-
1
-
-
0023053503
-
Profiling steroid hormones and urinary steroids
-
C.H.L. Shackleton Profiling steroid hormones and urinary steroids J Chromatogr B Biomed Appl 379 1986 91 156
-
(1986)
J Chromatogr B Biomed Appl
, vol.379
, pp. 91-156
-
-
Shackleton, C.H.L.1
-
2
-
-
71849112937
-
Steroids excreted in urine by neonates with 21-hydroxylase deficiency: Characterization, using GC-MS and GC-MS/MS, of the D-ring and side chain structure of pregnanes and pregnenes
-
S. Christakoudi, D.A. Cowan, and N.F. Taylor Steroids excreted in urine by neonates with 21-hydroxylase deficiency: characterization, using GC-MS and GC-MS/MS, of the D-ring and side chain structure of pregnanes and pregnenes Steroids 75 2010 34 52
-
(2010)
Steroids
, vol.75
, pp. 34-52
-
-
Christakoudi, S.1
Cowan, D.A.2
Taylor, N.F.3
-
3
-
-
84858336160
-
Steroids excreted in urine by neonates with 21-hydroxylase deficiency. 2. Characterization, using GC-MS and GC-MS/MS, of pregnanes and pregnenes with an oxo-group on the A- or B-ring
-
S. Christakoudi, D.A. Cowan, and N.F. Taylor Steroids excreted in urine by neonates with 21-hydroxylase deficiency. 2. Characterization, using GC-MS and GC-MS/MS, of pregnanes and pregnenes with an oxo-group on the A- or B-ring Steroids 77 2012 382 393
-
(2012)
Steroids
, vol.77
, pp. 382-393
-
-
Christakoudi, S.1
Cowan, D.A.2
Taylor, N.F.3
-
4
-
-
84867599967
-
Steroids excreted in urine by neonates with 21-hydroxylase deficiency. 3. Characterization, using GC-MS and GC-MS/MS, of androstanes and androstenes
-
S. Christakoudi, D.A. Cowan, and N.F. Taylor Steroids excreted in urine by neonates with 21-hydroxylase deficiency. 3. Characterization, using GC-MS and GC-MS/MS, of androstanes and androstenes Steroids 77 2012 1487 1501
-
(2012)
Steroids
, vol.77
, pp. 1487-1501
-
-
Christakoudi, S.1
Cowan, D.A.2
Taylor, N.F.3
-
6
-
-
34447128813
-
Newborn screening for congenital adrenal hyperplasia: Additional steroid profile using liquid chromatography-tandem mass spectrometry
-
N. Janzen, M. Peter, S. Sander, U. Steuerwald, M. Terhardt, U. Holtkamp, and J. Sander Newborn screening for congenital adrenal hyperplasia: additional steroid profile using liquid chromatography-tandem mass spectrometry J Clin Endocrinol Metab 92 2007 2581 2589
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 2581-2589
-
-
Janzen, N.1
Peter, M.2
Sander, S.3
Steuerwald, U.4
Terhardt, M.5
Holtkamp, U.6
Sander, J.7
-
7
-
-
0017260324
-
Congenital adrenal hyperplasia caused by defect in steroid 21-hydroxylase. Establishment of definitive urinary steroid excretion pattern during first weeks of life
-
C.H.L. Shackleton Congenital adrenal hyperplasia caused by defect in steroid 21-hydroxylase. Establishment of definitive urinary steroid excretion pattern during first weeks of life Clin Chim Acta 67 1976 287 298
-
(1976)
Clin Chim Acta
, vol.67
, pp. 287-298
-
-
Shackleton, C.H.L.1
-
8
-
-
3042535976
-
Biochemical diagnosis of Antley-Bixler syndrome by steroid analysis
-
C.H.L. Shackleton, J. Marcos, E.M. Malunowicz, M. Szarras-Czapnik, P. Jira, and N.F. Taylor Biochemical diagnosis of Antley-Bixler syndrome by steroid analysis Am J Med Genet 128 A3 2004 223 231
-
(2004)
Am J Med Genet
, vol.128
, Issue.3
, pp. 223-231
-
-
Shackleton, C.H.L.1
Marcos, J.2
Malunowicz, E.M.3
Szarras-Czapnik, M.4
Jira, P.5
Taylor, N.F.6
-
9
-
-
0014353495
-
Steroids in germfree and conventional rats. 6. Identification of 15α- and 21-hydroxylated C21 steroids in faeces from germ free rats
-
J.A. Gustafsson, and J. Sjovall Steroids in germfree and conventional rats. 6. Identification of 15α- and 21-hydroxylated C21 steroids in faeces from germ free rats Eur J Biochem 6 1968 236 247
-
(1968)
Eur J Biochem
, vol.6
, pp. 236-247
-
-
Gustafsson, J.A.1
Sjovall, J.2
-
10
-
-
0018100488
-
Analysis of glucocorticoid metabolites in the neonatal period: Catabolism of cortisone acetate by an infant with 21-hydroxylase deficiency
-
N.F. Taylor, D.H. Curnow, and C.H.L. Shackleton Analysis of glucocorticoid metabolites in the neonatal period: catabolism of cortisone acetate by an infant with 21-hydroxylase deficiency Clin Chim Acta 85 1978 219 229
-
(1978)
Clin Chim Acta
, vol.85
, pp. 219-229
-
-
Taylor, N.F.1
Curnow, D.H.2
Shackleton, C.H.L.3
-
11
-
-
0141723941
-
0-Methyloximes as carbonyl derivatives in gas chromatography, mass spectrometry, and nuclear magnetic resonance
