Gene expression and cancer: getting it together (Englisch)
In:
NATURE GENETICS
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31
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1-2
;
2002
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ISSN:
- Aufsatz (Zeitschrift) / Print
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Titel:Gene expression and cancer: getting it together
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Erschienen in:NATURE GENETICS ; 31 ; 1-2
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Verlag:
- Neue Suche nach: NATURE PUBLISHING CO.
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Erscheinungsdatum:01.01.2002
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Format / Umfang:2 pages
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ISSN:
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Medientyp:Aufsatz (Zeitschrift)
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Format:Print
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Sprache:Englisch
- Neue Suche nach: 576.5
- Weitere Informationen zu Dewey Decimal Classification
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Klassifikation:
DDC: 576.5 -
Datenquelle:
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Inhaltsverzeichnis – Band 31
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Gene expression and cancer: getting it together| 2002
- 3
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CHEKs and balances: accounting for breast cancerBrody, Lawrence C. et al. | 2002
- 5
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Positioned to expandMirkin, Sergei M. / Smirnova, Ekaterina V. et al. | 2002
- 7
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Retinoid metabolism: a balancing actPerlmann, Thomas et al. | 2002
- 9
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Human mutation—blame (mostly) menEllegren, Hans et al. | 2002
- 11
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Dissecting Hirschsprung diseasePassarge, Eberhard et al. | 2002
- 13
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Translating the noiseHasty, Jeff / Collins, James J. et al. | 2002
- 15
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Touching base| 2002
- 17
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Otherness, biology and eugenicsWaller, John et al. | 2002
- 19
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GenMAPP, a new tool for viewing and analyzing microarray data on biological pathwaysDahlquist, Kam D. / Salomonis, Nathan / Vranizan, Karen / Lawlor, Steven C. / Conklin, Bruce R. et al. | 2002
- 21
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AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34Agarwal, Anil K. / Arioglu, Elif / de Almeida, Salome / Akkoc, Nurullah / Taylor, Simeon I. / Bowcock, Anne M. / Barnes, Robert I. / Garg, Abhimanyu et al. | 2002
- 25
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Bop encodes a muscle-restricted protein containing MYND and SET domains and is essential for cardiac differentiation and morphogenesisGottlieb, Paul D. / Pierce, Stephanie A. / Sims, Robert J. / Yamagishi, Hiroyuki / Weihe, Elizabeth K. / Harriss, June V. / Maika, Shanna D. / Kuziel, William A. / King, Heather L. / Olson, Eric N. et al. | 2002
- 33
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Polygenic susceptibility to breast cancer and implications for preventionPharoah, Paul D.P. / Antoniou, Antonis / Bobrow, Martin / Zimmern, Ron L. / Easton, Douglas F. / Ponder, Bruce A.J. et al. | 2002
- 37
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Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cellsCleary, John D. / Nichol, Kerrie / Wang, Yuh-Hwa / Pearson, Christopher E. et al. | 2002
- 47
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Disruption of CREB function in brain leads to neurodegenerationMantamadiotis, Theo / Lemberger, Thomas / Bleckmann, Susanne C. / Kern, Heidrun / Kretz, Oliver / Villalba, Ana Martin / Tronche, François / Kellendonk, Christoph / Gau, Daniel / Kapfhammer, Josef et al. | 2002
- 55
