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Items: 1 to 20 of 54

1.
Differential molecular regulation of processing and membrane expression of Type-I BMP receptors: implications for signaling
Tal Hirschhorn, Michal Levi-Hofman, Oded Danziger, Nechama I. Smorodinsky, Marcelo Ehrlich
Cell Mol Life Sci. 2017 Jul; 74(14): 2645–2662. Published online 2017 Mar 29. doi: 10.1007/s00018-017-2488-y
PMCID:
PMC11107780
AbstractArticlePDF–3.6M
2.
Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome
Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2022 May 27.
Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011
PMCID:
PMC8165030
AbstractArticlePDF–2.2M
3.
BMPR1B gene in brachydactyly type 2–A family with de novo R486W mutation and a disease phenotype
Marcin Bednarek, Marek Trybus, Monika Kolanowska, Mateusz Koziej, Beata Kiec‐Wilk, Artur Dobosz, Marta Kotlarek‐Łysakowska, Anna Kubiak‐Dydo, Ewelina Użarowska‐Gąska, Julia Staręga‐Rosłan, Paweł Gaj, Izabela Górzyńska, Katarzyna Serwan, Michał Świerniak, Adam Kot, Krystian Jażdżewski, Anna Wójcicka
Mol Genet Genomic Med. 2021 Mar; 9(3): e1594. Published online 2021 Jan 24. doi: 10.1002/mgg3.1594
PMCID:
PMC8104157
AbstractArticlePDF–1.0M
4.
SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling
Yuh-Charn Lin, Marcello Niceta, Valentina Muto, Barbara Vona, Alistair T. Pagnamenta, Reza Maroofian, Christian Beetz, Hermine van Duyvenvoorde, Maria Lisa Dentici, Peter Lauffer, Sadeq Vallian, Andrea Ciolfi, Simone Pizzi, Peter Bauer, Nana-Maria Grüning, Emanuele Bellacchio, Andrea Del Fattore, Stefania Petrini, Ranad Shaheen, Dov Tiosano, Rana Halloun, Ben Pode-Shakked, Hatice Mutlu Albayrak, Emregül Işık, Jan M. Wit, Marcus Dittrich, Bruna L. Freire, Debora R. Bertola, Alexander A.L. Jorge, Ortal Barel, Ataf H. Sabir, Amal M.J. Al Tenaiji, Sulaima M. Taji, Nouriya Al-Sannaa, Hind Al-Abdulwahed, Maria Cristina Digilio, Melita Irving, Yair Anikster, Gandham S.L. Bhavani, Katta M. Girisha, Genomics England Research Consortium, Thomas Haaf, Jenny C. Taylor, Bruno Dallapiccola, Fowzan S. Alkuraya, Ruey-Bing Yang, Marco Tartaglia
Am J Hum Genet. 2021 Jan 7; 108(1): 115–133. Published online 2020 Dec 11. doi: 10.1016/j.ajhg.2020.11.015
PMCID:
PMC7820739
AbstractArticlePDF–4.2M
5.
The quiescent fraction of chronic myeloid leukemic stem cells depends on BMPR1B, Stat3 and BMP4-niche signals to persist in patients in remission
Sandrine Jeanpierre, Kawtar Arizkane, Supat Thongjuea, Elodie Grockowiak, Kevin Geistlich, Lea Barral, Thibault Voeltzel, Anissa Guillemin, Sandrine Gonin-Giraud, Olivier Gandrillon, Franck-Emmanuel Nicolini, Adam J. Mead, Véronique Maguer-Satta, Sylvain Lefort
Haematologica. 2021 Jan 1; 106(1): 111–122. Published online 2020 Jan 30. doi: 10.3324/haematol.2019.232793
PMCID:
PMC7776261
AbstractArticlePDF–2.1M
6.
A novel homozygous variant in BMPR1B underlies acromesomelic dysplasia Hunter–Thompson type
Asmat Ullah, Muhammad Umair, Dost Muhammad, Muhammad Bilal, Kwanghyuk Lee, Suzanne M Leal, Wasim Ahmad
Ann Hum Genet. Author manuscript; available in PMC 2018 Sep 17.
Published in final edited form as: Ann Hum Genet. 2018 May; 82(3): 129–134. Published online 2018 Jan 10. doi: 10.1111/ahg.12233
PMCID:
PMC6141004
AbstractArticlePDF–983K
7.
