| Year |
Citation |
Score |
| 2019 |
Goring A, Sharma A, Javaheri B, Smith RC, Kanczler JM, Boyde A, Hesse E, Mahajan S, Olsen BR, Pitsillides AA, Schneider P, Oreffo RO, Clarkin CE. Regulation of the bone vascular network is sexually dimorphic. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 31269275 DOI: 10.1002/Jbmr.3825 |
0.314 |
|
| 2017 |
Nagao M, Hamilton JL, Kc R, Berendsen AD, Duan X, Cheong CW, Li X, Im HJ, Olsen BR. Vascular Endothelial Growth Factor in Cartilage Development and Osteoarthritis. Scientific Reports. 7: 13027. PMID 29026147 DOI: 10.1038/S41598-017-13417-W |
0.325 |
|
| 2016 |
Hu K, Olsen BR, Besschetnova TY. Cell autonomous ANTXR1-mediated regulation of extracellular matrix components in primary fibroblasts. Matrix Biology : Journal of the International Society For Matrix Biology. PMID 28011198 DOI: 10.1016/J.Matbio.2016.12.002 |
0.356 |
|
| 2016 |
Hu K, Olsen BR. Vascular Endothelial Growth Factor Control Mechanisms in Skeletal Growth and Repair. Developmental Dynamics : An Official Publication of the American Association of Anatomists. PMID 27750398 DOI: 10.1002/Dvdy.24463 |
0.315 |
|
| 2016 |
Hu K, Besschetnova TY, Olsen BR. Soluble VEGFR1 reverses BMP2 inhibition of intramembranous ossification during healing of cortical bone defects. Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society. PMID 27658810 DOI: 10.1002/Jor.23416 |
0.316 |
|
| 2016 |
Olsen BR, Berendsen AD, Besschetnova TY, Duan X, Hu K. Regulatory mechanisms of skeletal and connective tissue development and homeostasis - lessons from studies of human disorders. International Journal of Experimental Pathology. PMID 27581728 DOI: 10.1111/Iep.12198 |
0.336 |
|
| 2016 |
Hu K, Olsen BR. The roles of vascular endothelial growth factor in bone repair and regeneration. Bone. PMID 27353702 DOI: 10.1016/J.Bone.2016.06.013 |
0.311 |
|
| 2016 |
Duan X, Bradbury SR, Olsen BR, Berendsen AD. VEGF stimulates intramembranous bone formation during craniofacial skeletal development. Matrix Biology : Journal of the International Society For Matrix Biology. PMID 26899202 DOI: 10.1016/J.Matbio.2016.02.005 |
0.359 |
|
| 2016 |
Hu K, Olsen BR. Osteoblast-derived VEGF regulates osteoblast differentiation and bone formation during bone repair. The Journal of Clinical Investigation. 126: 509-26. PMID 26731472 DOI: 10.1172/Jci82585 |
0.325 |
|
| 2015 |
Agarwal S, Loder S, Brownley C, Cholok D, Mangiavini L, Li J, Breuler C, Sung HH, Li S, Ranganathan K, Peterson J, Tompkins R, Herndon D, Xiao W, Jumlongras D, ... Olsen BR, et al. Inhibition of Hif1α prevents both trauma-induced and genetic heterotopic ossification. Proceedings of the National Academy of Sciences of the United States of America. PMID 26721400 DOI: 10.1073/Pnas.1515397113 |
0.793 |
|
| 2015 |
Lloyd WR, Agarwal S, Nigwekar SU, Esmonde-White K, Loder S, Fagan S, Goverman J, Olsen BR, Jumlongras D, Morris MD, Levi B. Raman spectroscopy for label-free identification of calciphylaxis. Journal of Biomedical Optics. 20: 80501. PMID 26263412 DOI: 10.1117/1.Jbo.20.8.080501 |
0.756 |
|
| 2015 |
Duan X, Murata Y, Liu Y, Nicolae C, Olsen BR, Berendsen AD. Vegfa regulates perichondrial vascularity and osteoblast differentiation in bone development. Development (Cambridge, England). 142: 1984-91. PMID 25977369 DOI: 10.1242/Dev.117952 |
0.542 |
|
| 2015 |
Agarwal S, Loder S, Brownley C, Peterson J, Oluwatobi E, Tompkins R, Herndon D, Sung H, Zeng W, Jumlongras D, Olsen B, Cederna PS, Buchman SR, Levi B. Abstract 20: Defining the Role of the Vasculogenic Niche in Trauma-induced Heterotopic Ossification using Novel Imaging and Lineage-tracing Mice. Plastic and Reconstructive Surgery. 135: 24. PMID 25915234 DOI: 10.1097/01.Prs.0000465468.77621.1C |
0.763 |
|
| 2015 |
Berendsen AD, Olsen BR. Regulation of adipogenesis and osteogenesis in mesenchymal stem cells by vascular endothelial growth factor A. Journal of Internal Medicine. 277: 674-80. PMID 25779338 DOI: 10.1111/Joim.12364 |
0.332 |
|
| 2015 |
Besschetnova TY, Ichimura T, Katebi N, St Croix B, Bonventre JV, Olsen BR. Regulatory mechanisms of anthrax toxin receptor 1-dependent vascular and connective tissue homeostasis. Matrix Biology : Journal of the International Society For Matrix Biology. 42: 56-73. PMID 25572963 DOI: 10.1016/J.Matbio.2014.12.002 |
0.33 |
|
| 2014 |
Olsen BR. Disease models: Statins give bone growth a boost. Nature. 513: 494-5. PMID 25231860 DOI: 10.1038/Nature13750 |
0.33 |
|
| 2014 |
Dubail J, Aramaki-Hattori N, Bader HL, Nelson CM, Katebi N, Matuska B, Olsen BR, Apte SS. A new Adamts9 conditional mouse allele identifies its non-redundant role in interdigital web regression. Genesis (New York, N.Y. : 2000). 52: 702-12. PMID 24753090 DOI: 10.1002/Dvg.22784 |
0.317 |
|
| 2014 |
Liu Y, Olsen BR. Distinct VEGF functions during bone development and homeostasis. Archivum Immunologiae Et Therapiae Experimentalis. 62: 363-8. PMID 24699630 DOI: 10.1007/S00005-014-0285-Y |
0.534 |
|
| 2014 |
Berendsen AD, Olsen BR. How vascular endothelial growth factor-A (VEGF) regulates differentiation of mesenchymal stem cells. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 62: 103-8. PMID 24309509 DOI: 10.1369/0022155413516347 |
