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Results of search for 'au:"TASHIAN, R E"', page 7 of 7
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Authors
Bergenhem, N C
Brewer, G J
Carter, N D
Chegwidden, W R
DeSimone, J
Erickson, R P
Ferrell, R E
Goodman, M
Headings, V E
Hewett-Emmett, D
Lakkis, M M
Montgomery, J C
Osborne, W R
Shows, T B
Sly, W S
TASHIAN, R E
Tanis, R J
Tashian, R E
Venta, P J
Yu, Y S
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Topics
Amino Acid Sequence
Animals
Base Sequence
Biological Evolution
Carbonic Anhydrases
Electrophoresis
Erythrocytes
Female
Genetic Variation
Humans
Isoenzymes
Male
Mice
Molecular Sequence Data
analysis
blood
enzymology
genetics
metabolism
pharmacology
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English
Your search returned 132 results.
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121.
Novel inhibition of carbonic anhydrase isozymes I, II and III by carbamoyl phosphate.
[electronic resource]
by
Carter, N D
Chegwidden, W R
Hewett-Emmett, D
Jeffery, S
Shiels, A
Tashian, R E
Producer:
19840305
In:
FEBS letters
vol. 165
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122.
Comparative distribution of carbonic anhydrase isozymes III and II in rodent tissues.
[electronic resource]
by
Spicer, S S
Ge, Z H
Tashian, R E
Hazen-Martin, D J
Schulte, B A
Producer:
19900212
In:
The American journal of anatomy
vol. 187
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123.
Phylogenetic origins and adaptive evolution of avian and mammalian haemoglobin genes.
[electronic resource]
by
Czelusniak, J
Goodman, M
Hewett-Emmett, D
Weiss, M L
Venta, P J
Tashian, R E
Producer:
19820826
In:
Nature
vol. 298
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124.
Characterization of the human gene for a newly discovered carbonic anhydrase, CA VII, and its localization to chromosome 16.
[electronic resource]
by
Montgomery, J C
Venta, P J
Eddy, R L
Fukushima, Y S
Shows, T B
Tashian, R E
Producer:
19920313
In:
Genomics
vol. 11
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125.
Carbonic anhydrase II deficiency: single-base deletion in exon 7 is the predominant mutation in Caribbean Hispanic patients.
[electronic resource]
by
Hu, P Y
Ernst, A R
Sly, W S
Venta, P J
Skaggs, L A
Tashian, R E
Producer:
19940413
In:
American journal of human genetics
vol. 54
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126.
Marked zinc activation of ester hydrolysis by a mutation, 67-His (CAT) to Arg (CGT), in the active site of human carbonic anhydrase I.
[electronic resource]
by
Chegwidden, W R
Wagner, L E
Venta, P J
Bergenhem, N C
Yu, Y S
Tashian, R E
Producer:
19950329
In:
Human mutation
vol. 4
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127.
Red cells genetically deficient in carbonic anhydrase II have elevated levels of a carbonic anhydrase indistinguishable from muscle CA III.
[electronic resource]
by
Carter, N D
Heath, R
Welty, R J
Hewett-Emmett, D
Jeffery, S
Shiels, A
Tashian, R E
Producer:
19840813
In:
Annals of the New York Academy of Sciences
vol. 429
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128.
Evolutionarily conserved, "acatalytic" carbonic anhydrase-related protein XI contains a sequence motif present in the neuropeptide sauvagine: the human CA-RP XI gene (CA11) is embedded between the secretor gene cluster and the DBP gene at 19q13.3.
[electronic resource]
by
Lovejoy, D A
Hewett-Emmett, D
Porter, C A
Cepoi, D
Sheffield, A
Vale, W W
Tashian, R E
Producer:
19990223
In:
Genomics
vol. 54
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129.
Carbonic anhydrase isozymes in cultured Friend leukemic cells (39873).
[electronic resource]
by
Stern, R H
Boyer, S H
Conscience, J F
Friend, C
Margolet, L
Tashian, R E
Ruddle, F H
Producer:
19771130
In:
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)
vol. 156
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130.
A splice junction mutation in intron 2 of the carbonic anhydrase II gene of osteopetrosis patients from Arabic countries.
[electronic resource]
by
Hu, P Y
Roth, D E
Skaggs, L A
Venta, P J
Tashian, R E
Guibaud, P
Sly, W S
Producer:
19930610
In:
Human mutation
vol. 1
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131.
The catalytic properties of murine carbonic anhydrase VII.
[electronic resource]
by
Earnhardt, J N
Qian, M
Tu, C
Lakkis, M M
Bergenhem, N C
Laipis, P J
Tashian, R E
Silverman, D N
Producer:
19980821
In:
Biochemistry
vol. 37
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132.
Carbonic anhydrase II deficiency in 12 families with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.
[electronic resource]
by
Sly, W S
Whyte, M P
Sundaram, V
Tashian, R E
Hewett-Emmett, D
Guibaud, P
Vainsel, M
Baluarte, H J
Gruskin, A
Al-Mosawi, M
Producer:
19850801
In:
The New England journal of medicine
vol. 313
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