Rights-Protecting iCourts: The Curious Case of the OP-ICESCR

Autor: Benjamin Perryman

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4f0e2f2aa7ffdca0a4afb743720ea301
https://doi.org/10.1017/9781108590396.007

Deletion ofJAM-C, a candidate gene for heart defects in Jacobsen syndrome, results in a normal cardiac phenotype in mice

Autor: Maoqing Ye, Nissi Varki, Amy E. Geddis, M. Benjamin Perryman, Paul Grossfeld, Rabih Hamzeh

Publikováno v: American Journal of Medical Genetics Part A. :1438-1443

The 11q terminal deletion disorder (11q-) is a rare chromosomal disorder caused by a deletion in distal 11q. Fifty-six percent of patients have clinically significant congenital heart defects. A cardiac "critical region" has been identified in distal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2be5e2453717c2bd2cd4ddce55644dab
https://doi.org/10.1002/ajmg.a.32913

Simultaneous Quantification of Human Cardiac α- and β-Myosin Heavy Chain Proteins by MALDI-TOF Mass Spectrometry

Autor: Chia-Yu Yen, Steve M. Helmke, Karin Nunley, Krzysztof J. Cios, Mark W. Duncan, M. Benjamin Perryman, Michael R. Bristow

Publikováno v: Analytical Chemistry. 76:1683-1689

We have developed a novel method for quantifying protein isoforms, in both relative and absolute terms, based on MALDI-TOF mass spectrometry. The utility of the approach is demonstrated by quantifying the alpha and beta protein isoforms of myosin hea

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::305d43cb4b112f5dfd0044ecf74c54fc
https://doi.org/10.1021/ac035144l

Hypoplastic left heart syndrome myocytes are differentiated but possess a unique phenotype

Autor: Shuping Ge, Wayne Minobe, Steve M. Helmke, Michael R. Bristow, M. Benjamin Perryman, Alastair D. Robertson, Gary Brodsky, Teresa J. Bohlmeyer, Jennifer Lynch, James H Sederberg

Publikováno v: Cardiovascular Pathology. 12:23-31

Introduction: Hypoplastic left heart syndrome (HLHS) is the term used to describe a group of congenital malformations characterized by marked underdevelopment of the left side of the heart. HLHS accounts for nearly 25% of cardiac deaths in the first

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d91467b9f5fb45840b79e3167f2448a
https://doi.org/10.1016/s1054-8807(02)00127-8

Use of gene targeting for compromising energy homeostasis in neuro-muscular tissues: The role of sarcomeric mitochondrial creatine kinase

Autor: J.M.A. van Deursen, M.L.P. Brückwilder, Arend Heerschap, J.C.M. Koudijs, Benjamin Perryman, Dirk Pette, Karen Steeghs, B. Wieringa, Frank Oerlemans, Paul H.K. Jap, A.F.J. de Haan, Wim Ruitenbeek

Publikováno v: Journal of Neuroscience Methods, 71, 29-41. Elsevier
Journal of Neuroscience Methods, 71, 1, pp. 29-41
Journal of Neuroscience Methods, 71, 29-41
Steeghs, K, Heerschap, A, de Haan, A, Ruitenbeek, W, Oerlemans, F, Deursen, J, Perryman, B, Pette, D, Br|ckwilder, M, Koudijs, J, Jap, P & Wieringa, B 1997, ' Use of gene targeting for compromising energy homeostasis in neuromuscular tissues:The role of sarcomeric mitochondrial creatine kinase ', Journal of Neuroscience Methods, vol. 71, pp. 29-41 . https://doi.org/10.1016/S0165-0270(96)00124-0
Journal of Neuroscience Methods, 71, pp. 29-41

We have introduced a single knock-out mutation in the mitochondrial creatine kinase gene (ScCKmit) in the mouse germ line via targeted mutagenesis in mouse embryonic stem (ES) cells. Surprisingly, ScCKmit -/- muscles, unlike muscles of mice with a de

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d426a4028c2686ff0ba6b416f176c7ed
https://doi.org/10.1016/s0165-0270(96)00124-0