Bruno Reversade - Publications

Affiliations: 
Institute of Medical Biology, A*STAR 

57 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Sahni G, Chang SY, Meng JTC, Tan JZY, Fatien JJC, Bonnard C, Utami KH, Chan PW, Tan TT, Altunoglu U, Kayserili H, Pouladi M, Reversade B, Toh YC. A Micropatterned Human-Specific Neuroepithelial Tissue for Modeling Gene and Drug-Induced Neurodevelopmental Defects. Advanced Science (Weinheim, Baden-Wurttemberg, Germany). 8: 2001100. PMID 33717833 DOI: 10.1002/advs.202001100  0.36
2020 Trott J, Alpagu Y, Tan EK, Shboul M, Dawood Y, Elsy M, Wollmann H, Tano V, Bonnard C, Eng S, Narayanan G, Junnarkar S, Wearne S, Strutt J, Kumar A, ... ... Reversade B, et al. Mitchell-Riley syndrome iPSC exhibit reduced pancreatic endoderm differentiation due to an mutation. Development (Cambridge, England). PMID 33033118 DOI: 10.1242/dev.194878  0.52
2020 Al Sayed ZR, Canac R, Cimarosti B, Bonnard C, Gourraud JB, Hamamy H, Kayserili H, Girardeau A, Jouni M, Jacob N, Gaignerie A, Chariau C, David L, Forest V, Marionneau C, ... ... Reversade B, et al. Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conduction. Cardiovascular Research. PMID 32898233 DOI: 10.1093/Cvr/Cvaa259  0.36
2020 Bonnard C, Navaratnam N, Ghosh K, Chan PW, Tan TT, Pomp O, Ng AYJ, Tohari S, Changede R, Carling D, Venkatesh B, Altunoglu U, Kayserili H, Reversade B. A loss-of-function NUAK2 mutation in humans causes anencephaly due to impaired Hippo-YAP signaling. The Journal of Experimental Medicine. 217. PMID 32845958 DOI: 10.1084/Jem.20191561  0.36
2020 Tan EEK, Hopkins R, Lim CK, Jamuar S, Ong C, Thoon KC, Koh MJ, Shin EM, Lian DWQ, Weerasooriya M, Lee CZ, Soetedjo AAP, Lim CS, Au VB, Chua WME, ... ... Reversade B, et al. Dominant-negative NFKBIA mutation promotes IL-1β production causing hepatic disease with severe immunodeficiency. The Journal of Clinical Investigation. PMID 32750042 DOI: 10.1172/Jci98882  0.36
2020 Koh AL, Bonnard C, Lim JY, Liew WK, Thoon KC, Thomas T, Ali NAB, Ng AYJ, Tohari S, Phua KB, Venkatesh B, Reversade B, Jamuar SS. Heterozygous missense variant in EIF6 gene: A novel form of Shwachman-Diamond syndrome? American Journal of Medical Genetics. Part A. PMID 32657013 DOI: 10.1002/Ajmg.A.61758  0.36
2020 Kariminejad A, Ghaderi-Sohi S, Keshavarz E, Hashemi SA, Parsimehr E, Szenker-Ravi E, Khatoo M, Faraji Zonooz M, Reversade B, Najmabadi H, Hennekam RC. A GLI3 variant leading to polydactyly in heterozygotes and Pallister-Hall-like syndrome in a homozygote. Clinical Genetics. PMID 32112393 DOI: 10.1111/Cge.13730  0.36
2020 Hengel H, Bosso-Lefèvre C, Grady G, Szenker-Ravi E, Li H, Pierce S, Lebigot É, Tan TT, Eio MY, Narayanan G, Utami KH, Yau M, Handal N, Deigendesch W, Keimer R, ... ... Reversade B, et al. Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy. Nature Communications. 11: 595. PMID 32001716 DOI: 10.1038/S41467-020-14360-7  0.36
2019 Masri A, Shboul M, Khasawneh A, Jadallah R, ALmustafa A, Escande-Beillard N, Hamamy H, Bakri F, Reversade B. Congenital insensitivity to pain with anhidrosis syndrome: A series from Jordan. Clinical Neurology and Neurosurgery. 189: 105636. PMID 31841741 DOI: 10.1016/J.Clineuro.2019.105636  0.32
2019 Kariminejad A, Szenker-Ravi E, Lekszas C, Tajsharghi H, Moslemi AR, Naert T, Tran HT, Ahangari F, Rajaei M, Nasseri M, Haaf T, Azad A, Superti-Furga A, Maroofian R, Ghaderi-Sohi S, ... ... Reversade B, et al. Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia. American Journal of Human Genetics. 105: 1294-1301. PMID 31761294 DOI: 10.1016/j.ajhg.2019.10.013  0.36
2019 Ziaei A, Xu X, Dehghani L, Bonnard C, Zellner A, Jin Ng AY, Tohari S, Venkatesh B, Haffner C, Reversade B, Shaygannejad V, Pouladi MA. Novel mutation in in a family with diffuse white matter lesions and inflammatory features. Neurology. Genetics. 5: e345. PMID 31403081 DOI: 10.1212/Nxg.0000000000000345  0.36
2018 Shboul M, Roschger P, Ganger R, Paschalis L, Rokidi S, Zandieh S, Behunova J, Muschitz C, Fahrleitner-Pammer A, Ng AYJ, Tohari S, Venkatesh B, Bonnard C, Reversade B, Klaushofer K, et al. Bone matrix hypermineralization associated with low bone turnover in a case of Nasu-Hakola disease. Bone. PMID 30316000 DOI: 10.1016/J.Bone.2018.10.008  0.36
2018 Hettiaracchchi D, Bonnard C, Jayawardana SMA, Ng AYJ, Tohari S, Venkatesh B, Reversade B, Singaraja R, Dissanayake VHW. Cenani-Lenz syndactyly syndrome - a case report of a family with isolated syndactyly. Bmc Medical Genetics. 19: 125. PMID 30041615 DOI: 10.1186/S12881-018-0646-1  0.36
2018 Chia PH, Zhong FL, Niwa S, Bonnard C, Utami KH, Zeng R, Lee H, Eskin A, Nelson SF, Xie WH, Al-Tawalbeh S, El-Khateeb M, Shboul M, Pouladi MA, Al-Raqad M, ... Reversade B, et al. A homozygous loss-of-function mutation causes growth delay, frequent seizures and severe intellectual disability. Elife. 7. PMID 29784083 DOI: 10.7554/Elife.32451  0.52
2018 Bonnard C, Shboul M, Tonekaboni SH, Ng AYJ, Tohari S, Ghosh K, Lai A, Lim JY, Tan EC, Devisme L, Stichelbout M, Alkindi A, Banu N, Yüksel Z, Ghoumid J, ... ... Reversade B, et al. Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome. European Journal of Medical Genetics. PMID 29605658 DOI: 10.1016/J.Ejmg.2018.03.012  0.36
2017 Gueneau L, Fish RJ, Shamseldin HE, Voisin N, Tran Mau-Them F, Preiksaitiene E, Monroe GR, Lai A, Putoux A, Allias F, Ambusaidi Q, Ambrozaityte L, Cimbalistienė L, Delafontaine J, Guex N, ... ... Reversade B, et al. KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis. American Journal of Human Genetics. PMID 29290337 DOI: 10.1016/J.Ajhg.2017.12.002  0.36
2017 Chourabi M, Liew MS, Lim S, H'mida-Ben Brahim D, Boussofara L, Dai L, Wong PM, Foo JN, Sriha B, Robinson KS, Denil S, Common JE, Mamaï O, Ben Khalifa Y, Bollen M, ... ... Reversade B, et al. ENPP1 Mutation Causes Recessive Cole Disease by Altering Melanogenesis. The Journal of Investigative Dermatology. PMID 28964717 DOI: 10.1016/J.Jid.2017.08.045  0.36