0.327 |
|
| 2014 |
Berendsen AD, Olsen BR. Osteoblast-adipocyte lineage plasticity in tissue development, maintenance and pathology. Cellular and Molecular Life Sciences : Cmls. 71: 493-7. PMID 23934155 DOI: 10.1007/S00018-013-1440-Z |
0.316 |
|
| 2013 |
Adams A, McBratney-Owen B, Newby B, Bowen ME, Olsen BR, Warman ML. Presphenoidal synchondrosis fusion in DBA/2J mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 24: 54-62. PMID 23179633 DOI: 10.1007/S00335-012-9437-8 |
0.756 |
|
| 2012 |
Medici D, Olsen BR. Rapamycin inhibits proliferation of hemangioma endothelial cells by reducing HIF-1-dependent expression of VEGF. Plos One. 7: e42913. PMID 22900063 DOI: 10.1371/Journal.Pone.0042913 |
0.723 |
|
| 2012 |
Liu Y, Berendsen AD, Jia S, Lotinun S, Baron R, Ferrara N, Olsen BR. Intracellular VEGF regulates the balance between osteoblast and adipocyte differentiation. The Journal of Clinical Investigation. 122: 3101-13. PMID 22886301 DOI: 10.1172/Jci61209 |
0.534 |
|
| 2012 |
Medici D, Olsen BR. The role of endothelial-mesenchymal transition in heterotopic ossification. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 27: 1619-22. PMID 22806925 DOI: 10.1002/Jbmr.1691 |
0.744 |
|
| 2012 |
Jumlongras D, Lachke SA, O'Connell DJ, Aboukhalil A, Li X, Choe SE, Ho JW, Turbe-Doan A, Robertson EA, Olsen BR, Bulyk ML, Amendt BA, Maas RL. An evolutionarily conserved enhancer regulates Bmp4 expression in developing incisor and limb bud. Plos One. 7: e38568. PMID 22701669 DOI: 10.1371/Journal.Pone.0038568 |
0.774 |
|
| 2012 |
Reichenberger EJ, Levine MA, Olsen BR, Papadaki ME, Lietman SA. The role of SH3BP2 in the pathophysiology of cherubism. Orphanet Journal of Rare Diseases. 7: S5. PMID 22640988 DOI: 10.1186/1750-1172-7-S1-S5 |
0.317 |
|
| 2012 |
Ionescu A, Kozhemyakina E, Nicolae C, Kaestner KH, Olsen BR, Lassar AB. FoxA family members are crucial regulators of the hypertrophic chondrocyte differentiation program. Developmental Cell. 22: 927-39. PMID 22595668 DOI: 10.1016/J.Devcel.2012.03.011 |
0.308 |
|
| 2012 |
Jeng L, Olsen BR, Spector M. Engineering endostatin-expressing cartilaginous constructs using injectable biopolymer hydrogels. Acta Biomaterialia. 8: 2203-12. PMID 22370447 DOI: 10.1016/J.Actbio.2012.02.015 |
0.303 |
|
| 2011 |
Medici D, Olsen BR. Transforming blood vessels into bone. Cell Cycle (Georgetown, Tex.). 10: 362-3. PMID 21239889 DOI: 10.4161/Cc.10.3.14519 |
0.742 |
|
| 2011 |
Medici D, Shore EM, Lounev VY, Kaplan FS, Kalluri R, Olsen BR. Erratum: Corrigendum: Conversion of vascular endothelial cells into multipotent stem-like cells Nature Medicine. 17: 514-514. DOI: 10.1038/Nm0411-514D |
0.717 |
|
| 2010 |
Medici D, Shore EM, Lounev VY, Kaplan FS, Kalluri R, Olsen BR. Conversion of vascular endothelial cells into multipotent stem-like cells. Nature Medicine. 16: 1400-6. PMID 21102460 DOI: 10.1038/nm.2252 |
0.728 |
|
| 2010 |
Mauney J, Olsen BR, Volloch V. Matrix remodeling as stem cell recruitment event: a novel in vitro model for homing of human bone marrow stromal cells to the site of injury shows crucial role of extracellular collagen matrix. Matrix Biology : Journal of the International Society For Matrix Biology. 29: 657-63. PMID 20828613 DOI: 10.1016/J.Matbio.2010.08.008 |
0.332 |
|
| 2010 |
Mukherjee PM, Wang CJ, Chen IP, Jafarov T, Olsen BR, Ueki Y, Reichenberger EJ. Cherubism gene Sh3bp2 is important for optimal bone formation, osteoblast differentiation, and function. American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics. 138: 140.e1-140.e11; disc. PMID 20691350 DOI: 10.1016/J.Ajodo.2009.05.021 |
0.32 |
|
| 2010 |
Nicolae C, Olsen BR. Unexpected matrix diseases and novel therapeutic strategies. Cell and Tissue Research. 339: 155-65. PMID 19813027 DOI: 10.1007/S00441-009-0874-Y |
0.324 |
|
| 2010 |
Mukherjee PM, Wang CJ, Chen I-, Jafarov T, Olsen BR, Ueki Y, Reichenberger EJ. Editor's Comment and Q&A: Cherubism gene Sh3bp2 is important for optimal bone formation, osteoblast differentiation, and function American Journal of Orthodontics and Dentofacial Orthopedics. 138: 140-141. DOI: 10.1016/J.Ajodo.2010.04.004 |
0.348 |
|
| 2009 |
Gebauer JM, Keene DR, Olsen BR, Sorokin LM, Paulsson M, Wagener R. Mouse AMACO, a kidney and skin basement membrane associated molecule that mediates RGD-dependent cell attachment. Matrix Biology : Journal of the International Society For Matrix Biology. 28: 456-62. PMID 19651211 DOI: 10.1016/J.Matbio.2009.07.006 |
0.301 |
|
| 2009 |
Griekspoor P, Olsen B, Waldenström J. Campylobacter jejuni in Penguins, Antarctica Emerging Infectious Diseases. 15: 847-849. PMID 19402996 DOI: 10.3201/Eid1505.081160 |
0.306 |
|
| 2009 |
Galli C, Fu Q, Wang W, Olsen BR, Manolagas SC, Jilka RL, O'Brien CA. Commitment to the osteoblast lineage is not required for RANKL gene expression. The Journal of Biological Chemistry. 284: 12654-62. PMID 19279010 DOI: 10.1074/Jbc.M806628200 |
0.319 |
|
| 2009 |
