| Year |
Citation |
Score |
| 2020 |
Zhang A, Berardinelli SJ, Leonhard-Melief C, Vasudevan D, Liu TW, Taibi A, Giannone S, Apte SS, Holdener BC, Haltiwanger RS. -Fucosylation of ADAMTSL2 is required for secretion and is impacted by geleophysic dysplasia-causing mutations. The Journal of Biological Chemistry. PMID 32913123 DOI: 10.1074/Jbc.Ra120.014557 |
0.331 |
|
| 2019 |
Holdener BC, Percival CJ, Grady RC, Cameron DC, Berardinelli SJ, Zhang A, Neupane S, Takeuchi M, Jimenez-Vega JC, Uddin SMZ, Komatsu DE, Honkanen R, Dubail J, Apte SS, Sato T, et al. ADAMTS9 and ADAMTS20 are differentially affected by loss of B3GLCT in a mouse model of Peters Plus Syndrome. Human Molecular Genetics. PMID 31600785 DOI: 10.1093/Hmg/Ddz225 |
0.416 |
|
| 2017 |
Siller SS, Sharma H, Li S, Yang J, Zhang Y, Holtzman MJ, Winuthayanon W, Colognato H, Holdener BC, Li FQ, Takemaru KI. Conditional knockout mice for the distal appendage protein CEP164 reveal its essential roles in airway multiciliated cell differentiation. Plos Genetics. 13: e1007128. PMID 29244804 DOI: 10.1371/Journal.Pgen.1007128 |
0.332 |
|
| 2016 |
Benz BA, Nandadasa S, Takeuchi M, Grady RC, Takeuchi H, LoPilato RK, Kakuda S, Somerville RP, Apte SS, Haltiwanger RS, Holdener BC. Genetic and biochemical evidence that gastrulation defects in Pofut2 mutants result from defects in ADAMTS9 secretion. Developmental Biology. PMID 27297885 DOI: 10.1016/J.Ydbio.2016.05.038 |
0.424 |
|
| 2013 |
Taibi AV, Lighthouse JK, Grady RC, Shroyer KR, Holdener BC. Development of a conditional Mesd (mesoderm development) allele for functional analysis of the low-density lipoprotein receptor-related family in defined tissues. Plos One. 8: e75782. PMID 24124512 DOI: 10.1371/Journal.Pone.0075782 |
0.75 |
|
| 2011 |
Köhler C, Lighthouse JK, Werther T, Andersen OM, Diehl A, Schmieder P, Du J, Holdener BC, Oschkinat H. The structure of MESD45-184 brings light into the mechanism of LDLR family folding. Structure (London, England : 1993). 19: 337-48. PMID 21397185 DOI: 10.1016/J.Str.2010.12.022 |
0.726 |
|
| 2011 |
Lighthouse JK, Zhang L, Hsieh JC, Rosenquist T, Holdener BC. MESD is essential for apical localization of megalin/LRP2 in the visceral endoderm. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 240: 577-88. PMID 21337463 DOI: 10.1002/Dvdy.22477 |
0.776 |
|
| 2011 |
Koehler C, Lighthouse J, Werther T, Andersen O, Diehl A, Schmieder P, Holdener B, Oschkinat H. NMR based model structure of mesoderm development (MESD) in solution. Journal of Back and Musculoskeletal Rehabilitation. DOI: 10.13018/Bmr11076 |
0.688 |
|
| 2010 |
Du J, Takeuchi H, Leonhard-Melief C, Shroyer KR, Dlugosz M, Haltiwanger RS, Holdener BC. O-fucosylation of thrombospondin type 1 repeats restricts epithelial to mesenchymal transition (EMT) and maintains epiblast pluripotency during mouse gastrulation. Developmental Biology. 346: 25-38. PMID 20637190 DOI: 10.1016/J.Ydbio.2010.07.008 |
0.385 |
|
| 2003 |
Hsieh JC, Lee L, Zhang L, Wefer S, Brown K, DeRossi C, Wines ME, Rosenquist T, Holdener BC. Mesd encodes an LRP5/6 chaperone essential for specification of mouse embryonic polarity. Cell. 112: 355-67. PMID 12581525 DOI: 10.1016/S0092-8674(03)00045-X |
0.7 |
|
| 2002 |