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Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutationsMeijers-Heijboer, Hanne / van den Ouweland, Ans / Klijn, Jan / Wasielewski, Marijke / de Snoo, Anja / Oldenburg, Rogier / Hollestelle, Antoinette / Houben, Mark / Crepin, Ellen / van Veghel-Plandsoen, Monique et al. | 2002
- 60
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Topological and causal structure of the yeast transcriptional regulatory networkGuelzim, Nabil / Bottani, Samuele / Bourgine, Paul / Képès, François et al. | 2002
- 64
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Network motifs in the transcriptional regulation network of Escherichia coliShen-Orr, Shai S. / Milo, Ron / Mangan, Shmoolik / Alon, Uri et al. | 2002
- 69
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Regulation of noise in the expression of a single geneOzbudak, Ertugrul M. / Thattai, Mukund / Kurtser, Iren / Grossman, Alan D. / van Oudenaarden, Alexander et al. | 2002
- 79
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Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndromeHearn, Tom / Renforth, Glenn L. / Spalluto, Cosma / Hanley, Neil A. / Piper, Karen / Brickwood, Sarah / White, Chris / Connolly, Vincent / Taylor, James F.N. / Russell-Eggitt, Isabelle et al. | 2002
- 84
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Genetic evidence that oxidative derivatives of retinoic acid are not involved in retinoid signaling during mouse developmentNiederreither, Karen / Abu-Abed, Suzan / Schuhbaur, Brigitte / Petkovich, Martin / Chambon, Pierre / Dollé, Pascal et al. | 2002
- 89
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Segregation at three loci explains familial and population risk in Hirschsprung diseaseGabriel, Stacey Bolk / Salomon, Rémi / Pelet, Anna / Angrist, Misha / Amiel, Jeanne / Fornage, Myriam / Attié-Bitach, Tania / Olson, Jane M. / Hofstra, Robert / Buys, Charles et al. | 2002
- 94
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Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase–deficient micePendás, Alberto M. / Zhou, Zhongjun / Cadiñanos, Juan / Freije, José M.P. / Wang, Jianming / Hultenby, Kjell / Astudillo, Aurora / Wernerson, Annika / Rodríguez, Francisco / Tryggvason, Karl et al. | 2002
- 100
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Evidence of en bloc duplication in vertebrate genomesAbi-Rached, Laurent / Gilles, André / Shiina, Takashi / Pontarotti, Pierre / Inoko, Hidetoshi et al. | 2002
- 106
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Cardiac troponin T is essential in sarcomere assembly and cardiac contractilitySehnert, Amy J. / Huq, Anja / Weinstein, Brant M. / Walker, Charline / Fishman, Mark / Stainier, Didier Y. R. et al. | 2002
- 111
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beta-cell-specific deletion of the Igf1 receptor leads to hyperinsulinemia and glucose intolerance but does not alter beta-cell massKulkarni, R. N. / Holzenberger, M. / Shih, D. Q. / Ozcan, U. / Stoffel, M. / Magnuson, M. A. / Kahn, C. R. et al. | 2002
- 111
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β-cell–specific deletion of the Igf1 receptor leads to hyperinsulinemia and glucose intolerance but does not alter β-cell massKulkarni, Rohit N. / Holzenberger, Martin / Shih, David Q. / Ozcan, Umut / Stoffel, Markus / Magnuson, Mark A. / Kahn, C. Ronald et al. | 2002
- 117
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Oncogenomics: cancer and technology| 2002
- 121
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Plant morphogenesis and KNOX genesHake, Sarah / Ori, Naomi et al. | 2002
- 123
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Methylation matters: a new spin on maspinCostello, Joseph F. / Vertino, Paula M. et al. | 2002
- 125
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Building-blocks of embryogenesisMullins, Mary C. et al. | 2002
- 126
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Repair by retrotranspositionEickbush, Thomas H. et al. | 2002
- 128