骨形成蛋白7通过激活Ⅰ型受体BMPR1A、BMPR1B抑制肺大细胞癌NCI-H460细胞的增殖
徐 慧慧, 齐 艳丽, 顿 嵩, 高 英, 邱 雪杉
Zhongguo Fei Ai Za Zhi. 2010 Jul 20; 13(7): 659–664. Chinese. doi: 10.3779/j.issn.1009-3419.2010.07.01
PMCID:
PMC6000380
AbstractArticlePDF–2.2M
8.
Linked homozygous BMPR1B and PDHA2 variants in a consanguineous family with complex digit malformation and male infertility
Yeşerin Yıldırım, Toufik Ouriachi, Ute Woehlbier, Wahiba Ouahioune, Mahmut Balkan, Sajid Malik, Aslıhan Tolun
Eur J Hum Genet. 2018 Jun; 26(6): 876–885. Published online 2018 Mar 26. doi: 10.1038/s41431-018-0121-7
PMCID:
PMC5973948
AbstractArticlePDF–1.4M
9.
Architecture of the human interactome defines protein communities and disease networks
Edward L. Huttlin, Raphael J. Bruckner, Joao A. Paulo, Joe R. Cannon, Lily Ting, Kurt Baltier, Greg Colby, Fana Gebreab, Melanie P. Gygi, Hannah Parzen, John Szpyt, Stanley Tam, Gabriela Zarraga, Laura Pontano-Vaites, Sharan Swarup, Anne E. White, Devin K. Schweppe, Ramin Rad, Brian K. Erickson, Robert A. Obar, K.G. Guruharsha, Kejie Li, Spyros Artavanis-Tsakonas, Steven P. Gygi, J. Wade Harper
Nature. Author manuscript; available in PMC 2017 Nov 17.
Published in final edited form as: Nature. 2017 May 25; 545(7655): 505–509. Published online 2017 May 17. doi: 10.1038/nature22366
PMCID:
PMC5531611
AbstractArticlePDF–2.7M
10.
Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing
Teng Fei, Yiwen Chen, Tengfei Xiao, Wei Li, Laura Cato, Peng Zhang, Maura B. Cotter, Michaela Bowden, Rosina T. Lis, Shuang G. Zhao, Qiu Wu, Felix Y. Feng, Massimo Loda, Housheng Hansen He, X. Shirley Liu, Myles Brown
Proc Natl Acad Sci U S A. 2017 Jun 27; 114(26): E5207–E5215. Published online 2017 Jun 13. doi: 10.1073/pnas.1617467114
PMCID:
PMC5495225
AbstractArticlePDF–1.3M
11.
BMPR1B mutation causes Pierre Robin sequence
Yongjia Yang, Jianying Yuan, Xu Yao, Rong Zhang, Hui Yang, Rui Zhao, Jihong Guo, Ke Jin, Haibo Mei, Yongqi Luo, Liu Zhao, Ming Tu, Yimin Zhu
Oncotarget. 2017 Apr 18; 8(16): 25864–25871. Published online 2017 Mar 23. doi: 10.18632/oncotarget.16531
PMCID:
PMC5432222
AbstractArticlePDF–1.8M
12.
Low expression of BMPRIB indicates poor prognosis of breast cancer and is insensitive to taxane-anthracycline chemotherapy
Kun Dai, Fengxia Qin, Huikun Zhang, Xiaoli Liu, Caixia Guo, Ming Zhang, Feng Gu, Fu Li, Yongjie Ma
Oncotarget. 2016 Jan 26; 7(4): 4770–4784. Published online 2015 Dec 14. doi: 10.18632/oncotarget.6613
PMCID:
PMC4826242
AbstractArticlePDF–8.4M
13.
The protein kinase LKB1 negatively regulates bone morphogenetic protein receptor signaling
Erna Raja, Kalliopi Tzavlaki, Robin Vuilleumier, Karolina Edlund, Kaoru Kahata, Agata Zieba, Anita Morén, Yukihide Watanabe, Iryna Voytyuk, Johan Botling, Ola Söderberg, Patrick Micke, George Pyrowolakis, Carl-Henrik Heldin, Aristidis Moustakas
Oncotarget. 2016 Jan 12; 7(2): 1120–1143. Published online 2015 Dec 19. doi: 10.18632/oncotarget.6683
PMCID:
PMC4811448
AbstractArticlePDF–8.3M
14.
