35. Colacino J. M. and Kraus D. w.: Hemoglobincontaining cells of Neodasys (Gastrotricha, Chaetonotida) - II. Respiratory significance. Compo Biochern. Physiol. Pt. A 79: 363-369 (1984)
36. Coletta M. et al.: Ligand-dependent behaviour of the
hemoglobin from the ascarid Parascaris equorum.
Biochim. biophys. Acta 870: 169-175 (1986)
37. Coletta M. et al.: A novel mechanism of heme-heme
interaction in the homodimeric hemoglobin from Scapharca inaequivalis as manifested upon cleavage of
the proximal Fe-N bond at low pH. J. BioI. Chern.
265: 4828-30 (1990)
38. Dafre A. L. and F 0 D. w.: Root effect hemoglobins
in marine fish. Compo Biochem. Physiol. Pt. A 92:
267-471 (1989)
39. Darawshe S., Tsafahdya Yand Daniel E.: Quaternary
structure of erythrocruorin from the nematode Ascaris suum. Evidence for unsaturated haem-binding
sites. Biochem. J. 242: 689-694 (1987)
40. Decker H. and Sterner R.: Nested allostery of arthropodan hemocyanin (Eurypelma californicum and
Homarus americanus). J. mol. BioI. 211: 281-293
(1990)
41. Douglas E. L. et al.: Myoglobin in the heart tissue of
fishes lacking hemoglobin. Compo Biochem. Physiol.
Pt. A 81: 885-888 (1985)
42. Drexel R. et al.: Complete amino-acid sequence of a
functional unit from a molluscan hemocyanin (Helix
pomatia). BioI. Chern. Hoppe-Seyler 368: 617-635
(1987)
43. Ellerton H. D., Bearman C. H. and Loong P. c.:
Erythrocruorin from the New Zealand earthworm
Maoridrilus montanus: a multi-subunit annelid extracellular hemoglobin. Compo Biochem. Physiol. Pt. B
87: 1017-23 (1987)
44. Fitch D. H. A et al.: Molecular history of gene conversions in the primate fetal gamma-globin genes.
Nucleotide sequences from the common gibbon,
Hylobates lar. J. BioI. Chern. 265: 781-793 (1990)
45. Focesi A. jr., Ogo S. H. and Matsuura M. S. A:
Dimer-tetramer transition in hemoglobins from Liophis miliaris. II. Evidence with the stripped proteins.
Compo Biochem. Physiol. Pt. B 96: 119-122 (1990)
46. Garey J. R. and Riggs A F.: The hemoglobin of Urechis caupo. The cDNA-derived amino acid sequence.
J. bioI. Chern. 261: 16446-50 (1986)
47. Garner K. J. and Lingrei J. B.: A comparison of the
~A- and ~B-globin gene clusters of sheep. J. mol.
Evol. 28: 175-184 (1989)
48. Gelissen G., Hennecke R. and Spindler K. D.: The
site of synthesis of hemocyanin in the crayfish, Astacus leptodactylus. Experientia 47: 194-/195 (1991)
49. Giardina B. et al.: Interaction of hemoglobin with
chloride and 2,3-bisphophoglycerate: A comparative
approach. Eur. J. Biochem. 194: 61-65 (1990)
50. Gibson Q. H. et al.: Ligand binding in a hierarchy of
globin complexes: The hexagonal bilayer hemoglobin
of Lumbricus terrestris and its heme-containing subunits. J. BioI. Chern. 266: 13097-102 (1991)
51. Gielens C. et al.: Identification, separation and characterization of the haemocyanin components of Helix
aspersa. Compo Biochem. Physiol. Pt. B 88: 181-186
(1987)
52. Gonzalez-Redondo J. M. et al.: Nucleotide sequence
of the human theta-l globin gene. Biochem. Genet.
26: 207-211 (1988)
References
283
53. Goodman M. et al.: Amino acid sequence evidence
on the phylogeny of primates and other eutherians.
In: Goodman M. (ed.): Macromolecular sequences in
systematics and evolutionary biology, pp. 115-191.
Plenum, New York 1982
54. Goodman M. et al.: The eta-globin gene. Its long
evolutionary history in the ~-globin gene family of
mammals. J. mol. BioI. 180: 803-823 (1984)
55. Goodman M. et al.: An evolutionary tree for invertebrate globin sequences. J. mol. Evol. 27: 236-249
(1988)
56. Gotoh T. and Suzuki T.: Molecular assembly and
evolution of multi-subunit extracellular annelid
hemoglobines. Zool. Sci. 7: 1-16 (1990)
57. Grinich N. P., Terwilliger R. C. and Terwilliger N. B.:
Oxygen equilibria and structural characteristics of the
tetrameric and polymeric intracellular hemoglobins
from the bivalve mollusc Barbatia reeveana. J. compo
Physiol. B 156: 675-682 (1986)
58. Hardison R. C. and Gelinas R. E.: Assignment of
orthologous relationships among mammalian aglobin genes by examining flanking regions reveals a
rapid rate of evolution. Mol. BioI. Evol. 3: 243-261
(1986)
59. Hardison R. C. et al.: A previously undetected pseudogen in the human alpha globin gene cluster.
Nucleic Acids Res. 14: 1903-11 (1986)
60. Harris S. et al.: Nucleotide sequence analysis of the
lemur ~-globin gene family: Evidence for major rate
fluctuations in globin polypeptide evolution. Mol.