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Genome duplication strikes backSpring, Jürg et al. | 2002
- 133
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Oncogenic properties of PPM1D located within a breast cancer amplification epicenter at 17q23Li, Jing / Yang, Ying / Peng, Yue / Austin, Richard J. / van Eyndhoven, Winfried G. / Nguyen, Ken C. Q. / Gabriele, Tim / McCurrach, Mila E. / Marks, Jeffrey R. / Hoey, Timothy et al. | 2002
- 135
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Insertional mutagenesis in zebrafish rapidly identifies genes essential for early vertebrate developmentGolling, Gregory / Amsterdam, Adam / Sun, Zhaoxia / Antonelli, Marcelo / Maldonado, Ernesto / Chen, Wenbiao / Burgess, Shawn / Haldi, Maryann / Artzt, Karen / Farrington, Sarah et al. | 2002
- 141
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A genomic screen for genes upregulated by demethylation and histone deacetylase inhibition in human colorectal cancerSuzuki, Hiromu / Gabrielson, Edward / Chen, Wei / Anbazhagan, Ramaswamy / van Engeland, Manon / Weijenberg, Matty P. / Herman, James G. / Baylin, Stephen B. et al. | 2002
- 150
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nagie oko, encoding a MAGUK-family protein, is essential for cellular patterning of the retinaWei, Xiangyun / Malicki, Jarema et al. | 2002
- 159
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DNA repair mediated by endonuclease-independent LINE-1 retrotranspositionMorrish, Tammy A. / Gilbert, Nicolas / Myers, Jeremy S. / Vincent, Bethaney J. / Stamato, Thomas D. / Taccioli, Guillermo E. / Batzer, Mark A. / Moran, John V. et al. | 2002
- 166
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Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene familySchlingmann, Karl P. / Weber, Stefanie / Peters, Melanie / Niemann Nejsum, Lene / Vitzthum, Helga / Klingel, Karin / Kratz, Markus / Haddad, Elie / Ristoff, Ellinor / Dinour, Dganit et al. | 2002
- 171
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Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemiaWalder, Roxanne Y. / Landau, Daniel / Meyer, Peter / Shalev, Hanna / Tsolia, Maria / Borochowitz, Zvi / Boettger, Melanie Barbara / Beck, Gretel E. / Englehardt, Richard K. / Carmi, Rivka et al. | 2002
- 175
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Role for DNA methylation in the control of cell type–specific maspin expressionFutscher, Bernard W. / Oshiro, Marc M. / Wozniak, Ryan J. / Holtan, Nicholas / Hanigan, Christin L. / Duan, Hong / Domann, Frederick E. et al. | 2002
- 180
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Clustering of housekeeping genes provides a unified model of gene order in the human genomeLercher, Martin J. / Urrutia, Araxi O. / Hurst, Laurence D. et al. | 2002
- 184
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Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsyCossette, Patrick / Liu, Lidong / Brisebois, Katéri / Dong, Haiheng / Lortie, Anne / Vanasse, Michel / Saint-Hilaire, Jean-Marc / Carmant, Lionel / Verner, Andrei / Lu, Wei-Yang et al. | 2002
- 190
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Suppression of the p53- or pRB-mediated G1 checkpoint is required for E2F-induced S-phase entryLomazzi, Marina / Moroni, M. Cristina / Jensen, Michael R. / Frittoli, Emanuela / Helin, Kristian et al. | 2002
- 195
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Tbx24, encoding a T-box protein, is mutated in the zebrafish somite-segmentation mutant fused somitesNikaido, Masataka / Kawakami, Atsushi / Sawada, Atsushi / Furutani-Seiki, Makoto / Takeda, Hiroyuki / Araki, Kazuo et al. | 2002
- 205
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Age distribution of human gene families shows significant roles of both large- and small-scale duplications in vertebrate evolutionGu, Xun / Wang, Yufeng / Gu, Jianying et al. | 2002
- 210
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Amplification of PPM1D in human tumors abrogates p53 tumor-suppressor activityBulavin, Dmitry V. / Demidov, Oleg N. / Saito, Shin'ichi / Kauraniemi, Paivikki / Phillips, Crissy / Amundson, Sally A. / Ambrosino, Concetta / Sauter, Guido / Nebreda, Angel R. / Anderson, Carl W. et al. | 2002
