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Items: 1 to 20 of 29

1.
PROKR1–CREB–NR4A2 axis for oxidative muscle fiber specification and improvement of metabolic function
Jongsoo Mok, Jeong Hwan Park, Su Chong Yeom, Joonghoon Park
Proc Natl Acad Sci U S A. 2024 Jan 23; 121(4): e2308960121. Published online 2024 Jan 17. doi: 10.1073/pnas.2308960121
PMCID:
PMC10823220
AbstractArticlePDF–6.7M
2.
Impaired Nociception and Inflammatory Pain Sensation in Mice Lacking the Prokineticin Receptor PKR1: Focus on Interaction between PKR1 and the Capsaicin Receptor TRPV1 in Pain Behavior
Lucia Negri, Roberta Lattanzi, Elisa Giannini, Mariantonella Colucci, Federica Margheriti, Pietro Melchiorri, Vittorio Vellani, Hui Tian, Milena De Felice, Frank Porreca
J Neurosci. 2006 Jun 21; 26(25): 6716–6727. doi: 10.1523/JNEUROSCI.5403-05.2006
PMCID:
PMC6673825
AbstractArticlePDF–781K
3.
Prokineticin Receptor 1 as a Novel Suppressor of Preadipocyte Proliferation and Differentiation to Control Obesity
Cécilia Szatkowski, Judith Vallet, Mojdeh Dormishian, Nadia Messaddeq, Phillippe Valet, Mounia Boulberdaa, Daniel Metzger, Pierre Chambon, Canan G. Nebigil
PLoS One. 2013; 8(12): e81175. Published online 2013 Dec 4. doi: 10.1371/journal.pone.0081175
PMCID:
PMC3852222
AbstractArticlePDF–1.6M
4.
Prokineticin Receptor‐1 Is a New Regulator of Endothelial Insulin Uptake and Capillary Formation to Control Insulin Sensitivity and Cardiovascular and Kidney Functions
Mojdeh Dormishian, Gulen Turkeri, Kyoji Urayama, Thu Lan Nguyen, Mounia Boulberdaa, Nadia Messaddeq, Gilles Renault, Daniel Henrion, Canan G. Nebigil
J Am Heart Assoc. 2013 Oct; 2(5): e000411. Published online 2013 Oct 25. doi: 10.1161/JAHA.113.000411
PMCID:
PMC3835255
AbstractArticlePDF–4.0M
5.
Bv8, the amphibian homologue of the mammalian prokineticins, induces a proinflammatory phenotype of mouse macrophages
Cataldo Martucci, Silvia Franchi, Elisa Giannini, Hui Tian, Pietro Melchiorri, Lucia Negri, Paola Sacerdote
Br J Pharmacol. 2006 Jan; 147(2): 225–234. Published online 2005 Nov 21. doi: 10.1038/sj.bjp.0706467
PMCID:
PMC1615858
AbstractArticlePDF–271K
6.
Prokineticin receptor-1-dependent paracrine and autocrine pathways control cardiac tcf21+ fibroblast progenitor cell transformation into adipocytes and vascular cells
Rehana Qureshi, Michel Kindo, Himanshu Arora, Mounia Boulberdaa, Marja Steenman, Canan G. Nebigil
Sci Rep. 2017; 7: 12804. Published online 2017 Oct 16. doi: 10.1038/s41598-017-13198-2
PMCID:
PMC5643307
AbstractArticlePDF–16M
7.
The Melanocortin Receptor Accessory Protein 2 promotes food intake through inhibition of the Prokineticin Receptor-1
Anna L Chaly, Dollada Srisai, Ellen E Gardner, Julien A Sebag
eLife. 2016; 5: e12397. Published online 2016 Feb 1. doi: 10.7554/eLife.12397
PMCID:
PMC4786424
AbstractArticlePDF–3.4M
8.
Antagonism of the Prokineticin System Prevents and Reverses Allodynia and Inflammation in a Mouse Model of Diabetes
Mara Castelli, Giada Amodeo, Lucia Negri, Roberta Lattanzi, Daniela Maftei, Cecilia Gotti, Francesco Pistillo, Valentina Onnis, Cenzo Congu, Alberto E. Panerai, Paola Sacerdote, Silvia Franchi
PLoS One. 2016; 11(1): e0146259. Published online 2016 Jan 5. doi: 10.1371/journal.pone.0146259
PMCID:
PMC4701417
AbstractArticlePDF–2.7M
9.
