about
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formationThree-Dimensional Structure of Vertebrate Muscle Z-Band: The Small-Square Lattice Z-Band in Rat Cardiac Muscle.Mutations in REEP6 Cause Autosomal-Recessive Retinitis PigmentosaEndothelial MAPKs Direct ICAM-1 Signaling to Divergent Inflammatory Functions.Probing the Heterogeneity of Protein Kinase Activation in Cells by Super-resolution MicroscopyTargeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects.Generation of a three-dimensional ultrastructural model of human respiratory cilia.Characterizing the ultrastructure of primary ciliary dyskinesia transposition defect using electron tomography.Rod disc renewal occurs by evagination of the ciliary plasma membrane that makes cadherin-based contacts with the inner segment.Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry.Methamphetamine-induced nitric oxide promotes vesicular transport in blood-brain barrier endothelial cells.The relationship between ER-multivesicular body membrane contacts and the ESCRT machinery.Calcium signaling at ER membrane contact sites.REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking.WASH and Tsg101/ALIX-dependent diversion of stress-internalized EGFR from the canonical endocytic pathway.Regulation of melanosome number, shape and movement in the zebrafish retinal pigment epithelium by OA1 and PMEL.Differential apicobasal VEGF signaling at vascular blood-neural barriers.New light on photoreceptor renewal.Retinal Pigment Epithelial Cells Mitigate the Effects of Complement Attack by Endocytosis of C5b-9.Expression of OA1 limits the fusion of a subset of MVBs with lysosomes - a mechanism potentially involved in the initial biogenesis of melanosomes.Gene discovery for motile cilia disorders: mutation spectrum in primary ciliary dyskinesia and discovery of mutations in CCDC151.Correlative light and immuno-electron microscopy of retinal tissue cryostat sections.HtrA1 Mediated Intracellular Effects on Tubulin Using a Polarized RPE Disease Model.Phenotypic variability of CCDC103 mutation in British Pakistani children with Primary Ciliary Dyskinesia (PCD).Primary Cilia Mediate Diverse Kinase Inhibitor Resistance Mechanisms in Cancer.ALIX Regulates Tumor-Mediated Immunosuppression by Controlling EGFR Activity and PD-L1 PresentationPrimary ciliary dyskinesia with normal ultrastructure: three-dimensional tomography detects absence of DNAH11Selective Ablation of Megalin in the Retinal Pigment Epithelium Results in Megaophthalmos, Macromelanosome Formation and Severe Retina DegenerationPhagosomal and mitochondrial alterations in RPE may contribute to KCNJ13 retinopathyMutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus.NPC1 regulates ER contacts with endocytic organelles to mediate cholesterol egressThree-dimensional structure of the basketweave Z-band in midshipman fish sonic muscleAgonist-induced membrane nanodomain clustering drives GLP-1 receptor responses in pancreatic beta cellsThree dimensional ultrastructure of human respiratory cilia in health and disease
P50
Q24303570-96E4EDB6-7CB5-481F-8A36-9FA8C43245F6Q27309649-DE1F94FD-FE41-4DA3-9B0E-4D2043249D5EQ29147466-00D1C5DE-1967-4EA6-84C5-1376404F20A6Q30352832-A8E3B55C-5DF8-4C4F-AEC6-6F7B232E0DF2Q30364872-7660F685-3B76-41FE-B3C8-6536AE41E7F0Q30580167-1357DB6F-0B7B-45F5-90FA-AD71B68A9F84Q34398642-05D225EB-D1BB-4E0F-B3D9-7F6DD481250BQ35116940-6F179273-80CB-452F-9B34-39F2BFFEBF3CQ35868909-1C1CA794-A1C5-450E-8612-1CB925F780BBQ36358455-039464B1-F95B-4D16-BBEC-C5C9C3436B4CQ36536592-F71AF177-8803-47DB-A137-9C3838773E77Q37995738-0DD6944F-B9DD-4D51-9FBC-594C4545E834Q38348273-B36E3C78-9EB2-4936-8AA4-C9BC1500A3EAQ38802085-B1CE516C-0BAE-4A7C-827F-03D0C1E98F9EQ41458080-92056584-7D32-4D50-B65F-579848E67174Q41818361-EDCA541B-86D7-47C1-9E7C-9D329866D0BAQ42030071-D84F2A9B-DA00-49C3-8B3B-B3F406C58970Q42430967-0F3E542B-11D8-4884-A413-F80B37280B1FQ42481764-583E72A2-0553-4732-BC6C-4F3862E3E827Q42906442-E62FE7A0-AD63-40E4-87A6-48AF13DD2223Q47101945-E0867FF4-C638-4F37-8C7C-B6AE3BEC987FQ47190367-B19E1917-AB6C-480A-B84A-F7F386CB6C26Q47263577-9D937F9A-D732-4341-BF5B-23E5F449E058Q54700112-0FB6F444-256B-43D9-9533-100CA2E4BD23Q54976883-F4607B72-0549-4E11-A973-F73D98D0421FQ57950156-4CBAC8C7-96F1-425B-97B5-8B4032A28E79Q60409319-E524FC55-C0E5-4518-AB99-DCEBF066A434Q61452852-4E381ED7-99D2-4701-A941-56FA1182DF1CQ64054587-2637AC69-E413-4E79-A234-88C70E32A16FQ64914313-AC1645AE-67A8-4D7C-A691-B40C0918B637Q90183088-282A460E-D579-480F-8834-E35AC037DD13Q92002246-6CFB13E6-A5FF-422F-957B-F004E88ED779Q92726723-27946292-F1B9-440A-83C4-7E8E48AEFF68Q93572572-56678448-18BF-42FA-AC97-BAA15C83ED3B
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Thomas Burgoyne
@ast
Thomas Burgoyne
@en
Thomas Burgoyne
@es
Thomas Burgoyne
@nl
Thomas Burgoyne
@sl
type
label
Thomas Burgoyne
@ast
Thomas Burgoyne
@en
Thomas Burgoyne
@es
Thomas Burgoyne
@nl
Thomas Burgoyne
@sl
altLabel
Tom Burgoyne
@en
prefLabel
Thomas Burgoyne
@ast
Thomas Burgoyne
@en
Thomas Burgoyne
@es
Thomas Burgoyne
@nl
Thomas Burgoyne
@sl
P108
P106
P21
P31
P496
0000-0002-8428-720X