Two novel disease-causing variants in BMPR1B are associated with brachydactyly type A1
Lemuel Racacho, Ashley M Byrnes, Heather MacDonald, Helen J Dranse, Sarah M Nikkel, Judith Allanson, Elisabeth Rosser, T Michael Underhill, Dennis E Bulman
Eur J Hum Genet. 2015 Dec; 23(12): 1640–1645. Published online 2015 Mar 11. doi: 10.1038/ejhg.2015.38
PMCID:
PMC4795202
AbstractArticlePDF–3.6M
15.
HFE interacts with the BMP type I receptor ALK3 to regulate hepcidin expression
Xing-gang Wu, Yang Wang, Qian Wu, Wai-Hang Cheng, Wenjing Liu, Yueshui Zhao, Claire Mayeur, Paul J. Schmidt, Paul B. Yu, Fudi Wang, Yin Xia
Blood. 2014 Aug 21; 124(8): 1335–1343. Prepublished online 2014 Jun 5. doi: 10.1182/blood-2014-01-552281
PMCID:
PMC4624447
AbstractArticle
16.
The BioPlex Network: A Systematic Exploration of the Human Interactome
Edward L. Huttlin, Lily Ting, Raphael J. Bruckner, Fana Gebreab, Melanie P. Gygi, John Szpyt, Stanley Tam, Gabriela Zarraga, Greg Colby, Kurt Baltier, Rui Dong, Virginia Guarani, Laura Pontano Vaites, Alban Ordureau, Ramin Rad, Brian K. Erickson, Martin Wühr, Joel Chick, Bo Zhai, Deepak Kolippakkam, Julian Mintseris, Robert A. Obar, Tim Harris, Spyros Artavanis-Tsakonas, Mathew E. Sowa, Pietro DeCamilli, Joao A. Paulo, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2016 Jul 16.
Published in final edited form as: Cell. 2015 Jul 16; 162(2): 425–440. doi: 10.1016/j.cell.2015.06.043
PMCID:
PMC4617211
AbstractArticlePDF–2.2M
17.
A hypomorphic BMPR1B mutation causes du Pan acromesomelic dysplasia
Katja Stange, Julie Désir, Naseebullah Kakar, Thomas D. Mueller, Birgit S. Budde, Christopher T. Gordon, Denise Horn, Petra Seemann, Guntram Borck
Orphanet J Rare Dis. 2015; 10: 84. Published online 2015 Jun 24. doi: 10.1186/s13023-015-0299-5
PMCID:
PMC4482310
AbstractArticlePDF–1.8M
18.
Casein kinase 2 (CK2) phosphorylates the deubiquitylase OTUB1 at Ser16 to trigger its nuclear localization
Lina Herhaus, Ana B. Perez-Oliva, Giorgio Cozza, Robert Gourlay, Simone Weidlich, David G. Campbell, Lorenzo A. Pinna, Gopal P. Sapkota
Sci Signal. Author manuscript; available in PMC 2015 Oct 14.
Published in final edited form as: Sci Signal. 2015; 8(372): ra35. Published online 2015 Apr 14. doi: 10.1126/scisignal.aaa0441
PMCID:
PMC4421874
AbstractArticlePDF–3.4M
19.
Disequilibrium of BMP2 Levels in the Breast Stem Cell Niche Launches Epithelial Transformation by Overamplifying BMPR1B Cell Response
Marion Chapellier, Elodie Bachelard-Cascales, Xenia Schmidt, Flora Clément, Isabelle Treilleux, Emmanuel Delay, Alexandre Jammot, Christine Ménétrier-Caux, Gaëtan Pochon, Roger Besançon, Thibault Voeltzel, Claude Caron de Fromentel, Christophe Caux, Jean-Yves Blay, Richard Iggo, Véronique Maguer-Satta
Stem Cell Reports. 2015 Feb 10; 4(2): 239–254. Published online 2015 Jan 15. doi: 10.1016/j.stemcr.2014.12.007
PMCID:
PMC4325271
AbstractArticlePDF–6.1M
20.
USP15 targets ALK3/BMPR1A for deubiquitylation to enhance bone morphogenetic protein signalling
Lina Herhaus, Mazin A. Al-Salihi, Kevin S. Dingwell, Timothy D. Cummins, Lize Wasmus, Janis Vogt, Richard Ewan, David Bruce, Thomas Macartney, Simone Weidlich, James C. Smith, Gopal P. Sapkota
Open Biol. 2014 May; 4(5): 140065. Published online 2014 May 21. doi: 10.1098/rsob.140065
PMCID:
PMC4042855
AbstractArticlePDF–1015K

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