Pritchard H - Search Results

1

The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes.

Kuivenhoven JA, Pritchard H, Hill J, Frohlich J, Assmann G, Kastelein J. Kuivenhoven JA, et al. Among authors: pritchard h. J Lipid Res. 1997 Feb;38(2):191-205. J Lipid Res. 1997. PMID: 9162740 Free article. Review.

2

Study of the components of reverse cholesterol transport in lecithin:cholesterol acyltransferase deficiency.

Park MS, Kudchodkar BJ, Frohlich J, Pritchard H, Lacko AG. Park MS, et al. Among authors: pritchard h. Arch Biochem Biophys. 1987 Nov 1;258(2):545-54. doi: 10.1016/0003-9861(87)90376-6. Arch Biochem Biophys. 1987. PMID: 3674887

3

Markedly accelerated catabolism of apolipoprotein A-II (ApoA-II) and high density lipoproteins containing ApoA-II in classic lecithin: cholesterol acyltransferase deficiency and fish-eye disease.

Rader DJ, Ikewaki K, Duverger N, Schmidt H, Pritchard H, Frohlich J, Clerc M, Dumon MF, Fairwell T, Zech L, et al. Rader DJ, et al. Among authors: pritchard h. J Clin Invest. 1994 Jan;93(1):321-30. doi: 10.1172/JCI116962. J Clin Invest. 1994. PMID: 8282802 Free PMC article.

4

LCAT synthesized by primary astrocytes esterifies cholesterol on glia-derived lipoproteins.

Hirsch-Reinshagen V, Donkin J, Stukas S, Chan J, Wilkinson A, Fan J, Parks JS, Kuivenhoven JA, Lütjohann D, Pritchard H, Wellington CL. Hirsch-Reinshagen V, et al. Among authors: pritchard h. J Lipid Res. 2009 May;50(5):885-93. doi: 10.1194/jlr.M800584-JLR200. Epub 2008 Dec 8. J Lipid Res. 2009. PMID: 19065001 Free PMC article.

5

Familial defective apolipoprotein B-100 in hypercholesterolemic Chinese Canadians: identification of a unique haplotype of the apolipoprotein B-100 allele.

Abdel-Wareth LO, Pimstone SN, Lagarde JP, Raisonnier A, Benlian P, Pritchard H, Hayden MR, Frohlich JJ. Abdel-Wareth LO, et al. Among authors: pritchard h. Atherosclerosis. 1997 Dec;135(2):181-5. doi: 10.1016/s0021-9150(97)00159-7. Atherosclerosis. 1997. PMID: 9430367

6

Interaction of high density lipoprotein with adipocytes in a new patient with Tangier disease.

Frohlich J, Fong B, Julien P, Despres JP, Angel A, Hayden M, McLeod R, Chow C, Davison RH, Pritchard H. Frohlich J, et al. Among authors: pritchard h. Clin Invest Med. 1987 Sep;10(5):377-82. Clin Invest Med. 1987. PMID: 3677505

7

Acute dyslipoproteinemia induced by interleukin-2: lecithin:cholesteryl acyltransferase, lipoprotein lipase, and hepatic lipase deficiencies.

Kwong LK, Ridinger DN, Bandhauer M, Ward JH, Samlowski WE, Iverius PH, Pritchard H, Wilson DE. Kwong LK, et al. Among authors: pritchard h. J Clin Endocrinol Metab. 1997 May;82(5):1572-81. doi: 10.1210/jcem.82.5.3937. J Clin Endocrinol Metab. 1997. PMID: 9141552

8

A novel TC deletion resulting in Pro(260)-->Stop in the human LCAT gene is associated with a dominant effect on HDL-cholesterol.

Kasid A, Rhyne J, Zeller K, Pritchard H, Miller M. Kasid A, et al. Among authors: pritchard h. Atherosclerosis. 2001 May;156(1):127-32. doi: 10.1016/s0021-9150(00)00640-7. Atherosclerosis. 2001. PMID: 11369005

9

Apolipoprotein A-I(Zavalla) (Leu159-->Pro): HDL cholesterol deficiency in a kindred associated with premature coronary artery disease.

Miller M, Aiello D, Pritchard H, Friel G, Zeller K. Miller M, et al. Among authors: pritchard h. Arterioscler Thromb Vasc Biol. 1998 Aug;18(8):1242-7. doi: 10.1161/01.atv.18.8.1242. Arterioscler Thromb Vasc Biol. 1998. PMID: 9714130

10

The proton NMR of blood plasma and the test for cancer.

Herring FG, Phillips PS, Pritchard H, Silver H, Whittal KP. Herring FG, et al. Among authors: pritchard h. Magn Reson Med. 1990 Oct;16(1):35-48. doi: 10.1002/mrm.1910160105. Magn Reson Med. 1990. PMID: 2175009

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