| Year |
Citation |
Score |
| 2024 |
Dimori M, Toulany M, Sultana LS, Onal M, Thostenson JD, Carroll JL, O'Brien CA, Morello R. A new Col1a1 conditional knock-in mouse model to study osteogenesis imperfecta. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 39566076 DOI: 10.1093/jbmr/zjae189 |
0.344 |
|
| 2023 |
Dimori M, Pokrovskaya ID, Liu S, Sherrill JT, Gomez-Acevedo H, Fu Q, Storrie B, Lupashin VV, Morello R. A missense mouse model for Smith-McCort dysplasia shows bone resorption defects and altered protein glycosylation. Frontiers in Genetics. 14: 1204296. PMID 37359363 DOI: 10.3389/fgene.2023.1204296 |
0.372 |
|
| 2023 |
Warren A, Porter RM, Reyes-Castro O, Ali MM, Marques-Carvalho A, Kim HN, Gatrell LB, Schipani E, Nookaew I, O'Brien CA, Morello R, Almeida M. The NAD salvage pathway in mesenchymal cells is indispensable for skeletal development in mice. Nature Communications. 14: 3616. PMID 37330524 DOI: 10.1038/s41467-023-39392-7 |
0.3 |
|
| 2020 |
Marom R, Rabenhorst BM, Morello R. Osteogenesis imperfecta: an update on clinical features and therapies. European Journal of Endocrinology. 183: R95-R106. PMID 32621590 DOI: 10.1530/Eje-20-0299 |
0.408 |
|
| 2020 |
Xu H, Lenhart SA, Chu EY, Chavez MB, Wimer HF, Dimori M, Somerman MJ, Morello R, Foster BL, Hatch NE. Dental and Craniofacial Defects in the Crtap Mouse Model of Osteogenesis Imperfecta Type VII. Developmental Dynamics : An Official Publication of the American Association of Anatomists. PMID 32133710 DOI: 10.1002/Dvdy.166 |
0.42 |
|
| 2020 |
Dimori M, Heard-Lipsmeyer ME, Byrum SD, Mackintosh SG, Kurten RC, Carroll JL, Morello R. Respiratory defects in the KO mouse model of Osteogenesis Imperfecta. American Journal of Physiology. Lung Cellular and Molecular Physiology. PMID 32022592 DOI: 10.1152/Ajplung.00313.2019 |
0.389 |
|
| 2019 |
Zimmerman SM, Dimori M, Heard-Lipsmeyer ME, Morello R. The Osteocyte Transcriptome Is Extensively Dysregulated in Mouse Models of Osteogenesis Imperfecta. Jbmr Plus. 3: e10171. PMID 31372585 DOI: 10.1002/jbm4.10171 |
0.39 |
|
| 2018 |
Zimmerman SM, Besio R, Heard-Lipsmeyer ME, Dimori M, Castagnola P, Swain FL, Gaddy D, Diekman AB, Morello R. Expression characterization and functional implication of the collagen-modifying Leprecan proteins in mouse gonadal tissue and mature sperm. Aims Genetics. 5: 24-40. PMID 30417103 DOI: 10.3934/genet.2018.1.24 |
0.358 |
|
| 2018 |
Zimmerman SM, Heard-Lipsmeyer ME, Dimori M, Thostenson JD, Mannen EM, O'Brien CA, Morello R. Loss of RANKL in osteocytes dramatically increases cancellous bone mass in the osteogenesis imperfecta mouse (oim). Bone Reports. 9: 61-73. PMID 30105276 DOI: 10.1016/J.Bonr.2018.06.008 |
0.398 |
|
| 2018 |
O'Brien CA, Morello R. Modeling Rare Bone Diseases in Animals. Current Osteoporosis Reports. 16: 458-465. PMID 29802575 DOI: 10.1007/S11914-018-0452-X |
0.317 |
|
| 2018 |
Morello R. Osteogenesis imperfecta and therapeutics. Matrix Biology : Journal of the International Society For Matrix Biology. 71: 294-312. PMID 29540309 DOI: 10.1016/J.Matbio.2018.03.010 |
0.439 |
|
| 2017 |
Hudson DM, Weis M, Rai J, Joeng KS, Dimori M, Lee BH, Morello R, Eyre DR. P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA. The Journal of Biological Chemistry. PMID 28115524 DOI: 10.1074/Jbc.M116.762245 |