- 216
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Aberrant patterns of X chromosome inactivation in bovine clonesXue, F. / Tian, X. C. / Du, F. / Kubota, C. / Taneja, M. / Dinnyes, A. / Dai, Y. / Levine, H. / Pereira, L. V. / Yang, X. et al. | 2002
- 223
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When public goes private| 2002
- 225
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The Iceland mapWeber, J. L. et al. | 2002
- 227
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The ABcs of mitochondrial transcriptionShoubridge, Eric A. et al. | 2002
- 228
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Saving sulfurJamieson, Derek et al. | 2002
- 230
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Reversing Babel with GOGresham, David et al. | 2002
- 233
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Learning to be a principal investigatorBargmann, Cori et al. | 2002
- 235
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From QTL to gene: the harvest beginsKorstanje, Ron / Paigen, Beverly et al. | 2002
- 237
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The MHC and body odors: arbitrary effects caused by shifts of mean pleasantnessWedekind, Claus et al. | 2002
- 239
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Identification of SLC39A4, a gene involved in acrodermatitis enteropathicaKüry, Sébastien / Dréno, Brigitte / Bézieau, Stéphane / Giraudet, Stéphanie / Kharfi, Monia / Kamoun, Ridha / Moisan, Jean-Paul et al. | 2002
- 241
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A high-resolution recombination map of the human genomeKong, Augustine / Gudbjartsson, Daniel F. / Sainz, Jesus / Jonsdottir, Gudrun M. / Gudjonsson, Sigurjon A. / Richardsson, Bjorgvin / Sigurdardottir, Sigrun / Barnard, John / Hallbeck, Bjorn / Masson, Gisli et al. | 2002
- 248
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Genome-wide binding map of the histone deacetylase Rpd3 in yeastKurdistani, Siavash K. / Robyr, Daniel / Tavazoie, Saeed / Grunstein, Michael et al. | 2002
- 255
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Large-scale prediction of Saccharomyces cerevisiae gene function using overlapping transcriptional clustersWu, Lani F. / Hughes, Timothy R. / Davierwala, Armaity P. / Robinson, Mark D. / Stoughton, Roland / Altschuler, Steven J. et al. | 2002
- 267
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Reciprocal crossover asymmetry and meiotic drive in a human recombination hot spotJeffreys, Alec J. / Neumann, Rita et al. | 2002
- 272
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Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOXMay, Celia A. / Shone, Angela C. / Kalaydjieva, Luba / Sajantila, Antti / Jeffreys, Alec J. et al. | 2002
- 276
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Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataractBu, Lei / Jin, Yiping / Shi, Yuefeng / Chu, Renyuan / Ban, Airong / Eiberg, Hans / Andres, Lisa / Jiang, Haisong / Zheng, Guangyong / Qian, Meiqian et al. | 2002
- 279
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Deletion in Catna2, encoding alphaN-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulationPark, C. / Falls, W. / Finger, J. H. / Longo-Guess, C. M. / Ackerman, S. L. et al. | 2002
- 279
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Deletion in Catna2, encoding αN-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulationPark, Chankyu / Falls, William / Finger, Jacqueline H. / Longo-Guess, Chantal M. / Ackerman, Susan L. et al. | 2002
- 285
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Truncating mutations of RB1CC1 in human breast cancerChano, Tokuhiro / Kontani, Keiichi / Teramoto, Koji / Okabe, Hidetoshi / Ikegawa, Shiro et al. | 2002
- 289
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Mitochondrial transcription factors B1 and B2 activate transcription of human mtDNAFalkenberg, Maria / Gaspari, Martina / Rantanen, Anja / Trifunovic, Aleksandra / Larsson, Nils-Göran / Gustafsson, Claes M. et al. | 2002