The chemokine Bv8/prokineticin 2 is up-regulated in inflammatory granulocytes and modulates inflammatory pain
Elisa Giannini, Roberta Lattanzi, Annalisa Nicotra, Antonio F. Campese, Paola Grazioli, Isabella Screpanti, Gianfranco Balboni, Severo Salvadori, Paola Sacerdote, Lucia Negri
Proc Natl Acad Sci U S A. 2009 Aug 25; 106(34): 14646–14651. Published online 2009 Aug 10. doi: 10.1073/pnas.0903720106
PMCID:
PMC2731841
AbstractArticlePDF–1.3M
10.
Abnormal development of the olfactory bulb and reproductive system in mice lacking prokineticin receptor PKR2
Shun-ichiro Matsumoto, Chihiro Yamazaki, Koh-hei Masumoto, Mamoru Nagano, Masanori Naito, Takatoshi Soga, Hideki Hiyama, Mitsuyuki Matsumoto, Jun Takasaki, Masazumi Kamohara, Ayako Matsuo, Hiroyuki Ishii, Masato Kobori, Masao Katoh, Hitoshi Matsushime, Kiyoshi Furuichi, Yasufumi Shigeyoshi
Proc Natl Acad Sci U S A. 2006 Mar 14; 103(11): 4140–4145. Published online 2006 Mar 2. doi: 10.1073/pnas.0508881103
PMCID:
PMC1449660
AbstractArticlePDF–1.6M
11.
The endocrine-gland-derived VEGF homologue Bv8 promotes angiogenesis in the testis: Localization of Bv8 receptors to endothelial cells
Jennifer LeCouter, Rui Lin, Max Tejada, Gretchen Frantz, Franklin Peale, Kenneth J. Hillan, Napoleone Ferrara
Proc Natl Acad Sci U S A. 2003 Mar 4; 100(5): 2685–2690. Published online 2003 Feb 25. doi: 10.1073/pnas.0337667100
PMCID:
PMC151401
AbstractArticlePDF–635K
12.
Quantitative genetics of age-related retinal degeneration: a second F1 intercross between the A/J and C57BL/6 strains
M. Danciger, H. Yang, R. Ralston, Y. Liu, M. T. Matthes, J. Peirce, M. M. LaVail
Mol Vis. 2007; 13: 79–85. Published online 2007 Jan 25.
PMCID:
PMC2503185
AbstractArticlePDF–118K
13.
Prokineticin receptor-1 signaling promotes Epicardial to Mesenchymal Transition during heart development
Himanshu Arora, Mounia Boulberdaa, Rehana Qureshi, Verda Bitirim, Adeline Gasser, Nadia Messaddeq, Pascal Dolle, Canan G. Nebigil
Sci Rep. 2016; 6: 25541. Published online 2016 May 6. doi: 10.1038/srep25541
PMCID:
PMC4858698
AbstractArticlePDF–3.2M
14.
Epicardial-Myocardial Signaling Directing Coronary Vasculogenesis
Harold E. Olivey, Eric C. Svensson
Circ Res. Author manuscript; available in PMC 2011 Mar 19.
Published in final edited form as: Circ Res. 2010 Mar 19; 106(5): 818–832. doi: 10.1161/CIRCRESAHA.109.209197
PMCID:
PMC2843003
AbstractArticlePDF–2.2M
15.
Brn3a regulates the transition from neurogenesis to terminal differentiation and represses non-neural gene expression in the trigeminal ganglion
Jason Lanier, Iain M. Dykes, Stephanie Nissen, S. Raisa Eng, Eric E. Turner
Dev Dyn. Author manuscript; available in PMC 2010 Jul 27.
Published in final edited form as: Dev Dyn. 2009 Dec; 238(12): 3065–3079. doi: 10.1002/dvdy.22145
PMCID:
PMC2910251
AbstractArticlePDF–5.5M
16.
MAPPING OF QTLs FOR ORAL ALCOHOL SELF-ADMINISTRATION IN B6.C AND B6.I QUASI-CONGENIC RQI STRAINS
Csaba Vadasz, Mariko Saito, Beatrix M. Gyetvai, Melinda Oros, Istvan Szakall, Krisztina M. Kovacs, Vidudala V.T.S. Prasad, Grant Morahan, Reka Toth
Neurochem Res. Author manuscript; available in PMC 2008 Dec 4.
Published in final edited form as: Neurochem Res. 2007 Jul; 32(7): 1099–1112. Published online 2007 Feb 2. doi: 10.1007/s11064-006-9234-4
PMCID:
PMC2595145
AbstractArticlePDF–344K
17.