BioI. Evol. 3: 465-484 (1986)
61. Herskovits T. T. and Hamilton M. G.: The hemoglobin of the aquatic snail, Planorbella duryi
(Wetherby). Compo Biochem. Physiol. Pt. B 95:
321-326 (1990)
62. Herskovits T. T. et al: Light-scattering and scanning
transmission electron microscopic investigation of the
hemocyanin of the bivalve, Yoldia limatula (Say).
Compo Biochem. Physiol. Pt. B 96: 497-503 (1990)
63. Herskovits T. T. and Hamilton M. G.: Higher order
assemblies of molluscan hemocyanins (Minireview).
Compo Biochem. Physiol. Pt. B 99: 19-34 (1991)
64. Hirsch R. E. and Noble R. W.: Intrinsic fluorescence
of carp hemoglobin: a study of the R-T-transition.
Biochim. biophys. Acta 914: 213-219 (1987)
65. Hombrados I. et al.: Primary structure of the minor
hemoglobins from the sea lamprey (Petromyzon marinus, Cyclostomata). BioI. Chern. Hoppe-Seyler 368:
145-154 (1987)
66. Honig G. R. and Adams J. G. (eds.): Human hemoglobin genetics. Springer, Wien 1986
67. Honzatko R. B. and Hendrickson W. A.: Molecular
models for the putative dimer of sea lamprey hemoglobin. Proc. Nat. Acad. Sci. USA83: 8487-91 (1986)
68. Hsu L. et al.: Structure and expression of the human
theta-globin gene. Nature 331: 94-96 (1988)
69. Huber F. and Braunitzer G.: The primary structure of
the hemoglobin of the electric eel (Electrophorus
electricus). BioI. Chern. Hoppe-Seyler 370: 245-250
(1989)
70. Huisman T. H. J.: A comprehensive list of all hemoglobin variants and their references. Hemoglobin 13:
221-323 (1989)
71. van Iersel A A J. and Blaauboer B. J.: NADHferrihemoglobin reductase in avian erythrocytes.
Compo Biochem. Physiol. Pt. B 81: 1027-31 (1985)
36. Coletta M. et al.: Ligand-dependent behaviour of the
hemoglobin from the ascarid Parascaris equorum.
Biochim. biophys. Acta 870: 169-175 (1986)
37. Coletta M. et al.: A novel mechanism of heme-heme
interaction in the homodimeric hemoglobin from Scapharca inaequivalis as manifested upon cleavage of
the proximal Fe-N bond at low pH. J. BioI. Chern.
265: 4828-30 (1990)
38. Dafre A. L. and F 0 D. w.: Root effect hemoglobins
in marine fish. Compo Biochem. Physiol. Pt. A 92:
267-471 (1989)
39. Darawshe S., Tsafahdya Yand Daniel E.: Quaternary
structure of erythrocruorin from the nematode Ascaris suum. Evidence for unsaturated haem-binding
sites. Biochem. J. 242: 689-694 (1987)
40. Decker H. and Sterner R.: Nested allostery of arthropodan hemocyanin (Eurypelma californicum and
Homarus americanus). J. mol. BioI. 211: 281-293
(1990)
41. Douglas E. L. et al.: Myoglobin in the heart tissue of
fishes lacking hemoglobin. Compo Biochem. Physiol.
Pt. A 81: 885-888 (1985)
42. Drexel R. et al.: Complete amino-acid sequence of a
functional unit from a molluscan hemocyanin (Helix
pomatia). BioI. Chern. Hoppe-Seyler 368: 617-635
(1987)
43. Ellerton H. D., Bearman C. H. and Loong P. c.:
Erythrocruorin from the New Zealand earthworm
Maoridrilus montanus: a multi-subunit annelid extracellular hemoglobin. Compo Biochem. Physiol. Pt. B
87: 1017-23 (1987)
44. Fitch D. H. A et al.: Molecular history of gene conversions in the primate fetal gamma-globin genes.
Nucleotide sequences from the common gibbon,
Hylobates lar. J. BioI. Chern. 265: 781-793 (1990)
45. Focesi A. jr., Ogo S. H. and Matsuura M. S. A:
Dimer-tetramer transition in hemoglobins from Liophis miliaris. II. Evidence with the stripped proteins.