Hou B, Kolpakova-Hart E, Fukai N, Wu K, Olsen BR. The polycystic kidney disease 1 (Pkd1) gene is required for the responses of osteochondroprogenitor cells to midpalatal suture expansion in mice. Bone. 44: 1121-33. PMID 19264154 DOI: 10.1016/J.Bone.2009.02.018 |
0.339 |
|
| 2009 |
Sun XD, Jeng L, Bolliet C, Olsen BR, Spector M. Non-viral endostatin plasmid transfection of mesenchymal stem cells via collagen scaffolds. Biomaterials. 30: 1222-31. PMID 19059640 DOI: 10.1016/J.Biomaterials.2008.10.020 |
0.331 |
|
| 2008 |
Jinnin M, Medici D, Park L, Limaye N, Liu Y, Boscolo E, Bischoff J, Vikkula M, Boye E, Olsen BR. Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma. Nature Medicine. 14: 1236-46. PMID 18931684 DOI: 10.1038/Nm.1877 |
0.766 |
|
| 2008 |
Aliprantis AO, Ueki Y, Sulyanto R, Park A, Sigrist KS, Sharma SM, Ostrowski MC, Olsen BR, Glimcher LH. NFATc1 in mice represses osteoprotegerin during osteoclastogenesis and dissociates systemic osteopenia from inflammation in cherubism. The Journal of Clinical Investigation. 118: 3775-89. PMID 18846253 DOI: 10.1172/Jci35711 |
0.332 |
|
| 2008 |
Medici D, Hay ED, Olsen BR. Snail and Slug promote epithelial-mesenchymal transition through beta-catenin-T-cell factor-4-dependent expression of transforming growth factor-beta3. Molecular Biology of the Cell. 19: 4875-87. PMID 18799618 DOI: 10.1091/Mbc.E08-05-0506 |
0.707 |
|
| 2008 |
McBratney-Owen B, Iseki S, Bamforth SD, Olsen BR, Morriss-Kay GM. Development and tissue origins of the mammalian cranial base. Developmental Biology. 322: 121-32. PMID 18680740 DOI: 10.1016/J.Ydbio.2008.07.016 |
0.778 |
|
| 2008 |
Medici D, Razzaque MS, Deluca S, Rector TL, Hou B, Kang K, Goetz R, Mohammadi M, Kuro-O M, Olsen BR, Lanske B. FGF-23-Klotho signaling stimulates proliferation and prevents vitamin D-induced apoptosis. The Journal of Cell Biology. 182: 459-65. PMID 18678710 DOI: 10.1083/Jcb.200803024 |
0.716 |
|
| 2008 |
Kolpakova-Hart E, McBratney-Owen B, Hou B, Fukai N, Nicolae C, Zhou J, Olsen BR. Growth of cranial synchondroses and sutures requires polycystin-1. Developmental Biology. 321: 407-19. PMID 18652813 DOI: 10.1016/J.Ydbio.2008.07.005 |
0.772 |
|
| 2007 |
Kolpakova-Hart E, Jinnin M, Hou B, Fukai N, Olsen BR. Kinesin-2 controls development and patterning of the vertebrate skeleton by Hedgehog- and Gli3-dependent mechanisms. Developmental Biology. 309: 273-84. PMID 17698054 DOI: 10.1016/J.Ydbio.2007.07.018 |
0.3 |
|
| 2007 |
Li Y, Xu L, Olsen BR. Lessons from genetic forms of osteoarthritis for the pathogenesis of the disease. Osteoarthritis and Cartilage / Oars, Osteoarthritis Research Society. 15: 1101-5. PMID 17572112 DOI: 10.1016/J.Joca.2007.04.013 |
0.303 |
|
| 2007 |
Marneros AG, She H, Zambarakji H, Hashizume H, Connolly EJ, Kim I, Gragoudas ES, Miller JW, Olsen BR. Endogenous endostatin inhibits choroidal neovascularization. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 21: 3809-18. PMID 17526870 DOI: 10.1096/Fj.07-8422Com |
0.302 |
|
| 2007 |
Hou B, Fukai N, Olsen BR. Mechanical force-induced midpalatal suture remodeling in mice. Bone. 40: 1483-93. PMID 17398175 DOI: 10.1016/J.Bone.2007.01.019 |
0.314 |
|
| 2007 |
Ueki Y, Lin CY, Senoo M, Ebihara T, Agata N, Onji M, Saheki Y, Kawai T, Mukherjee PM, Reichenberger E, Olsen BR. Increased myeloid cell responses to M-CSF and RANKL cause bone loss and inflammation in SH3BP2 "cherubism" mice. Cell. 128: 71-83. PMID 17218256 DOI: 10.1016/J.Cell.2006.10.047 |
0.324 |
|
| 2007 |
Lam NP, Li Y, Waldman AB, Brussiau J, Lee PL, Olsen BR, Xu L. Age-dependent increase of discoidin domain receptor 2 and matrix metalloproteinase 13 expression in temporomandibular joint cartilage of type IX and type XI collagen-deficient mice. Archives of Oral Biology. 52: 579-84. PMID 17125729 DOI: 10.1016/J.Archoralbio.2006.10.014 |
0.301 |
|
| 2005 |
Hopfer U, Fukai N, Hopfer H, Wolf G, Joyce N, Li E, Olsen BR. Targeted disruption of Col8a1 and Col8a2 genes in mice leads to anterior segment abnormalities in the eye. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 19: 1232-44. PMID 16051690 DOI: 10.1096/Fj.04-3019Com |
0.317 |
|
| 2005 |
Marneros AG, Olsen BR. Physiological role of collagen XVIII and endostatin. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 19: 716-28. PMID 15857886 DOI: 10.1096/Fj.04-2134Rev |
0.35 |
|
| 2005 |
Gaetzner S, Deckers MM, Stahl S, Löwik C, Olsen BR, Felbor U. Endostatin's heparan sulfate-binding site is essential for inhibition of angiogenesis and enhances in situ binding to capillary-like structures in bone explants. Matrix Biology : Journal of the International Society For Matrix Biology. 23: 557-61. PMID 15694132 DOI: 10.1016/J.Matbio.2004.10.001 |
0.311 |
|
| 2005 |
Zelzer E, Olsen BR. Multiple roles of vascular endothelial growth factor (VEGF) in skeletal development, growth, and repair. Current Topics in Developmental Biology. 65: 169-87. PMID 15642383 DOI: 10.1016/S0070-2153(04)65006-X |
0.314 |
|
| 2005 |
Xu L, Peng H, Wu D, Hu K, Goldring MB, Olsen BR, Li Y. Activation of the discoidin domain receptor 2 induces expression of matrix metalloproteinase 13 associated with osteoarthritis in mice. The Journal of Biological Chemistry. 280: 548-55. PMID 15509586 DOI: 10.1074/Jbc.M411036200 |
