Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 25 to 36 of 56 entries
Sorted by: Best Match Show Resources per page
Revisiting the variation of clustering coefficient of biological networks suggests new modular structure.

BMC systems biology

Hao D, Ren C, Li C.
PMID: 22548803
BMC Syst Biol. 2012 May 01;6:34. doi: 10.1186/1752-0509-6-34.

BACKGROUND: A central idea in biology is the hierarchical organization of cellular processes. A commonly used method to identify the hierarchical modular organization of network relies on detecting a global signature known as variation of clustering coefficient (so-called modularity...

Cite
Hao D, Ren C, Li C. Revisiting the variation of clustering coefficient of biological networks suggests new modular structure. BMC Syst Biol. 2012;6:34doi: 10.1186/1752-0509-6-34.
Hao, D., Ren, C., & Li, C. (2012). Revisiting the variation of clustering coefficient of biological networks suggests new modular structure. BMC systems biology, 634. https://doi.org/10.1186/1752-0509-6-34
Hao, Dapeng, et al. "Revisiting the variation of clustering coefficient of biological networks suggests new modular structure." BMC systems biology vol. 6 (2012): 34. doi: https://doi.org/10.1186/1752-0509-6-34
Hao D, Ren C, Li C. Revisiting the variation of clustering coefficient of biological networks suggests new modular structure. BMC Syst Biol. 2012 May 01;6:34. doi: 10.1186/1752-0509-6-34. PMID: 22548803; PMCID: PMC3465239.
Copy Download .nbib Format: NLM
The metabolic world of Escherichia coli is not small.

Proceedings of the National Academy of Sciences of the United States of America

Arita M.
PMID: 14757824
Proc Natl Acad Sci U S A. 2004 Feb 10;101(6):1543-7. doi: 10.1073/pnas.0306458101. Epub 2004 Feb 02.

To elucidate the organizational and evolutionary principles of the metabolism of living organisms, recent studies have addressed the graph-theoretic analysis of large biochemical networks responsible for the synthesis and degradation of cellular building blocks [Jeong, H., Tombor, B., Albert,...

Cite
Arita M. The metabolic world of Escherichia coli is not small. Proc Natl Acad Sci U S A. 2004;101(6):1543-7doi: 10.1073/pnas.0306458101.
Arita, M. (2004). The metabolic world of Escherichia coli is not small. Proceedings of the National Academy of Sciences of the United States of America, 101(6), 1543-7. https://doi.org/10.1073/pnas.0306458101
Arita, Masanori. "The metabolic world of Escherichia coli is not small." Proceedings of the National Academy of Sciences of the United States of America vol. 101,6 (2004): 1543-7. doi: https://doi.org/10.1073/pnas.0306458101
Arita M. The metabolic world of Escherichia coli is not small. Proc Natl Acad Sci U S A. 2004 Feb 10;101(6):1543-7. doi: 10.1073/pnas.0306458101. Epub 2004 Feb 02. PMID: 14757824; PMCID: PMC341771.
Copy Download .nbib Format: NLM
Do fully synthetic and genetically synthesised human insulin differ?.

Lancet (London, England)

Teuscher A, Diem P.
PMID: 6107781
Lancet. 1980 Nov 29;2(8205):1186. doi: 10.1016/s0140-6736(80)92612-4.

No abstract available.

Cite
Teuscher A, Diem P. Do fully synthetic and genetically synthesised human insulin differ?. Lancet. 1980;2(8205):1186doi: 10.1016/s0140-6736(80)92612-4.
Teuscher, A., & Diem, P. (1980). Do fully synthetic and genetically synthesised human insulin differ?. Lancet (London, England), 2(8205), 1186. https://doi.org/10.1016/s0140-6736(80)92612-4
Teuscher, A, and Diem, P. "Do fully synthetic and genetically synthesised human insulin differ?." Lancet (London, England) vol. 2,8205 (1980): 1186. doi: https://doi.org/10.1016/s0140-6736(80)92612-4
Teuscher A, Diem P. Do fully synthetic and genetically synthesised human insulin differ?. Lancet. 1980 Nov 29;2(8205):1186. doi: 10.1016/s0140-6736(80)92612-4. PMID: 6107781.
Copy Download .nbib Format: NLM
Visualizing multi-omics data in metabolic networks with the software Omix: a case study.

Bio Systems

Droste P, Miebach S, Niedenführ S, Wiechert W, Nöh K.
PMID: 21575673
Biosystems. 2011 Aug;105(2):154-61. doi: 10.1016/j.biosystems.2011.04.003. Epub 2011 May 07.

