-
1
-
-
0026701911
-
A novel complex locus UGT1 encodes human bilirubin, phenol, and other UDP-glucuronosyltransferase isoenzymes with identical carboxyl termini
-
Ritter J., Chen Y., Sheen H., Tran S., Kimura M., Yeatman M., Owens S. A novel complex locus UGT1 encodes human bilirubin, phenol, and other UDP-glucuronosyltransferase isoenzymes with identical carboxyl termini. J. Biol. Chem. 267:1992;3257-3261.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 3257-3261
-
-
Ritter, J.1
Chen, Y.2
Sheen, H.3
Tran, S.4
Kimura, M.5
Yeatman, M.6
Owens, S.7
-
2
-
-
0026764632
-
Identification of a genetic alteration in the code for bilirubin UDP-glucuronosyltransferase in the UGT1 gene complex of a Crigler-Najjar type I patient
-
Ritter J., Yeatman M., Ferreira P., Owens I. Identification of a genetic alteration in the code for bilirubin UDP-glucuronosyltransferase in the UGT1 gene complex of a Crigler-Najjar type I patient. J. Clin. Invest. 90:1992;150-155.
-
(1992)
J. Clin. Invest.
, vol.90
, pp. 150-155
-
-
Ritter, J.1
Yeatman, M.2
Ferreira, P.3
Owens, I.4
-
3
-
-
0028867826
-
The genetic basis of the reduced expression of bilirubin UDP-glucoronosyltransferase 1 in Gilbert's syndrome
-
Bosma P., Chowdhury J., Bakker C., Gantla S.h., De Boer A., Oostra B., Linhout D., Tytgat G., et al. The genetic basis of the reduced expression of bilirubin UDP-glucoronosyltransferase 1 in Gilbert's syndrome. N. Engl. J. Med. 333:1995;1171-1175.
-
(1995)
N. Engl. J. Med.
, vol.333
, pp. 1171-1175
-
-
Bosma, P.1
Chowdhury, J.2
Bakker, C.3
Gantla, S.H.4
De Boer, A.5
Oostra, B.6
Linhout, D.7
Tytgat, G.8
-
4
-
-
0032880196
-
(TA)8 allele in the UGT1 A1 gene promoter of a Caucasian with Gilbert's syndrome
-
Iolascon A., Fainenza M.F., Centra M., Storelli S., Zelante L., Savoia A. (TA)8 allele in the UGT1 A1 gene promoter of a Caucasian with Gilbert's syndrome. Haematologica. 84:1999;106-109.
-
(1999)
Haematologica
, vol.84
, pp. 106-109
-
-
Iolascon, A.1
Fainenza, M.F.2
Centra, M.3
Storelli, S.4
Zelante, L.5
Savoia, A.6
-
5
-
-
0034085045
-
A Caucasian boy with Gilbert's syndrome heterozygous for the (TA)8 allele
-
Tsezou A., Tzetis M., Kitsiou M., Kavazarakis E., Galla A., Kanavakis E. A Caucasian boy with Gilbert's syndrome heterozygous for the (TA)8 allele. Heamatologica. 85:2000;319-336.
-
(2000)
Heamatologica
, vol.85
, pp. 319-336
-
-
Tsezou, A.1
Tzetis, M.2
Kitsiou, M.3
Kavazarakis, E.4
Galla, A.5
Kanavakis, E.6
-
6
-
-
0020049449
-
Construction of human gene libraries from small amounts of peripheral blood: Analysis of β-like globin genes
-
Poncz M., Solowiejczyk D., Harpel B., Mory Y., Schwartz E., Surrey S. Construction of human gene libraries from small amounts of peripheral blood analysis of β-like globin genes . Hemoglobin. 6:1982;27-36.
-
(1982)
Hemoglobin
, vol.6
, pp. 27-36
-
-
Poncz, M.1
Solowiejczyk, D.2
Harpel, B.3
Mory, Y.4
Schwartz, E.5
Surrey, S.6
-
8
-
-
0032493441
-
Racial variability in the UDP-glucoronosyltransferase 1 (UGT1 A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism?
-
Beutler E., Gelbart T., Demina A. Racial variability in the UDP-glucoronosyltransferase 1 (UGT1 A1) promoter a balanced polymorphism for regulation of bilirubin metabolism? Proc. Natl. Acad. Sci. USA. 95:1998;8170-8174.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 8170-8174
-
-
Beutler, E.1
Gelbart, T.2
Demina, A.3
-
9
-
-
0030698230
-
Hyperbilirubinaemia in heterozygous β-thalassemia is related to co-inherited Gilbert's syndrome
-
Galanello R., Perseu M., Melis A., Cipollina L., Barella S., Giagu N., Turco M.P., Maccioni O., Cao A. Hyperbilirubinaemia in heterozygous β-thalassemia is related to co-inherited Gilbert's syndrome. Br. J. Hematol. 99:1997;433-436.