Compo Biochem. Physiol. Pt. B 96: 119-122 (1990)
46. Garey J. R. and Riggs A F.: The hemoglobin of Urechis caupo. The cDNA-derived amino acid sequence.
J. bioI. Chern. 261: 16446-50 (1986)
47. Garner K. J. and Lingrei J. B.: A comparison of the
~A- and ~B-globin gene clusters of sheep. J. mol.
Evol. 28: 175-184 (1989)
48. Gelissen G., Hennecke R. and Spindler K. D.: The
site of synthesis of hemocyanin in the crayfish, Astacus leptodactylus. Experientia 47: 194-/195 (1991)
49. Giardina B. et al.: Interaction of hemoglobin with
chloride and 2,3-bisphophoglycerate: A comparative
approach. Eur. J. Biochem. 194: 61-65 (1990)
50. Gibson Q. H. et al.: Ligand binding in a hierarchy of
globin complexes: The hexagonal bilayer hemoglobin
of Lumbricus terrestris and its heme-containing subunits. J. BioI. Chern. 266: 13097-102 (1991)
51. Gielens C. et al.: Identification, separation and characterization of the haemocyanin components of Helix
aspersa. Compo Biochem. Physiol. Pt. B 88: 181-186
(1987)
52. Gonzalez-Redondo J. M. et al.: Nucleotide sequence
of the human theta-l globin gene. Biochem. Genet.
26: 207-211 (1988)
References
283
53. Goodman M. et al.: Amino acid sequence evidence
on the phylogeny of primates and other eutherians.
In: Goodman M. (ed.): Macromolecular sequences in
systematics and evolutionary biology, pp. 115-191.
Plenum, New York 1982
54. Goodman M. et al.: The eta-globin gene. Its long
evolutionary history in the ~-globin gene family of
mammals. J. mol. BioI. 180: 803-823 (1984)
55. Goodman M. et al.: An evolutionary tree for invertebrate globin sequences. J. mol. Evol. 27: 236-249
(1988)
56. Gotoh T. and Suzuki T.: Molecular assembly and
evolution of multi-subunit extracellular annelid
hemoglobines. Zool. Sci. 7: 1-16 (1990)
57. Grinich N. P., Terwilliger R. C. and Terwilliger N. B.:
Oxygen equilibria and structural characteristics of the
tetrameric and polymeric intracellular hemoglobins
from the bivalve mollusc Barbatia reeveana. J. compo
Physiol. B 156: 675-682 (1986)
58. Hardison R. C. and Gelinas R. E.: Assignment of
orthologous relationships among mammalian aglobin genes by examining flanking regions reveals a
rapid rate of evolution. Mol. BioI. Evol. 3: 243-261
(1986)
59. Hardison R. C. et al.: A previously undetected pseudogen in the human alpha globin gene cluster.
Nucleic Acids Res. 14: 1903-11 (1986)
60. Harris S. et al.: Nucleotide sequence analysis of the
lemur ~-globin gene family: Evidence for major rate
fluctuations in globin polypeptide evolution. Mol.
BioI. Evol. 3: 465-484 (1986)
61. Herskovits T. T. and Hamilton M. G.: The hemoglobin of the aquatic snail, Planorbella duryi
(Wetherby). Compo Biochem. Physiol. Pt. B 95:
321-326 (1990)
62. Herskovits T. T. et al: Light-scattering and scanning
transmission electron microscopic investigation of the
hemocyanin of the bivalve, Yoldia limatula (Say).
Compo Biochem. Physiol. Pt. B 96: 497-503 (1990)
63. Herskovits T. T. and Hamilton M. G.: Higher order
assemblies of molluscan hemocyanins (Minireview).
Compo Biochem. Physiol. Pt. B 99: 19-34 (1991)
64. Hirsch R. E. and Noble R. W.: Intrinsic fluorescence
of carp hemoglobin: a study of the R-T-transition.
Biochim. biophys. Acta 914: 213-219 (1987)
65. Hombrados I. et al.: Primary structure of the minor
hemoglobins from the sea lamprey (Petromyzon marinus, Cyclostomata). BioI. Chern. Hoppe-Seyler 368:
145-154 (1987)
66. Honig G. R. and Adams J. G. (eds.): Human hemoglobin genetics. Springer, Wien 1986
67. Honzatko R. B. and Hendrickson W. A.: Molecular
models for the putative dimer of sea lamprey hemoglobin. Proc. Nat. Acad. Sci. USA83: 8487-91 (1986)
68. Hsu L. et al.: Structure and expression of the human
theta-globin gene. Nature 331: 94-96 (1988)
69. Huber F. and Braunitzer G.: The primary structure of
the hemoglobin of the electric eel (Electrophorus
electricus). BioI. Chern. Hoppe-Seyler 370: 245-250
(1989)
70. Huisman T. H. J.: A comprehensive list of all hemoglobin variants and their references. Hemoglobin 13:
221-323 (1989)
71. van Iersel A A J. and Blaauboer B. J.: NADHferrihemoglobin reductase in avian erythrocytes.
Compo Biochem. Physiol. Pt. B 81: 1027-31 (1985)