J W Halliday
Overview
Explore the profile of J W Halliday including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
159
Citations
1508
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
11.
Ramm G, Powell L, Halliday J
J Gastroenterol Hepatol
. 1996 Nov;
11(11):1072-8.
PMID: 8985833
We have previously demonstrated that colchicine inhibits ferritin clearance from the circulation of normal and iron-loaded rats and stimulates endogenous ferritin release into both the serum and bile of iron-loaded...
12.
Halliday J, Searle J
Biometals
. 1996 Apr;
9(2):205-9.
PMID: 8744902
Iron deposition occurs in parenchymal cells of the liver in two major defects in human subjects (i) in primary iron overload (genetic haemochromatosis) and (ii) secondary to anaemias in which...
13.
Powell L, Burt M, Halliday J, Jazwinska E
Semin Liver Dis
. 1996 Feb;
16(1):55-63.
PMID: 8723324
No abstract available.
14.
Crawford D, Powell L, Halliday J
Annu Rev Nutr
. 1996 Jan;
16:139-60.
PMID: 8839923
Genetic hemochromatosis is one of the most common inherited disorders in Caucasian populations. The disease frequency in Caucasian populations in Australia, Europe, and the United States is 1:300-400. The basic...
15.
Crawford D, Powell L, Leggett B, Francis J, Fletcher L, Webb S, et al.
Am J Hum Genet
. 1995 Aug;
57(2):362-7.
PMID: 7668262
Hemochromatosis (HC) is a common inherited disorder of iron metabolism for which neither the gene nor biochemical defect have yet been identified. The aim of this study was to look...
16.
Caldwell S, Halliday J, Fletcher L, Kulaga M, MURPHY T, Li X, et al.
J Gastroenterol Hepatol
. 1995 Mar;
10(2):174-8.
PMID: 7787164
To assess the relationship between carbohydrate-deficient transferrin (CDT) and alcoholic liver disease, we measured the ratio of carbohydrate-deficient transferrin to total transferrin (rCDT) in 32 male alcoholics with liver disease...
17.
Jazwinska E, Pyper W, Burt M, Francis J, Goldwurm S, Webb S, et al.
Am J Hum Genet
. 1995 Feb;
56(2):428-33.
PMID: 7847378
Hemochromatosis (HC), an inherited disorder of iron metabolism, shows a very strong founder effect in Australia, with the majority of patients being of Celtic (Scots/Irish) origin. Australian HC patients thus...
18.
Moss D, Hibbs A, Stenzel D, Powell L, Halliday J
Br J Haematol
. 1994 Dec;
88(4):746-53.
PMID: 7819099
We have established the intracellular destination of the putative immunoregulatory protein, human recombinant H (heavy)-ferritin, in the transformed T-cell line MOLT-4, by laser scanning confocal microscopy of live cells. A...
19.
Stone C, Pointon J, Jazwinska E, Halliday J, Powell L, Robson K, et al.
Hum Mol Genet
. 1994 Nov;
3(11):2043-6.
PMID: 7874124
The gene for hereditary haemochromatosis (HC) is linked to HLA-A and D6S105 on chromosome 6p. Both markers have also been reported to display linkage disequilibrium with the disease. However, their...
20.
Kluck R, McDougall C, Harmon B, Halliday J
Biochim Biophys Acta
. 1994 Sep;
1223(2):247-54.
PMID: 8086495
A moderate sustained rise in intracellular ionised calcium has been observed to be associated with apoptosis occurring in many experimental systems. The application of extracellular and intracellular chelators of calcium...