David P. Witte mainly focuses on Internal medicine, Endocrinology, Immunology, Pathology and Molecular biology. In his study, Eosinophilia and Cohort study is inextricably linked to Gastroenterology, which falls within the broad field of Internal medicine. His Endocrinology research is multidisciplinary, incorporating perspectives in Inclusion bodies, Ubiquitin, Lysosome and Null allele.
His Immunology research integrates issues from Andrology and Fibrinogen. His study in the fields of Biopsy and Soft tissue under the domain of Pathology overlaps with other disciplines such as Blind study and Rhabdomyosarcoma. His Molecular biology research includes themes of Homeobox, ROR1, Receptor tyrosine kinase and In situ hybridization.
The scientist’s investigation covers issues in Internal medicine, Molecular biology, Immunology, Endocrinology and Pathology. Many of his studies on Internal medicine apply to Gastroenterology as well. He has researched Molecular biology in several fields, including In situ hybridization, Gene expression, Northern blot and Biochemistry.
In his study, which falls under the umbrella issue of In situ hybridization, Cell culture is strongly linked to Cell biology. David P. Witte combines topics linked to Fibrinogen with his work on Immunology. His Endocrinology study combines topics from a wide range of disciplines, such as Glucocerebrosidase, Receptor and Spleen.
His primary scientific interests are in Internal medicine, Pathology, Immunology, Biopsy and Lupus nephritis. His studies in Internal medicine integrate themes in fields like Gastroenterology, Endocrinology and Oncology. His research integrates issues of Missense mutation and Compound heterozygosity in his study of Endocrinology.
The study of Pathology is intertwined with the study of Astrogliosis in a number of ways. His studies deal with areas such as Lung and Lymph as well as Immunology. His work deals with themes such as Biomarker, Systemic lupus erythematosus, Nephrology and Kidney, which intersect with Lupus nephritis.
His scientific interests lie mostly in Immunology, Biopsy, Pathology, Cancer research and Biomarker. His Immunology research integrates issues from Lung and Lymph. His Biopsy study incorporates themes from Immunohistochemistry, Exome sequencing, Urology, Renal function and Glioma.
Pathology is frequently linked to Astrogliosis in his study. The study incorporates disciplines such as Genotype-phenotype distinction, Haematopoiesis, Stem cell and Myelodysplastic syndromes in addition to Cancer research. His Biomarker study necessitates a more in-depth grasp of Internal medicine.
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.
ALK , the chromosome 2 gene locus altered by the t(2;5) in non-Hodgkin's lymphoma, encodes a novel neural receptor tyrosine kinase that is highly related to leukocyte tyrosine kinase (LTK)
Stephan W Morris;Clayton Naeve;Prasad Mathew;Payton L James.
Absence of radius and ulna in mice lacking hoxa-11 and hoxd-11
Allan Peter Davis;David P. Witte;Hsiu M. Hsieh-Li;S. Steven Potter.
Dissection of experimental asthma with DNA microarray analysis identifies arginase in asthma pathogenesis
Nives Zimmermann;Nina E. King;Johanne Laporte;Ming Yang.
Journal of Clinical Investigation (2003)
Mutation of an axonemal dynein affects left–right asymmetry in inversus viscerum mice
Dorothy M. Supp;David P. Witte;S. Steven Potter;Martina Brueckner.
Leukocyte engagement of fibrin(ogen) via the integrin receptor αMβ2/Mac-1 is critical for host inflammatory response in vivo
Matthew J. Flick;Xin Li Du;David P. Witte;Markéta Jiroušková.
Journal of Clinical Investigation (2004)
Hoxa 11 structure, extensive antisense transcription, and function in male and female fertility
H.M. Hsieh-Li;D.P. Witte;M. Weinstein;W. Branford.
Fatal embryonic bleeding events in mice lacking tissue factor, the cell-associated initiator of blood coagulation
Thomas H. Bugge;Qing Xiao;Keith W. Kombrinck;Matthew J. Flick.
Proceedings of the National Academy of Sciences of the United States of America (1996)
Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping.
H. J. Scrable;D. P. Witte;B. C. Lampkin;W. K. Cavenee.
Prothrombin deficiency results in embryonic and neonatal lethality in mice
William Y. Sun;David P. Witte;Jay L. Degen;Melissa C. Colbert.
Proceedings of the National Academy of Sciences of the United States of America (1998)
Targeted overexpression of IGF-I evokes distinct patterns of organ remodeling in smooth muscle cell tissue beds of transgenic mice.
Jianwei Wang;Wen Niu;Yuri Nikiforov;Shinji Naito.
Journal of Clinical Investigation (1997)
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