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Integrating large-scale functional genomic data to dissect the complexity of yeast regulatory networks (English)
National licence
- New search for: Zhu, Jun
- New search for: Zhang, Bin
- New search for: Smith, Erin N
- New search for: Drees, Becky
- New search for: Brem, Rachel B
- New search for: Kruglyak, Leonid
- New search for: Bumgarner, Roger E
- New search for: Schadt, Eric E
- New search for: Zhu, Jun
- New search for: Zhang, Bin
- New search for: Smith, Erin N
- New search for: Drees, Becky
- New search for: Brem, Rachel B
- New search for: Kruglyak, Leonid
- New search for: Bumgarner, Roger E
- New search for: Schadt, Eric E
In:
Nature Genetics
;
40
, 7
;
854-861
;
2008
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ISSN:
- Article (Journal) / Electronic Resource
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Title:Integrating large-scale functional genomic data to dissect the complexity of yeast regulatory networks
-
Contributors:Zhu, Jun ( author ) / Zhang, Bin ( author ) / Smith, Erin N ( author ) / Drees, Becky ( author ) / Brem, Rachel B ( author ) / Kruglyak, Leonid ( author ) / Bumgarner, Roger E ( author ) / Schadt, Eric E ( author )
-
Published in:Nature Genetics ; 40, 7 ; 854-861
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Publisher:
- New search for: Nature Publishing Group
-
Publication date:2008-07-01
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Size:8 pages
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ISSN:
-
DOI:
-
Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 40, Issue 7
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 805
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All in the mind| 2008
- 806
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ESR1 gene amplification in breast cancer: a common phenomenon?Brown, Lindsay A / Hoog, Jeremy / Chin, Suet-Feung / Tao, Yu / Zayed, Abd Alnaser / Chin, Koei / Teschendorff, Andrew E / Quackenbush, John F / Marioni, John C / Leung, Samuel et al. | 2008
- 810
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Reply to “ESR1 gene amplification in breast cancer: a common phenomenon?”Holst, Frederik / Stahl, Phillip / Hellwinkel, Olaf / Dancau, Ana-Maria / Krohn, Antje / Wuth, Laura / Heupel, Christian / Lebeau, Annette / Terracciano, Luigi / Al-Kuraya, Khawla et al. | 2008
- 812
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HDAC2 deficiency and histone acetylationRee, Anne Hansen / Folkvord, Sigurd / Flatmark, Kjersti et al. | 2008
- 813
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Reply to “HDAC2 deficiency and histone acetylation”Ropero, Santiago / Esteller, Manel et al. | 2008
- 814
-
Giuseppe Attardi 1923–2008Wallace, Douglas C et al. | 2008
- 815
-
Blood-strong loveTerry, Sharon F et al. | 2008
- 817
-
Shedding light on skin cancerPharoah, Paul D P et al. | 2008
- 818
-
A new identity for the elusive intestinal stem cellBatlle, Eduard et al. | 2008
- 820
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Bringing age-related macular degeneration into focusAllikmets, Rando / Dean, Michael et al. | 2008
- 821
-
Conflicting evidence on the frequency of ESR1 amplification in breast cancerAlbertson, Donna G et al. | 2008
- 822
-
Lung stem cells in the balanceBellusci, Saverio et al. | 2008
- 825
-
Research highlights| 2008
- 827
-
Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene databaseAllen, Nicole C / Bagade, Sachin / McQueen, Matthew B / Ioannidis, John P A / Kavvoura, Fotini K / Khoury, Muin J / Tanzi, Rudolph E / Bertram, Lars et al. | 2008
- 835
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Two newly identified genetic determinants of pigmentation in EuropeansSulem, Patrick / Gudbjartsson, Daniel F / Stacey, Simon N / Helgason, Agnar / Rafnar, Thorunn / Jakobsdottir, Margret / Steinberg, Stacy / Gudjonsson, Sigurjon A / Palsson, Arnar / Thorleifsson, Gudmar et al. | 2008
- 838
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Common sequence variants on 20q11.22 confer melanoma susceptibilityBrown, Kevin M / MacGregor, Stuart / Montgomery, Grant W / Craig, David W / Zhao, Zhen Zhen / Iyadurai, Kelly / K Henders, Anjali / Homer, Nils / Campbell, Megan J / Stark, Mitchell et al. | 2008
- 841
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Estimating coverage and power for genetic association studies using near-complete variation dataBhangale, Tushar R / Rieder, Mark J / Nickerson, Deborah A et al. | 2008