0.569 |
|
| 2016 |
Loughran AJ, Gaddy D, Beenken KE, Meeker DG, Morello R, Zhao H, Byrum SD, Tackett AJ, Cassat JE, Smeltzer MS. Impact of sarA and phenol-soluble modulins in the pathogenesis of osteomyelitis in diverse clinical isolates of Staphylococcus aureus. Infection and Immunity. PMID 27354444 DOI: 10.1128/Iai.00152-16 |
0.392 |
|
| 2016 |
Heard ME, Besio R, Weis M, Rai J, Hudson DM, Dimori M, Zimmerman SM, Kamykowski JA, Hogue WR, Swain FL, Burdine MS, Mackintosh SG, Tackett AJ, Suva LJ, Eyre DR, ... Morello R, et al. Sc65-Null Mice Provide Evidence for a Novel Endoplasmic Reticulum Complex Regulating Collagen Lysyl Hydroxylation. Plos Genetics. 12: e1006002. PMID 27119146 DOI: 10.1371/Journal.Pgen.1006002 |
0.411 |
|
| 2014 |
Homan EP, Lietman C, Grafe I, Lennington J, Morello R, Napierala D, Jiang MM, Munivez EM, Dawson B, Bertin TK, Chen Y, Lua R, Lichtarge O, Hicks J, Weis MA, et al. Differential effects of collagen prolyl 3-hydroxylation on skeletal tissues. Plos Genetics. 10: e1004121. PMID 24465224 DOI: 10.1371/Journal.Pgen.1004121 |
0.621 |
|
| 2014 |
Gruenwald K, Castagnola P, Besio R, Dimori M, Chen Y, Akel NS, Swain FL, Skinner RA, Eyre DR, Gaddy D, Suva LJ, Morello R. Sc65 is a novel endoplasmic reticulum protein that regulates bone mass homeostasis. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 29: 666-75. PMID 23959653 DOI: 10.1002/Jbmr.2075 |
0.435 |
|
| 2011 |
Amor IMB, Rauch F, Gruenwald K, Weis M, Eyre DR, Roughley P, Glorieux FH, Morello R. Severe osteogenesis imperfecta caused by a small in-frame deletion in CRTAP. American Journal of Medical Genetics Part A. 155: 2865-2870. PMID 21964860 DOI: 10.1002/Ajmg.A.34269 |
0.479 |
|
| 2011 |
Homan EP, Rauch F, Grafe I, Lietman C, Doll JA, Dawson B, Bertin T, Napierala D, Morello R, Gibbs R, White L, Miki R, Cohn DH, Crawford S, Travers R, et al. Mutations in SERPINF1 cause osteogenesis imperfecta type VI Journal of Bone and Mineral Research. 26: 2798-2803. PMID 21826736 DOI: 10.1002/Jbmr.487 |
0.59 |
|
| 2010 |
Monticone M, Panfoli I, Ravera S, Puglisi R, Jiang MM, Morello R, Candiani S, Tonachini L, Biticchi R, Fabiano A, Cancedda R, Boitani C, Castagnola P. The nuclear genes Mtfr1 and Dufd1 regulate mitochondrial dynamic and cellular respiration. Journal of Cellular Physiology. 225: 767-76. PMID 20568109 DOI: 10.1002/Jcp.22279 |
0.315 |
|
| 2010 |
Baldridge D, Lennington J, Weis M, Homan EP, Jiang MM, Munivez E, Keene DR, Hogue WR, Pyott S, Byers PH, Krakow D, Cohn DH, Eyre DR, Lee B, Morello R. Generalized connective tissue disease in Crtap-/- mouse. Plos One. 5: e10560. PMID 20485499 DOI: 10.1371/Journal.Pone.0010560 |
0.56 |
|
| 2010 |
Morello R, Rauch F. Role of cartilage-associated protein in skeletal development. Current Osteoporosis Reports. 8: 77-83. PMID 20425614 DOI: 10.1007/S11914-010-0010-7 |
0.477 |
|
| 2010 |
Gabbay KH, Bohren KM, Morello R, Bertin T, Liu J, Vogel P. Ascorbate synthesis pathway: dual role of ascorbate in bone homeostasis. The Journal of Biological Chemistry. 285: 19510-20. PMID 20410296 DOI: 10.1074/Jbc.M110.110247 |
0.425 |
|
| 2010 |