0.303 |
|
| 2004 |
Li Q, Olsen BR. Increased angiogenic response in aortic explants of collagen XVIII/endostatin-null mice. The American Journal of Pathology. 165: 415-24. PMID 15277216 DOI: 10.1016/S0002-9440(10)63307-X |
0.349 |
|
| 2004 |
Nawshad A, LaGamba D, Olsen BR, Hay ED. Laser capture microdissection (LCM) for analysis of gene expression in specific tissues during embryonic epithelial-mesenchymal transformation. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 230: 529-34. PMID 15188437 DOI: 10.1002/Dvdy.20064 |
0.303 |
|
| 2004 |
Wang W, Wang YG, Reginato AM, Glotzer DJ, Fukai N, Plotkina S, Karsenty G, Olsen BR. Groucho homologue Grg5 interacts with the transcription factor Runx2-Cbfa1 and modulates its activity during postnatal growth in mice. Developmental Biology. 270: 364-81. PMID 15183720 DOI: 10.1016/J.Ydbio.2004.03.003 |
0.333 |
|
| 2004 |
Pfander D, Kobayashi T, Knight MC, Zelzer E, Chan DA, Olsen BR, Giaccia AJ, Johnson RS, Haase VH, Schipani E. Deletion of Vhlh in chondrocytes reduces cell proliferation and increases matrix deposition during growth plate development. Development (Cambridge, England). 131: 2497-508. PMID 15128677 DOI: 10.1242/Dev.01138 |
0.361 |
|
| 2004 |
Zelzer E, Mamluk R, Ferrara N, Johnson RS, Schipani E, Olsen BR. VEGFA is necessary for chondrocyte survival during bone development. Development (Cambridge, England). 131: 2161-71. PMID 15073147 DOI: 10.1242/Dev.01053 |
0.359 |
|
| 2004 |
Jumlongras D, Lin JY, Chapra A, Seidman CE, Seidman JG, Maas RL, Olsen BR. A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia. Human Genetics. 114: 242-9. PMID 14689302 DOI: 10.1007/S00439-003-1066-6 |
0.764 |
|
| 2003 |
Ylikärppä R, Eklund L, Sormunen R, Muona A, Fukai N, Olsen BR, Pihlajaniemi T. Double knockout mice reveal a lack of major functional compensation between collagens XV and XVIII. Matrix Biology : Journal of the International Society For Matrix Biology. 22: 443-8. PMID 14614990 DOI: 10.1016/S0945-053X(03)00074-X |
0.309 |
|
| 2003 |
Ylikärppä R, Eklund L, Sormunen R, Kontiola AI, Utriainen A, Määttä M, Fukai N, Olsen BR, Pihlajaniemi T. Lack of type XVIII collagen results in anterior ocular defects. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 17: 2257-9. PMID 14525950 DOI: 10.1096/Fj.02-1001Fje |
0.308 |
|
| 2003 |
Rice R, Rice DP, Olsen BR, Thesleff I. Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4. Developmental Biology. 262: 75-87. PMID 14512019 DOI: 10.1016/S0012-1606(03)00355-5 |
0.329 |
|
| 2003 |
Marneros AG, Olsen BR. Age-dependent iris abnormalities in collagen XVIII/endostatin deficient mice with similarities to human pigment dispersion syndrome. Investigative Ophthalmology & Visual Science. 44: 2367-72. PMID 12766032 DOI: 10.1167/Iovs.02-1180 |
0.314 |
|
| 2003 |
Czipri M, Otto JM, Cs-Szabó G, Kamath RV, Vermes C, Firneisz G, Kolman KJ, Watanabe H, Li Y, Roughley PJ, Yamada Y, Olsen BR, Glant TT. Genetic rescue of chondrodysplasia and the perinatal lethal effect of cartilage link protein deficiency. The Journal of Biological Chemistry. 278: 39214-23. PMID 12732630 DOI: 10.1074/Jbc.M303329200 |
0.302 |
|
| 2003 |
Rossi M, Morita H, Sormunen R, Airenne S, Kreivi M, Wang L, Fukai N, Olsen BR, Tryggvason K, Soininen R. Heparan sulfate chains of perlecan are indispensable in the lens capsule but not in the kidney. The Embo Journal. 22: 236-45. PMID 12514129 DOI: 10.1093/Emboj/Cdg019 |
0.314 |
|
| 2002 |
Suzuki OT, Sertié AL, Der Kaloustian VM, Kok F, Carpenter M, Murray J, Czeizel AE, Kliemann SE, Rosemberg S, Monteiro M, Olsen BR, Passos-Bueno MR. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome American Journal of Human Genetics. 71: 1320-1329. PMID 12415512 DOI: 10.1086/344695 |
0.323 |
|
| 2002 |
Wang WF, Wang YG, Reginato AM, Plotkina S, Gridley T, Olsen BR. Growth defect in Grg5 null mice is associated with reduced Ihh signaling in growth plates. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 224: 79-89. PMID 11984876 DOI: 10.1002/Dvdy.10089 |
0.327 |
|
| 2002 |
Brouillard P, Boon LM, Mulliken JB, Enjolras O, Ghassibé M, Warman ML, Tan OT, Olsen BR, Vikkula M. Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas"). American Journal of Human Genetics. 70: 866-74. PMID 11845407 DOI: 10.1086/339492 |
0.321 |
|
| 2001 |
Gong Y, Slee RB, Fukai N, Rawadi G, Roman-Roman S, Reginato AM, Wang H, Cundy T, Glorieux FH, Lev D, Zacharin M, Oexle K, Marcelino J, Suwairi W, Heeger S, ... ... Olsen BR, et al. LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development. Cell. 107: 513-23. PMID 11719191 DOI: 10.1016/S0092-8674(01)00571-2 |
0.303 |
|
| 2001 |
McLean W, Olsen BR. Mouse models of abnormal skeletal development and homeostasis. Trends in Genetics : Tig. 17: S38-43. PMID 11585675 DOI: 10.1016/S0168-9525(01)02458-1 |
0.305 |
|
| 2001 |
Marneros AG, Olsen BR. The role of collagen-derived proteolytic fragments in angiogenesis Matrix Biology. 20: 337-345. PMID 11566268 DOI: 10.1016/S0945-053X(01)00151-2 |
0.315 |
|
| 2001 |
