His study in Dna testing extends to Genetics with its themes. His research brings together the fields of Genetics and Dna testing. He integrates several fields in his works, including Fetus and Obstetrics. He integrates Obstetrics and Fetus in his studies. His German research extends to the thematically linked field of Archaeology. His research on German often connects related areas such as Archaeology. His work in Prenatal diagnosis is not limited to one particular discipline; it also encompasses Prenatal screening. His study connects Prenatal diagnosis and Prenatal screening. Peter E. Newburger integrates several fields in his works, including Pregnancy and Cell-free fetal DNA.
Amniocentesis, Cell-free fetal DNA and Prenatal screening are the main areas of his Prenatal diagnosis studies. Peter E. Newburger integrates Amniocentesis and Prenatal diagnosis in his research. Research on Complete remission and Granulocyte colony-stimulating factor is a part of his Chemotherapy study. In his works, Peter E. Newburger undertakes multidisciplinary study on Genetics and Cancer research. Peter E. Newburger integrates Cancer research with Genetics in his study. Gene and Fluorescence in situ hybridization are two areas of study in which Peter E. Newburger engages in interdisciplinary research. Pathology and Papilloma are frequently intertwined in his study. His Pathology research extends to the thematically linked field of Papilloma. His Internal medicine study frequently intersects with other fields, such as Discontinuation.
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.
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
Ewan Birney;John A. Stamatoyannopoulos;Anindya Dutta;Roderic Guigó.
A User's Guide to the Encyclopedia of DNA Elements (ENCODE)
Richard M. Myers;John Stamatoyannopoulos;Michael Snyder;Ian Dunham.
PLOS Biology (2011)
Cloning the gene for an inherited human disorder—chronic granulomatous disease—on the basis of its chromosomal location
B. Royerpokora;L. M. Kunkel;A. P. Monaco;S. C. Goff.
Cloning the gene for the inherited disorder chronic granulomatous disease on the basis of its chromosomal location.
B Royer-Pokora;L M Kunkel;A P Monaco;S C Goff.
Cold Spring Harbor Symposia on Quantitative Biology (1986)
Ribosomal Protein L5 and L11 Mutations Are Associated with Cleft Palate and Abnormal Thumbs in Diamond-Blackfan Anemia Patients
Hanna T. Gazda;Hanna T. Gazda;Mee Rie Sheen;Adrianna Vlachos;Adrianna Vlachos;Valerie Choesmel;Valerie Choesmel.
American Journal of Human Genetics (2008)
Role of toll-like receptor 2 (TLR2) in neutrophil activation: GM-CSF enhances TLR2 expression and TLR2-mediated interleukin 8 responses in neutrophils.
Evelyn A. Kurt-Jones;Leisa Mandell;Constance Whitney;Alison Padgett.
A myelopoiesis-associated regulatory intergenic noncoding RNA transcript within the human HOXA cluster
Xueqing Zhang;Zheng Lian;Carolyn Padden;Mark B. Gerstein.
Functional changes in human leukemic cell line HL-60. A model for myeloid differentiation.
PE Newburger;ME Chovaniec;JS Greenberger;HJ Cohen.
Journal of Cell Biology (1979)
Partial Correction of the Phagocyte Defect in Patients with X-Linked Chronic Granulomatous Disease by Subcutaneous Interferon Gamma
R A Ezekowitz;M C Dinauer;H S Jaffe;S H Orkin.
The New England Journal of Medicine (1988)
Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia
Leana Doherty;Mee Rie Sheen;Adrianna Vlachos;Adrianna Vlachos;Valerie Choesmel;Valerie Choesmel.
American Journal of Human Genetics (2010)
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: