| An FGF response pathway that mediates hepatic gene induction in embryonic endoderm cells A Calmont, E Wandzioch, KD Tremblay, G Minowada, KH Kaestner, ... Developmental cell 11 (3), 339-348, 2006 | 203 | 2006 |
| Defective ciliogenesis, embryonic lethality and severe impairment of the Sonic Hedgehog pathway caused by inactivation of the mouse complex A intraflagellar transport gene … S Cortellino, C Wang, B Wang, MR Bassi, E Caretti, D Champeval, ... Developmental biology 325 (1), 225-237, 2009 | 146 | 2009 |
| Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm A Calmont, S Ivins, KL Van Bueren, I Papangeli, V Kyriakopoulou, ... Development 136 (18), 3173-3183, 2009 | 145 | 2009 |
| An Ift80 mouse model of short rib polydactyly syndromes shows defects in hedgehog signalling without loss or malformation of cilia S Rix, A Calmont, PJ Scambler, PL Beales Human molecular genetics 20 (7), 1306-1314, 2011 | 108 | 2011 |
| Neural crest–derived SEMA3C activates endothelial NRP1 for cardiac outflow tract septation A Plein, A Calmont, A Fantin, L Denti, NA Anderson, PJ Scambler, ... The Journal of clinical investigation 125 (7), 2661-2676, 2015 | 81 | 2015 |
| Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome KL van Bueren, I Papangeli, F Rochais, K Pearce, C Roberts, A Calmont, ... Developmental biology 340 (2), 369-380, 2010 | 63 | 2010 |
| Decreased expression of connexin 43 blunts the progression of experimental GN P Kavvadas, A Abed, C Poulain, F Authier, LP Labéjof, A Calmont, C Afieri, ... Journal of the American Society of Nephrology 28 (10), 2915-2930, 2017 | 37 | 2017 |
| Vascular permeability: regulation pathways and role in kidney diseases A Cai, C Chatziantoniou, A Calmont Nephron 145 (3), 297-310, 2021 | 24 | 2021 |
| Transcriptional control of epithelial differentiation during kidney development D Ribes, E Fischer, J Rossert Journal of the American Society of Nephrology 14 (suppl_1), S9-S15, 2003 | 23 | 2003 |
| Absence of the vagus nerve in the stomach of Tbx1−/− mutant mice A Calmont, N Thapar, PJ Scambler, AJ Burns Neurogastroenterology & Motility 23 (2), 125-130, 2011 | 14 | 2011 |
| Genetic inactivation of Semaphorin 3C protects mice from acute kidney injury A Cai, G Ye, S Placier, P Frère, B Surin, S Vandermeersch, R Kormann, ... Kidney International 101 (4), 720-732, 2022 | 7 | 2022 |
| Defective Vagal Innervation in Murine Tbx1 Mutant Hearts A Calmont, N Anderson, JP Suntharalingham, R Ang, A Tinker, ... Journal of Cardiovascular Development and Disease 5 (4), 49, 2018 | 7 | 2018 |
| Identification of a Short cis-Acting Element in the Human Vasopressin Type 2 Receptor Gene Which Confers High-Level Expression of a Reporter Gene Specifically … A Calmont, K Reichwald, P Ronco, J Rossert Molecular Endocrinology 14 (10), 1682-1695, 2000 | 6 | 2000 |
| Neuropilin‐1 regulates renin synthesis in juxtaglomerular cells Y Shen, K Lotenberg, J Zaworski, KAE Broeker, F Vasseur, L Louedec, ... The Journal of Physiology, 2024 | 1 | 2024 |
| 22q11 Deletion Syndrome: A Role for Tbx1 in Pharynx and Cardiovascular Development A Calmont, P Scambler eLS, 2010 | 1 | 2010 |
| Identification of potential Tbx1 targets in a mouse model of DiGeorge syndrome KL van Bueren, S Ivins, C Roberts, A Calmont, K Pearce, E Lindsay, ... Developmental Biology 1 (306), 323, 2007 | 1 | 2007 |
| A Novel Role of Semaphorin 3C in Modulating Systemic and Renal Hemodynamics A Cai, S Placier, L Louedec, P Frère, S Ouchelouche, C Chatziantoniou, ... Nephron 147 (7), 434-440, 2023 | | 2023 |
| Sema4A-Nrp1 versus Sema4A-plexinB2 in the acutely damaged kidney A Calmont Kidney International 101 (2), 419, 2022 | | 2022 |
| 13-P005 Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm A Calmont, S Ivins, KL Van Bueren, I Papangeli, V Kyriakopoulou, ... Mechanisms of Development, S195-S196, 2009 | | 2009 |
| Gbx2: a modifier of Tbx1 happloinsufficiency phenotype A Calmont, S Ivins, C Roberts, KL Van Bueren, E Lindsay, A Baldini, ... GENETICAL RESEARCH 90 (3), 288-288, 2008 | | 2008 |
Peter ScamblerEmeritus Professor of Molecular MedicineVerified email at ich.ucl.ac.uk
