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Items: 19

1.
Endothelial cell expression of hemoglobin a regulates nitric oxide signaling
Adam C. Straub, Alexander W. Lohman, Marie Billaud, Scott R. Johnstone, Scott T. Dwyer, Monica Y. Lee, Pamela Schoppee Bortz, Angela K. Best, Linda Columbus, Benjamin Gaston, Brant E. Isakson
Nature. Author manuscript; available in PMC 2013 May 15.
Published in final edited form as: Nature. 2012 Nov 15; 491(7424): 473–477. Published online 2012 Oct 31. doi: 10.1038/nature11626
PMCID:
PMC3531883
ArticlePDF–1.5M
2.
Four Haemoglobins in One Individual
A. B. Raper, D. B. Gammack, E. R. Huehns, E. M. Shooter
Br Med J. 1960 Oct 29; 2(5208): 1257-1260, 1260-2-1261. doi: 10.1136/bmj.2.5208.1257
PMCID:
PMC2097059
SummaryPage BrowsePDF–1.6M
3.
Stanleyville I and II
Paulette Dherte, J. Vandepitte, J. A. M. Ager, H. Lehmann
Br Med J. 1959 Aug 29; 2(5147): 282–284. doi: 10.1136/bmj.2.5147.282
PMCID:
PMC1990126
SummaryPage BrowsePDF–1.0M
4.
Hemoglobin Koya Dora: high frequency of a chain termination mutant.
W W De Jong, P Meera Khan, L F Bernini
Am J Hum Genet. 1975 Jan; 27(1): 81–90.
PMCID:
PMC1762765
SummaryPage BrowsePDF–978K
5.
Hemoglobin sealy (alpha 2-47His-beta 2): a new variant in a Jewish family.
R G Schneider, S Ueda, J B Alperin, B Brimhall, R T Jones
Am J Hum Genet. 1968 Mar; 20(2): 151–156.
PMCID:
PMC1706261
SummaryPage BrowsePDF–756K
6.
Development of a somatic mutation screening system using Hb mutants. IV. Successful detection of red cells containing the human frameshift mutants Hb Wayne and Hb Cranston using monospecific fluorescent antibodies.
G Stamatoyannopoulos, P E Nute, T Papayannopoulou, T McGuire, G Lim, H F Bunn, D Rucknagel
Am J Hum Genet. 1980 Jul; 32(4): 484–496.
PMCID:
PMC1686139
SummaryPage BrowsePDF–1.4M
7.
The occurrence of the alpha G-Philadelphia-globin allele on a double-locus chromosome.
C J Bruzdzinski, K L Sisco, S J Ferrucci, D L Rucknagel
Am J Hum Genet. 1984 Jan; 36(1): 101–109.
PMCID:
PMC1684377
SummaryPage BrowsePDF–925K
8.
Alpha-thalassaemia caused by a poly(A) site mutation reveals that transcriptional termination is linked to 3' end processing in the human alpha 2 globin gene.
E Whitelaw, N Proudfoot
EMBO J. 1986 Nov; 5(11): 2915–2922. doi: 10.1002/j.1460-2075.1986.tb04587.x
PMCID:
PMC1167242
SummaryPage BrowsePDF–1.9M
9.
Molecular basis for nondeletion alpha-thalassemia in American blacks. Alpha 2(116GAG----UAG).
S A Liebhaber, M B Coleman, J G Adams, 3rd, F E Cash, M H Steinberg
J Clin Invest. 1987 Jul; 80(1): 154–159. doi: 10.1172/JCI113041
PMCID:
PMC442213
SummaryPage BrowsePDF–1.5M
10.
Hematologic and biosynthetic studies in homozygous hemoglobin Constant Spring.
S Derry, W G Wood, M Pippard, J B Clegg, D J Weatherall, S N Wickramasinghe, J Darley, S Fucharoen, P Wasi
J Clin Invest. 1984 Jun; 73(6): 1673–1682. doi: 10.1172/JCI111374
PMCID:
PMC437078
SummaryPage BrowsePDF–1.7M
11.
Trimodality in the proportion of hemoglobin G Philadelphia in heterozygotes: evidence for heterogeneity in the number of human alpha chain loci.
R M Baine, D L Rucknagel, P A Dublin, Jr, J G Adams, 3rd
Proc Natl Acad Sci U S A. 1976 Oct; 73(10): 3633–3636. doi: 10.1073/pnas.73.10.3633
PMCID:
PMC431172
SummaryPage BrowsePDF–833K
12.
Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.
D K Bowden, A V Hill, D R Higgs, S J Oppenheimer, D J Weatherall, J B Clegg
J Clin Invest. 1987 Jan; 79(1): 39–43. doi: 10.1172/JCI112804
PMCID:
PMC423981
SummaryPage BrowsePDF–1.0M
13.
Locus assignment of alpha-globin structural mutations by hybrid-selected translation.
S A Liebhaber, F E Cash
J Clin Invest. 1985 Jan; 75(1): 64–70. doi: 10.1172/JCI111698
PMCID:
PMC423400
SummaryPage BrowsePDF–1.5M
14.
Proportion of hemoglobin G Philadelphia (alpha 268 Asn leads to Lys beta 2) in heterozygotes is determined by alpha-globin gene deletions.
G B Sancar, B Tatsis, M M Cedeno, R F Rieder
Proc Natl Acad Sci U S A. 1980 Nov; 77(11): 6874–6878. doi: 10.1073/pnas.77.11.6874
PMCID:
PMC350393
SummaryPage BrowsePDF–1.1M
15.
Linkage of alpha G-Philadelphia to alpha-thalassemia in African-Americans .
S Surrey, K Ohene-Frempong, E Rappaport, J Atwater, E Schwartz
Proc Natl Acad Sci U S A. 1980 Aug; 77(8): 4885–4889. doi: 10.1073/pnas.77.8.4885
PMCID:
PMC349953
SummaryPage BrowsePDF–1.0M
16.
Hemoglobin Wayne: a frameshift mutation detected in human hemoglobin alpha chains.
M Seid-Akhavan, W P Winter, R K Abramson, D L Rucknagel
Proc Natl Acad Sci U S A. 1976 Mar; 73(3): 882–886. doi: 10.1073/pnas.73.3.882
PMCID:
PMC336023
SummaryPage BrowsePDF–1.0M
17.
Hemoglobin Hasharon (α247 his(CD5)β2): a hemoglobin found in low concentration
S. Charache, A. M. Mondzac, U. Gessner
J Clin Invest. 1969 May; 48(5): 834–847. doi: 10.1172/JCI106041
PMCID:
PMC322291
SummaryPage BrowsePDF–2.3M
18.
Mutation in an intervening sequence splice junction in man.
S H Orkin, S C Goff, R L Hechtman
Proc Natl Acad Sci U S A. 1981 Aug; 78(8): 5041–5045. doi: 10.1073/pnas.78.8.5041
PMCID:
PMC320328
SummaryPage BrowsePDF–1.3M
19.
Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies
George P. Patrinos, Belinda Giardine, Cathy Riemer, Webb Miller, David H. K. Chui, Nicholas P. Anagnou, Henri Wajcman, Ross C. Hardison
Nucleic Acids Res. 2004 Jan 1; 32(Database issue): D537–D541. doi: 10.1093/nar/gkh006
PMCID:
PMC308741
AbstractArticlePDF–300K

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