S. C. Goff

发表

Beta-thalassemia due to two novel nucleotide substitutions in consensus acceptor splice sequences of the beta-globin gene.

S. Orkin, S. Antonarakis, D. Nathan, 1989, Blood.

Molecular cloning of human adenosine deaminase gene sequences.

G. Bruns, P. Daddona, A. Markham, 1983, The Journal of biological chemistry.

Abnormal RNA processing due to the exon mutation of beta E-globin gene.

H. Ostrer, S. Orkin, S. Antonarakis, 1982, Nature.

Cloning the gene for the inherited disorder chronic granulomatous disease on the basis of its chromosomal location.

A. Monaco, L. Kunkel, S. Orkin, 1986, Cold Spring Harbor symposia on quantitative biology.

Mutation in an intervening sequence splice junction in man.

S. Orkin, S. C. Goff, R. Hechtman, 1981, Proceedings of the National Academy of Sciences of the United States of America.

Production of mouse globin in heterokaryons of mouse erythroleukaemia cells and human fibroblasts.

A. Deisseroth, B. Alter, B. Forget, 1977, Journal of cell science.

Heterogeneity of DNA deletion in gamma delta beta-thalassemia.

S. Orkin, D. Nathan, S. C. Goff, 1981, The Journal of clinical investigation.

On the origin and spread of beta-thalassemia: recurrent observation of four mutations in different ethnic groups.

S. Orkin, S. Antonarakis, C. Boehm, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Nonsense and frameshift mutations in beta 0-thalassemia detected in cloned beta-globin genes.

S. Orkin, S. C. Goff, 1981, The Journal of biological chemistry.

Evidence for multiple origins of the beta E-globin gene in Southeast Asia.

H. Ostrer, A. Chakravarti, S. Orkin, 1982, Proceedings of the National Academy of Sciences of the United States of America.

Transient expression of human adenosine deaminase cDNAs: identification of a nonfunctional clone resulting from a single amino acid substitution

P. Daddona, W. N. Kelley, S. C. Goff, 1985, Molecular and cellular biology.

A murine model for the switch from fetal to adult hemoglobin during ontogeny.

B. Alter, S. C. Goff, S. Goff, 1980, Blood.

Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster

S. Orkin, S. Antonarakis, H. Kazazian, 1982, Nature.

Variable globin chain synthesis in mouse erythroleukemia cells.

B. Alter, S. C. Goff, 1978, Blood.

Globin Chain Electrophoresis: a New Approach to the Determination of the Gγ/Aγ Ratio in Fetal Haemoglobin and to Studies of Globin Synthesis

B. Alter, S. C. Goff, G. Efremov, 1980 .

Abnormal RNA processing due to the exon mutation of βE-globin gene

Stylianos E. Antonarakis, Stuart H. Orkin, Haig H. Kazazian, 1982, Nature.

Globin synthesis in mouse erythroleukemia cells in vitro: a switch in beta chains due to inducing agent.

B. Alter, S. C. Goff, 1977, Blood.

Molecular characterization of seven beta‐thalassemia mutations in Asian Indians.

S. Orkin, S. Antonarakis, P. Waber, 1984, The EMBO journal.

ATA box transcription mutation in β-thalassemia

S. Orkin, P. Giardina, S. C. Goff, 1983 .

The duplicated human α-globin genes: Their relative expression as measured by RNA analysis

S. Orkin, S. C. Goff, 1981, Cell.

Cloning the gene for an inherited human disorder—chronic granulomatous disease—on the basis of its chromosomal location

A. Monaco, L. Kunkel, S. Orkin, 1986, Nature.

Electrophoretic separation of human embryonic globin demonstrates "alpha-thalassemia" in human leukemia cell line K562.

B. Alter, S. C. Goff, 1980, Biochemical and biophysical research communications.

Chemical evidence for the separation of G gamma and A gamma globin chains by polyacrylamide gel electrophoresis in urea and Triton X-100.

B. Alter, S. C. Goff, T. J. Klonowski, 1981, Preparative biochemistry.

Hemoglobin switching: a cellular model.

B. Alter, S. C. Goff, 1980, Science.

Globin chain electrophoresis: a new approach to the determination of the G gamma/A gamma ratio in fetal haemoglobin and to studies of globin synthesis.

B. Alter, S. C. Goff, G. Efremov, 1980, British journal of haematology.

Characterization of a spontaneous mutation to a beta-thalassemia allele.

S. Orkin, P. Newburger, C. Boehm, 1986, American journal of human genetics.

Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster.

S. Orkin, S. Antonarakis, P. Waber, 1982, Nature.

Purification of the human NF-E2 complex: cDNA cloning of the hematopoietic cell-specific subunit and evidence for an associated partner

S. Orkin, N. Andrews, S. Weremowicz, 1993, Molecular and cellular biology.

Arrested development of embryonic red cell precursors in mouse embryos lacking transcription factor GATA-1.

Y Fujiwara, S. Orkin, Y. Fujiwara, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Inactivation of an acceptor RNA splice site by a short deletion in beta-thalassemia.

S. Orkin, H. Kazazian, H. Kazazian, 1983, The Journal of biological chemistry.

ATA box transcription mutation in beta-thalassemia.

S. Orkin, H. Kazazian, P. Giardina, 1983, Nucleic acids research.

The duplicated human alpha-globin genes: their relative expression as measured by RNA analysis.

S. Orkin, S. C. Goff, 1981, Cell.