Fratzl-Zelman N, Morello R, Lee B, Rauch F, Glorieux FH, Misof BM, Klaushofer K, Roschger P. CRTAP deficiency leads to abnormally high bone matrix mineralization in a murine model and in children with osteogenesis imperfecta type VII Bone. 46: 820-826. PMID 19895918 DOI: 10.1016/J.Bone.2009.10.037 |
0.459 |
|
| 2009 |
Ferlin A, Pepe A, Gianesello L, Garolla A, Feng S, Facciolli A, Morello R, Agoulnik AI, Foresta C. New roles for INSL3 in adults. Annals of the New York Academy of Sciences. 1160: 215-8. PMID 19416191 DOI: 10.1111/J.1749-6632.2008.03787.X |
0.375 |
|
| 2009 |
Fratzl-Zelman N, Morello R, Lee B, Rauch F, Glorieux FH, Misof BM, Klaushofer K, Roschger P. CRTAP deficiency leads to high bone matrix mineralization in children (Osteogenesis imperfecta type VII) and mice Bone. 44. DOI: 10.1016/J.Bone.2009.03.133 |
0.532 |
|
| 2008 |
Baldridge D, Schwarze U, Morello R, Lennington J, Bertin TK, Pace JM, Pepin MG, Weis M, Eyre DR, Walsh J, Lambert D, Green A, Robinson H, Michelson M, Houge G, et al. CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta. Human Mutation. 29: 1435-42. PMID 18566967 DOI: 10.1002/Humu.20799 |
0.604 |
|
| 2008 |
Morello R, Bertin TK, Schlaubitz S, Shaw CA, Kakuru S, Munivez E, Hermanns P, Chen Y, Zabel B, Lee B. Brachy-syndactyly caused by loss of Sfrp2 function. Journal of Cellular Physiology. 217: 127-37. PMID 18446812 DOI: 10.1002/Jcp.21483 |
0.52 |
|
| 2008 |
Ferlin A, Pepe A, Gianesello L, Garolla A, Feng S, Giannini S, Zaccolo M, Facciolli A, Morello R, Agoulnik AI, Foresta C. Mutations in the insulin-like factor 3 receptor are associated with osteoporosis. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 23: 683-93. PMID 18433302 DOI: 10.1359/Jbmr.080204 |
0.455 |
|
| 2008 |
Napierala D, Sam K, Morello R, Zheng Q, Munivez E, Shivdasani RA, Lee B. Uncoupling of chondrocyte differentiation and perichondrial mineralization underlies the skeletal dysplasia in tricho-rhino-phalangeal syndrome. Human Molecular Genetics. 17: 2244-54. PMID 18424451 DOI: 10.1093/Hmg/Ddn125 |
0.592 |
|
| 2008 |
Lennington J, Morello R, Jiang M, Baldridge D, Bertin T, Lee B. 141: Prolyl-3 Hydroxylase Expression in the Mouse Kidney and Developing Embryo American Journal of Kidney Diseases. 51. DOI: 10.1053/J.Ajkd.2008.02.149 |
0.499 |
|
| 2006 |
Barnes AM, Chang W, Morello R, Cabral WA, Weis M, Eyre DR, Leikin S, Makareeva E, Kuznetsova N, Uveges TE, Ashok A, Flor AW, Mulvihill JJ, Wilson PL, Sundaram UT, et al. Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta. The New England Journal of Medicine. 355: 2757-64. PMID 17192541 DOI: 10.1056/Nejmoa063804 |
0.614 |
|
| 2006 |
Morello R, Bertin TK, Chen Y, Hicks J, Tonachini L, Monticone M, Castagnola P, Rauch F, Glorieux FH, Vranka J, Bächinger HP, Pace JM, Schwarze U, Byers PH, Weis M, et al. CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta. Cell. 127: 291-304. PMID 17055431 DOI: 10.1016/J.Cell.2006.08.039 |
0.626 |
|
| 2006 |
Tavella S, Biticchi R, Morello R, Castagnola P, Musante V, Costa D, Cancedda R, Garofalo S. Forced chondrocyte expression of sonic hedgehog impairs joint formation affecting proliferation and apoptosis. Matrix Biology. 25: 389-397. PMID 16962305 DOI: 10.1016/J.Matbio.2006.07.005 |
0.395 |
|
| 2006 |
Kang JS, Wang XP, Miner JH, Morello R, Sado Y, Abrahamson DR, Borza DB. Loss of alpha3/alpha4(IV) collagen from the glomerular basement membrane induces a strain-dependent isoform switch to alpha5alpha6(IV) collagen associated with longer renal survival in Col4a3-/- Alport mice. Journal of the American Society of Nephrology : Jasn. 17: 1962-9. PMID 16769745 DOI: 10.1681/Asn.2006020165 |
0.377 |
|
| 2006 |
Morello R, Bertin T, Hicks J, Castagnola P, Glorieux FH, Bachinger H, Byers PH, Eyre DR, Boyce BF, Lee B. Prolyl 3_hydroxylation and recessive osteogenesis imperfecta Matrix Biology. 25. DOI: 10.1016/J.Matbio.2006.08.176 |
0.539 |
|
| 2006 |
Barnes A, Chang W, Morello R, Cabral W, Weis M, Eyre D, Leikin S, Mulvihill J, Lee B, Marini J. Recessive lethal form of OI caused by null mutations in CRTAP Matrix Biology. 25. DOI: 10.1016/J.Matbio.2006.08.170 |
0.52 |
|
| 2004 |
Dreyer SD, Naruse T, Morello R, Zabel B, Winterpacht A, Johnson RL, Lee B, Oberg KC. Lmx1b expression during joint and tendon formation: localization and evaluation of potential downstream targets. Gene Expression Patterns : Gep. 4: 397-405. PMID 15183306 DOI: 10.1016/J.Modgep.2004.01.006 |
0.521 |
|
| 2003 |
Zheng Q, Zhou G, Morello R, Chen Y, Garcia-Rojas X, Lee B. Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte-specific expression in vivo. The Journal of Cell Biology. 162: 833-42. PMID 12952936 DOI: 10.1083/Jcb.200211089 |
0.551 |
|
| 2002 |
Hamano Y, Grunkemeyer JA, Sudhakar A, Zeisberg M, Cosgrove D, Morello R, Lee B, Sugimoto H, Kalluri R. Determinants of vascular permeability in the kidney glomerulus. The Journal of Biological Chemistry. 277: 31154-62. PMID 12039968 DOI: 10.1074/Jbc.M204806200 |
0.541 |
|
| 2002 |
Morello R, Lee B. Insight into podocyte differentiation from the study of human genetic disease: nail-patella syndrome and transcriptional regulation in podocytes. Pediatric Research. 51: 551-8. PMID 11978876 DOI: 10.1203/00006450-200205000-00002 |
0.531 |
|
| 2002 |
Miner JH, Morello R, Andrews KL, Li C, Antignac C, Shaw AS, Lee B. Transcriptional induction of slit diaphragm genes by Lmx1b is required in podocyte differentiation. The Journal of Clinical Investigation. 109: 1065-72. PMID 11956244 DOI: 10.1172/Jci13954 |
0.572 |
|
| 2001 |
Morello R, Zhou G, Dreyer SD, Harvey SJ, Ninomiya Y, Thorner PS, Miner JH, Cole W, Winterpacht A, Zabel B, Oberg KC, Lee B. Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome Nature Genetics. 27: 205-208. PMID 11175791 DOI: 10.1038/84853 |
0.516 |
|
| 2000 |
Dreyer SD, Morello R, German MS, Zabel B, Winterpacht A, Lunstrum GP, Horton WA, Oberg KC, Lee B. LMX1B transactivation and expression in nail-patella syndrome Human Molecular Genetics. 9: 1067-1074. PMID 10767331 DOI: 10.1093/Hmg/9.7.1067 |
0.562 |
|
| 1999 |
Tonachini L, Morello R, Monticone M, Skaug J, Scherer SW, Cancedda R, Castagnola P. cDNA cloning, characterization and chromosome mapping of the gene encoding human cartilage associated protein (CRTAP). Cytogenetic and Genome Research. 87: 191-194. PMID 10702664 DOI: 10.1159/000015463 |
0.327 |
|
| 1999 |
Morello R, Tonachini L, Monticone M, Viggiano L, Rocchi M, Cancedda R, Castagnola P. cDNA cloning, characterization and chromosome mapping of Crtap encoding the mouse cartilage associated protein. Matrix Biology. 18: 319-324. PMID 10429950 DOI: 10.1016/S0945-053X(99)00002-5 |
0.34 |
|
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