2017 Windpassinger C, Piard J, Bonnard C, Alfadhel M, Lim S, Bisteau X, Blouin S, Ali NB, Ng AYJ, Lu H, Tohari S, Talib SZA, van Hul N, Caldez MJ, Van Maldergem L, ... ... Reversade B, et al. CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays. American Journal of Human Genetics. 101: 391-403. PMID 28886341 DOI: 10.1016/J.Ajhg.2017.08.003  0.36
2017 Xue S, Maluenda J, Marguet F, Shboul M, Quevarec L, Bonnard C, Ng AY, Tohari S, Tan TT, Kong MK, Monaghan KG, Cho MT, Siskind CE, Sampson JB, Rocha CT, ... ... Reversade B, et al. Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita. American Journal of Human Genetics. PMID 28318499 DOI: 10.1016/J.Ajhg.2017.02.006  0.36
2017 Kariminejad A, Afroozan F, Bozorgmehr B, Ghanadan A, Akbaroghli S, Khorram Khorshid HR, Mojahedi F, Setoodeh A, Loh A, Tan YX, Escande-Beillard N, Malfait F, Reversade B, Gardeitchik T, Morava E. Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica. International Journal of Molecular Sciences. 18. PMID 28294978 DOI: 10.3390/Ijms18030635  0.36
2017 Gordon CT, Xue S, Yigit G, Filali H, Chen K, Rosin N, Yoshiura KI, Oufadem M, Beck TJ, McGowan R, Magee AC, Altmüller J, Dion C, Thiele H, Gurzau AD, ... ... Reversade B, et al. De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development. Nature Genetics. PMID 28067911 DOI: 10.1038/Ng.3765  0.36
2016 Perez-Camps M, Tian J, Chng SC, Sem KP, Sudhaharan T, Teh C, Wachsmuth M, Korzh V, Ahmed S, Reversade B. Quantitative imaging reveals real-time Pou5f3-Nanog complexes driving dorsoventral mesendoderm patterning in zebrafish. Elife. 5. PMID 27684073 DOI: 10.7554/Elife.11475  0.56
2016 Zhong FL, Mamaï O, Sborgi L, Boussofara L, Hopkins R, Robinson K, Szeverényi I, Takeichi T, Balaji R, Lau A, Tye H, Roy K, Bonnard C, Ahl PJ, Jones LA, ... ... Reversade B, et al. Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation. Cell. 167: 187-202.e17. PMID 27662089 DOI: 10.1016/J.Cell.2016.09.001  0.56
2016 Cain CJ, Gaborit N, Lwin W, Barruet E, Ho S, Bonnard C, Hamamy H, Shboul M, Reversade B, Kayserili H, Bruneau BG, Hsiao EC. Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralization. Bone Reports. 5: 86-95. PMID 27453922 DOI: 10.1016/J.Bonr.2016.02.005  0.36
2016 Mbarek H, Steinberg S, Nyholt DR, Gordon SD, Miller MB, McRae AF, Hottenga JJ, Day FR, Willemsen G, de Geus EJ, Davies GE, Martin HC, Penninx BW, Jansen R, McAloney K, ... ... Reversade B, et al. Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility. American Journal of Human Genetics. PMID 27132594 DOI: 10.1016/J.Ajhg.2016.03.008  0.56
2016 Jamuar SS, Kuan JL, Brett M, Tiang Z, Tan WL, Lim JY, Liew WK, Javed A, Liew WK, Law HY, Tan ES, Lai A, Ng I, Teo YY, Venkatesh B, ... Reversade B, et al. Incidentalome from Genomic Sequencing: A Barrier to Personalized Medicine? Ebiomedicine. 5: 211-6. PMID 27077130 DOI: 10.1016/J.Ebiom.2016.01.030  0.56
2016 Oud MM, Bonnard C, Mans DA, Altunoglu U, Tohari S, Ng AY, Eskin A, Lee H, Rupar CA, de Wagenaar NP, Wu KM, Lahiry P, Pazour GJ, Nelson SF, Hegele RA, ... ... Reversade B, et al. A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome. Cilia. 5: 8. PMID 27069622 DOI: 10.1186/S13630-016-0029-1  0.52
