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1. |
β-Chain Variants in Jamaican Newborns |
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Hemoglobin,
Volume 2,
Issue 6,
1978,
Page 495-502
AhernE.,
AhernV.,
SerjeantG. R.,
SerjeantB. E.,
SeakinsM.,
DarbreP.,
MiddletonA.,
LehmannH.,
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摘要:
In an electrophoretic study of 15,661 Jamaican cord bloods, 8 rareβ-chain variants were found in 18 subjects in addition to the commonβ-chain variants, Hb S and Hb C. The heterozygote frequencies for Hb S and Hb C were 10.1% and 3.7% respectively. The most frequent of the rareβ-chain variants were Hb Korle Bu (β73 Asp→Asn) (7 cases) and Hb Osu-Christiansborg (β52 Asp→Asn) (3 cases). One new B-chain variant, Hb Caribbean (8 91 Leu→Arg) was found.
ISSN:0363-0269
DOI:10.3109/03630267809005351
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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2. |
Synthesis of Fetal and Adult Hemoglobins in Culture by Human Umbilical Cord Blood Erythropoietic Precursors |
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Hemoglobin,
Volume 2,
Issue 6,
1978,
Page 503-512
KidoguchiK.,
OgawaM.,
KaramJ. D.,
WilsonJ. M.,
FitchM. S.,
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摘要:
We cultured human umbilical cord blood and adult peripheral blood erythropoietic precursors in methylcellulose clonal assay and measured the synthetic rates of HbA, A2, and F. Hb was labeled with14C-amino acid in culture and separated by slab-gel isoelectric focusing and quantitated by autoradiography. While the mean percentage of HbF synthesized by adult cells was only 20.1%, that of umbilical cord blood cells was 53.9%, which corresponds closely to the biosynthetic capabilities of umbilical cord blood reticulocytes. Variations in the erythropoietin concentrations did not influence the percentage of HbF. Erythropoietic cell cultures of human umbilical cord blood may provide an important means for studying the molecular mechanisms controlling physiological Hb switching in the perinatal period.
ISSN:0363-0269
DOI:10.3109/03630267809005352
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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3. |
δβ-Thalassemia in a Mexican Family: Clinical Differences Among Homozygotes |
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Hemoglobin,
Volume 2,
Issue 6,
1978,
Page 513-529
ReyesGuillermo Ruiz,
PiñaArturo,
FeliceA. E.,
GravelyM. E.,
HuismanT. H. J.,
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摘要:
Three→β-thalassemia homozygotes were found in a Mexican family. Both parents and two siblings had heterozygous 63-thalassemia with about 10% Hb F, mild microcytosis and mild hypochromia, while three siblings were normal. Hb F, which was the only Hb component in the homozygotes, had equal quantities of Gγand Aγchains as in GγAγ-→β-thalassemia. The homozygotes had comparable erythrocytic indices which were about the same as those of the heterozygotes. However, two were clinically and hematologically healthy but the third had a severe chronic hemolytic anemia and a more severein vitrochain synthesis imbalance than her homozygous sisters. Comparison of these cases with other GγAγ63-thalassemia homozygotes and with GγAγHPFH homozygotes indicates the possibility that the proliferation of F-cell precursors may be defective in→β-thalassemia.
ISSN:0363-0269
DOI:10.3109/03630267809005353
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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4. |
Hemoglobins AIDA (α64 ASP→ASN) and D-Los Angeles (β121 Glu→Glu) in an Asian-Indian Family |
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Hemoglobin,
Volume 2,
Issue 6,
1978,
Page 531-540
BunnH. F.,
AltmanA. J.,
StanglandK.,
FirsheinS. I.,
ForgetB.,
SchmidtG. J.,
JonesR. T.,
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摘要:
Hemoglobins D-Los Angeles (β121 Gin) and Aida (α64 Asn) were encountered in an Asian Indian, unassociated with any clinical manifestations. These hemoglobins had normal oxygen affinities and were stable to heat and isopropanol. The ratio ofαchain synthesis toβchain synthesis was close to unity. The identical change in isoelectric points of the two variants produced an interesting electrophoretic pattern.The coexistance of more than one hemoglobin variant in an individual or family has provided valuable
ISSN:0363-0269
DOI:10.3109/03630267809005354
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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5. |
Hemoglobin Hofu orαβ[126 (H4) Val→Glu] Found in Combination with Hemoglobin S |
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Hemoglobin,
Volume 2,
Issue 6,
1978,
Page 541-549
BrittenhamG.,
LozoffB.,
HarrisJ. W.,
NayuduN. V. S.,
GravelyM.,
WilsonJ. B.,
LamH.,
HuismanT. H. J.,
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摘要:
Hb Hofu,αβ[126 (H4) Val→Glu], was found in 10 members of 2 apparently unrelated Valmiki families in central India. None showed evidence of hemolysis and hemoglobin levels were normal in most. In two individuals, Hb Hofu occurred in combination with Hb S, but neither had clinical manifestations of sickle cell disease. In samples containing Hb Hofu, the isopropanol precipitation test was positive. Quantitation of the hemoglobin fractions by DEAE-cellulose chromatography showed that Hb Hofu constituted a mean of 23-25% of the total whether in combination with Hb A or Hb S.
ISSN:0363-0269
DOI:10.3109/03630267809005355
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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6. |
Another Case of Hemoglobin M Iwate in a Japanese Family |
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Hemoglobin,
Volume 2,
Issue 6,
1978,
Page 551-555
ShihT. B.,
ImaiK.,
TyumaI.,
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ISSN:0363-0269
DOI:10.3109/03630267809005356
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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7. |
A Second Patient with Hemoglobin Alberta, a High-Oxygen-Affinity Variant Causing Erythrocytosis and Forming Asymmetric Tetramers |
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Hemoglobin,
Volume 2,
Issue 6,
1978,
Page 557-559
WongS. C.,
AliM. A. R.,
NicholsonW.,
WilsonJ. B.,
LamH.,
HuismanT. N. J.,
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PDF (130KB)
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ISSN:0363-0269
DOI:10.3109/03630267809005357
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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8. |
HB UBE-4 (α116 Glu→Ala): A Second Independent Instance Found in a Korean Family of Japan |
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Hemoglobin,
Volume 2,
Issue 6,
1978,
Page 561-563
IuchiI.,
HidakaK.,
UedaS.,
ShibataS.,
HitomiF.,
TakesueA.,
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ISSN:0363-0269
DOI:10.3109/03630267809005358
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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9. |
International Hemoglobin Information Center Policies Ihic |
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Hemoglobin,
Volume 2,
Issue 6,
1978,
Page 565-566
BlackwellR. Q.,
BunnH. F.,
HellerP.,
HuismanT. H. J.,
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PDF (71KB)
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ISSN:0363-0269
DOI:10.3109/03630267809005359
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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10. |
Variant Lists |
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Hemoglobin,
Volume 2,
Issue 6,
1978,
Page 567-598
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PDF (1076KB)
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ISSN:0363-0269
DOI:10.3109/03630267809005360
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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