Nguyen thi Man
Overview
Explore the profile of Nguyen thi Man including associated specialties, affiliations and a list of published articles.
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Articles
19
Citations
193
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Recent Articles
1.
Lynch T, Lam L, Man N, Kobayashi K, Toda T, Morris G
Biochem Biophys Res Commun
. 2012 Jul;
424(2):354-7.
PMID: 22771323
Mutations in the gene encoding fukutin protein cause Fukuyama muscular dystrophy, a severe congenital disorder that occurs mainly in Japan. A major consequence of the mutation is reduced glycosylation of...
2.
Morris G, Man N, Sewry C
Methods Mol Biol
. 2011 Jan;
709:39-61.
PMID: 21194020
Several molecular approaches to Duchenne muscular dystrophy (DMD) therapy are at or near the point of clinical trial and usually involve attempts to replace the missing dystrophin protein. Although improved...
3.
Fuller H, Man N, Lam L, Shamanin V, Androphy E, Morris G
J Proteome Res
. 2010 Jun;
9(8):4228-33.
PMID: 20568814
Valproate is commonly used as an anticonvulsant and mood stabilizer, but its long-term side-effects can include bone loss. As a histone deacetylase (HDAC) inhibitor, valproate has also been considered for...
4.
Fuller H, Man N, Lam L, Thanh L, Keough R, Asperger A, et al.
J Proteome Res
. 2009 Nov;
9(1):556-63.
PMID: 19928837
Understanding networks of interacting proteins is a major goal in cell biology. The survival of motor neurons protein (SMN) interacts, directly or indirectly, with a large number of other proteins...
5.
Man N, Humphrey E, Lam L, Fuller H, Lynch T, Sewry C, et al.
Neurology
. 2008 Jul;
71(22):1757-63.
PMID: 18633133
Objectives: Spinal muscular atrophy (SMA) is an autosomal recessive disorder characterized by loss of lower motor neurons during early or postnatal development. Severity is variable and is inversely related to...
6.
Wolstencroft E, Simic G, Man N, Holt I, Lam L, Buckland P, et al.
J Mol Histol
. 2007 Jun;
38(4):333-40.
PMID: 17593530
Five subtypes of dopamine receptor exist in two subfamilies: two D(1)-like (D(1) and D(5)) and three D(2)-like (D(2), D(3) and D(4)). We produced novel monoclonal antibodies against all three D(2)-like...
7.
Pham Y, Man N, Holt I, Sewry C, Pall G, Johnson K, et al.
J Cell Biochem
. 2005 Jun;
95(5):990-1001.
PMID: 15962300
SIX5 is a member of the human SIX family of transcription factors, many of which are involved in eye development. However, SIX5 transcripts are known to be present at very...
8.
Lunn M, Root D, Martino A, Flaherty S, Kelley B, Coovert D, et al.
Chem Biol
. 2004 Nov;
11(11):1489-93.
PMID: 15555999
Most patients with the pediatric neurodegenerative disease spinal muscular atrophy have a homozygous deletion of the survival motor neuron 1 (SMN1) gene, but retain one or more copies of the...
9.
Holt I, Ostlund C, Stewart C, Man N, Worman H, Morris G
J Cell Sci
. 2003 Jun;
116(Pt 14):3027-35.
PMID: 12783988
Mutations in lamin A/C can cause Emery-Dreifuss muscular dystrophy (EDMD) or a related cardiomyopathy (CMD1A). Using transfection of lamin-A/C-deficient fibroblasts, we have studied the effects of nine pathogenic mutations on...
10.
Morris G, Sedgwick S, Ellis J, Pereboev A, Chamberlain J, Man N
Biochemistry
. 1998 Aug;
37(31):11117-27.
PMID: 9693008
The muscular dystrophy protein, dystrophin, and the closely related protein, utrophin, are large cytoskeletal proteins which link actin microfilaments to the plasma membrane. A panel of 38 monoclonal antibodies (mAbs)...