Zelzer E, Glotzer DJ, Hartmann C, Thomas D, Fukai N, Soker S, Olsen BR. Tissue specific regulation of VEGF expression during bone development requires Cbfa1/Runx2 Mechanisms of Development. 106: 97-106. PMID 11472838 DOI: 10.1016/S0925-4773(01)00428-2 |
0.333 |
|
| 2001 |
Lavrin IO, McLean W, Seegmiller RE, Olsen BR, Hay ED. The mechanism of palatal clefting in the Col11a1 mutant mouse. Archives of Oral Biology. 46: 865-9. PMID 11420059 DOI: 10.1016/S0003-9969(01)00044-9 |
0.343 |
|
| 2001 |
Jumlongras D, Bei M, Stimson JM, Wang WF, DePalma SR, Seidman CE, Felbor U, Maas R, Seidman JG, Olsen BR. A nonsense mutation in MSX1 causes Witkop syndrome. American Journal of Human Genetics. 69: 67-74. PMID 11369996 DOI: 10.1086/321271 |
0.781 |
|
| 2001 |
Reichenberger E, Tiziani V, Watanabe S, Park L, Ueki Y, Santanna C, Baur ST, Shiang R, Grange DK, Beighton P, Gardner J, Hamersma H, Sellars S, Ramesar R, Lidral AC, ... ... Olsen BR, et al. Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANK. American Journal of Human Genetics. 68: 1321-6. PMID 11326338 DOI: 10.1086/320612 |
0.317 |
|
| 2001 |
Rieger DK, Reichenberger E, McLean W, Sidow A, Olsen BR. A double-deletion mutation in the Pitx3 gene causes arrested lens development in aphakia mice. Genomics. 72: 61-72. PMID 11247667 DOI: 10.1006/Geno.2000.6464 |
0.316 |
|
| 2000 |
Reichenberger E, Baur S, Sukotjo C, Olsen BR, Karimbux NY, Nishimura I. Collagen XII mutation disrupts matrix structure of periodontal ligament and skin. Journal of Dental Research. 79: 1962-8. PMID 11201046 DOI: 10.1177/00220345000790120701 |
0.304 |
|
| 2000 |
Zatterstrom UK, Felbor U, Fukai N, Olsen BR. Collagen XVIII/endostatin structure and functional role in angiogenesis Cell Structure and Function. 25: 97-101. PMID 10885579 DOI: 10.1247/Csf.25.97 |
0.321 |
|
| 2000 |
Spayde EC, Joshi AP, Wilcox WR, Briggs M, Cohn DH, Olsen BR. Exon skipping mutation in the COL9A2 gene in a family with multiple epiphyseal dysplasia Matrix Biology. 19: 121-128. PMID 10842095 DOI: 10.1016/S0945-053X(00)00055-X |
0.322 |
|
| 1999 |
Ting K, Ramachandran H, Chung KS, Shah-Hosseini N, Olsen BR, Nishimura I. A short isoform of Col9a1 supports alveolar bone repair. The American Journal of Pathology. 155: 1993-9. PMID 10595929 DOI: 10.1016/S0002-9440(10)65518-6 |
0.333 |
|
| 1999 |
Annunen S, Körkkö J, Czarny M, Warman ML, Brunner HG, Kääriäinen H, Mulliken JB, Tranebjærg L, Brooks DG, Cox GF, Cruysberg JR, Curtis MA, Davenport SLH, Friedrich CA, Kaitila I, ... ... Olsen BR, et al. Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes American Journal of Human Genetics. 65: 974-983. PMID 10486316 DOI: 10.1086/302585 |
0.449 |
|
| 1999 |
Olsen BR. Genetic regulation of skeletal patterning, differentiation, and growth Bone. 25: 77-79. PMID 10423025 DOI: 10.1016/S8756-3282(99)00114-3 |
0.39 |
|
| 1999 |
Kania AM, Reichenberger E, Baur ST, Karimbux NY, Taylor RW, Olsen BR, Nishimura I. Structural variation of type XII collagen at its carboxyl-terminal NC1 domain generated by tissue-specific alternative splicing. The Journal of Biological Chemistry. 274: 22053-9. PMID 10419532 DOI: 10.1074/Jbc.274.31.22053 |
0.301 |
|
| 1999 |
Boon LM, Brouillard P, Irrthum A, Karttunen L, Warman ML, Rudolph R, Mulliken JB, Olsen BR, Vikkula M. A gene for inherited cutaneous venous anomalies ('Glomangiomas') localizes to chromosome 1p21-22 American Journal of Human Genetics. 65: 125-133. PMID 10364524 DOI: 10.1086/302450 |
0.308 |
|
| 1998 |
Gorski JP, Olsen BR. Mutations in extracellular matrix molecules Current Opinion in Cell Biology. 10: 586-593. PMID 9818168 DOI: 10.1016/S0955-0674(98)80033-1 |
0.314 |
|
| 1998 |
Yu J, Madison JM, Mundlos S, Winston F, Olsen BR. Characterization of a human homologue of the Saccharomyces cerevisiae transcription factor Spt3 (SUPT3H) Genomics. 53: 90-96. PMID 9787080 DOI: 10.1006/Geno.1998.5500 |
0.492 |
|
| 1998 |
Fülöp C, Kamath RV, Li Y, Otto JM, Salustri A, Olsen BR, Glant TT, Hascall VC. Coding sequence, exon-intron structure and chromosomal localization of murine TNF-stimulated gene 6 that is specifically expressed by expanding cumulus cell-oocyte complexes. Gene. 202: 95-102. PMID 9427551 DOI: 10.1016/S0378-1119(97)00459-9 |
0.312 |
|
| 1997 |
Huang LF, Fukai N, Selby PB, Olsen BR, Mundlos S. Mouse clavicular development: analysis of wild-type and cleidocranial dysplasia mutant mice. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 210: 33-40. PMID 9286593 DOI: 10.1002/(Sici)1097-0177(199709)210:1<33::Aid-Aja4>3.0.Co;2-2 |
0.544 |
|
| 1997 |
Goodman FR, Mundlos S, Muragaki Y, Donnai D, Giovannucci-Uzielli ML, Lapi E, Majewski F, McGaughran J, McKeown C, Reardon W, Upton J, Winter RM, Olsen BR, Scambler PJ. Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract. Proceedings of the National Academy of Sciences of the United States of America. 94: 7458-63. PMID 9207113 DOI: 10.1073/Pnas.94.14.7458 |
0.486 |
|
| 1997 |
Weed M, Mundlos S, Olsen BR. The role of sonic hedgehog in vertebrate development Matrix Biology. 16: 53-58. PMID 9205942 DOI: 10.1016/S0945-053X(97)90072-X |
0.492 |
|
| 1997 |
Li Y, Olsen BR. Murine models of human genetic skeletal disorders Matrix Biology. 16: 49-52. PMID 9205941 DOI: 10.1016/S0945-053X(97)90071-8 |