Laiosa MD, Lai ZW, Thurmond TS, Fiore NC, DeRossi C, Holdener BC, Gasiewicz TA, Silverstone AE. 2,3,7,8-tetrachlorodibenzo-p-dioxin causes alterations in lymphocyte development and thymic atrophy in hemopoietic chimeras generated from mice deficient in ARNT2. Toxicological Sciences : An Official Journal of the Society of Toxicology. 69: 117-24. PMID 12215665 DOI: 10.1093/Toxsci/69.1.117 |
0.447 |
|
| 2002 |
Barrow LL, Wines ME, Romitti PA, Holdener BC, Murray JC. Aryl hydrocarbon receptor nuclear translocator 2 (ARNT2): structure, gene mapping, polymorphisms, and candidate evaluation for human orofacial clefts. Teratology. 66: 85-90. PMID 12210012 DOI: 10.1002/Tera.10062 |
0.739 |
|
| 2001 |
Wines ME, Lee L, Katari MS, Zhang L, DeRossi C, Shi Y, Perkins S, Feldman M, McCombie WR, Holdener BC. Identification of mesoderm development (mesd) candidate genes by comparative mapping and genome sequence analysis. Genomics. 72: 88-98. PMID 11247670 DOI: 10.1006/Geno.2000.6466 |
0.704 |
|
| 2000 |
Wines ME, Shi Y, Lindor M, Holdener BC. Physical localization of the mesoderm development (mesd) functional region. Genomics. 68: 322-9. PMID 10995574 DOI: 10.1006/Geno.2000.6264 |
0.742 |
|
| 2000 |
DeRossi C, Laiosa MD, Silverstone AE, Holdener BC. Mouse fzd4 maps within a region of chromosome 7 important for thymus and cardiac development. Genesis. 27: 64-75. PMID 10890980 DOI: 10.1002/1526-968X(200006)27:2<64::Aid-Gene30>3.0.Co;2-I |
0.481 |
|
| 2000 |
Grimes JA, Nielsen SJ, Battaglioli E, Miska EA, Speh JC, Berry DL, Atouf F, Holdener BC, Mandel G, Kouzarides T. The co-repressor mSin3A is a functional component of the REST-CoREST repressor complex. The Journal of Biological Chemistry. 275: 9461-7. PMID 10734093 DOI: 10.1074/Jbc.275.13.9461 |
0.334 |
|
| 2000 |
Michaud JL, DeRossi C, May NR, Holdener BC, Fan CM. ARNT2 acts as the dimerization partner of SIM1 for the development of the hypothalamus. Mechanisms of Development. 90: 253-61. PMID 10640708 DOI: 10.1016/S0925-4773(99)00328-7 |
0.354 |
|
| 1998 |
Wines ME, Tiffany AM, Holdener BC. Physical localization of the mouse aryl hydrocarbon receptor nuclear translocator-2 (Arnt2) gene within the c112K deletion. Genomics. 51: 223-32. PMID 9722945 DOI: 10.1006/Geno.1998.5347 |
0.749 |
|
| 1998 |
Williams RW, Holdener BC, Angel JM, Oakey R, Hunter KW. Encyclopedia of the mouse genome VII. Mouse chromosome 7. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: S136-59. PMID 9662624 DOI: 10.1007/S003359900652 |
0.413 |
|
| 1995 |
Holdener BC, Rinchik EM, Magnuson T. Phenotypic and physical analysis of a chemically induced mutation disrupting anterior axial development in the mouse. Mammalian Genome. 6: 474-475. PMID 7579891 DOI: 10.1007/Bf00360658 |
0.317 |
|
| 1995 |
Holdener BC, Thomas JW, Schumacher A, Potter MD, Rinchik EM, Sharan SK, Magnuson T. Physical localization of eed: a region of mouse chromosome 7 required for gastrulation. Genomics. 27: 447-56. PMID 7558026 DOI: 10.1006/Geno.1995.1076 |
0.492 |
|
| 1994 |
Thomas JW, Holdener BC, Magnuson T. Sequence analysis of a radiation-induced deletion breakpoint fusion in mouse Mammalian Genome. 5: 518-519. PMID 7949739 DOI: 10.1007/Bf00369324 |
0.333 |
|
| 1993 |
Holdener BC, Brown SD, Angel JM, Nicholls RD, Kelsey G, Magnuson T. Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 7. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: S110-20. PMID 8268667 DOI: 10.1007/Bf00360833 |
0.404 |
|
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