohistochemistry using the polyclonal antibody HB-6.
Autor:
Katalin Csiszar, Masando Hayashi, Charles D. Boyd, Keith S. K. Fong, Frederic Mercier, Kimiko Hayashi
Publikováno v:
Journal of Molecular Histology. 35:845-855
Lysyl oxidase (LOX) and lysyl oxidase-like (LOXL) are extracellular enzymes that deaminate peptidyl lysyl residues involved in the cross-linking of fibrillar collagens and elastin. While LOX is required for the survival of newborn mice, the role of L
Autor:
C. Sung, Steven Robinow, Charles D. Boyd, András Váradi, J. N. Tarnay, Attila Iliás, Flóra Szeri, Tarmo Annilo, Michael Dean, O. Le Saux
Publikováno v:
Insect Molecular Biology. 13:539-548
ATP-binding cassette (ABC) transporters are involved in the transport of substrates across biological membranes and are essential for many cellular processes. Of the fifty-six Drosophila ABC transporter genes only white, brown, scarlet, E23 and Atet
Autor:
Olivier Le Saux, Konstanze Beck, Brian Nishiguchi, Charles D. Boyd, Masando Hayashi, Kimiko Hayashi
Publikováno v:
Journal of Histochemistry & Cytochemistry. 51:887-902
We have studied the tissue distribution of Abcc6, a member of the ABC transmembrane transporter subfamily C, in normal C57BL/6 mice. RNase protection assays revealed that although almost all tissues studied contained detectable levels of the mRNA enc
Autor:
Christine Sachsinger, Anna Susan Marais, Eric W. Johnson, Lionel Bercovitch, Sharon F. Terry, Carina Treiber, Harald H H Göring, Konstanze Beck, Charles D. Boyd, Katie Curry, Denis Viljoen, Olivier Le Saux
Publikováno v:
Human Genetics. 111:331-338
Pseudoxanthoma elasticum (PXE) is a heritable elastic tissue disorder recently shown to be attributable to mutations in the ABCC6 ( MRP6) gene. Whereas PXE has been identified in all ethnic groups studied to date, the prevalence of this disease in va
Autor:
Katalin Csiszar, Chia Granda, Zsolt Urban, Johann Urschitz, Susanne Teklits Iobst, Claudia Lupp, Charles D. Boyd, Kathleen A Souza, Kurt Matthew Schilling, Ian Richard Scott
Publikováno v:
Journal of Investigative Dermatology. 119:3-13
To study the phenotypic changes in human skin associated with repeated sun exposure at the transcription level, we have undertaken a comparative serial analysis of gene expression of sun-damaged preauricular skin and sun-protected postauricular skin
Autor:
Olivier Le Saux, Thomas L. Seidl, Zsolt Urban, Balázs Sarkadi, András Váradi, Attila Iliás, Emese Sinkó, Charles D. Boyd
Publikováno v:
Journal of Biological Chemistry. 277:16860-16867
Mutations in the ABCC6 (MRP6) gene cause pseudoxanthoma elasticum (PXE), a rare heritable disorder resulting in the calcification of elastic fibers. In the present study a cDNA encoding a full-length normal variant of ABCC6 was amplified from a human
Autor:
Margaret R. Wallace, Gregg K. Maeda, Zsolt Urban, Elaine C. Davis, Heather J. Stalker, Jun Zhang, Charles D. Boyd, Anil Kumar, John W. Belmont
Publikováno v:
Human Genetics. 109:512-520
We have identified two elastin gene (ELN) mutations located in cis in two related families with supravalvular aortic stenosis (SVAS). These mutations included an in-frame duplication in exon 18 (1034-1057dup) and a single base substitution in exon 26