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Results of search for 'au:"Nicholson, D C"', page 2 of 2
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Authors
ACKNER, B
Andrews, J
BILLING, B H
COLE, W J
COOPER, J E
Chanarin, I
Clark, K G
Cole, W J
Cowger, M L
GRAY, C H
Gray, C H
Halliday, D
Jackson, A H
KULCZYCKA, A
Lim, C K
NICHOLSON, D C
Nicholson, D C
Samson, D
Thompson, R P
Williams, R
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Topics
Adolescent
Adult
Animals
Bile Pigments
Bilirubin
Erythropoiesis
Feces
Female
Glycine
Heme
Humans
Male
Middle Aged
Photosensitivity Disorders
Porphyrias
Porphyrins
Urobilin
analysis
biosynthesis
metabolism
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Your search returned 34 results.
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21.
The IX-alpha structure of the common bile pigments.
[electronic resource]
by
GRAY, C H
NICHOLSON, D C
NICOLAUS, R A
Producer:
20000701
In:
Nature
vol. 181
Online resources:
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22.
The orientation of the alkyl groups of the end rings of natural and racemic stercobilin.
[electronic resource]
by
Gray, C H
Lemmon, G A
Nicholson, D C
Producer:
19670317
In:
Journal of the Chemical Society. Perkin transactions 1
vol. 2
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23.
The chemistry of the bile pigments. VI. The effect of metal complex formation upon optical activity and spectral absorption of urobilins.
[electronic resource]
by
Cole, W J
Gray, C H
Nicholson, D C
Norman, M
Producer:
19660928
In:
Journal of the Chemical Society. Perkin transactions 1
vol. 15
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24.
Isotopic studies of the conversion of oxophlorins and their ferrihaems into bile pigments in the rat.
[electronic resource]
by
Kondo, T
Nicholson, D C
Jackson, A H
Kenner, G W
Producer:
19720108
In:
The Biochemical journal
vol. 121
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25.
Optical activity of stercobilin and d-urobilin.
[electronic resource]
by
GRAY, C H
JONES, P M
KLYNE, W
NICHOLSON, D C
Producer:
19981101
In:
Nature
vol. 184
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26.
Congenital erythropoietic porphyria (Günther disease).
[electronic resource]
by
Murphy, G M
Hawk, J L
Nicholson, D C
Magnus, I A
Producer:
19871112
In:
Clinical and experimental dermatology
vol. 12
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27.
Molecular species of the urobilins.
[electronic resource]
by
Jackson, A H
Smith, K M
Gray, C H
Nicholson, D C
Producer:
19670108
In:
Nature
vol. 209
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28.
'Erythropoietic' protoporphyria and cirrhosis in sisters.
[electronic resource]
by
Thompson, R P
Molland, E A
Nicholson, D C
Gray, C H
Producer:
19740528
In:
Gut
vol. 14
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29.
ISOTOPE STUDIES ON A CASE OF ERYTHROPOIETIC PROTOPORPHYRIA.
[electronic resource]
by
GRAY, C H
KULCZYCKA, A
NICHOLSON, D C
MAGNUS, I A
RIMINGTON, C
Producer:
19961201
In:
Clinical science
vol. 26
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30.
Cutaneous porphyria due to a malignant primary hepatoma.
[electronic resource]
by
Thompson, R P
Nicholson, D C
Farnan, T
Whitmore, D N
Williams, R
Producer:
19701212
In:
Gastroenterology
vol. 59
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31.
THE METABOLISM OF (14C)-BILIRUBIN IN CONGENITAL NON-HAEMOLYTIC HYPERBILIRUBINAEMIA.
[electronic resource]
by
BILLING, B H
GRAY, C H
KULCZYCKA, A
MANFIELD, P
NICHOLSON, D C
Producer:
19961201
In:
Clinical science
vol. 27
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32.
Excretion of porphobilinogen and 5-aminolaevulinic acid in acute porphyria.
[electronic resource]
by
ACKNER, B
COOPER, J E
GRAY, C H
KELLY, M
NICHOLSON, D C
Producer:
19981101
In:
Lancet (London, England)
vol. 1
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33.
Isotopic studies of the erythropoietic and hepatic components of congenital porphyria and 'erythropoietic' protoporphyria.
[electronic resource]
by
Nicholson, D C
Cowger, M L
Kalivas, J
Thompson, R P
Gray, C H
Producer:
19731010
In:
Clinical science
vol. 44
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34.
Congenital erythropoietic uroporphyria (Günther's disease) presenting in a middle aged man.
[electronic resource]
by
Weston, M J
Nicholson, D C
Lim, C K
Clark, K G
Macdonald, A
Henderson, M A
Williams, R
Producer:
19790516
In:
The International journal of biochemistry
vol. 9
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