Hideki Enomoto spends much of his time researching Neurotrophic factors, Cell biology, Persephin, Neurturin and Glial cell line-derived neurotrophic factor. His Neurotrophic factors study incorporates themes from Endocrinology and Enteric nervous system. His work in Enteric nervous system addresses issues such as Immunology, which are connected to fields such as Cell division.
His work on Stem cell and Lamin as part of his general Cell biology study is frequently connected to Population and Nuclear matrix, thereby bridging the divide between different branches of science. Hideki Enomoto combines subjects such as Tyrosine kinase, Artemin and GDNF family of ligands with his study of Persephin. Hideki Enomoto is involved in the study of Glial cell line-derived neurotrophic factor that focuses on Proto-Oncogene Proteins c-ret in particular.
His primary scientific interests are in Cell biology, Neurotrophic factors, Enteric nervous system, Glial cell line-derived neurotrophic factor and Neural crest. His Cell biology course of study focuses on Nervous system and Apoptosis. The Neurotrophic factors study combines topics in areas such as Cell and Neurotrophin.
His research in Enteric nervous system intersects with topics in Cancer research, Tyrosine kinase, Neurogenesis, Programmed cell death and MAPK/ERK pathway. The various areas that Hideki Enomoto examines in his Glial cell line-derived neurotrophic factor study include Endocrinology, Signal transduction and Neuroscience. His study looks at the intersection of Neurturin and topics like Artemin with Persephin.
Hideki Enomoto mostly deals with Enteric nervous system, Neural crest, Cancer research, Neurotrophic factors and Cell biology. Hideki Enomoto works mostly in the field of Enteric nervous system, limiting it down to topics relating to Schwann cell and, in certain cases, Neurogenesis and Nervous system, as a part of the same area of interest. His Cancer research research incorporates themes from Phenotype, Gene, Mutant and Pathogenesis.
His study of Glial cell line-derived neurotrophic factor is a part of Neurotrophic factors. His Glial cell line-derived neurotrophic factor research integrates issues from Endocrinology, Signal transduction and Neurotrophin. His work on RHOA is typically connected to Confocal as part of general Cell biology study, connecting several disciplines of science.
His main research concerns Neural crest, Enteric nervous system, Schwann cell, Neurotrophic factors and Neuroscience. His Neural crest research is included under the broader classification of Cell biology. His study on Receptor tyrosine kinase is often connected to Hindgut, Crest and Vagus nerve as part of broader study in Cell biology.
The Glial cell line-derived neurotrophic factor research Hideki Enomoto does as part of his general Neurotrophic factors study is frequently linked to other disciplines of science, such as Hes3 signaling axis, therefore creating a link between diverse domains of science. His work deals with themes such as Neurotrophin, Trk receptor and Cell type, which intersect with Neuroscience. His biological study spans a wide range of topics, including Low-affinity nerve growth factor receptor and Gastrointestinal tract.
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A promoter-level mammalian expression atlas
Alistair R.R. Forrest;Hideya Kawaji;Michael Rehli;J. Kenneth Baillie.
Nature (2014)
Artemin, a Novel Member of the GDNF Ligand Family, Supports Peripheral and Central Neurons and Signals through the GFRα3–RET Receptor Complex
Robert H Baloh;Malú G Tansey;Patricia A Lampe;Timothy J Fahrner.
Neuron (1998)
The GDNF family ligands and receptors - implications for neural development.
Robert H Baloh;Hideki Enomoto;Eugene M Johnson;Jeffrey Milbrandt.
Current Opinion in Neurobiology (2000)
GFRα1-Deficient Mice Have Deficits in the Enteric Nervous System and Kidneys
Hideki Enomoto;Toshiyuki Araki;Alana Jackman;Robert O Heuckeroth.
Neuron (1998)
Gene Targeting Reveals a Critical Role for Neurturin in the Development and Maintenance of Enteric, Sensory, and Parasympathetic Neurons
Robert O Heuckeroth;Hideki Enomoto;John R Grider;Judith P Golden.
Neuron (1999)
RET signaling is essential for migration, axonal growth and axon guidance of developing sympathetic neurons
Hideki Enomoto;Peter A. Crawford;Alexander Gorodinsky;Robert O. Heuckeroth.
Development (2001)
A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3
White Ps;Maris Jm;Beltinger C;Sulman E.
Proceedings of the National Academy of Sciences of the United States of America (1995)
Complex formation between lamin A and the retinoblastoma gene product: identification of the domain on lamin A required for its interaction.
Ozaki T;Saijo M;Murakami K;Enomoto H.
Oncogene (1994)
Dynamics of neural crest-derived cell migration in the embryonic mouse gut.
H.M. Young;A.J. Bergner;R.B. Anderson;H. Enomoto.
Developmental Biology (2004)
GDNF availability determines enteric neuron number by controlling precursor proliferation
Scott Gianino;John R. Grider;Jennifer Cresswell;Hideki Enomoto.
Development (2003)
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