- 844
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NAD(P)H:quinone oxidoreductase 1 NQO1*2 genotype (P187S) is a strong prognostic and predictive factor in breast cancerFagerholm, Rainer / Hofstetter, Barbara / Tommiska, Johanna / Aaltonen, Kirsimari / Vrtel, Radek / Syrjäkoski, Kirsi / Kallioniemi, Anne / Kilpivaara, Outi / Mannermaa, Arto / Kosma, Veli-Matti et al. | 2008
- 854
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Integrating large-scale functional genomic data to dissect the complexity of yeast regulatory networksZhu, Jun / Zhang, Bin / Smith, Erin N / Drees, Becky / Brem, Rachel B / Kruglyak, Leonid / Bumgarner, Roger E / Schadt, Eric E et al. | 2008
- 862
-
A Gata6-Wnt pathway required for epithelial stem cell development and airway regenerationZhang, Yuzhen / Goss, Ashley M / Cohen, Ethan David / Kadzik, Rachel / Lepore, John J / Muthukumaraswamy, Karthika / Yang, Jifu / DeMayo, Francesco J / Whitsett, Jeffrey A / Parmacek, Michael S et al. | 2008
- 871
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Dishevelled controls apical docking and planar polarization of basal bodies in ciliated epithelial cellsPark, Tae Joo / Mitchell, Brian J / Abitua, Philip B / Kintner, Chris / Wallingford, John B et al. | 2008
- 880
-
Strong association of de novo copy number mutations with sporadic schizophreniaXu, Bin / Roos, J Louw / Levy, Shawn / van Rensburg, E J / Gogos, Joseph A / Karayiorgou, Maria et al. | 2008
- 886
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ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinomaGudbjartsson, Daniel F / Sulem, Patrick / Stacey, Simon N / Goldstein, Alisa M / Rafnar, Thorunn / Sigurgeirsson, Bardur / Benediktsdottir, Kristrun R / Thorisdottir, Kristin / Ragnarsson, Rafn / Sveinsdottir, Steinunn G et al. | 2008
- 892
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Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNAFritsche, Lars G / Loenhardt, Thomas / Janssen, Andreas / Fisher, Sheila A / Rivera, Andrea / Keilhauer, Claudia N / Weber, Bernhard H F et al. | 2008
- 897
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Combinatorial patterns of histone acetylations and methylations in the human genomeWang, Zhibin / Zang, Chongzhi / Rosenfeld, Jeffrey A / Schones, Dustin E / Barski, Artem / Cuddapah, Suresh / Cui, Kairong / Roh, Tae-Young / Peng, Weiqun / Zhang, Michael Q et al. | 2008
- 904
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Genomic surveys by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methylationKerkel, Kristi / Spadola, Alexandra / Yuan, Eric / Kosek, Jolanta / Jiang, Le / Hod, Eldad / Li, Kerry / Murty, Vundavalli V / Schupf, Nicole / Vilain, Eric et al. | 2008
- 909
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Mouse segmental duplication and copy number variationShe, Xinwei / Cheng, Ze / Zöllner, Sebastian / Church, Deanna M / Eichler, Evan E et al. | 2008
- 915
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Bmi1 is expressed in vivo in intestinal stem cellsSangiorgi, Eugenio / Capecchi, Mario R et al. | 2008
- 921
-
Ras-MAPK signaling promotes trophectoderm formation from embryonic stem cells and mouse embryosLu, Chi-Wei / Yabuuchi, Akiko / Chen, Lingyi / Viswanathan, Srinivas / Kim, Kitai / Daley, George Q et al. | 2008
- 927
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Corrigendum: Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndromeLeitch, Carmen C / Zaghloul, Norann A / Davis, Erica E / Stoetzel, Corinne / Diaz-Font, Anna / Rix, Suzanne / Al-Fadhel, Majid / Lewis, Richard Alan / Eyaid, Wafaa / Banin, Eyal et al. | 2008
- 927
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Corrigendum: Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathyUppal, Sandeep / Diggle, Christine P / Carr, Ian M / Fishwick, Colin W G / Ahmed, Mushtaq / Ibrahim, Gamal H / Helliwell, Philip S / Latos-Bieleńska, Anna / Phillips, Simon E V / Markham, Alexander F et al. | 2008
- 927
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Corrigendum: Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfectaCabral, Wayne A / Chang, Weizhong / Barnes, Aileen M / Weis, MaryAnn / Scott, Melissa A / Leikin, Sergey / Makareeva, Elena / Kuznetsova, Natalia V / Rosenbaum, Kenneth N / Tifft, Cynthia J et al. | 2008