-
(1997)
Br. J. Hematol.
, vol.99
, pp. 433-436
-
-
Galanello, R.1
Perseu, M.2
Melis, A.3
Cipollina, L.4
Barella, S.5
Giagu, N.6
Turco, M.P.7
Maccioni, O.8
Cao, A.9
-
10
-
-
0030663191
-
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous β-thalassaemia and in glucose-6-phospate dehydrogenase deficiency
-
Sampieto M., Lupica L., Perrero L., Comino A., Montemuros F., Cappelini M.D., Fiorelli G. The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous β-thalassaemia and in glucose-6-phospate dehydrogenase deficiency. Br. J. Hematol. 99:1997;437-439.
-
(1997)
Br. J. Hematol.
, vol.99
, pp. 437-439
-
-
Sampieto, M.1
Lupica, L.2
Perrero, L.3
Comino, A.4
Montemuros, F.5
Cappelini, M.D.6
Fiorelli, G.7
-
11
-
-
0032852420
-
Co-inherited Gilbert's syndrome: A factor determining hyperbilirubinemia in homozygous beta-thalassemia
-
Galanello R., Cipollina M.D., Dessi C., Giagu N., Lai E., Cao A. Co-inherited Gilbert's syndrome a factor determining hyperbilirubinemia in homozygous beta-thalassemia . Heamatologica. 84:1999;103-105.
-
(1999)
Heamatologica
, vol.84
, pp. 103-105
-
-
Galanello, R.1
Cipollina, M.D.2
Dessi, C.3
Giagu, N.4
Lai, E.5
Cao, A.6
-
12
-
-
17944368760
-
Gilbert syndrome associated with beta-thalassemia
-
Tzetis M., Kanavakis E., Tsezou A., Ladis V., Pateraki E., Georgakopoulos T., Kavazarakis E., Maragoudaki E., Karpathios T., Kitsiou-Tzeli S. Gilbert syndrome associated with beta-thalassemia. Pediatr. Hematol. Oncol. 18:2001;477-484.
-
(2001)
Pediatr. Hematol. Oncol.
, vol.18
, pp. 477-484
-
-
Tzetis, M.1
Kanavakis, E.2
Tsezou, A.3
Ladis, V.4
Pateraki, E.5
Georgakopoulos, T.6
Kavazarakis, E.7
Maragoudaki, E.8
Karpathios, T.9
Kitsiou-Tzeli, S.10
-
13
-
-
0034760144
-
Influence of bilirubin uridine diphosphate-glucoronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in children with sickle cell anemia
-
Passon R., Howard T.h., Zimmerman S.h., Schultz W., Ware R. Influence of bilirubin uridine diphosphate-glucoronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in children with sickle cell anemia. J. Pediatr. Hematol. Oncol. 23:2001;448-451.
-
(2001)
J. Pediatr. Hematol. Oncol.
, vol.23
, pp. 448-451
-
-
Passon, R.1
Howard, T.H.2
Zimmerman, S.H.3
Schultz, W.4
Ware, R.5
-
14
-
-
0035676442
-
Cholelithiasis and Gilbert's syndrome in homozygous β-thalassemia
-
Galanello R., Piras S., Barella S., Leoni G., Cipollina M., Perseu L., Cao A. Cholelithiasis and Gilbert's syndrome in homozygous β-thalassemia. Br. J. Hematol. 115:2001;926-928.
-
(2001)
Br. J. Hematol.
, vol.115
, pp. 926-928
-
-
Galanello, R.1
Piras, S.2
Barella, S.3
Leoni, G.4
Cipollina, M.5
Perseu, L.6
Cao, A.7
-
15
-
-
0038157469
-
Causes of mortality
-
G. Serjeant (Ed.), Oxford Univ. Press, New York
-
G. Serjeant, Causes of mortality, in: G. Serjeant (Ed.), Sickle Cell Disease, Oxford Univ. Press, New York, 1985, pp. 344-348.
-
(1985)
Sickle Cell Disease
, pp. 344-348
-
-
Serjeant, G.1
-
16
-
-
12444279408
-
-
Th. Andreoli, C. Bennet, Ch. Carpenter, F. Plum, L. Smith (Eds.), Saunders, Philadelphia
-
Th. Andreoli, C. Bennet, Ch. Carpenter, F. Plum, L. Smith, Jaundice, in: Th. Andreoli, C. Bennet, Ch. Carpenter, F. Plum, L. Smith (Eds.), Cecil Essentials of Medicine, 3rd ed., Saunders, Philadelphia, 1993, pp. 323-327.
-
(1993)
Cecil Essentials of Medicine, 3rd Ed.
, pp. 323-327
-
-
Andreoli, Th.1
Bennet, C.2
Carpenter, Ch.3
Plum, F.4
Smith, L.5
Jaundice6
|