Papers associated with acvr1

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	Uncoupling the BMP receptor antagonist function from the WNT agonist function of R-spondin 2 using the inhibitory peptide dendrimer RWd., Lee H, Lee H, Sun R, Niehrs C., J Biol Chem. February 1, 2022; 298 (2): 101586.
	The molecular dynamics of subdistal appendages in multi-ciliated cells., Ryu H, Lee H, Lee H, Lee J, Noh H, Shin M, Kumar V, Hong S, Kim J, Park S., Nat Commun. January 27, 2021; 12 (1): 612.
	R-spondins are BMP receptor antagonists in Xenopus early embryonic development., Lee H, Lee H, Seidl C, Sun R, Glinka A, Niehrs C., Nat Commun. November 4, 2020; 11 (1): 5570.
	TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis., Chen M, Amado N, Tan J, Reis A, Ge M, Abreu JG, He X., Elife. September 14, 2020; 9
	Natural size variation among embryos leads to the corresponding scaling in gene expression., Leibovich A, Edri T, Klein SL, Moody SA, Fainsod A., Dev Biol. June 15, 2020; 462 (2): 165-179.
	Biology of multiciliated cells., Boutin C, Kodjabachian L., Curr Opin Genet Dev. June 1, 2019; 56 1-7.
	Barhl2 maintains T cell factors as repressors and thereby switches off the Wnt/β-Catenin response driving Spemann organizer formation., Sena E, Rocques N, Borday C, Muhamad Amin HS, Parain K, Sitbon D, Chesneau A, Durand BC., Development. May 22, 2019; 146 (10):
	Transcriptome analysis of regeneration during Xenopus laevis experimental twinning., Sosa EA, Moriyama Y, Ding Y, Tejeda-Muñoz N, Colozza G, De Robertis EM., Int J Dev Biol. January 1, 2019; 63 (6-7): 301-309.
	CDC20B is required for deuterosome-mediated centriole production in multiciliated cells., Revinski DR, Zaragosi LE, Boutin C, Ruiz-Garcia S, Deprez M, Thomé V, Rosnet O, Gay AS, Mercey O, Paquet A, Pons N, Ponzio G, Marcet B, Kodjabachian L, Barbry P., Nat Commun. November 7, 2018; 9 (1): 4668.
	ADMP controls the size of Spemann's organizer through a network of self-regulating expansion-restriction signals., Leibovich A, Kot-Leibovich H, Ben-Zvi D, Fainsod A., BMC Biol. January 22, 2018; 16 (1): 13.
	Maternal Gdf3 is an obligatory cofactor in Nodal signaling for embryonic axis formation in zebrafish., Bisgrove BW, Su YC, Yost HJ., Elife. November 15, 2017; 6
	Dissecting BMP signaling input into the gene regulatory networks driving specification of the blood stem cell lineage., Kirmizitas A, Meiklejohn S, Ciau-Uitz A, Stephenson R, Patient R., Proc Natl Acad Sci U S A. June 6, 2017; 114 (23): 5814-5821.
	High-throughput analysis reveals novel maternal germline RNAs crucial for primordial germ cell preservation and proper migration., Owens DA, Butler AM, Aguero TH, Newman KM, Van Booven D, King ML., Development. January 15, 2017; 144 (2): 292-304.
	Expression of the ALK1 family of type I BMP/ADMP receptors during gastrula stages in Xenopus embryos., Leibovich A, Steinbeißer H, Fainsod A., Int J Dev Biol. January 1, 2017; 61 (6-7): 465-470.
	Rapid and efficient analysis of gene function using CRISPR-Cas9 in Xenopus tropicalis founders., Shigeta M, Sakane Y, Iida M, Suzuki M, Kashiwagi K, Kashiwagi A, Fujii S, Yamamoto T, Suzuki KT., Genes Cells. July 1, 2016; 21 (7): 755-71.
	Differential requirement of bone morphogenetic protein receptors Ia (ALK3) and Ib (ALK6) in early embryonic patterning and neural crest development., Schille C, Heller J, Schambony A., BMC Dev Biol. January 19, 2016; 16 1.
	Antisense Oligonucleotide-Mediated Transcript Knockdown in Zebrafish., Pauli A, Montague TG, Lennox KA, Behlke MA, Schier AF., PLoS One. January 1, 2015; 10 (10): e0139504.
	USP15 targets ALK3/BMPR1A for deubiquitylation to enhance bone morphogenetic protein signalling., Herhaus L, Al-Salihi MA, Dingwell KS, Cummins TD, Wasmus L, Vogt J, Ewan R, Bruce D, Macartney T, Weidlich S, Smith JC, Sapkota GP., Open Biol. May 1, 2014; 4 (5): 140065.
