M B Perryman
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Explore the profile of M B Perryman including associated specialties, affiliations and a list of published articles.
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58
Citations
776
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Recent Articles
1.
Perryman M, Friedman D, Fu Y, Caskey C
Trends Cardiovasc Med
. 2011 Jan;
3(3):82-4.
PMID: 21244944
Myotonic muscular dystrophy (DM) has been shown to be caused by the expansion of an unstable triplet nucleotide repeat sequence located in the 3' untranslated region of a gene coding...
2.
Hamburg R, Friedman D, Perryman M
Trends Cardiovasc Med
. 2011 Jan;
1(5):195-200.
PMID: 21239310
Creatine kinase isoenzyme content is frequently used to assess the state of differentiation of muscle and neural tissue and following release into plasma as diagnostic markers for acute myocardial infarction,...
3.
Ye M, Coldren C, Liang X, Mattina T, Goldmuntz E, Benson D, et al.
Hum Mol Genet
. 2009 Nov;
19(4):648-56.
PMID: 19942620
Congenital heart defects comprise the most common form of major birth defects, affecting 0.7% of all newborn infants. Jacobsen syndrome (11q-) is a rare chromosomal disorder caused by deletions in...
4.
Bush E, Helmke S, Birnbaum R, Perryman M
Biochemistry
. 2000 Jul;
39(29):8480-90.
PMID: 10913253
Human myotonic dystrophy protein kinase (DMPK) is a member of a novel class of multidomain protein kinases that regulate cell size and shape in a variety of organisms. However, little...
5.
MOUNSEY J, John 3rd J, Helmke S, Bush E, Gilbert J, Roses A, et al.
J Biol Chem
. 2000 May;
275(30):23362-7.
PMID: 10811636
The genetic abnormality in myotonic muscular dystrophy, multiple CTG repeats lie upstream of a gene that encodes a novel protein kinase, myotonic dystrophy protein kinase (DMPK). Phospholemman (PLM), a major...
6.
Pahl P, Hodges Y, Meltesen L, Perryman M, Horwitz K, Horwitz L
Genomics
. 1998 Nov;
53(3):410-2.
PMID: 9799612
No abstract available.
7.
Zisman L, Asano K, Dutcher D, Ferdensi A, Robertson A, Jenkin M, et al.
Circulation
. 1998 Oct;
98(17):1735-41.
PMID: 9788827
Background: The regulation and interaction of ACE and the angiotensin II (Ang II) type I (AT1) receptor in the failing human heart are not understood. Methods And Results: Radioligand binding...
8.
Asano K, Dutcher D, Port J, Minobe W, Tremmel K, Roden R, et al.
Circulation
. 1997 Mar;
95(5):1193-200.
PMID: 9054849
Background: The regulation of angiotensin II receptors and the two major subtypes (AT1 and AT2) in chronically failing human ventricular myocardium has not been previously examined. Methods And Results: Angiotensin...
9.
Bush E, Taft C, Meixell G, Perryman M
J Biol Chem
. 1996 Jan;
271(1):548-52.
PMID: 8550617
Myotonic muscular dystrophy is an autosomal dominant defect that produces muscle wasting, myotonia, and cardiac conduction abnormalities. The myotonic dystrophy locus codes for a putative serine-threonine protein kinase of unknown...
10.
Raynolds M, Perryman M
Eur Heart J
. 1995 Nov;
16 Suppl K:23-30.
PMID: 8869132
The cardiac vasculature and myocardium contain components of the renin-angiotensin system (RAS), which may regulate local growth and cellular function. Alterations in the expression or action of these components, which...