Dlx1&2 and Mash1 Transcription Factors Control MGE and CGE Patterning and Differentiation through Parallel and Overlapping Pathways
Jason E. Long, Inma Cobos, Greg B. Potter, John L. R. Rubenstein
Cereb Cortex. 2009 Jul; 19(Suppl 1): i96–i106. Published online 2009 Apr 22. doi: 10.1093/cercor/bhp045
PMCID:
PMC2693539
AbstractArticlePDF–838K
18.
Dlx1&2 and Mash1 Transcription Factors Control Striatal Patterning and Differentiation Through Parallel and Overlapping Pathways
Jason E. Long, Christo Swan, Winnie S. Liang, Inma Cobos, Gregory B. Potter, John L. R. Rubenstein
J Comp Neurol. Author manuscript; available in PMC 2010 Feb 1.
Published in final edited form as: J Comp Neurol. 2009 Feb 1; 512(4): 556–572. doi: 10.1002/cne.21854
PMCID:
PMC2761428
AbstractArticlePDF–8.6M
19.
High-throughput discovery of novel developmental phenotypes
Mary E. Dickinson, Ann M. Flenniken, Xiao Ji, Lydia Teboul, Michael D. Wong, Jacqueline K. White, Terrence F. Meehan, Wolfgang J. Weninger, Henrik Westerberg, Hibret Adissu, Candice N. Baker, Lynette Bower, James M. Brown, L. Brianna Caddle, Francesco Chiani, Dave Clary, James Cleak, Mark J. Daly, James M. Denegre, Brendan Doe, Mary E. Dolan, Sarah M. Edie, Helmut Fuchs, Valerie Gailus-Durner, Antonella Galli, Alessia Gambadoro, Juan Gallegos, Shiying Guo, Neil R. Horner, Chih-wei Hsu, Sara J. Johnson, Sowmya Kalaga, Lance C. Keith, Louise Lanoue, Thomas N. Lawson, Monkol Lek, Manuel Mark, Susan Marschall, Jeremy Mason, Melissa L. McElwee, Susan Newbigging, Lauryl M.J. Nutter, Kevin A. Peterson, Ramiro Ramirez-Solis, Douglas J. Rowland, Edward Ryder, Kaitlin E. Samocha, John R. Seavitt, Mohammed Selloum, Zsombor Szoke-Kovacs, Masaru Tamura, Amanda G Trainor, Ilinca Tudose, Shigeharu Wakana, Jonathan Warren, Olivia Wendling, David B. West, Leeyean Wong, Atsushi Yoshiki, The International Mouse Phenotyping Consortium, Daniel G. MacArthur, Glauco P. Tocchini-Valentini, Xiang Gao, Paul Flicek, Allan Bradley, William C. Skarnes, Monica J. Justice, Helen E. Parkinson, Mark Moore, Sara Wells, Robert E. Braun, Karen L. Svenson, Martin Hrabe de Angelis, Yann Herault, Tim Mohun, Ann-Marie Mallon, R. Mark Henkelman, Steve D.M. Brown, David J. Adams, K.C. Kent Lloyd, Colin McKerlie, Arthur L. Beaudet, Maja Bucan, Stephen A. Murray
Nature. Author manuscript; available in PMC 2017 Mar 14.
Published in final edited form as: Nature. 2016 Sep 22; 537(7621): 508–514. Published online 2016 Sep 14. doi: 10.1038/nature19356
Correction in:
Nature. 2017 Nov 16; 551(7680): 398.
PMCID:
PMC5295821
AbstractArticlePDF–3.0M
20.
The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data
Gautier Koscielny, Gagarine Yaikhom, Vivek Iyer, Terrence F. Meehan, Hugh Morgan, Julian Atienza-Herrero, Andrew Blake, Chao-Kung Chen, Richard Easty, Armida Di Fenza, Tanja Fiegel, Mark Grifiths, Alan Horne, Natasha A. Karp, Natalja Kurbatova, Jeremy C. Mason, Peter Matthews, Darren J. Oakley, Asfand Qazi, Jack Regnart, Ahmad Retha, Luis A. Santos, Duncan J. Sneddon, Jonathan Warren, Henrik Westerberg, Robert J. Wilson, David G. Melvin, Damian Smedley, Steve D. M. Brown, Paul Flicek, William C. Skarnes, Ann-Marie Mallon, Helen Parkinson
Nucleic Acids Res. 2014 Jan 1; 42(Database issue): D802–D809. Published online 2013 Nov 3. doi: 10.1093/nar/gkt977
PMCID:
PMC3964955
AbstractArticlePDF–5.7M

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