about
Genetics of human neural tube defectsCLN-1 and CLN-5, genes for infantile and variant late infantile neuronal ceroid lipofuscinoses, are expressed in the embryonic human brainMutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisisThe Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formationMutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouseCordon-bleu is a conserved gene involved in neural tube formationDisruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouseFOXP2 and the neuroanatomy of speech and languageThe chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migrationCurly tail: a 50-year history of the mouse spina bifida modelSpina bifidaDisruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebratesSyndecan 4 interacts genetically with Vangl2 to regulate neural tube closure and planar cell polarityLamin b1 polymorphism influences morphology of the nuclear envelope, cell cycle progression, and risk of neural tube defects in miceVangl2 acts via RhoA signaling to regulate polarized cell movements during development of the proximal outflow tractConvergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closureCardiovascular defects associated with abnormalities in midline development in the Loop-tail mouse mutantOver-expression of Grhl2 causes spina bifida in the Axial defects mutant mouseCloning and characterization of Igsf9 in mouse and human: a new member of the immunoglobulin superfamily expressed in the developing nervous system.Is LMNB1 a susceptibility gene for neural tube defects in humans?Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screeningNeural tube defects--disorders of neurulation and related embryonic processes.Neural tube defects: recent advances, unsolved questions, and controversies.Novel exomphalos genetic mouse model: the importance of accurate phenotypic classificationFemale predisposition to cranial neural tube defects is not because of a difference between the sexes in the rate of embryonic growth or development during neurulation.Planar cell polarity and the kidney.Physical and transcriptional map of a 3-Mb region of mouse chromosome 1 containing the gene for the neural tube defect mutant loop-tail (Lp).Neurulation and neural tube closure defects.Neural tube defects: prevention by folic acid and other vitamins.Genetic interactions between planar cell polarity genes cause diverse neural tube defects in mice.A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36.Vangl-dependent planar cell polarity signalling is not required for neural crest migration in mammals.Genetics and development of neural tube defects.Integrity of the methylation cycle is essential for mammalian neural tube closure.The genetic background of the curly tail strain confers susceptibility to folate-deficiency-induced exencephaly.Planar cell polarity aligns osteoblast division in response to substrate strainGlycine decarboxylase deficiency causes neural tube defects and features of non-ketotic hyperglycinemia in miceThe genetic basis of mammalian neurulation.Tethering of the spinal cord in mouse fetuses and neonates with spina bifidaCellular basis of neuroepithelial bending during mouse spinal neural tube closure.
P50
Q22337140-4726DC56-866C-4ADD-8E32-A1628FB91DC0Q24290264-5C2928B1-F563-4FBB-8813-EA8855375D92Q24297844-D08D1738-6DC0-40EE-8EDF-37B64460E6B2Q24337819-389C80E4-B0D7-4223-A54A-0D4417779764Q28184694-BC5B6360-059E-4C3E-B65D-F179D11C2B31Q28205077-54A4B047-613E-4328-80FF-4B8044601885Q28218970-9B11D90D-0341-439F-BD39-4E538AA05D00Q28305278-5C100625-D80D-41E6-8309-0BA7E39515C1Q28306226-FB08DA78-8F01-47B3-8EDD-27286AA9AF70Q28366531-4F0F74BC-C83C-4DD8-8F8C-87F0C729F2C1Q28396364-A43F07CE-A389-4C56-A308-7A73D1452A67Q28506652-B4E18E15-F9B9-43B9-A2E8-BB2BBD9B8D83Q28512411-1B2979DB-60F8-4871-A64E-0BD0C3B8ECAAQ28513087-13AF4F76-27C4-49A7-B3B1-CF56D941D4A5Q28587502-363FE0E2-F625-471E-B045-C2A6147DB5C6Q28588549-1DD770F4-A7C8-407D-878E-07A5CEE791DFQ28593171-06DF0151-2537-41EA-A8E8-59BB31FEFCDDQ28594231-6B3D2731-6A35-4FF6-B5F9-ABCB437111BAQ30330276-C593A971-A5AE-4667-A366-A9773FDAA981Q30431444-0B9E3F27-3CD2-4D8A-88E4-B15E4E0652F9Q30486034-66AF15E9-A199-42BB-AB62-4F0CECEDAC84Q33620903-4D039896-BA71-4C81-8B3C-44AF7593B17EQ33620909-129BBC49-42CB-4085-A09B-F0CC838B536CQ33648735-C8F669C2-D23C-46DF-9667-07B211DC6E68Q33648735-CF6B172C-440F-4E16-AE26-30829974CC72Q33674175-F74A11E7-7B0C-48F5-AC1D-92A44E70139DQ33807051-86899AA7-B9B9-4835-9AB4-D96233ABCB0FQ33853622-AE935D92-6348-44DE-9776-D3EC25755ADDQ33935718-4E093FF5-8A12-4556-B884-00674591B3F0Q34192070-31F336DC-632F-4C0F-B6B1-56D5BBEAD88EQ34241126-B3826F31-2794-4898-BE69-6122B5C6810FQ34294770-955B0589-E68A-48DE-9671-DA9013D335FBQ34341283-3903C4E4-42CF-450A-9D19-869B82AF9406Q34552276-D2DC6682-6D90-409A-8DE5-CC5F75D5007DQ34560587-C98DB3D1-3E25-4161-ADEC-EE64825A89FEQ34768495-42053F8C-7AA0-424C-89D8-4746BF90B4C2Q35097037-11D485AA-8BAC-48E4-A62A-71080E968661Q35196989-EA506D48-52E7-46E9-812C-D7D7A62E9CA2Q35298412-6A9176C4-BD65-47AA-AC7D-3AD72AB5C8BFQ35608352-59AD2901-BCF2-4A3B-9C4A-85C27E6FAA86
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Andrew J Copp
@ast
Andrew J Copp
@en
Andrew J Copp
@es
Andrew J Copp
@nl
Andrew J Copp
@sl
type
label
Andrew J Copp
@ast
Andrew J Copp
@en
Andrew J Copp
@es
Andrew J Copp
@nl
Andrew J Copp
@sl
altLabel
Andrew Copp
@en
prefLabel
Andrew J Copp
@ast
Andrew J Copp
@en
Andrew J Copp
@es
Andrew J Copp
@nl
Andrew J Copp
@sl
P106
P21
P31
P496
0000-0002-2544-9117