Bok S, Sun J, Greenblatt M
J Bone Miner Res. 2024; 39(10):1386-1392.
PMID: 39052334
PMC: 11425698.
DOI: 10.1093/jbmr/zjae109.
Sun J, Hu L, Bok S, Yallowitz A, Cung M, McCormick J
Nature. 2023; 621(7979):602-609.
PMID: 37704733
PMC: 10829697.
DOI: 10.1038/s41586-023-06519-1.
Sun J, Hu L, Bok S, Yallowitz A, Cung M, McCormick J
Res Sq. 2023; .
PMID: 36747772
PMC: 9901027.
DOI: 10.21203/rs.3.rs-2106142/v1.
Wu W, Kong X, Jia Y, Jia Y, Ou W, Dai C
Front Cell Dev Biol. 2022; 10:1051102.
PMID: 36393845
PMC: 9649799.
DOI: 10.3389/fcell.2022.1051102.
Ochi S, Manabe S, Kikkawa T, Osumi N
Int J Mol Sci. 2022; 23(11).
PMID: 35682795
PMC: 9181425.
DOI: 10.3390/ijms23116115.
Epigenetic remodeling regulates transcriptional changes between ovarian cancer and benign precursors.
Elias K, Emori M, Westerling T, Long H, Budina-Kolomets A, Li F
JCI Insight. 2016; 1(13).
PMID: 27617304
PMC: 5017158.
DOI: 10.1172/jci.insight.87988.
Making no bones about it: Transcription factors in vertebrate skeletogenesis and disease.
Chatterjee S, Sivakamasundari V, Lee W, Chan H, Lufkin T
Trends Dev Biol. 2013; 6:45-52.
PMID: 23950621
PMC: 3742036.
A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome.
Pohl E, Aykut A, Beleggia F, Karaca E, Durmaz B, Keupp K
Hum Genet. 2013; 132(11):1311-20.
PMID: 23851939
DOI: 10.1007/s00439-013-1337-9.
Functional redundancy of two Pax-like proteins in transcriptional activation of cyst wall protein genes in Giardia lamblia.
Chuang S, Su L, Cho C, Pan Y, Sun C
PLoS One. 2012; 7(2):e30614.
PMID: 22355320
PMC: 3280250.
DOI: 10.1371/journal.pone.0030614.
Noggin is novel inducer of mesenchymal stem cell adipogenesis: implications for bone health and obesity.
Sawant A, Chanda D, Isayeva T, Tsuladze G, Garvey W, Ponnazhagan S
J Biol Chem. 2012; 287(15):12241-9.
PMID: 22351751
PMC: 3320975.
DOI: 10.1074/jbc.M111.293613.
AKT and PAX3-FKHR cooperation enforces myogenic differentiation blockade in alveolar rhabdomyosarcoma cell.
Jothi M, Nishijo K, Keller C, Mal A
Cell Cycle. 2012; 11(5):895-908.
PMID: 22333587
PMC: 3323795.
DOI: 10.4161/cc.11.5.19346.
Control of pelvic girdle development by genes of the Pbx family and Emx2.
Capellini T, Handschuh K, Quintana L, Ferretti E, Di Giacomo G, Fantini S
Dev Dyn. 2011; 240(5):1173-89.
PMID: 21455939
PMC: 3081414.
DOI: 10.1002/dvdy.22617.
A novel pax-like protein involved in transcriptional activation of cyst wall protein genes in Giardia lamblia.
Wang Y, Pan Y, Cho C, Lin B, Su L, Huang Y
J Biol Chem. 2010; 285(42):32213-26.
PMID: 20699219
PMC: 2952222.
DOI: 10.1074/jbc.M110.156620.
Mitochondrial retention of Opa1 is required for mouse embryogenesis.
Moore B, Aviles G, Larkins C, Hillman M, Caspary T
Mamm Genome. 2010; 21(7-8):350-60.
PMID: 20652258
DOI: 10.1007/s00335-010-9272-8.
Scapula development is governed by genetic interactions of Pbx1 with its family members and with Emx2 via their cooperative control of Alx1.
Capellini T, Vaccari G, Ferretti E, Fantini S, He M, Pellegrini M
Development. 2010; 137(15):2559-69.
PMID: 20627960
PMC: 2927673.
DOI: 10.1242/dev.048819.
Comparative study of Pax2 expression in glial cells in the retina and optic nerve of birds and mammals.
Stanke J, Moose H, El-Hodiri H, Fischer A
J Comp Neurol. 2010; 518(12):2316-33.
PMID: 20437530
PMC: 3840394.
DOI: 10.1002/cne.22335.
Pbx1/Pbx2 govern axial skeletal development by controlling Polycomb and Hox in mesoderm and Pax1/Pax9 in sclerotome.
Capellini T, Zewdu R, Di Giacomo G, Asciutti S, Kugler J, Di Gregorio A
Dev Biol. 2008; 321(2):500-14.
PMID: 18691704
PMC: 5918304.
DOI: 10.1016/j.ydbio.2008.04.005.
Reciprocal inhibition between Pax7 and muscle regulatory factors modulates myogenic cell fate determination.
Olguin H, Yang Z, Tapscott S, Olwin B
J Cell Biol. 2007; 177(5):769-79.
PMID: 17548510
PMC: 2064278.
DOI: 10.1083/jcb.200608122.
Current perspectives on the genetic causes of neural tube defects.
De Marco P, Merello E, Mascelli S, Capra V
Neurogenetics. 2006; 7(4):201-21.
PMID: 16941185
DOI: 10.1007/s10048-006-0052-2.
A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia.
Jumlongras D, Lin J, Chapra A, Seidman C, Seidman J, Maas R
Hum Genet. 2003; 114(3):242-9.
PMID: 14689302
DOI: 10.1007/s00439-003-1066-6.