-
H.M. Fales, and T. Luukkainen 0-Methyloximes as carbonyl derivatives in gas chromatography, mass spectrometry, and nuclear magnetic resonance Anal Chem 37 1965 955 957
-
(1965)
Anal Chem
, vol.37
, pp. 955-957
-
-
Fales, H.M.1
Luukkainen, T.2
-
12
-
-
0020073338
-
The diagnosis of 21-hydroxylase deficiency in a prematurely born infant on the basis of the urinary steroid excretion pattern
-
K.R. Van der Ploeg, B.G. Wolthers, G.T. Nagel, M. Volmer, and N.M. Drayer The diagnosis of 21-hydroxylase deficiency in a prematurely born infant on the basis of the urinary steroid excretion pattern Clin Chim Acta 120 1982 341 353
-
(1982)
Clin Chim Acta
, vol.120
, pp. 341-353
-
-
Van Der Ploeg, K.R.1
Wolthers, B.G.2
Nagel, G.T.3
Volmer, M.4
Drayer, N.M.5
-
13
-
-
0015547351
-
Influence of 11-trimethylsilyloxy- or 11-hydroxy-substituents on the electron-impact-induced fragmentation of trimethylsilyl derivatives of some androstanols
-
P. Vouros, and D.J. Harvey Influence of 11-trimethylsilyloxy- or 11-hydroxy-substituents on the electron-impact-induced fragmentation of trimethylsilyl derivatives of some androstanols J Chem Soc Perkin 1 1973 727 732
-
(1973)
J Chem Soc Perkin
, vol.1
, pp. 727-732
-
-
Vouros, P.1
Harvey, D.J.2
-
14
-
-
0016213263
-
Steroid excretion by an infant with an unusual salt-losing syndrome: A gas chromatographic-mass spectrometric study
-
C.H.L. Shackleton, and G.H. Snodgrass Steroid excretion by an infant with an unusual salt-losing syndrome: a gas chromatographic-mass spectrometric study Ann Clin Biochem 11 1974 91 99
-
(1974)
Ann Clin Biochem
, vol.11
, pp. 91-99
-
-
Shackleton, C.H.L.1
Snodgrass, G.H.2
-
15
-
-
31544457026
-
Electron ionization
-
J.T. Watson, O.D. Sparkman, John Willey & Sons, Ltd. Chichester
-
J.T. Watson, and O.D. Sparkman Electron ionization J.T. Watson, O.D. Sparkman, Introduction to mass spectrometry: instrumentation, applications and strategies for data interpretation 2007 John Willey & Sons, Ltd. Chichester 317 443
-
(2007)
Introduction to Mass Spectrometry: Instrumentation, Applications and Strategies for Data Interpretation
, pp. 317-443
-
-
Watson, J.T.1
Sparkman, O.D.2
-
16
-
-
0026001618
-
Steroid hormone hydroxylase specificities of eleven cDNA-expressed human cytochrome P450s
-
D.J. Waxman, D.P. Lapenson, T. Aoyama, H.V. Gelboin, F.J. Gonzalez, and K. Korzekwa Steroid hormone hydroxylase specificities of eleven cDNA-expressed human cytochrome P450s Arch Biochem Biophys 290 1991 160 166
-
(1991)
Arch Biochem Biophys
, vol.290
, pp. 160-166
-
-
Waxman, D.J.1
Lapenson, D.P.2
Aoyama, T.3
Gelboin, H.V.4
Gonzalez, F.J.5
Korzekwa, K.6
-
17
-
-
0142210233
-
Developmental expression of the major human hepatic CYP3A enzymes
-
J.C. Stevens, R.N. Hines, C. Gu, S.B. Koukouritaki, J.R. Manro, and P.J. Tandler Developmental expression of the major human hepatic CYP3A enzymes J Pharmacol Exp Ther 307 2003 573 582
-
(2003)
J Pharmacol Exp Ther
, vol.307
, pp. 573-582
-
-
Stevens, J.C.1
Hines, R.N.2
Gu, C.3
Koukouritaki, S.B.4
Manro, J.R.5
Tandler, P.J.6
-
18
-
-
0032452471
-
Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency
-
T.A.S.S. Bachega, A.E. Billerbeck, G. Madureira, J.A.M. Marcondes, C.A. Longui, M.V. Leite, I.J.P. Arnhold, and B.B. Mendonca Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency J Clin Endocrinol Metab 83 1998 4416 4419
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 4416-4419
-
-
Bachega, T.A.S.S.1
Billerbeck, A.E.2
Madureira, G.3
Marcondes, J.A.M.4
Longui, C.A.5
Leite, M.V.6
Arnhold, I.J.P.7
Mendonca, B.B.8
-
19
-
-
0032452922
-
Expression of type 2 11β-hydroxysteroid dehydrogenase and corticosteroid hormone receptors in early human fetal life
-
J. Condon, C. Gosden, D. Gardener, P. Nickson, M. Hewison, and A.J. Howie Expression of type 2 11β-hydroxysteroid dehydrogenase and corticosteroid hormone receptors in early human fetal life J Clin Endocrinol Metab 83 1998 4490 4497
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 4490-4497
-
-
Condon, J.1
Gosden, C.2
Gardener, D.3
Nickson, P.4
Hewison, M.5
Howie, A.J.6
-
20
-
-
79951665862
-
The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders
-
W.L. Miller, and R.J. Auchus The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders Endocr Rev 32 2011 81 151
-
(2011)
Endocr Rev
, vol.32
, pp. 81-151
-
-
Miller, W.L.1
Auchus, R.J.2
|