654
16 Sterols and Steroids
38. Goad L. J. et al.: Composition of free, esterified and
sulphated sterols from the sea cucumber Psolus fabricii. Compo Biochem. Physiol. Pt. B 84: 189-196 (1986)
39. Gorbman A. (ed.): Comparative endocrinology. Wiley
& Sons, New York 1983
40. Grieneisen M. L. et al.: A putative role to ecdysteroids. Metabolism of cholesterol invitro by mildly disrupted prothoracic glands of Manduca sexta. Insect
Biochem. 21: 41-51 (1991)
41. Griffin P. R. et al.: The amino acid sequence of the sex
steroid-binding protein of rabbit serum. J. BioI. Chem.
264: 19066-75 (1989)
42. Guerriero A. and Pietra F.: Isolation in large amounts
of the rare plant ecdysteroid ajugasterone C from the
Mediterranean zoanthid Gerardia savaglia. Compo
Biochem. Physiol. Pt. B 80: 277-278 (1985)
43. Habermehl G.: Toxic animals and their weapons (In
German). 4th ed. Springer, Berlin 1987
44. Hammond G. L. et al.: Primary structure of human
corticosteroid binding globulin, deduced from hepatic
and pulmonary cDNAs, exhibits homology with serine
protease inhibitors. Proc. Nat. Acad. Sci. USA 84:
5153-57 (1987)
45. Hammond G. L. et al.: The cDNA-deduced primary
structure of human sex hormone-binding globulin and
location of its steroid-binding domain. FEBS Letters
215: 100-104 (1987)
46. Haslewood G. A. D.: The biological importance of
bile salts. North-Holland, Amsterdam 1978
47. Hellou J., King A. and Ni I. H.: Bile acids from the
harp seals, Phoca groenlandica. Compo Biochem. Physiol. Pt. A 89: 211-214 (1988)
48. Henrich V. C. et al.: A steroid/thyroid hormone receptor superfamily member in Drosophila melanogaster
that shares extensive sequence similarity with a mammalian homologue. Nucleic Acids Res. 18: 4143-48
(1990)
49. Hoffmann J. A.: Ten years of ecdysone workshop.
Insect Biochem. 16: 1-9 (1986)
50. Hoffmann K. H., Thiry E. and Lafont R.: 14Deoxyecdysteroids in an insect (Gryllus bimaculatus).
z. Naturforsch. Sect. C 45: 703-708 (1990)
51. Itoh T., Sica D. and Djerassi c.: Minor and trace sterols in marine invertebrates, part 35. Isolation and
structure elucidation of 74 sterols from the sponge Axinella cannabina. J. chem. Soc. Perkin Trans. II. 1983:
147-153
52. Jarzebski A. et al.: Sterol composition of Mesidothea
entomon L. (Isopoda, Crustacea). Compo Biochem.
Physiol. Pt. B 81: 733-735 (1985)
53. Jarzebski A., Polak L. and Habermehl G.: Free and
esterified sterols of Macoma balthica (L.). Compo Biochem. Physiol. Pt. B 86: 561-563 (1987)
54. Jeltsch J. M. et al.: Characterization of multiple
mRNAs originating from the chicken progesterone
receptor gene. Evidence for a specific transcript
encoding form A. J. BioI. Chem. 265: 3967-74 (1990)
55. Jirsa M. et al.: Classical bile acids in animals, ~phocaecholic acid in ducks. Compo Biochem. Physiol.
Pt. B 92: 357-360 (1989)
56. Johnson W. J. and Cain G. D.: Biosynthesis of polyisoprenoid lipids in the rat tapeworm Hymenolepis
diminuta. Compo Biochem. Physiol. Pt. B 82: 487-495
(1985)
57. Joseph D. R., Hall S. H. and French F. S.: Rats
androgen-binding protein: evidence for identical subunits and amino acid sequence homology with human
sex hormone-binding globulin. Proc. Nat. Acad. Sci.