- 295
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Ptprj is a candidate for the mouse colon-cancer susceptibility locus Scc1 and is frequently deleted in human cancersRuivenkamp, Claudia A.L. / van Wezel, Tom / Zanon, Carlo / Stassen, Alphons P.M. / Vlcek, Cestmir / Csikós, Tamás / Klous, Anita M. / Tripodis, Nikos / Perrakis, Anastassis / Boerrigter, Lucie et al. | 2002
- 301
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Protein elongation factor EEF1A2 is a putative oncogene in ovarian cancerAnand, Nisha / Murthy, Sabita / Amann, Gudrun / Wernick, Meredith / Porter, Lisa A. / Cukier, I. Howard / Collins, Colin / Gray, Joe W. / Diebold, Joachim / Demetrick, Doug J. et al. | 2002
- 301
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Gene encoding protein elongation factor EEF1A2 is a putative oncogene in ovarian cancerAnand, N. / Murthy, S. / Amann, G. / Wernick, M. / Porter, L. A. / Cukier, I. H. / Collins, C. / Gray, J. W. / Diebold, J. / Demetrick, D. J. et al. | 2002
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Mutations in SUFU predispose to medulloblastomaTaylor, Michael D. / Liu, Ling / Raffel, Corey / Hui, Chi-chung / Mainprize, Todd G. / Zhang, Xiaoyun / Agatep, Ron / Chiappa, Sharon / Gao, Luzhang / Lowrance, Anja et al. | 2002
- 311
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Placental alpha~2-adrenoceptors control vascular development at the interface between mother and embryoPhilipp, M. / Brede, M. E. / Hadamek, K. / Gessler, M. / Lohse, M. J. / Hein, L. et al. | 2002
- 311
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Placental α2-adrenoceptors control vascular development at the interface between mother and embryoPhilipp, Melanie / Brede, Marc E. / Hadamek, Kerstin / Gessler, Manfred / Lohse, Martin J. / Hein, Lutz et al. | 2002
- 316
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Association of genes to genetically inherited diseases using data miningPerez-Iratxeta, Carolina / Bork, Peer / Andrade, Miguel A. et al. | 2002
- 320
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Radixin deficiency causes conjugated hyperbilirubinemia with loss of Mrp2 from bile canalicular membranesKikuchi, S. / Hata, M. / Fukumoto, K. / Yamane, Y. / Matsui, T. / Tamura, A. / Yonemura, S. / Yamagishi, H. / Keppler, D. / Tsukita, S. et al. | 2002
- 327
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Making connections| 2002
- 329
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Unifying the genetics of behaviorde Belle, J. Steven et al. | 2002
- 331
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The genome's best friendJinks-Robertson, S. et al. | 2002
- 333
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Complement in glomerulonephritisWelch, Thomas R. et al. | 2002
- 335
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Strabismus shows the wayPacker, Alan et al. | 2002
- 339
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Molecular pathogenesis of human hepatocellular carcinomaThorgeirsson, Snorri S. / Grisham, Joe W. et al. | 2002
- 347
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SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegiaPatel, Heema / Cross, Harold / Proukakis, Christos / Hershberger, Ruth / Bork, Peer / Ciccarelli, Francesca D. / Patton, Michael A. / McKusick, Victor A. / Crosby, Andrew H. et al. | 2002
- 349
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Identification of genes involved in Drosophila melanogaster geotaxis, a complex behavioral traitToma, Daniel P. / White, Kevin P. / Hirsch, Jerry / Greenspan, Ralph J. et al. | 2002
- 354
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Paxillin binds schwannomin and regulates its density-dependent localization and effect on cell morphologyFernandez-Valle, Cristina / Tang, Yong / Ricard, Jerome / Rodenas-Ruano, Alma / Taylor, Anna / Hackler, Elizabeth / Biggerstaff, John / Iacovelli, Jared et al. | 2002
- 363
