2006 - Fellow of John Simon Guggenheim Memorial Foundation
As part of her studies on Genetics, Jane Gitschier often connects relevant areas like Thalassemia. Her study brings together the fields of Genetics and Thalassemia. In her papers, she integrates diverse fields, such as Gene and Duchenne muscular dystrophy. She performs integrative Duchenne muscular dystrophy and Gene research in her work. Her research is interdisciplinary, bridging the disciplines of Pathology and Neurodegeneration. She combines Pathology and Disease in her studies. Her Disease study frequently involves adjacent topics like Parkinsonism. In her articles, she combines various disciplines, including Parkinsonism and Neurodegeneration. Her research brings together the fields of Radiology and Hyperintensity.
Much of her study explores Genetics relationship to Transporter. Jane Gitschier integrates Gene and Polymerase chain reaction in her studies. Jane Gitschier performs integrative Polymerase chain reaction and Molecular biology research in her work. In her study, she carries out multidisciplinary Molecular biology and Gel electrophoresis research. While working in this field, Jane Gitschier studies both Gel electrophoresis and Temperature gradient gel electrophoresis. Mutation and Missense mutation are two areas of study in which Jane Gitschier engages in interdisciplinary work. She combines Factor IX and Haemophilia A in her studies. In her research, Jane Gitschier performs multidisciplinary study on Haemophilia A and Haemophilia. She conducted interdisciplinary study in her works that combined Haemophilia and Haemophilia B.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase.
Christopher Vulpe;Barbara Levinson;Barbara Levinson;Susan Whitney;Seymour Packman.
Nature Genetics (1993)
Characterization of the human factor VIII gene
Jane Gitschier;William I. Wood;Therese M. Goralka;Karen L. Wion.
Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse.
Christopher D. Vulpe;Yien-Ming Kuo;Therese L. Murphy;Lex Cowley.
Nature Genetics (1999)
Base composition-independent hybridization in tetramethylammonium chloride: a method for oligonucleotide screening of highly complex gene libraries.
William I. Wood;Jane Gitschier;Laurence A. Lasky;Richard M. Lawn.
Proceedings of the National Academy of Sciences of the United States of America (1985)
An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.
Scott C. Kogan;Marie Doherty;Jane Gitschier.
The New England Journal of Medicine (1987)
Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A.
Delia Lakich;Haig H. Kazazian;Stylianos E. Antonarakis;Stylianos E. Antonarakis;Jane Gitschier.
Nature Genetics (1993)
Expression of active human factor VIII from recombinant DNA clones
William I. Wood;Daniel J. Capon;Christian C. Simonsen;Dan L. Eaton.
A novel pantothenate kinase gene ( PANK2 ) is defective in Hallervorden-Spatz syndrome
Bing Zhou;Shawn K. Westaway;Barbara Levinson;Monique A. Johnson.
Nature Genetics (2001)
Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.
Susan J. Hayflick;Shawn K. Westaway;Barbara Levinson;Bing Zhou.
The New England Journal of Medicine (2003)
hCTR1: A human gene for copper uptake identified by complementation in yeast
Bing Zhou;Jane Gitschier.
Proceedings of the National Academy of Sciences of the United States of America (1997)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: