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Items: 17

1.
OCRL deficiency impairs endolysosomal function in a humanized mouse model for Lowe syndrome and Dent disease
Beatrice Paola Festa, Marine Berquez, Alkaly Gassama, Irmgard Amrein, Hesham M Ismail, Marijana Samardzija, Leopoldo Staiano, Alessandro Luciani, Christian Grimm, Robert L Nussbaum, Maria Antonietta De Matteis, Olivier M Dorchies, Leonardo Scapozza, David Paul Wolfer, Olivier Devuyst
Hum Mol Genet. 2019 Jun 15; 28(12): 1931–1946. Published online 2018 Dec 26. doi: 10.1093/hmg/ddy449
PMCID:
PMC6548226
AbstractArticlePDF–48M
2.
Prosapip1-Dependent Synaptic Adaptations in the Nucleus Accumbens Drive Alcohol Intake, Seeking, and Reward
Sophie Laguesse, Nadege Morisot, Jung Hoon Shin, Feng Liu, Martin F. Adrover, Samuel A. Sakhai, Marcelo F. Lopez, Khanhky Phamluong, William C. Griffin, III, Howard C. Becker, Kevin J. Bender, Veronica A. Alvarez, Dorit Ron
Neuron. Author manuscript; available in PMC 2018 Jun 22.
Published in final edited form as: Neuron. 2017 Sep 27; 96(1): 145–159.e8. Published online 2017 Sep 8. doi: 10.1016/j.neuron.2017.08.037
PMCID:
PMC6014831
AbstractArticlePDF–1.0M
3.
Mexneurin is a novel precursor of peptides in the central nervous system of rodents
Maura Epifanía Matus-Ortega, Philippe Leff Gelman, Juan Carlos Calva-Nieves, Anabel Flores-Zamora, Alberto Salazar-Juárez, Carlos-Alejandro Torner-Aguilar, Gerardo Gamba, Paola De Los Heros, Bonnie Peng, John E. Pintar, Heinrich S. Gompf, Charles N. Allen, Benito Antón-Palma
FEBS Lett. Author manuscript; available in PMC 2018 Jun 1.
Published in final edited form as: FEBS Lett. 2017 Jun; 591(12): 1627–1636. Published online 2017 Jun 1. doi: 10.1002/1873-3468.12679
PMCID:
PMC5509056
AbstractArticlePDF–1.6M
4.
Kidney Tubular Ablation of Ocrl/Inpp5b Phenocopies Lowe Syndrome Tubulopathy
Kazunori Inoue, Daniel M. Balkin, Lijuan Liu, Ramiro Nandez, Yumei Wu, Xuefei Tian, Tong Wang, Robert Nussbaum, Pietro De Camilli, Shuta Ishibe
J Am Soc Nephrol. 2017 May; 28(5): 1399–1407. Published online 2016 Nov 28. doi: 10.1681/ASN.2016080913
PMCID:
PMC5407733
AbstractArticle
5.
Mouse Model for Lowe Syndrome/Dent Disease 2 Renal Tubulopathy
Susan P. Bothwell, Emily Chan, Isa M. Bernardini, Yien-Ming Kuo, William A. Gahl, Robert L. Nussbaum
J Am Soc Nephrol. 2011 Mar; 22(3): 443–448. doi: 10.1681/ASN.2010050565
PMCID:
PMC3060438
AbstractArticle
6.
Species-specific difference in expression and splice-site choice in Inpp5b, an inositol polyphosphate 5-phosphatase paralogous to the enzyme deficient in Lowe Syndrome
Susan P. Bothwell, Leslie W. Farber, Adam Hoagland, Robert L. Nussbaum
Mamm Genome. 2010; 21(9): 458–466. Published online 2010 Sep 26. doi: 10.1007/s00335-010-9281-7
PMCID:
PMC2974198
AbstractArticlePDF–546K
7.
Cracking the egg: molecular dynamics and evolutionary aspects of the transition from the fully grown oocyte to embryo
Alexei V. Evsikov, Joel H. Graber, J. Michael Brockman, Aleš Hampl, Andrea E. Holbrook, Priyam Singh, John J. Eppig, Davor Solter, Barbara B. Knowles
Genes Dev. 2006 Oct 1; 20(19): 2713–2727. doi: 10.1101/gad.1471006
PMCID:
PMC1578697
AbstractArticlePDF–1.7M
8.
Mammalian inositol polyphosphate 5-phosphatase II can compensate for the absence of all three yeast Sac1-like-domain-containing 5-phosphatases.
C J O'Malley, B K McColl, A M Kong, S L Ellis, A P Wijayaratnam, J Sambrook, C A Mitchell
Biochem J. 2001 May 1; 355(Pt 3): 805–817. doi: 10.1042/bj3550805
PMCID:
PMC1221798
SummaryPDF–411K
9.
Functional overlap between murine Inpp5b and Ocrl1 may explain why deficiency of the murine ortholog for OCRL1 does not cause Lowe syndrome in mice.
P A Jänne, S F Suchy, D Bernard, M MacDonald, J Crawley, A Grinberg, A Wynshaw-Boris, H Westphal, R L Nussbaum
J Clin Invest. 1998 May 15; 101(10): 2042–2053. doi: 10.1172/JCI2414
PMCID:
PMC508792
SummaryPDF–397K
10.