USA 84: 339-343 (1987)
58. Kabbouh M. et al.: Further characterization of the 2deoxyecdysone C-2 hydroxylase from Locusta migratoria. Insect Biochem. 17: 1155-61 (1987)
59. Kabbouh M. and Rees H. H.: Characterization of the
ATP-2-deoxyecdysone
22-phosphotransferase
(2deoxyecdysone 22-kinase) in the follicle cells of Schistocerca gregaria. Insect Biochem. 21: 57-64 (1991)
60. Kalinovskaya N. I. et al.: Steroid metabolites of the far
eastern holothurian Stichopus japonicus Selenka.
Compo Biochem. Physiol. Pt. B 76: 167-171 (1983)
61. Karlaganis G. et al.: A bile alcohol sulfate as a major
component in the bile of the small skate (Raja erinacea). J. Lipid Res. 30: 317-322 (1989)
62. Kihira K. et al.: Bile salts of the coelacanth, Latimeria
chalumnae. J. Lipid Res. 25: 1330--36 (1985)
63. Kiriishi S. et al.: Prothoracic gland synthesis of 3dehydroecdysone and its hemolymph 3-beta-reductase
mediated conversion to ecdysone in representative
insects. Experientia 46: 716-721 (1990)
64. Kljajic Z., Dogovic N. and Gasic M. J.: Sterols in
Adriatic sea ascidians. Compo Biochem. Physiol. Pt. B
75: 519-521 (1983)
65. KooIman J.: Ecdysteroids (Review). Zool. Sci. 7:
563-580 (1990)
66. Krust A. et al.: The chicken oestrogen receptor
sequence: homology with v-erbA and the human oestrogen and glucocorticoid receptors. Embo J. 5:
891-897 (1986)
67. Ksebati M. B. and Schmitz F. J.: 24-Methyl-5acholestane-3B,5,6B,22R,24-pentol 6-acetate: new
polyhydroxylated sterol from the soft coral Asterospicularia randalli. Steroids 43: 639-649 (1984)
68. Lachaise F. and Lafont R.: Ecdysteroid metabolism in
a crab: Carcinus maenas L. Steroids 43: 243-259
(1984)
69. Lee H. M., Parish E. J. and Bone L. w.: Occurrence
of mammalian sex steroids in the free-living nematode,
Turbatrix aceti. Compo Biochem. Physiol. Pt. A 97:
115-117 (1990)
70. Lehtovaara I and Koskinen T.: Demonstration of vitamin D3 metabolism in Mytilus edulis. Experientia 42:
147-148 (1986)
71. de Loof A., Briers T. and Huybrechts R.: Presence and
function of ecdysteroids in adult insects. Compo Biochem. Physiol. Pt. B 79: 505-509 (1984)
72. Lopez de Haro M. S. and Nieto A.: Nucleotide and
derived amino acid sequences of a cDNA coding for
the pre-utero globin from the lung of the hare (Lepus
capensis). Biochem. J. 235: 895-898 (1986)
73. Mak P and Callard G. v.: A novel steroid-binding protein in the testis of the dogfish Squalus acanthias. Gen
compo Endocrinol. 68: 104-112 (1987)
74. Makin H. L. J. (ed.): Biochemistry of steroid hormones. Blackwell, Oxford 1984
75. Manconi R. et al.: Steroids in porifera. Sterols from
freshwater sponges Ephydatia fluviatilis (L.) and
Spongilla lacustris (L.). Compo Biochem. Physiol. Pt.
