Gene Expression Literature Summary

Summary by Gene and Reference: Number indicates the number of results matching the search criteria recorded for each reference.
* Indicates detailed expression data entries available

Sox10  SRY (sex determining region Y)-box 10   (Synonyms: gt, Sox21)
Results	Reference
1*	J:132978 Corpening JC, Cantrell VA, Deal KK, Southard-Smith EM, A Histone2BCerulean BAC transgene identifies differential expression of Phox2b in migrating enteric neural crest derivatives and enteric glia. Dev Dyn. 2008 Apr;237(4):1119-32
1*	J:269500 Hao MM, Capoccia E, Cirillo C, Boesmans W, Vanden Berghe P, Arundic Acid Prevents Developmental Upregulation of S100B Expression and Inhibits Enteric Glial Development. Front Cell Neurosci. 2017;11:42
1	J:265501 Kim H, Langohr IM, Faisal M, McNulty M, Thorn C, Kim J, Ablation of Ezh2 in neural crest cells leads to aberrant enteric nervous system development in mice. PLoS One. 2018;13(8):e0203391
1	J:295923 McMenamin PG, Shields GT, Seyed-Razavi Y, Kalirai H, Insall RH, Machesky LM, Coupland SE, Melanoblasts Populate the Mouse Choroid Earlier in Development Than Previously Described. Invest Ophthalmol Vis Sci. 2020 Aug 3;61(10):33
1	J:284087 Schill EM, Wright CM, Jamil A, LaCombe JM, Roper RJ, Heuckeroth RO, Down syndrome mouse models have an abnormal enteric nervous system. JCI Insight. 2019 Apr 18;5
1	J:224366 Uesaka T, Nagashimada M, Enomoto H, Neuronal Differentiation in Schwann Cell Lineage Underlies Postnatal Neurogenesis in the Enteric Nervous System. J Neurosci. 2015 Jul 8;35(27):9879-88
1	J:287295 Wright CM, Garifallou JP, Schneider S, Mentch HL, Kothakapa DR, Maguire BA, Heuckeroth RO, Dlx1/2 mice have abnormal enteric nervous system function. JCI Insight. 2020 Feb 27;5(4)
1	J:81003 Young HM, Bergner AJ, Muller T, Acquisition of neuronal and glial markers by neural crest-derived cells in the mouse intestine. J Comp Neurol. 2003 Jan 27;456(1):1-11
1	J:316159 Yu Q, Du M, Zhang W, Liu L, Gao Z, Chen W, Gu Y, Zhu K, Niu X, Sun Q, Wang L, Mesenteric Neural Crest Cells Are the Embryological Basis of Skip Segment Hirschsprung's Disease. Cell Mol Gastroenterol Hepatol. 2021;12(1):1-24