2016 Murza A, Sainsily X, Coquerel D, Côté J, Marx P, Besserer-Offroy É, Longpre JM, Lainé J, Reversade B, Salvail D, Leduc R, Dumaine R, Lesur O, Auger-Messier M, Sarret P, et al. Discovery and Structure-Activity Relationship of a Bioactive Fragment of ELABELA that Modulates Vascular and Cardiac Functions. Journal of Medicinal Chemistry. PMID 26986036 DOI: 10.1021/Acs.Jmedchem.5B01549  0.56
2016 Tafakhori A, Yu Jin Ng A, Tohari S, Venkatesh B, Lee H, Eskin A, Nelson SF, Bonnard C, Reversade B, Kariminejad A. Mutation in TWINKLE in a Large Iranian Family with Progressive External Ophthalmoplegia, Myopathy, Dysphagia and Dysphonia, and Behavior Change. Archives of Iranian Medicine. 19: 87-91. PMID 26838077 DOI: 0161902/AIM.004  0.52
2016 Reijnders MR, Zachariadis V, Latour B, Jolly L, Mancini GM, Pfundt R, Wu KM, van Ravenswaaij-Arts CM, Veenstra-Knol HE, Anderlid BM, Wood SA, Cheung SW, Barnicoat A, Probst F, Magoulas P, ... ... Reversade B, et al. De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations. American Journal of Human Genetics. PMID 26833328 DOI: 10.1016/J.Ajhg.2015.12.015  0.56
2015 Zhou F, Narasimhan V, Shboul M, Chong YL, Reversade B, Roy S. Gmnc Is a Master Regulator of the Multiciliated Cell Differentiation Program. Current Biology : Cb. PMID 26778655 DOI: 10.1016/J.Cub.2015.10.062  0.56
2015 Ho L, Tan SY, Wee S, Wu Y, Tan SJ, Ramakrishna NB, Chng SC, Nama S, Sczerbineska I, Chan W, Avery S, Tsuneyoshi N, Ng HH, Gunaratne J, Dunn NR, ... Reversade B, et al. ELABELA Is an Endogenous Growth Factor that Sustains hESC Self-Renewal via the PI3K/AKT Pathway. Cell Stem Cell. PMID 26387754 DOI: 10.1016/J.Stem.2015.08.010  0.56
2015 Fischer-Zirnsak B, Escande-Beillard N, Ganesh J, Tan YX, Al Bughaili M, Lin AE, Sahai I, Bahena P, Reichert SL, Loh A, Wright GD, Liu J, Rahikkala E, Pivnick EK, Choudhri AF, ... ... Reversade B, et al. Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa. American Journal of Human Genetics. 97: 483-92. PMID 26320891 DOI: 10.1016/J.Ajhg.2015.08.001  0.56
2015 Kariminejad A, Nafissi S, Nilipoor Y, Tavasoli A, Van Veldhoven PP, Bonnard C, Ng YT, Majoie CB, Reversade B, Hennekam RC. Intellectual disability, muscle weakness and characteristic face in three siblings: A newly described recessive syndrome mapping to 3p24.3-p25.3. American Journal of Medical Genetics. Part A. 167: 2508-15. PMID 26192890 DOI: 10.1002/Ajmg.A.37248  0.56
2015 Brown R, Lee H, Eskin A, Kichaev G, Lohmueller KE, Reversade B, Nelson SF, Pasaniuc B. Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders. European Journal of Human Genetics : Ejhg. PMID 25898925 DOI: 10.1038/Ejhg.2015.68  0.56
2015 Ng CK, Shboul M, Taverniti V, Bonnard C, Lee H, Eskin A, Nelson SF, Al-Raqad M, Altawalbeh S, Séraphin B, Reversade B. Loss of the scavenger mRNA decapping enzyme DCPS causes syndromic intellectual disability with neuromuscular defects. Human Molecular Genetics. 24: 3163-71. PMID 25712129 DOI: 10.1093/Hmg/Ddv067  0.56
