Y. Kan

发表

Butyrate infusions in the ovine fetus delay the biologic clock for globin gene switching.

S. J. Chen, Y. Kan, D. Faller, 1988, Proceedings of the National Academy of Sciences of the United States of America.

In vivo protein-DNA interactions at the beta-globin gene locus.

T. Ikuta, Y. Kan, 1991, Proceedings of the National Academy of Sciences of the United States of America.

SPONTANEOUS MUTATION IN β-THALASSAEMIA PRODUCING THE SAME NUCLEOTIDE SUBSTITUTION AS THAT IN A COMMON HEREDITARY FORM

F. Chehab, Y. Kan, G. Honig, 1986, The Lancet.

Detection of specific DNA sequences by fluorescence amplification: a color complementation assay.

F. Chehab, Y. Kan, Yuet Wai Kan, 1989, Proceedings of the National Academy of Sciences of the United States of America.

A SIMPLE SENSITIVE PRENATAL TEST FOR HYDROPS FETALIS CAUSED BY α-THALASSAEMIA

Y. Kan, E. Rubin, 1985, The Lancet.

ANTENATAL DIAGNOSIS OF SICKLE CELL ANAEMIA BY DIRECT ANALYSIS OF THE SICKLE MUTATION

Y. Kan, Judy C. Chang, 1981, The Lancet.

Identification of the multiple beta-thalassemia mutations by denaturing gradient gel electrophoresis.

S. Cai, Y. Kan, 1990, The Journal of clinical investigation.

[14] Amplification and detection of specific DNA sequences with fluorescent PCR primers: Application to ΔF508 mutation in cystic fibrosis

J. Wall, F. Chehab, Y. Kan, 1992 .

Introduction and expression of the human Bs-globin gene in transgenic mice.

E. Rubin, N. Mohandas, Y. Kan, 1988, American journal of human genetics.

Effect of Human #5-Globin Chains on Cellular Properties of Red Cells from #l-Thalassemic Mice

E. Rubin, N. Mohandas, Y. Kan, 1988 .

Detection of cytomegalovirus infection in paraffin-embedded tissue specimens with the polymerase chain reaction.

F. Chehab, T. Yen, Y. Kan, 1989, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Detection of sickle cell anaemia mutation by colour DNA amplification

F. Chehab, Y. Kan, 1990, The Lancet.

Deletion of the β-globin structure gene in hereditary persistence of foetal haemoglobin

S. Charache, H. Kazazian, A. Dozy, 1975, Nature.

α-Globin gene organisation in blacks precludes the severe form of α-thalassaemia

Y. Kan, S. Embury, A. Dozy, 1979, Nature.

Inhibition of fetal globin gene switching in vivo in human and ovine fetuses.

D. Faller, S. Perrine, M. Greene, 1987, Progress in clinical and biological research.

Alterations in protein-DNA interactions in the gamma-globin gene promoter in response to butyrate therapy.

D. Faller, P. Swerdlow, T. Ikuta, 1998, Blood.

Beta-thalassemia mutations in Indonesia and their linkage to beta haplotypes.

M. Lim, S. Cai, Y. Kan, 1989, American journal of human genetics.

A new TATA box mutation detected at prenatal diagnosis for beta-thalassemia.

S. Cai, J. Z. Zhang, Y. Kan, 1989, American journal of human genetics.

Butyric acid modulates developmental globin gene switching in man and sheep.

D. Faller, P. Swerdlow, S. Perrine, 1989, Advances in experimental medicine and biology.

Inactivation of mouse alpha-globin gene by homologous recombination: mouse model of hemoglobin H disease.

R. Pedersen, Y. Kan, J. Meneses, 1996, Blood.

UNBALANCED GLOBIN CHAIN SYNTHESIS IN ALPHA‐THALASSEMIA HETEROZYGOTES *

Y. Kan, E. Schwartz, D. Nathan, 1969, Annals of the New York Academy of Sciences.

Identification of the Multiple ,B-Thalassemia Mutations by Denaturing Gradient Gel Electrophoresis

S. Cai, Y. Kan, 2013 .

Rapid Effect of Human #5-Globin Chains on Cellular Properties of Red Cells from #l-Thalassemic Mice

N. Mohandas, Y. Kan, E. Rubin, 2022 .

Effect of human beta (s)-globin chains on cellular properties of red cells from beta-thalassemic mice.

E. Rubin, N. Mohandas, Y. Kan, 1988, Journal of Clinical Investigation.

The use of direct gene analysis to define beta-thalassemia.

F. Chehab, S. Cai, A. Dozy, 1990, Annals of the New York Academy of Sciences.