Systems Biology is a multi-disciplinary research field with the aim of understanding the function of complex processes in living organisms. These intracellular processes are described by biochemical networks. Experimental studies in alliance with computer simulation lead to a continually...

Cite
Droste P, Miebach S, Niedenführ S, et al. Visualizing multi-omics data in metabolic networks with the software Omix: a case study. Biosystems. 2011;105(2):154-61doi: 10.1016/j.biosystems.2011.04.003.
Droste, P., Miebach, S., Niedenführ, S., Wiechert, W., & Nöh, K. (2011). Visualizing multi-omics data in metabolic networks with the software Omix: a case study. Bio Systems, 105(2), 154-61. https://doi.org/10.1016/j.biosystems.2011.04.003
Droste, Peter, et al. "Visualizing multi-omics data in metabolic networks with the software Omix: a case study." Bio Systems vol. 105,2 (2011): 154-61. doi: https://doi.org/10.1016/j.biosystems.2011.04.003
Droste P, Miebach S, Niedenführ S, Wiechert W, Nöh K. Visualizing multi-omics data in metabolic networks with the software Omix: a case study. Biosystems. 2011 Aug;105(2):154-61. doi: 10.1016/j.biosystems.2011.04.003. Epub 2011 May 07. PMID: 21575673.
Copy Download .nbib Format: NLM
Systems-Level Annotation of a Metabolomics Data Set Reduces 25 000 Features to Fewer than 1000 Unique Metabolites.

Analytical chemistry

Mahieu NG, Patti GJ.
PMID: 28914531
Anal Chem. 2017 Oct 03;89(19):10397-10406. doi: 10.1021/acs.analchem.7b02380. Epub 2017 Sep 15.

When using liquid chromatography/mass spectrometry (LC/MS) to perform untargeted metabolomics, it is now routine to detect tens of thousands of features from biological samples. Poor understanding of the data, however, has complicated interpretation and masked the number of unique...

Cite
Mahieu NG, Patti GJ. Systems-Level Annotation of a Metabolomics Data Set Reduces 25 000 Features to Fewer than 1000 Unique Metabolites. Anal Chem. 2017;89(19):10397-10406doi: 10.1021/acs.analchem.7b02380.
Mahieu, N. G., & Patti, G. J. (2017). Systems-Level Annotation of a Metabolomics Data Set Reduces 25 000 Features to Fewer than 1000 Unique Metabolites. Analytical chemistry, 89(19), 10397-10406. https://doi.org/10.1021/acs.analchem.7b02380
Mahieu, Nathaniel G, and Patti, Gary J. "Systems-Level Annotation of a Metabolomics Data Set Reduces 25 000 Features to Fewer than 1000 Unique Metabolites." Analytical chemistry vol. 89,19 (2017): 10397-10406. doi: https://doi.org/10.1021/acs.analchem.7b02380
Mahieu NG, Patti GJ. Systems-Level Annotation of a Metabolomics Data Set Reduces 25 000 Features to Fewer than 1000 Unique Metabolites. Anal Chem. 2017 Oct 03;89(19):10397-10406. doi: 10.1021/acs.analchem.7b02380. Epub 2017 Sep 15. PMID: 28914531; PMCID: PMC6427824.
Copy Download .nbib Format: NLM
Density-Dependent Recycling Promotes the Long-Term Survival of Bacterial Populations during Periods of Starvation.

mBio

Takano S, Pawlowska BJ, Gudelj I, Yomo T, Tsuru S.
PMID: 28174316
mBio. 2017 Feb 07;8(1). doi: 10.1128/mBio.02336-16.

The amount of natural resources in the Earth's environment is in flux, which can trigger catastrophic collapses of ecosystems. How populations survive under nutrient-poor conditions is a central question in ecology. Curiously, some bacteria persist for a long time...