Targeting a Complex Transcriptome: The Construction of the Mouse Full-Length cDNA Encyclopedia
Piero Carninci, Kazunori Waki, Toshiyuki Shiraki, Hideaki Konno, Kazuhiro Shibata, Masayoshi Itoh, Katsunori Aizawa, Takahiro Arakawa, Yoshiyuki Ishii, Daisuke Sasaki, Hidemasa Bono, Shinji Kondo, Yuichi Sugahara, Rintaro Saito, Naoki Osato, Shiro Fukuda, Kenjiro Sato, Akira Watahiki, Tomoko Hirozane-Kishikawa, Mari Nakamura, Yuko Shibata, Ayako Yasunishi, Noriko Kikuchi, Atsushi Yoshiki, Moriaki Kusakabe, Stefano Gustincich, Kirk Beisel, William Pavan, Vassilis Aidinis, Akira Nakagawara, William A. Held, Hiroo Iwata, Tomohiro Kono, Hiromitsu Nakauchi, Paul Lyons, Christine Wells, David A. Hume, Michela Fagiolini, Takao K. Hensch, Michelle Brinkmeier, Sally Camper, Junji Hirota, Peter Mombaerts, Masami Muramatsu, Yasushi Okazaki, Jun Kawai, Yoshihide Hayashizaki
Genome Res. 2003 Jun; 13(6b): 1273–1289. doi: 10.1101/gr.1119703
PMCID:
PMC403712
AbstractArticlePDF–770K
11.
Large-Scale Identification of Disease Genes Involved in Acute Myeloid Leukemia
Stefan J. Erkeland, Marijke Valkhof, Claudia Heijmans-Antonissen, Antoinette van Hoven-Beijen, Ruud Delwel, Mirjam H. A. Hermans, Ivo P. Touw
J Virol. 2004 Feb; 78(4): 1971–1980. doi: 10.1128/JVI.78.4.1971-1980.2004
PMCID:
PMC369447
AbstractArticlePDF–210K
12.
Characterization of the mouse gene for the heavy metal-responsive transcription factor MTF-1
Adrian Auf der Maur, Tanja Belser, Ying Wang, Cagatay Günes, Peter Lichtlen, Oleg Georgiev, Walter Schaffner
Cell Stress Chaperones. 2000 Jul; 5(3): 196–206. doi: 10.1379/1466-1268(2000)005<0196:cotmgf>2.0.co;2
PMCID:
PMC312886
AbstractArticlePDF–458K
13.
Construction of Long-Transcript Enriched cDNA Libraries from Submicrogram Amounts of Total RNAs by a Universal PCR Amplification Method
Yulan Piao, Naomi T. Ko, Meng K. Lim, Minoru S.H. Ko
Genome Res. 2001 Sep; 11(9): 1553–1558. doi: 10.1101/gr.185501
PMCID:
PMC311119
AbstractArticlePDF–743K
14.
RIKEN Integrated Sequence Analysis (RISA) System—384-Format Sequencing Pipeline with 384 Multicapillary Sequencer
Kazuhiro Shibata, Masayoshi Itoh, Katsunori Aizawa, Sumiharu Nagaoka, Nobuya Sasaki, Piero Carninci, Hideaki Konno, Junichi Akiyama, Katsuo Nishi, Tokuji Kitsunai, Hideo Tashiro, Mari Itoh, Noriko Sumi, Yoshiyuki Ishii, Shin Nakamura, Makoto Hazama, Tsutomu Nishine, Akira Harada, Rintaro Yamamoto, Hiroyuki Matsumoto, Sumito Sakaguchi, Takashi Ikegami, Katsuya Kashiwagi, Syuji Fujiwake, Kouji Inoue, Yoshiyuki Togawa, Masaki Izawa, Eiji Ohara, Masanori Watahiki, Yuko Yoneda, Tomokazu Ishikawa, Kaori Ozawa, Takumi Tanaka, Shuji Matsuura, Jun Kawai, Yasushi Okazaki, Masami Muramatsu, Yorinao Inoue, Akira Kira, Yoshihide Hayashizaki
Genome Res. 2000 Nov; 10(11): 1757–1771. doi: 10.1101/gr.152600
PMCID:
PMC310992
AbstractArticlePDF–3.4M
15.
Normalization and Subtraction of Cap-Trapper-Selected cDNAs to Prepare Full-Length cDNA Libraries for Rapid Discovery of New Genes
Piero Carninci, Yuko Shibata, Norihito Hayatsu, Yuichi Sugahara, Kazuhiro Shibata, Masayoshi Itoh, Hideaki Konno, Yasushi Okazaki, Masami Muramatsu, Yoshihide Hayashizaki
Genome Res. 2000 Oct; 10(10): 1617–1630. doi: 10.1101/gr.145100
PMCID:
PMC310980
AbstractArticlePDF–1.4M
16.
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences
Mammalian Gene Collection (MGC) Program Team
Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899
PMCID:
PMC139241
AbstractArticlePDF–118K
17.
Gene expression in the developing mouse retina by EST sequencing and microarray analysis
Xiuqian Mu, Sheng Zhao, Rashmi Pershad, Tzung-Fu Hsieh, Ann Scarpa, Steven W. Wang, R. Allen White, Phillip D. Beremand, Terry L. Thomas, Lin Gan, William H. Klein
Nucleic Acids Res. 2001 Dec 15; 29(24): 4983–4993. doi: 10.1093/nar/29.24.4983
PMCID:
PMC97568
AbstractArticlePDF–412K

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