John Klingensmith mainly focuses on Cell biology, Segment polarity gene, Wnt signaling pathway, Genetics and Dishevelled. His Cell biology course of study focuses on Anatomy and Bone morphogenetic protein and Noggin. His work on Chordin as part of general Bone morphogenetic protein research is frequently linked to Prosencephalon, bridging the gap between disciplines.
Within one scientific family, he focuses on topics pertaining to Drosophila Protein under Segment polarity gene, and may sometimes address concerns connected to Imaginal disc, PORCN, Transmembrane protein and Peptide sequence. His studies deal with areas such as Phosphoprotein and engrailed as well as Dishevelled. His research integrates issues of Essential gene and Gene in his study of Signal transduction.
His primary scientific interests are in Cell biology, Genetics, Noggin, Bone morphogenetic protein and Anatomy. His Cell biology research includes themes of Endocrinology, Endoderm and Internal medicine. His work is connected to Segment polarity gene, Gene, engrailed, Wnt signaling pathway and Mutant, as a part of Genetics.
His Segment polarity gene research incorporates elements of Drosophila Protein, Dishevelled and Imaginal disc. His study in Bone morphogenetic protein is interdisciplinary in nature, drawing from both Neurulation, FGF8 and Neuroepithelial cell. He combines subjects such as Foregut morphogenesis, Notochord and Mesoderm with his study of Anatomy.
John Klingensmith mostly deals with Anatomy, Foregut morphogenesis, Esophagus, Foregut and Compartmentalization. His Anatomy research incorporates themes from Cranial neural crest, Pharyngeal arch, Neural crest, Noggin and Cell biology. The Cranial neural crest study combines topics in areas such as Chondrogenesis, Cartilage condensation, Cartilage, Sonic hedgehog and Ectoderm.
Noggin is a primary field of his research addressed under Bone morphogenetic protein. His Foregut morphogenesis study deals with the bigger picture of Endoderm. His Morphogenesis research includes elements of Process, Embryonic stem cell, Tracheoesophageal fistula and Lateral region.
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The organizer factors Chordin and Noggin are required for mouse forebrain development
Daniel Bachiller;John Klingensmith;C. Kemp;J. A. Belo.
The Drosophila segment polarity gene dishevelled encodes a novel protein required for response to the wingless signal.
J Klingensmith;R Nusse;N Perrimon.
Genes & Development (1994)
dishevelled and armadillo act in the Wingless signalling pathway in Drosophila
Jasprien Noordermeer;John Klingensmith;Norbert Perrimon;Roel Nusse.
The dishevelled protein is modified by wingless signaling in Drosophila.
Shin-Ichi Yanagawa;F. Van Leeuwen;A. Wodarz;J. Klingensmith.
Genes & Development (1995)
The segment polarity gene porcupine encodes a putative multitransmembrane protein involved in Wingless processing.
T Kadowaki;E Wilder;J Klingensmith;K Zachary.
Genes & Development (1996)
Mutations in the segment polarity genes wingless and porcupine impair secretion of the wingless protein.
M van den Heuvel;C Harryman-Samos;J Klingensmith;N Perrimon.
The EMBO Journal (1993)
Cordon-bleu is an actin nucleation factor and controls neuronal morphology.
Rashmi Ahuja;Rashmi Ahuja;Roser Pinyol;Roser Pinyol;Nicole Reichenbach;Nicole Reichenbach;Laura Custer.
Signaling by wingless in Drosophila
John Klingensmith;Roel Nusse.
Developmental Biology (1994)
Morphogenesis of the trachea and esophagus: current players and new roles for noggin and Bmps.
Jianwen Que;Murim Choi;Joshua W. Ziel;John Klingensmith.
Dorsalizing and neuralizing properties of Xdsh, a maternally expressed Xenopus homolog of dishevelled.
Sergei Y. Sokol;John Klingensmith;Norbert Perrimon;Keiji Itoh.
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