0.353 |
|
| 1997 |
Mundlos S, Otto F, Mundlos C, Mulliken JB, Aylsworth AS, Albright S, Lindhout D, Cole WG, Henn W, Knoll JH, Owen MJ, Mertelsmann R, Zabel BU, Olsen BR. Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia. Cell. 89: 773-9. PMID 9182765 DOI: 10.1016/S0092-8674(00)80260-3 |
0.485 |
|
| 1997 |
Otto F, Thornell AP, Crompton T, Denzel A, Gilmour KC, Rosewell IR, Stamp GW, Beddington RS, Mundlos S, Olsen BR, Selby PB, Owen MJ. Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development. Cell. 89: 765-71. PMID 9182764 DOI: 10.1016/S0092-8674(00)80259-7 |
0.533 |
|
| 1997 |
Gerecke DR, Olson PF, Koch M, Knoll JHM, Taylor R, Hudson DL, Champliaud MF, Olsen BR, Burgeson RE. Complete primary structure of two splice variants of collagen XII, and assignment of α1(XII) collagen (COL12A1), α1(IX) collagen (COL9A1), and α1(XIX) collagen (COL19a1) to human chromosome 6q12-q13 Genomics. 41: 236-242. PMID 9143499 DOI: 10.1006/Geno.1997.4638 |
0.315 |
|
| 1997 |
Chung KS, Jacenko O, Boyle P, Olsen BR, Nishimura I. Craniofacial abnormalities in mice carrying a dominant interference mutation in type X collagen. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 208: 544-52. PMID 9097026 DOI: 10.1002/(Sici)1097-0177(199704)208:4<544::Aid-Aja10>3.0.Co;2-X |
0.322 |
|
| 1997 |
Paschalis EP, Jacenko O, Olsen B, deCrombrugghe B, Boskey AL. The role of type X collagen in endochondral ossification as deduced by Fourier transform infrared microscopy analysis. Connective Tissue Research. 35: 371-7. PMID 9084677 DOI: 10.3109/03008209609029214 |
0.318 |
|
| 1997 |
Mundlos S, Olsen BR. Heritable diseases of the skeleton. Part I: Molecular insights into skeletal development-transcription factors and signaling pathways Faseb Journal. 11: 125-132. PMID 9039954 DOI: 10.1096/Fasebj.11.2.9039954 |
0.52 |
|
| 1997 |
Kwan KM, Pang MK, Zhou S, Cowan SK, Kong RY, Pfordte T, Olsen BR, Sillence DO, Tam PP, Cheah KS. Abnormal compartmentalization of cartilage matrix components in mice lacking collagen X: implications for function. The Journal of Cell Biology. 136: 459-71. PMID 9015315 DOI: 10.1083/Jcb.136.2.459 |
0.344 |
|
| 1997 |
Van Cappellen P, Ingall ED, Warren ST, Muragaki Y, Mundlos S, Upton J, Olsen BR. Polyalanine expansion in synpolydactyly might result from unequal crossing-over of HOXD13 Science. 275: 408-409. PMID 9005557 DOI: 10.1126/Science.275.5298.408 |
0.42 |
|
| 1997 |
Pace JM, Li Y, Seegmiller RE, Teuscher C, Taylor BA, Olsen BR. Disproportionate micromelia (Dmm) in mice caused by a mutation in the C-propeptide coding region of Col2a1. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 208: 25-33. PMID 8989518 DOI: 10.1002/(Sici)1097-0177(199701)208:1<25::Aid-Aja3>3.0.Co;2-3 |
0.347 |
|
| 1997 |
Paschalis EP, Jacenko O, Olsen B, Mendelsohn R, Boskey AL. Fourier transform infrared microspectroscopic analysis identifies alterations in mineral properties in bones from mice transgenic for type X collagen. Bone. 19: 151-6. PMID 8853859 DOI: 10.1016/8756-3282(96)00164-0 |
0.344 |
|
| 1997 |
Mundlos S, Olsen BR. Heritable diseases of the skeleton. Part II: Molecular insights into skeletal development‐matrix components and their homeostasis The Faseb Journal. 11: 227-233. DOI: 10.1096/Fasebj.11.4.9068611 |
0.513 |
|
| 1996 |
Vikkula M, Olsen BR. Unravelling the molecular genetics of osteoarthrosis Annals of Medicine. 28: 301-304. PMID 8862683 DOI: 10.3109/07853899608999084 |
0.311 |
|
| 1996 |
Mundlos S, Huang LF, Selby P, Olsen BR. Cleidocranial dysplasia in mice Annals of the New York Academy of Sciences. 785: 301-302. PMID 8702161 DOI: 10.1111/J.1749-6632.1996.Tb56290.X |
0.465 |
|
| 1996 |
Muragaki Y, Mundlos S, Upton J, Olsen BR. Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13 Science. 272: 548-551. PMID 8614804 DOI: 10.1126/Science.272.5261.548 |
0.522 |
|
| 1996 |
Muragaki Y, Mariman EC, van Beersum SE, Perälä M, van Mourik JB, Warman ML, Olsen BR, Hamel BC. A mutation in the gene encoding the alpha 2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2). Nature Genetics. 12: 103-5. PMID 8528240 DOI: 10.1038/Ng0196-103 |
0.309 |
|
| 1995 |
Böhme K, Li Y, Oh PS, Olsen BR. Primary structure of the long and short splice variants of mouse collagen XII and their tissue-specific expression during embryonic development. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 204: 432-45. PMID 8601036 DOI: 10.1002/Aja.1002040409 |
0.33 |
|
| 1995 |
Olsen BR. Mutations in collagen genes resulting in metaphyseal and epiphyseal dysplasias Bone. 17. PMID 8579897 DOI: 10.1016/8756-3282(95)00208-U |
0.367 |
|
| 1995 |
Mundlos S, Mulliken JB, Abramson DL, Warman ML, Knoll JH, Olsen BR. Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family. Human Molecular Genetics. 4: 71-5. PMID 7711736 DOI: 10.1093/Hmg/4.1.71 |
0.474 |
|
| 1995 |
Olsen BR. The roles of collagen genes in skeletal development and morphogenesis Experientia. 51: 194-195. PMID 7698270 DOI: 10.1007/Bf01931087 |
0.318 |
|
| 1995 |
Mallein-Gerin F, Ruggiero F, Quinn TM, Bard F, Grodzinsky AJ, Olsen BR, van der Rest M. Analysis of collagen synthesis and assembly in culture by immortalized mouse chondrocytes in the presence or absence of alpha 1(IX) collagen chains. Experimental Cell Research. 219: 257-65. PMID 7628541 DOI: 10.1006/Excr.1995.1226 |
0.32 |
|
| 1995 |
Wick M, Härönen R, Mumberg D, Bürger C, Olsen BR, Budarf ML, Apte SS, Müller R. Structure of the human TIMP-3 gene and its cell cycle-regulated promoter. The Biochemical Journal. 549-54. PMID 7487894 DOI: 10.1042/Bj3110549 |
0.313 |
|
| 1994 |
McIntosh I, Abbott MH, Warman ML, Olsen BR, Francomano CA. Additional mutations of type X collagen confirm COL10A1 as the Schmid metaphyseal chondrodysplasia locus. Human Molecular Genetics. 3: 303-7. PMID 8004099 DOI: 10.1093/Hmg/3.2.303 |
0.306 |
|
| 1994 |
Apte SS, Hayashi K, Seldin MF, Mattei MG, Hayashi M, Olsen BR. Gene encoding a novel murine tissue inhibitor of metalloproteinases (TIMP), TIMP-3, is expressed in developing mouse epithelia, cartilage, and muscle, and is located on mouse chromosome 10 Developmental Dynamics. 200: 177-197. PMID 7949367 DOI: 10.1002/Aja.1002000302 |
0.323 |
|
| 1994 |
Nishimura I, Ting K, Olsen BR. The role of short type IX collagen in alveolar bone repair examined in α1(IX) “knock-out” transgenic mice Matrix Biology. 14: 413. DOI: 10.1016/0945-053X(94)90157-0 |
0.312 |
|
| 1993 |
Lu Valle P, Iwamoto M, Fanning P, Pacifici M, Olsen BR. Multiple negative elements in a gene that codes for an extracellular matrix protein, collagen X, restrict expression to hypertrophic chondrocytes Journal of Cell Biology. 121: 1173-1179. PMID 8501122 DOI: 10.1083/Jcb.121.5.1173 |
0.315 |
|
| 1993 |
Apte SS, Olsen BR. Characterization of the mouse type X collagen gene Matrix. 13: 165-179. PMID 8492743 DOI: 10.1016/S0934-8832(11)80075-2 |
0.33 |
|
| 1993 |
Nakata K, Ono K, Miyazaki J, Olsen BR, Muragaki Y, Adachi E, Yamamura K, Kimura T. Osteoarthritis associated with mild chondrodysplasia in transgenic mice expressing alpha 1(IX) collagen chains with a central deletion. Proceedings of the National Academy of Sciences of the United States of America. 90: 2870-4. PMID 8464901 DOI: 10.1073/Pnas.90.7.2870 |
0.301 |
|
| 1993 |
Jacenko O, Luvalle PA, Olsen BR. Spondylometaphyseal dysplasia in mice carrying a dominant negative mutation in a matrix protein specific for cartilage-to-bone transition Nature. 365: 56-61. PMID 8361538 DOI: 10.1038/365056A0 |
0.355 |
|
| 1993 |
Oh SP, Griffith CM, Hay ED, Olsen BR. Tissue-specific expression of type XII collagen during mouse embryonic development. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 196: 37-46. PMID 8334298 DOI: 10.1002/Aja.1001960105 |
0.325 |
|
| 1993 |
Warman ML, Abbott M, Apte SS, Hefferon T, McIntosh I, Cohn DH, Hecht JT, Olsen BR, Francomano CA. A type X collagen mutation causes schmid metaphyseal chondrodysplasia Nature Genetics. 5: 79-82. PMID 8220429 DOI: 10.1038/Ng0993-79 |
0.335 |
|
| 1993 |
Mallein-Gerin F, Olsen BR. Expression of simian virus 40 large T (tumor) oncogene in mouse chondrocytes induces cell proliferation without loss of the differentiated phenotype Proceedings of the National Academy of Sciences of the United States of America. 90: 3289-3293. PMID 7682698 DOI: 10.1073/Pnas.90.8.3289 |
0.306 |
|
| 1992 |
Apte SS, Seldin MF, Hayashi M, Olsen BR. Cloning of the human and mouse type X collagen genes and mapping of the mouse type X collagen gene to chromosome 10 European Journal of Biochemistry. 206: 217-224. PMID 1587271 DOI: 10.1111/J.1432-1033.1992.Tb16919.X |
0.312 |
|
| 1992 |
Oh SP, Taylor RW, Gerecke DR, Rochelle JM, Seldin MF, Olsen BR. The mouse alpha 1(XII) and human alpha 1(XII)-like collagen genes are localized on mouse chromosome 9 and human chromosome 6. Genomics. 14: 225-31. PMID 1427837 DOI: 10.1016/S0888-7543(05)80210-1 |
0.311 |
|
| 1991 |
Nakahara H, Watanabe K, Sugrue SP, Olsen BR, Caplan AI. Temporal and spatial distribution of type XII collagen in high cell density culture of periosteal-derived cells. Developmental Biology. 142: 481-5. PMID 1701739 DOI: 10.1016/0012-1606(90)90370-X |
0.308 |
|
| 1989 |
Sugrue SP, Gordon MK, Seyer J, Dublet B, van der Rest M, Olsen BR. Immunoidentification of type XII collagen in embryonic tissues. The Journal of Cell Biology. 109: 939-45. PMID 2668306 DOI: 10.1083/Jcb.109.2.939 |
0.304 |
|
| 1989 |
Kimura T, Mattei MG, Stevens JW, Goldring MB, Ninomiya Y, Olsen BR. Molecular cloning of rat and human type IX collagen cDNA and localization of the alpha 1(IX) gene on the human chromosome 6. European Journal of Biochemistry / Febs. 179: 71-8. PMID 2465149 DOI: 10.1111/J.1432-1033.1989.Tb14522.X |
0.31 |
|
| 1987 |
Gordon MK, Gerecke DR, Olsen BR. Type XII collagen: distinct extracellular matrix component discovered by cDNA cloning. Proceedings of the National Academy of Sciences of the United States of America. 84: 6040-4. PMID 3476925 DOI: 10.1073/Pnas.84.17.6040 |
0.314 |
|
| 1986 |
Hayashi M, Ninomiya Y, Parsons J, Olsen BR, Trelstad RL. Differential localization of mRNAs of collagen types I and II in chick fibroblasts, chondrocytes, and corneal cells by in situ hybridization using cDNA probes Journal of Cell Biology. 102: 2302-2309. PMID 3011812 DOI: 10.1083/Jcb.102.6.2302 |
0.302 |
|
| 1985 |
Lozano G, Ninomiya Y, Thompson H, Olsen BR. A distinct class of vertebrate collagen genes encodes chicken type IX collagen polypeptides Proceedings of the National Academy of Sciences of the United States of America. 82: 4050-4054. PMID 3858862 DOI: 10.1073/Pnas.82.12.4050 |
0.314 |
|
| 1984 |
Ninomiya Y, Showalter AM, Van Der Rest M, Seidah NG, Chrétien M, Olsen BR. Structure of the carboxyl propeptide of chicken type II procollagen determined by DNA and protein sequence analysis Biochemistry. 23: 617-624. DOI: 10.1021/Bi00299A005 |
0.595 |
|
| 1982 |
Guzman NA, Oronsky AL, Suarez G, Meyerson LR, Cutroneo KR, Olsen BR, Prockop DJ. Prolyl 4-Hydroxylase from Human Placenta. Simultaneous Isolation of Immunoglobulin G which Binds to Ascaris Cuticle Collagen Collagen and Related Research. 2: 365-380. DOI: 10.1016/S0174-173X(82)80001-0 |
0.434 |
|
| 1981 |
Pesciotta DM, Dickson LA, Showalter AM, Eikenberry EF, De Crombrugghe B, Fietzek PP, Olsen BR. Primary structure of the carbohydrate-containing regions of the carboxyl propeptides of type I procollagen Febs Letters. 125: 170-174. PMID 7227547 DOI: 10.1016/0014-5793(81)80711-9 |
0.585 |
|
| 1981 |
Graves PN, Olsen BR, Fietzek PP, Prockop DJ, Monson JM. Comparison of the NH2-Terminal sequences of chick Type I preprocollagen chains synthesized in an nRNA-dependent reticulocyte lysate. European Journal of Biochemistry. 118: 363-9. PMID 6269854 DOI: 10.1111/J.1432-1033.1981.Tb06411.X |
0.425 |
|
| 1980 |
Showalter AM, Pesciotta DM, Eikenberry EF, Yamamoto T, Pastan I, DeCrombrugghe B, Fietzek PP, Olsen BR. Nucleotide sequence of a collagen cDNA-fragment coding for the carboxyl end of proα1(I)-chains Febs Letters. 111: 61-65. PMID 6987088 DOI: 10.1016/0014-5793(80)80761-7 |
0.577 |
|
| 1976 |
Hoffmann HP, Olsen BR, Chen HT, Prockop DJ. Segment long spacing aggregates and isolation of COOH terminal peptides from type I procollagen Proceedings of the National Academy of Sciences of the United States of America. 73: 4304-4308. PMID 1069985 DOI: 10.1073/Pnas.73.12.4304 |
0.451 |
|
| 1976 |
Olsen BR, Hoffmann HP, Prockop DJ. Interchain disulfide bonds at the COOH-terminal end of procollagen synthesized by matrix-free cells from chick embryonic tendon and cartilage Archives of Biochemistry and Biophysics. 175: 341-350. PMID 182083 DOI: 10.1016/0003-9861(76)90516-6 |
0.464 |
|
| 1975 |
Kishida Y, Olsen BR, Berg RA, Prockop DJ. Two improved methods for preparing ferritin protein conjugates for electron microscopy Journal of Cell Biology. 64: 331-339. PMID 803973 DOI: 10.1083/Jcb.64.2.331 |
0.417 |
|
| 1975 |
Olsen BR, Berg RA, Kishida Y, Prockop DJ. Further characterization of embryonic tendon fibroblasts and the use of immunoferritin techniques to study collagen biosynthesis Journal of Cell Biology. 64: 340-355. PMID 163830 DOI: 10.1083/Jcb.64.2.340 |
0.482 |
|
| 1974 |
Olsen BR, Prockop DJ. Ferritin conjugated antibodies used for labeling of organelles involved in the cellular synthesis and transport of procollagen Proceedings of the National Academy of Sciences of the United States of America. 71: 2033-2037. PMID 4525314 DOI: 10.1073/Pnas.71.5.2033 |
0.44 |
|
| 1974 |
Dehm P, Olsen BR, Prockop DJ. Antibodies to chick tendon procollagen. Affinity purification with the isolated disulfide linked NH2 terminal extensions and reactivity with a component in embryonic serum European Journal of Biochemistry. 46: 107-116. PMID 4136533 DOI: 10.1111/J.1432-1033.1974.Tb03602.X |
0.433 |
|
| 1973 |
Olsen BR, Berg RA, Kishida Y, Prockop DJ. Collagen synthesis: Localization of prolyl hydroxylase in tendon cells detected with ferritin labeled antibodies Science. 182: 825-827. PMID 4355681 DOI: 10.1126/Science.182.4114.825 |
0.441 |
|
| 1973 |
Olsen BR, Berg RA, Kivirikko KI, Prockop DJ. Structure of Protocollagen Proline Hydroxylase from Chick Embryos European Journal of Biochemistry. 35: 135-147. PMID 4351527 DOI: 10.1111/J.1432-1033.1973.Tb02819.X |
0.415 |
|
| 1972 |
Dehm P, Jimenez SA, Olsen BR, Prockop DJ. A transport form of collagen from embryonic tendon: electron microscopic demonstration of an NH 2 -terminal extension and evidence suggesting the presence of cystine in the molecule (chick embryo-tropocollagen-gel filtration) Proceedings of the National Academy of Sciences of the United States of America. 69: 60-64. PMID 4333046 DOI: 10.1073/Pnas.69.1.60 |
0.447 |
|
| 1972 |
Berg RA, Olsen BR, Prockop DJ. Labeled antibodies to protocollagen proline hydroxylase from chick embryos for intracellular localization of the enzyme Bba - Protein Structure. 285: 167-175. PMID 4120059 DOI: 10.1016/0005-2795(72)90188-2 |
0.424 |
|
| 1971 |
Olsen BR, Berg RA, Sakakibara S, Kishida Y, Prockop DJ. The synthetic polytripeptides (Pro-Pro-Gly)10 and (Pro-Pro-Gly)20 form micro-crystalline structures similar to segmental structures formed by collagen. Journal of Molecular Biology. 57: 589-95. PMID 4103752 DOI: 10.1016/0022-2836(71)90111-2 |
0.36 |
|
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