N Mian
Overview
Explore the profile of N Mian including associated specialties, affiliations and a list of published articles.
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Articles
36
Citations
367
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Recent Articles
1.
Metcalfe K, Poll A, Llacuachaqui M, Nanda S, Tulman A, Mian N, et al.
Clin Genet
. 2010 Jul;
78(5):411-7.
PMID: 20653694
It is not known to what extent participation in a genetic testing program for BRCA1 and BRCA2, which does not include an extensive pre-test counselling session, influences cancer-related distress, cancer...
2.
Mills P, Mills K, Mian N, Winchester B, Clayton P
J Inherit Metab Dis
. 2003 Aug;
26(2-3):119-34.
PMID: 12889655
The majority of secreted or membrane-bound proteins are glycosylated. The glycans attached to glycoproteins can affect a range of physicochemical and biological properties of the glycoprotein and appropriate glycosylation is...
3.
Cerutti L, Mian N, Bateman A
Trends Biochem Sci
. 2000 Oct;
25(10):481-2.
PMID: 11050429
No abstract available.
4.
Imtiaz F, Worthington V, Champion M, Beesley C, Charlwood J, Clayton P, et al.
J Inherit Metab Dis
. 2000 May;
23(2):162-74.
PMID: 10801058
18 UK patients (14 families) have been diagnosed with the carbohydrate-deficient glycoprotein syndrome (CDGS), type 1, on the basis of their clinical symptoms and/or abnormal electrophoretic patterns of serum transferrin....
5.
Zucker S, Mian N, Drews M, Conner C, Davidson A, Miller F, et al.
J Rheumatol
. 1999 Jan;
26(1):78-80.
PMID: 9918244
Objective: In view of evidence that stromelysin-1 and collagenase-1 are involved in tissue injury in inflammatory joint diseases, we sought to determine whether matrix metalloproteinases (MMP) are implicated in the...
6.
Charlwood J, Clayton P, Keir G, Mian N, Young E, Winchester B
Prenat Diagn
. 1998 Aug;
18(7):693-9.
PMID: 9706650
Two pregnancies at risk for the carbohydrate-deficient glycoprotein syndrome Type 1A (CDG1A, phosphomannomutase deficient) were monitored by enzyme and genetic linkage analyses. The index case in both families had a...
7.
Charlwood J, Clayton P, Keir G, Mian N, Winchester B
Glycobiology
. 1998 Jun;
8(4):351-7.
PMID: 9499382
The glycosylation of serum transferrin from galactosemic patients with a deficiency of galactose-1-phosphate uridyl transferase (EC 2. 7.7 12) is abnormal but becomes normal after treatment with a galactose-free diet....
8.
Charlwood J, Clayton P, Johnson A, Keir G, Mian N, Winchester B
J Inherit Metab Dis
. 1998 Jan;
20(6):817-26.
PMID: 9427152
The carbohydrate-deficient glycoprotein syndrome (CDGS) is a group of disorders characterized biochemically by abnormal glycosylation of serum and cellular glycoproteins. It has been classified into four forms on the basis...
9.
Iourin O, Mattu T, Mian N, Keir G, Winchester B, Dwek R, et al.
Glycoconj J
. 1996 Dec;
13(6):1031-42.
PMID: 8981095
One of the biochemical characteristics of carbohydrate deficient glycoprotein syndromes is the presence of abnormal glycoforms in serum transferrin. Both glycoform heterogeneity and variable site occupancy may, in principle, lead...
10.