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Urocortin-deficient mice show hearing impairment and increased anxiety-like behaviorVetter, Douglas E. / Li, Chien / Zhao, Lingyun / Contarino, Angelo / Liberman, M. Charles / Smith, George W. / Marchuk, Yelena / Koob, George F. / Heinemann, Stephen F. / Vale, Wylie et al. | 2002
- 370
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Revealing modular organization in the yeast transcriptional networkIhmels, Jan / Friedlander, Gilgi / Bergmann, Sven / Sarig, Ofer / Ziv, Yaniv / Barkai, Naama et al. | 2002
- 379
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Digenic inheritance of severe insulin resistance in a human pedigreeSavage, David B. / Agostini, Maura / Barroso, Inês / Gurnell, Mark / Luan, Jian'an / Meirhaeghe, Aline / Harding, Anne-Helen / Ihrke, Gudrun / Rajanayagam, Odelia / Soos, Maria A. et al. | 2002
- 385
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Meiotic arrest and aneuploidy in MLH3-deficient miceLipkin, Steven M. / Moens, Peter B. / Wang, Victoria / Lenzi, Michelle / Shanmugarajah, Dakshine / Gilgeous, Abigail / Thomas, James / Cheng, Jun / Touchman, Jeffrey W. / Green, Eric D. et al. | 2002
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Cblb is a major susceptibility gene for rat type 1 diabetes mellitusYokoi, Norihide / Komeda, Kajuro / Wang, He-Yao / Yano, Hideki / Kitada, Kazuhiro / Saitoh, Yuka / Seino, Yutaka / Yasuda, Kazuki / Serikawa, Tadao / Seino, Susumu et al. | 2002
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Genome-wide scan for familial nasopharyngeal carcinoma reveals evidence of linkage to chromosome 4Feng, Bing-Jian / Huang, Wei / Shugart, Yin Yao / Lee, Ming K. / Zhang, Feng / Xia, Jian-Chuan / Wang, Hui-Yun / Huang, Teng-Bo / Jian, Shao-Wen / Huang, Ping et al. | 2002
- 400
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Systematic screen for human disease genes in yeastSteinmetz, Lars M. / Scharfe, Curt / Deutschbauer, Adam M. / Mokranjac, Dejana / Herman, Zelek S. / Jones, Ted / Chu, Angela M. / Giaever, Guri / Prokisch, Holger / Oefner, Peter J. et al. | 2002
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Disruption of dog-1 in Caenorhabditis elegans triggers deletions upstream of guanine-rich DNACheung, Iris / Schertzer, Michael / Rose, Ann / Lansdorp, Peter M. et al. | 2002
- 410
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Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huet anomaly)Hoffmann, K. / Dreger, C. K. / Olins, A. L. / Olins, D. E. / Shultz, L. D. / Lucke, B. / Karl, H. / Kaps, R. / Muller, D. / Vaya, A. et al. | 2002
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Selection for short introns in highly expressed genesCastillo-Davis, Cristian I. / Mekhedov, Sergei L. / Hartl, Daniel L. / Koonin, Eugene V. / Kondrashov, Fyodor A. et al. | 2002
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PP1 binds Sara and negatively regulates Dpp signaling in Drosophila melanogasterBennett, Daimark / Alphey, Luke et al. | 2002
- 424
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Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor HPickering, M. C. / Cook, H. T. / Warren, J. / Bygrave, A. E. / Moss, J. / Walport, M. J. / Botto, M. et al. | 2002
- 429
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Epistatic interaction between KIR3DS1 and HLA-B delays the progression to AIDSMartin, Maureen P. / Gao, Xiaojiang / Lee, Jeong-Hee / Nelson, George W. / Detels, Roger / Goedert, James J. / Buchbinder, Susan / Hoots, Keith / Vlahov, David / Trowsdale, John et al. | 2002
- 435
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Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndromeMykytyn, Kirk / Nishimura, Darryl Y. / Searby, Charles C. / Shastri, Mythreyi / Yen, Hsan-jan / Beck, John S. / Braun, Terry / Streb, Luan M. / Cornier, Alberto S. / Cox, Gerald F. et al. | 2002
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A mouse model for the learning and memory deficits associated with neurofibromatosis type ISilva, A J / Frankland, P W / Marowitz, Z / Friedman, E / Lazlo, G / Cioffi, D / Jacks, T / Bourtchuladze, R et al. | 2002