2015 Mamaï O, Boussofara L, Denguezli M, Escande-Beillard N, Kraeim W, Merriman B, Ben Charfeddine I, Stevanin G, Bouraoui S, Amara A, Mili A, Nouira R, H'mida D, Sriha B, Gribaa M, ... ... Reversade B, et al. Multiple self-healing palmoplantar carcinoma: a familial predisposition to skin cancer with primary palmoplantar and conjunctival lesions. The Journal of Investigative Dermatology. 135: 304-8. PMID 25050600 DOI: 10.1038/Jid.2014.311  0.56
2014 Hu WF, Pomp O, Ben-Omran T, Kodani A, Henke K, Mochida GH, Yu TW, Woodworth MB, Bonnard C, Raj GS, Tan TT, Hamamy H, Masri A, Shboul M, Al Saffar M, ... ... Reversade B, et al. Katanin p80 regulates human cortical development by limiting centriole and cilia number. Neuron. 84: 1240-57. PMID 25521379 DOI: 10.1016/J.Neuron.2014.12.017  0.56
2014 Lopez E, Thauvin-Robinet C, Reversade B, Khartoufi NE, Devisme L, Holder M, Ansart-Franquet H, Avila M, Lacombe D, Kleinfinger P, Kaori I, Takanashi J, Le Merrer M, Martinovic J, Noël C, et al. C5orf42 is the major gene responsible for OFD syndrome type VI. Human Genetics. 133: 367-77. PMID 24178751 DOI: 10.1007/S00439-013-1385-1  0.56
2013 Jodoin JN, Shboul M, Albrecht TR, Lee E, Wagner EJ, Reversade B, Lee LA. The snRNA-processing complex, Integrator, is required for ciliogenesis and dynein recruitment to the nuclear envelope via distinct mechanisms. Biology Open. 2: 1390-6. PMID 24285713 DOI: 10.1242/Bio.20136981  0.56
2013 Jodoin JN, Sitaram P, Albrecht TR, May SB, Shboul M, Lee E, Reversade B, Wagner EJ, Lee LA. Nuclear-localized Asunder regulates cytoplasmic dynein localization via its role in the integrator complex. Molecular Biology of the Cell. 24: 2954-65. PMID 23904267 DOI: 10.1091/Mbc.E13-05-0254  0.56
2013 Lim CY, Reversade B, Knowles BB, Solter D. Optimal histone H3 to linker histone H1 chromatin ratio is vital for mesodermal competence in Xenopus. Development (Cambridge, England). 140: 853-60. PMID 23318639 DOI: 10.1242/Dev.086611  0.56
2012 Pohler E, Mamai O, Hirst J, Zamiri M, Horn H, Nomura T, Irvine AD, Moran B, Wilson NJ, Smith FJ, Goh CS, Sandilands A, Cole C, Barton GJ, Evans AT, ... ... Reversade B, et al. Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma. Nature Genetics. 44: 1272-6. PMID 23064416 DOI: 10.1038/Ng.2444  0.56
2012 Bonnard C, Strobl AC, Shboul M, Lee H, Merriman B, Nelson SF, Ababneh OH, Uz E, Güran T, Kayserili H, Hamamy H, Reversade B. Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1. Nature Genetics. 44: 709-13. PMID 22581230 DOI: 10.1038/Ng.2259  0.52
2011 Hamamy H, Antonarakis SE, Cavalli-Sforza LL, Temtamy S, Romeo G, Kate LP, Bennett RL, Shaw A, Megarbane A, van Duijn C, Bathija H, Fokstuen S, Engel E, Zlotogora J, Dermitzakis E, ... ... Reversade B, et al. Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 13: 841-7. PMID 21555946 DOI: 10.1097/Gim.0B013E318217477F  0.56