	β-Catenin-independent activation of TCF1/LEF1 in human hematopoietic tumor cells through interaction with ATF2 transcription factors., Grumolato L, Liu G, Haremaki T, Mungamuri SK, Mong P, Akiri G, Lopez-Bergami P, Arita A, Anouar Y, Mlodzik M, Ronai ZA, Brody J, Weinstein DC, Aaronson SA., PLoS Genet. January 1, 2013; 9 (8): e1003603.
	Self-regulation of the head-inducing properties of the Spemann organizer., Inui M, Montagner M, Ben-Zvi D, Martello G, Soligo S, Manfrin A, Aragona M, Enzo E, Zacchigna L, Zanconato F, Azzolin L, Dupont S, Cordenonsi M, Piccolo S., Proc Natl Acad Sci U S A. September 18, 2012; 109 (38): 15354-9.
	Thyroid hormone-dependent development in Xenopus laevis: a sensitive screen of thyroid hormone signaling disruption by municipal wastewater treatment plant effluent., Searcy BT, Beckstrom-Sternberg SM, Beckstrom-Sternberg JS, Stafford P, Schwendiman AL, Soto-Pena J, Owen MC, Ramirez C, Phillips J, Veldhoen N, Helbing CC, Propper CR., Gen Comp Endocrinol. May 1, 2012; 176 (3): 481-92.
	Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ, Hatayama M, Aruga J., Dev Biol. January 15, 2012; 361 (2): 220-31.
	The BMP pathway acts to directly regulate Tbx20 in the developing heart., Mandel EM, Kaltenbrun E, Callis TE, Zeng XX, Marques SR, Yelon D, Wang DZ, Conlon FL., Development. June 1, 2010; 137 (11): 1919-29.
	APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex., Shimomura Y, Agalliu D, Vonica A, Luria V, Wajid M, Baumer A, Belli S, Petukhova L, Schinzel A, Brivanlou AH, Brivanlou AH, Barres BA, Christiano AM., Nature. April 15, 2010; 464 (7291): 1043-7.
	Retinoid signaling can repress blastula Wnt signaling and impair dorsal development in Xenopus embryo., Li S, Lou X, Wang J, Liu B, Ma L, Su Z, Ding X., Differentiation. October 1, 2008; 76 (8): 897-907.
	Jade-1 inhibits Wnt signalling by ubiquitylating beta-catenin and mediates Wnt pathway inhibition by pVHL., Chitalia VC, Foy RL, Bachschmid MM, Zeng L, Panchenko MV, Zhou MI, Bharti A, Seldin DC, Lecker SH, Dominguez I, Cohen HT., Nat Cell Biol. October 1, 2008; 10 (10): 1208-16.
	Direct inhibition of GSK3beta by the phosphorylated cytoplasmic domain of LRP6 in Wnt/beta-catenin signaling., Piao S, Lee SH, Kim H, Yum S, Stamos JL, Xu Y, Xu Y, Lee SJ, Lee J, Lee J, Oh S, Han JK, Park BJ, Weis WI, Ha NC., PLoS One. January 1, 2008; 3 (12): e4046.
	Expression of Bmp ligands and receptors in the developing Xenopus retina., Hocking JC, McFarlane S., Int J Dev Biol. January 1, 2007; 51 (2): 161-5.
	Regulation of ADMP and BMP2/4/7 at opposite embryonic poles generates a self-regulating morphogenetic field., Reversade B, De Robertis EM., Cell. December 16, 2005; 123 (6): 1147-60.
	RanBP3 enhances nuclear export of active (beta)-catenin independently of CRM1., Hendriksen J, Fagotto F, van der Velde H, van Schie M, Noordermeer J, Fornerod M., J Cell Biol. December 5, 2005; 171 (5): 785-97.
	xBtg-x regulates Wnt/beta-Catenin signaling during early Xenopus development., Wessely O, Kim JI, Tran U, Fuentealba L, De Robertis EM., Dev Biol. July 1, 2005; 283 (1): 17-28.
	DRAGON, a bone morphogenetic protein co-receptor., Samad TA, Rebbapragada A, Bell E, Zhang Y, Zhang Y, Sidis Y, Jeong SJ, Campagna JA, Perusini S, Fabrizio DA, Schneyer AL, Lin HY, Brivanlou AH, Attisano L, Woolf CJ., J Biol Chem. April 8, 2005; 280 (14): 14122-9.