B 91: 237-245 (1988)
76. Martinez E., Givel F. and Wahli w.: A common ancestor DNA motif for invertebrate and vertebrate
hormone response elements. Embo J. 10: 263-268
(1991)
77. McDonnell D. P. et al.: Molecular cloning of complementary DNA encoding the avian receptor for vitamin
D. Science 235: 1214-17 (1987)
16 Sterols and Steroids
38. Goad L. J. et al.: Composition of free, esterified and
sulphated sterols from the sea cucumber Psolus fabricii. Compo Biochem. Physiol. Pt. B 84: 189-196 (1986)
39. Gorbman A. (ed.): Comparative endocrinology. Wiley
& Sons, New York 1983
40. Grieneisen M. L. et al.: A putative role to ecdysteroids. Metabolism of cholesterol invitro by mildly disrupted prothoracic glands of Manduca sexta. Insect
Biochem. 21: 41-51 (1991)
41. Griffin P. R. et al.: The amino acid sequence of the sex
steroid-binding protein of rabbit serum. J. BioI. Chem.
264: 19066-75 (1989)
42. Guerriero A. and Pietra F.: Isolation in large amounts
of the rare plant ecdysteroid ajugasterone C from the
Mediterranean zoanthid Gerardia savaglia. Compo
Biochem. Physiol. Pt. B 80: 277-278 (1985)
43. Habermehl G.: Toxic animals and their weapons (In
German). 4th ed. Springer, Berlin 1987
44. Hammond G. L. et al.: Primary structure of human
corticosteroid binding globulin, deduced from hepatic
and pulmonary cDNAs, exhibits homology with serine
protease inhibitors. Proc. Nat. Acad. Sci. USA 84:
5153-57 (1987)
45. Hammond G. L. et al.: The cDNA-deduced primary
structure of human sex hormone-binding globulin and
location of its steroid-binding domain. FEBS Letters
215: 100-104 (1987)
46. Haslewood G. A. D.: The biological importance of
bile salts. North-Holland, Amsterdam 1978
47. Hellou J., King A. and Ni I. H.: Bile acids from the
harp seals, Phoca groenlandica. Compo Biochem. Physiol. Pt. A 89: 211-214 (1988)
48. Henrich V. C. et al.: A steroid/thyroid hormone receptor superfamily member in Drosophila melanogaster
that shares extensive sequence similarity with a mammalian homologue. Nucleic Acids Res. 18: 4143-48
(1990)
49. Hoffmann J. A.: Ten years of ecdysone workshop.
Insect Biochem. 16: 1-9 (1986)
50. Hoffmann K. H., Thiry E. and Lafont R.: 14Deoxyecdysteroids in an insect (Gryllus bimaculatus).
z. Naturforsch. Sect. C 45: 703-708 (1990)
51. Itoh T., Sica D. and Djerassi c.: Minor and trace sterols in marine invertebrates, part 35. Isolation and
structure elucidation of 74 sterols from the sponge Axinella cannabina. J. chem. Soc. Perkin Trans. II. 1983:
147-153
52. Jarzebski A. et al.: Sterol composition of Mesidothea
entomon L. (Isopoda, Crustacea). Compo Biochem.
Physiol. Pt. B 81: 733-735 (1985)
53. Jarzebski A., Polak L. and Habermehl G.: Free and
esterified sterols of Macoma balthica (L.). Compo Biochem. Physiol. Pt. B 86: 561-563 (1987)
54. Jeltsch J. M. et al.: Characterization of multiple
mRNAs originating from the chicken progesterone
receptor gene. Evidence for a specific transcript
encoding form A. J. BioI. Chem. 265: 3967-74 (1990)
55. Jirsa M. et al.: Classical bile acids in animals, ~phocaecholic acid in ducks. Compo Biochem. Physiol.
Pt. B 92: 357-360 (1989)
56. Johnson W. J. and Cain G. D.: Biosynthesis of polyisoprenoid lipids in the rat tapeworm Hymenolepis
diminuta. Compo Biochem. Physiol. Pt. B 82: 487-495
(1985)
57. Joseph D. R., Hall S. H. and French F. S.: Rats
androgen-binding protein: evidence for identical subunits and amino acid sequence homology with human
sex hormone-binding globulin. Proc. Nat. Acad. Sci.
