Hamid Band mostly deals with Cell biology, Molecular biology, Tyrosine kinase, Cancer research and Receptor tyrosine kinase. His Cell biology study frequently draws connections to adjacent fields such as Ubiquitin ligase. His work deals with themes such as Amino acid, Tyrosine, Ubiquitin, Mutant and SH3 domain, which intersect with Molecular biology.
His studies deal with areas such as Binding site, Proto-oncogene tyrosine-protein kinase Src and Proto-Oncogene Proteins c-cbl as well as Tyrosine kinase. His Cancer research research is multidisciplinary, incorporating perspectives in Gene silencing, PI3K/AKT/mTOR pathway, PTEN and Downregulation and upregulation. His studies in Receptor tyrosine kinase integrate themes in fields like ROR1 and Platelet-derived growth factor receptor.
Hamid Band mainly investigates Cell biology, Molecular biology, Cancer research, Tyrosine kinase and Receptor tyrosine kinase. His study in Cell biology is interdisciplinary in nature, drawing from both Ubiquitin and Endocytic recycling. The Molecular biology study combines topics in areas such as DNA damage, Coactivator, Receptor, T-cell receptor and SH3 domain.
His biological study spans a wide range of topics, including Epithelial–mesenchymal transition, Carcinogenesis, Cancer, Breast cancer and Cell growth. His Tyrosine kinase study incorporates themes from Tyrosine, Tyrosine phosphorylation and RING finger domain. The concepts of his Receptor tyrosine kinase study are interwoven with issues in ROR1, Platelet-derived growth factor receptor, Epidermal growth factor and Protein tyrosine phosphatase.
His main research concerns Cell biology, Cancer research, Cell cycle, Carcinogenesis and Breast cancer. His Cell biology research is multidisciplinary, relying on both Endocytic cycle, Endocytic recycling and Ubiquitin. He combines subjects such as STUB1 and Ubiquitin ligase with his study of Cancer research.
His research in Breast cancer intersects with topics in Stromal cell, Mesenchymal stem cell, Pathology, Lysyl oxidase and Primary tumor. His study explores the link between Tyrosine kinase and topics such as Receptor tyrosine kinase that cross with problems in Epidermal growth factor. The Cell signaling study which covers Proto-oncogene tyrosine-protein kinase Src that intersects with Epidermal growth factor receptor.
Cell biology, Breast cancer, Endocytic recycling, Cancer and Carcinogenesis are his primary areas of study. His Cell biology research incorporates themes from Endocytic cycle and Skeletal muscle. The study incorporates disciplines such as Stromal cell, Cancer research, Lysyl oxidase, Mesenchymal stem cell and Tissue microarray in addition to Breast cancer.
He has included themes like Cilium and Morphogenesis in his Endocytic recycling study. Cancer cell is closely connected to Primary tumor in his research, which is encompassed under the umbrella topic of Carcinogenesis. His Tyrosine kinase study combines topics from a wide range of disciplines, such as Cell signaling, Receptor tyrosine kinase, Proto-oncogene tyrosine-protein kinase Src and Epidermal growth factor receptor.
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.
Direct presentation of nonpeptide prenyl pyrophosphate antigens to human γδ T cells
Craig T. Morita;Evan M. Beckman;Jack F. Bukowski;Yoshimasa Tanaka.
Immunity (1995)
Mutation of the c-Cbl TKB Domain Binding Site on the Met Receptor Tyrosine Kinase Converts It into a Transforming Protein
Pascal Peschard;Tanya M Fournier;Louie Lamorte;Monica A Naujokas.
Molecular Cell (2001)
The polycomb group protein Bmi-1 represses the tumor suppressor PTEN and induces epithelial-mesenchymal transition in human nasopharyngeal epithelial cells
Li Bing Song;Jun Li;Wen Ting Liao;Yan Feng.
Journal of Clinical Investigation (2009)
Histological, molecular and functional subtypes of breast cancers
Gautam K. Malhotra;Xiangshan Zhao;Hamid Band;Vimla Band.
Cancer Biology & Therapy (2010)
Regulation of CXCR4-mediated chemotaxis and chemoinvasion of breast cancer cells
Aaron Zefrin Fernandis;Anil Prasad;Hamid Band;Roland Klösel.
Oncogene (2004)
The tyrosine kinase regulator Cbl enhances the ubiquitination and degradation of the platelet-derived growth factor receptor α
Sachiko Miyake;Mark L. Lupher;Brian Druker;Hamid Band.
Proceedings of the National Academy of Sciences of the United States of America (1998)
Cbl-mediated Ubiquitinylation Is Required for Lysosomal Sorting of Epidermal Growth Factor Receptor but Is Dispensable for Endocytosis
Lei Duan;Yuko Miura;Manjari Dimri;Biswanath Majumder.
Journal of Biological Chemistry (2003)
Biology of the Human γ T‐Cell Receptor
Steven Porcelli;Michael B. Brenner;Hamid Band.
Immunological Reviews (1991)
The Cbl Phosphotyrosine-binding Domain Selects a D(N/D)XpY Motif and Binds to the Tyr292Negative Regulatory Phosphorylation Site of ZAP-70
Mark L. Lupher;Zhou Songyang;Steven E. Shoelson;Lewis C. Cantley.
Journal of Biological Chemistry (1997)
Tyrosine Phosphorylation of Cbl upon Epidermal Growth Factor (EGF) Stimulation and Its Association with EGF Receptor and Downstream Signaling Proteins
Toru Fukazawa;Sachiko Miyake;Vimla Band;Hamid Band.
Journal of Biological Chemistry (1996)
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