	PR72, a novel regulator of Wnt signaling required for Naked cuticle function., Creyghton MP, Roël G, Eichhorn PJ, Hijmans EM, Maurer I, Destrée O, Bernards R., Genes Dev. February 1, 2005; 19 (3): 376-86.
	Shisa promotes head formation through the inhibition of receptor protein maturation for the caudalizing factors, Wnt and FGF., Yamamoto A, Nagano T, Takehara S, Hibi M, Aizawa S., Cell. January 28, 2005; 120 (2): 223-35.
	Conditional BMP inhibition in Xenopus reveals stage-specific roles for BMPs in neural and neural crest induction., Wawersik S, Evola C, Whitman M., Dev Biol. January 15, 2005; 277 (2): 425-42.
	Cooperative inhibition of bone morphogenetic protein signaling by Smurf1 and inhibitory Smads., Murakami G, Watabe T, Takaoka K, Miyazono K, Imamura T., Mol Biol Cell. July 1, 2003; 14 (7): 2809-17.
	Endostatin is a potential inhibitor of Wnt signaling., Hanai J, Gloy J, Karumanchi SA, Kale S, Tang J, Hu G, Chan B, Ramchandran R, Jha V, Sukhatme VP, Sokol S., J Cell Biol. August 5, 2002; 158 (3): 529-39.
	Functional characterization and genetic mapping of alk8., Payne TL, Postlethwait JH, Yelick PC., Mech Dev. February 1, 2001; 100 (2): 275-89.
	Regulation of gut and heart left-right asymmetry by context-dependent interactions between xenopus lefty and BMP4 signaling., Branford WW, Essner JJ, Yost HJ., Dev Biol. July 15, 2000; 223 (2): 291-306.
	Mouse smad8 phosphorylation downstream of BMP receptors ALK-2, ALK-3, and ALK-6 induces its association with Smad4 and transcriptional activity., Kawai S, Faucheu C, Gallea S, Spinella-Jaegle S, Atfi A, Baron R, Roman SR., Biochem Biophys Res Commun. May 19, 2000; 271 (3): 682-7.
	Mechanisms of left-right determination in vertebrates., Capdevila J, Vogan KJ, Tabin CJ, Izpisúa Belmonte JC., Cell. March 31, 2000; 101 (1): 9-21.
	Cardiac looping and the vertebrate left-right axis: antagonism of left-sided Vg1 activity by a right-sided ALK2-dependent BMP pathway., Ramsdell AF, Yost HJ., Development. December 1, 1999; 126 (23): 5195-205.
	Neuralization of the Xenopus embryo by inhibition of p300/ CREB-binding protein function., Kato Y, Shi Y, Shi Y, He X., J Neurosci. November 1, 1999; 19 (21): 9364-73.
	A short loop on the ALK-2 and ALK-4 activin receptors regulates signaling specificity but cannot account for all their effects on early Xenopus development., Armes NA, Neal KA, Smith JC., J Biol Chem. March 19, 1999; 274 (12): 7929-35.
	Specific activation of Smad1 signaling pathways by the BMP7 type I receptor, ALK2., Macías-Silva M, Hoodless PA, Tang SJ, Buchwald M, Wrana JL., J Biol Chem. October 2, 1998; 273 (40): 25628-36.
	Direct binding of follistatin to a complex of bone-morphogenetic protein and its receptor inhibits ventral and epidermal cell fates in early Xenopus embryo., Iemura S, Yamamoto TS, Takagi C, Uchiyama H, Natsume T, Shimasaki S, Sugino H, Ueno N., Proc Natl Acad Sci U S A. August 4, 1998; 95 (16): 9337-42.
	Smad8 mediates the signaling of the ALK-2 [corrected] receptor serine kinase., Chen Y, Bhushan A, Vale W., Proc Natl Acad Sci U S A. November 25, 1997; 94 (24): 12938-43.
	The ALK-2 and ALK-4 activin receptors transduce distinct mesoderm-inducing signals during early Xenopus development but do not co-operate to establish thresholds., Armes NA, Smith JC., Development. October 1, 1997; 124 (19): 3797-804.
	A Xenopus type I activin receptor mediates mesodermal but not neural specification during embryogenesis., Chang C, Wilson PA, Mathews LS, Hemmati-Brivanlou A., Development. February 1, 1997; 124 (4): 827-37.
	Molecular cloning of Xenopus activin type I receptor and the analysis of its expression during embryogenesis., Kondo M, Semba K, Shiokawa K, Yamamoto T., Biochem Biophys Res Commun. January 17, 1996; 218 (2): 549-55.

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