USA 84: 339-343 (1987)
58. Kabbouh M. et al.: Further characterization of the 2deoxyecdysone C-2 hydroxylase from Locusta migratoria. Insect Biochem. 17: 1155-61 (1987)
59. Kabbouh M. and Rees H. H.: Characterization of the
ATP-2-deoxyecdysone
22-phosphotransferase
(2deoxyecdysone 22-kinase) in the follicle cells of Schistocerca gregaria. Insect Biochem. 21: 57-64 (1991)
60. Kalinovskaya N. I. et al.: Steroid metabolites of the far
eastern holothurian Stichopus japonicus Selenka.
Compo Biochem. Physiol. Pt. B 76: 167-171 (1983)
61. Karlaganis G. et al.: A bile alcohol sulfate as a major
component in the bile of the small skate (Raja erinacea). J. Lipid Res. 30: 317-322 (1989)
62. Kihira K. et al.: Bile salts of the coelacanth, Latimeria
chalumnae. J. Lipid Res. 25: 1330--36 (1985)
63. Kiriishi S. et al.: Prothoracic gland synthesis of 3dehydroecdysone and its hemolymph 3-beta-reductase
mediated conversion to ecdysone in representative
insects. Experientia 46: 716-721 (1990)
64. Kljajic Z., Dogovic N. and Gasic M. J.: Sterols in
Adriatic sea ascidians. Compo Biochem. Physiol. Pt. B
75: 519-521 (1983)
65. KooIman J.: Ecdysteroids (Review). Zool. Sci. 7:
563-580 (1990)
66. Krust A. et al.: The chicken oestrogen receptor
sequence: homology with v-erbA and the human oestrogen and glucocorticoid receptors. Embo J. 5:
891-897 (1986)
67. Ksebati M. B. and Schmitz F. J.: 24-Methyl-5acholestane-3B,5,6B,22R,24-pentol 6-acetate: new
polyhydroxylated sterol from the soft coral Asterospicularia randalli. Steroids 43: 639-649 (1984)
68. Lachaise F. and Lafont R.: Ecdysteroid metabolism in
a crab: Carcinus maenas L. Steroids 43: 243-259
(1984)
69. Lee H. M., Parish E. J. and Bone L. w.: Occurrence
of mammalian sex steroids in the free-living nematode,
Turbatrix aceti. Compo Biochem. Physiol. Pt. A 97:
115-117 (1990)
70. Lehtovaara I and Koskinen T.: Demonstration of vitamin D3 metabolism in Mytilus edulis. Experientia 42:
147-148 (1986)
71. de Loof A., Briers T. and Huybrechts R.: Presence and
function of ecdysteroids in adult insects. Compo Biochem. Physiol. Pt. B 79: 505-509 (1984)
72. Lopez de Haro M. S. and Nieto A.: Nucleotide and
derived amino acid sequences of a cDNA coding for
the pre-utero globin from the lung of the hare (Lepus
capensis). Biochem. J. 235: 895-898 (1986)
73. Mak P and Callard G. v.: A novel steroid-binding protein in the testis of the dogfish Squalus acanthias. Gen
compo Endocrinol. 68: 104-112 (1987)
74. Makin H. L. J. (ed.): Biochemistry of steroid hormones. Blackwell, Oxford 1984
75. Manconi R. et al.: Steroids in porifera. Sterols from
freshwater sponges Ephydatia fluviatilis (L.) and
Spongilla lacustris (L.). Compo Biochem. Physiol. Pt.
B 91: 237-245 (1988)
76. Martinez E., Givel F. and Wahli w.: A common ancestor DNA motif for invertebrate and vertebrate
hormone response elements. Embo J. 10: 263-268
(1991)
77. McDonnell D. P. et al.: Molecular cloning of complementary DNA encoding the avian receptor for vitamin
D. Science 235: 1214-17 (1987)