2011 Goudie DR, D'Alessandro M, Merriman B, Lee H, Szeverényi I, Avery S, O'Connor BD, Nelson SF, Coats SE, Stewart A, Christie L, Pichert G, Friedel J, Hayes I, Burrows N, ... ... Reversade B, et al. Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1. Nature Genetics. 43: 365-9. PMID 21358634 DOI: 10.1038/Ng.780  0.56
2010 Tian J, Ling L, Shboul M, Lee H, O'Connor B, Merriman B, Nelson SF, Cool S, Ababneh OH, Al-Hadidy A, Masri A, Hamamy H, Reversade B. Loss of CHSY1, a secreted FRINGE enzyme, causes syndromic brachydactyly in humans via increased NOTCH signaling. American Journal of Human Genetics. 87: 768-78. PMID 21129727 DOI: 10.1016/J.Ajhg.2010.11.005  0.52
2009 Reversade B, Escande-Beillard N, Dimopoulou A, Fischer B, Chng SC, Li Y, Shboul M, Tham PY, Kayserili H, Al-Gazali L, Shahwan M, Brancati F, Lee H, O'Connor BD, Schmidt-von Kegler M, et al. Mutations in PYCR1 cause cutis laxa with progeroid features. Nature Genetics. 41: 1016-21. PMID 19648921 DOI: 10.1038/Ng.413  0.56
2007 Sander V, Reversade B, De Robertis EM. The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning. The Embo Journal. 26: 2955-65. PMID 17525737 DOI: 10.1038/Sj.Emboj.7601705  0.56
2006 Lee HX, Ambrosio AL, Reversade B, De Robertis EM. Embryonic dorsal-ventral signaling: secreted frizzled-related proteins as inhibitors of tolloid proteinases. Cell. 124: 147-59. PMID 16413488 DOI: 10.1016/J.Cell.2005.12.018  0.56
2005 Reversade B, De Robertis EM. Regulation of ADMP and BMP2/4/7 at opposite embryonic poles generates a self-regulating morphogenetic field. Cell. 123: 1147-60. PMID 16360041 DOI: 10.1016/J.Cell.2005.08.047  0.56
2005 Reversade B, Kuroda H, Lee H, Mays A, De Robertis EM. Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos. Development (Cambridge, England). 132: 3381-92. PMID 15975940 DOI: 10.1242/Dev.01901  0.56
2005 Kuroda H, Fuentealba L, Ikeda A, Reversade B, De Robertis EM. Default neural induction: neuralization of dissociated Xenopus cells is mediated by Ras/MAPK activation. Genes & Development. 19: 1022-7. PMID 15879552 DOI: 10.1101/Gad.1306605  0.56
2005 Zakin L, Reversade B, Kuroda H, Lyons KM, De Robertis EM. Sirenomelia in Bmp7 and Tsg compound mutant mice: requirement for Bmp signaling in the development of ventral posterior mesoderm. Development (Cambridge, England). 132: 2489-99. PMID 15843411 DOI: 10.1242/Dev.01822  0.56
2003 Oelgeschläger M, Reversade B, Larraín J, Little S, Mullins MC, De Robertis EM. The pro-BMP activity of Twisted gastrulation is independent of BMP binding. Development (Cambridge, England). 130: 4047-56. PMID 12874126 DOI: 10.1242/Dev.00633  0.56
2003 Oelgeschläger M, Kuroda H, Reversade B, De Robertis EM. Chordin is required for the Spemann organizer transplantation phenomenon in Xenopus embryos. Developmental Cell. 4: 219-30. PMID 12586065 DOI: 10.1016/S1534-5807(02)00404-5  0.56
2002 Abreu JG, Ketpura NI, Reversade B, De Robertis EM. Connective-tissue growth factor (CTGF) modulates cell signalling by BMP and TGF-beta. Nature Cell Biology. 4: 599-604. PMID 12134160 DOI: 10.1038/Ncb826  0.56
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