Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Anatomy Item Literature (4897) Expression Attributions Wiki
XB-ANAT-3713

Papers associated with left (and npat)

Limit to papers also referencing gene:
Show all left papers
???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest Sort Oldest To Newest

Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease., Mishra-Gorur K., Proc Natl Acad Sci U S A. April 18, 2023; 120 (16): e2214997120.                                            


Systematic mapping of rRNA 2'-O methylation during frog development and involvement of the methyltransferase Fibrillarin in eye and craniofacial development in Xenopus laevis., Delhermite J., PLoS Genet. January 18, 2022; 18 (1): e1010012.                                                              


Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease., Coppenrath K., Genesis. December 1, 2021; 59 (12): e23453.        


Rare heterozygous GDF6 variants in patients with renal anomalies., Martens H., Eur J Hum Genet. December 1, 2020; 28 (12): 1681-1693.                      


STRAP regulates alternative splicing fidelity during lineage commitment of mouse embryonic stem cells., Jin L., Nat Commun. November 23, 2020; 11 (1): 5941.                


The Tudor-domain protein TDRD7, mutated in congenital cataract, controls the heat shock protein HSPB1 (HSP27) and lens fiber cell morphology., Barnum CE., Hum Mol Genet. July 29, 2020; 29 (12): 2076-2097.                        


Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome., Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.                  


Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility., Robson A., Proc Natl Acad Sci U S A. July 9, 2019; 116 (28): 14049-14054.                                  


A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation., Hou K., Cells. May 15, 2019; 8 (5):               


Serine Threonine Kinase Receptor-Associated Protein Deficiency Impairs Mouse Embryonic Stem Cells Lineage Commitment Through CYP26A1-Mediated Retinoic Acid Homeostasis., Jin L., Stem Cells. September 1, 2018; 36 (9): 1368-1379.                      


Evolution of the hypoxia-sensitive cells involved in amniote respiratory reflexes., Hockman D., Elife. April 7, 2017; 6                 


Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors., Kaminski MM., Nat Cell Biol. December 1, 2016; 18 (12): 1269-1280.                  


The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery., Toriyama M., Nat Genet. June 1, 2016; 48 (6): 648-56.                              


Six1 is a key regulator of the developmental and evolutionary architecture of sensory neurons in craniates., Yajima H., BMC Biol. May 29, 2014; 12 40.                        


Lung epithelial branching program antagonizes alveolar differentiation., Chang DR., Proc Natl Acad Sci U S A. November 5, 2013; 110 (45): 18042-51.    


Syndecan 4 interacts genetically with Vangl2 to regulate neural tube closure and planar cell polarity., Escobedo N., Development. July 1, 2013; 140 (14): 3008-17.            


CASZ1 promotes vascular assembly and morphogenesis through the direct regulation of an EGFL7/RhoA-mediated pathway., Charpentier MS., Dev Cell. April 29, 2013; 25 (2): 132-43.        


WNK2 kinase is a novel regulator of essential neuronal cation-chloride cotransporters., Rinehart J., J Biol Chem. August 26, 2011; 286 (34): 30171-80.              


Geminin-deficient neural stem cells exhibit normal cell division and normal neurogenesis., Schultz KM., PLoS One. March 9, 2011; 6 (3): e17736.          


Expression study of cadherin7 and cadherin20 in the embryonic and adult rat central nervous system., Takahashi M., BMC Dev Biol. June 23, 2008; 8 87.                


Bone density ligand, Sclerostin, directly interacts with LRP5 but not LRP5G171V to modulate Wnt activity., Ellies DL., J Bone Miner Res. November 1, 2006; 21 (11): 1738-49.              


Identification of neurogenin, a vertebrate neuronal determination gene., Ma Q., Cell. October 4, 1996; 87 (1): 43-52.                

???pagination.result.page??? 1