Shinya Yamamoto

Program in Developmental Biology, Baylor College of Medicine

Affiliated withBaylor College of Medicine Texas Children's Hospital

Research Area

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JoVE Journal Publications

ArticleTotal : 2	Year
Publication title Cited by 29	2019
Publication title Cited by 43	2019

Other Publications

Article	Year
Sequoia regulates cell fate decisions in the external sensory organs of adult Drosophila. EMBO reports\| PubMed ID: 19444309	2009
Endocytosis and intracellular trafficking of Notch and its ligands. Current topics in developmental biology\| PubMed ID: 20816395	2010
dEHBP1 controls exocytosis and recycling of Delta during asymmetric divisions. The Journal of cell biology\| PubMed ID: 22213802	2012
A mutation in EGF repeat-8 of Notch discriminates between Serrate/Jagged and Delta family ligands. Science (New York, N.Y.)\| PubMed ID: 23197537	2012
Crag is a GEF for Rab11 required for rhodopsin trafficking and maintenance of adult photoreceptor cells. PLoS biology\| PubMed ID: 23226104	2012
The C8ORF38 homologue Sicily is a cytosolic chaperone for a mitochondrial complex I subunit. The Journal of cell biology\| PubMed ID: 23509070	2013
Drosophila EHBP1 regulates Scabrous secretion during Notch-mediated lateral inhibition. Journal of cell science\| PubMed ID: 23788431	2013
Protein phosphatase 1ß limits ring canal constriction during Drosophila germline cyst formation. PloS one\| PubMed ID: 23936219	2013
Drosophila Tempura, a novel protein prenyltransferase α subunit, regulates notch signaling via Rab1 and Rab11. PLoS biology\| PubMed ID: 24492843	2014
Shared mechanisms between Drosophila peripheral nervous system development and human neurodegenerative diseases. Current opinion in neurobiology\| PubMed ID: 24762652	2014
Dopamine dynamics and signaling in Drosophila: an overview of genes, drugs and behavioral paradigms. Experimental animals\| PubMed ID: 24770636	2014
The retromer complex is required for rhodopsin recycling and its loss leads to photoreceptor degeneration. PLoS biology\| PubMed ID: 24781186	2014
Introduction to Notch signaling. Methods in molecular biology (Clifton, N.J.)\| PubMed ID: 25053477	2014
Large-scale identification of chemically induced mutations in Drosophila melanogaster. Genome research\| PubMed ID: 25258387	2014
A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases. Cell\| PubMed ID: 25259927	2014
Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production. eLife\| PubMed ID: 25313867	2014
Glial lipid droplets and ROS induced by mitochondrial defects promote neurodegeneration. Cell\| PubMed ID: 25594180	2015
Fruit flies in biomedical research. Genetics\| PubMed ID: 25624315	2015
A voltage-gated calcium channel regulates lysosomal fusion with endosomes and autophagosomes and is required for neuronal homeostasis. PLoS biology\| PubMed ID: 25811491	2015
Impaired Mitochondrial Energy Production Causes Light-Induced Photoreceptor Degeneration Independent of Oxidative Stress. PLoS biology\| PubMed ID: 26176594	2015
Morgan's legacy: fruit flies and the functional annotation of conserved genes. Cell\| PubMed ID: 26406362	2015
WAC Regulates mTOR Activity by Acting as an Adaptor for the TTT and Pontin/Reptin Complexes. Developmental cell\| PubMed ID: 26812014	2016
Ubr3, a Novel Modulator of Hh Signaling Affects the Degradation of Costal-2 and Kif7 through Poly-ubiquitination. PLoS genetics\| PubMed ID: 27195754	2016
Loss of Frataxin induces iron toxicity, sphingolipid synthesis, and Pdk1/Mef2 activation, leading to neurodegeneration. eLife\| PubMed ID: 27343351	2016
Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease. PLoS genetics\| PubMed ID: 27764101	2016
A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3. American journal of human genetics\| PubMed ID: 28017372	2017
Loss of Nardilysin, a Mitochondrial Co-chaperone for α-Ketoglutarate Dehydrogenase, Promotes mTORC1 Activation and Neurodegeneration. Neuron\| PubMed ID: 28017472	2017
MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome. American journal of human genetics\| PubMed ID: 28502612	2017
Neutral Competition for Drosophila Follicle and Cyst Stem Cell Niches Requires Vesicle Trafficking Genes. Genetics\| PubMed ID: 28512187	2017
Clinically severe CACNA1A alleles affect synaptic function and neurodegeneration differentially. PLoS genetics\| PubMed ID: 28742085	2017
Model Organisms Facilitate Rare Disease Diagnosis and Therapeutic Research. Genetics\| PubMed ID: 28874452	2017
Pleiotropic neuropathological and biochemical alterations associated with Myo5a mutation in a rat Model. Brain research\| PubMed ID: 29217155	2018
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder. American journal of human genetics\| PubMed ID: 29478781	2018
A gene-specific library for . eLife\| PubMed ID: 29565247	2018
Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder. Human molecular genetics\| PubMed ID: 29726930	2018
Integration of Drosophila and Human Genetics to Understand Notch Signaling Related Diseases. Advances in experimental medicine and biology\| PubMed ID: 30030826	2018
IRF2BPL Is Associated with Neurological Phenotypes. American journal of human genetics\| PubMed ID: 30057031	2018
Rapid and Integrative Discovery of Retina Regulatory Molecules. Cell reports\| PubMed ID: 30157441	2018
Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease. The New England journal of medicine\| PubMed ID: 30304647	2018
Unraveling Novel Mechanisms of Neurodegeneration Through a Large-Scale Forward Genetic Screen in . Frontiers in genetics\| PubMed ID: 30693015	2018
Unweaving the role of nuclear Lamins in neural circuit integrity. Cell stress\| PubMed ID: 31223139	2018
The fruit fly at the interface of diagnosis and pathogenic mechanisms of rare and common human diseases. Human molecular genetics\| PubMed ID: 31227826	2019
De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. American journal of human genetics\| PubMed ID: 31327508	2019