Cite
Takano S, Pawlowska BJ, Gudelj I, et al. Density-Dependent Recycling Promotes the Long-Term Survival of Bacterial Populations during Periods of Starvation. mBio. 2017;8(1)doi: 10.1128/mBio.02336-16.
Takano, S., Pawlowska, B. J., Gudelj, I., Yomo, T., & Tsuru, S. (2017). Density-Dependent Recycling Promotes the Long-Term Survival of Bacterial Populations during Periods of Starvation. mBio, 8(1), . https://doi.org/10.1128/mBio.02336-16
Takano, Sotaro, et al. "Density-Dependent Recycling Promotes the Long-Term Survival of Bacterial Populations during Periods of Starvation." mBio vol. 8,1 (2017). doi: https://doi.org/10.1128/mBio.02336-16
Takano S, Pawlowska BJ, Gudelj I, Yomo T, Tsuru S. Density-Dependent Recycling Promotes the Long-Term Survival of Bacterial Populations during Periods of Starvation. mBio. 2017 Feb 07;8(1). doi: 10.1128/mBio.02336-16. PMID: 28174316; PMCID: PMC5296608.
Copy Download .nbib Format: NLM
FLYCOP: metabolic modeling-based analysis and engineering microbial communities.

Bioinformatics (Oxford, England)

García-Jiménez B, García JL, Nogales J.
PMID: 30423096
Bioinformatics. 2018 Sep 01;34(17):i954-i963. doi: 10.1093/bioinformatics/bty561.

MOTIVATION: Synthetic microbial communities begin to be considered as promising multicellular biocatalysts having a large potential to replace engineered single strains in biotechnology applications, in pharmaceutical, chemical and living architecture sectors. In contrast to single strain engineering, the effective...

Cite
García-Jiménez B, García JL, Nogales J. FLYCOP: metabolic modeling-based analysis and engineering microbial communities. Bioinformatics. 2018;34(17):i954-i963doi: 10.1093/bioinformatics/bty561.
García-Jiménez, B., García, J. L., & Nogales, J. (2018). FLYCOP: metabolic modeling-based analysis and engineering microbial communities. Bioinformatics (Oxford, England), 34(17), i954-i963. https://doi.org/10.1093/bioinformatics/bty561
García-Jiménez, Beatriz, et al. "FLYCOP: metabolic modeling-based analysis and engineering microbial communities." Bioinformatics (Oxford, England) vol. 34,17 (2018): i954-i963. doi: https://doi.org/10.1093/bioinformatics/bty561
García-Jiménez B, García JL, Nogales J. FLYCOP: metabolic modeling-based analysis and engineering microbial communities. Bioinformatics. 2018 Sep 01;34(17):i954-i963. doi: 10.1093/bioinformatics/bty561. PMID: 30423096; PMCID: PMC6129290.
Copy Download .nbib Format: NLM
[Development of the screening system for the bacterial type III secretion apparatus inhibitor].

The Japanese journal of antibiotics

Abe A.
PMID: 12199117
Jpn J Antibiot. 2002 Jun;55(3):331-6.

No abstract available.

Cite
Abe A. [Development of the screening system for the bacterial type III secretion apparatus inhibitor]. Jpn J Antibiot. 2002;55(3):331-6
Abe, A. (2002). [Development of the screening system for the bacterial type III secretion apparatus inhibitor]. The Japanese journal of antibiotics, 55(3), 331-6.
Abe, Akio. "[Development of the screening system for the bacterial type III secretion apparatus inhibitor]." The Japanese journal of antibiotics vol. 55,3 (2002): 331-6.
Abe A. [Development of the screening system for the bacterial type III secretion apparatus inhibitor]. Jpn J Antibiot. 2002 Jun;55(3):331-6. Japanese. PMID: 12199117.
Copy Download .nbib Format: NLM
Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction.

The Journal of biological chemistry

BESSMAN MJ, LEHMAN IR, SIMMS ES, KORNBERG A.
PMID: 13563463
J Biol Chem. 1958 Jul;233(1):171-7.

No abstract available.

Cite
BESSMAN MJ, LEHMAN IR, SIMMS ES, et al. Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction. J Biol Chem. 1958;233(1):171-7
BESSMAN, M. J., LEHMAN, I. R., SIMMS, E. S., & KORNBERG, A. (1958). Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction. The Journal of biological chemistry, 233(1), 171-7.
BESSMAN, M J, et al. "Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction." The Journal of biological chemistry vol. 233,1 (1958): 171-7.
BESSMAN MJ, LEHMAN IR, SIMMS ES, KORNBERG A. Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction. J Biol Chem. 1958 Jul;233(1):171-7. PMID: 13563463.
Copy Download .nbib Format: NLM
Harry Miles Imboden, 1878-1951.

Medical radiography and photography

SPILLMAN R.
PMID: 13119051
Med Radiogr Photogr. 1953 Nov 04;29(4):Cover 2; passim, 110.

No abstract available.

Cite
SPILLMAN R. Harry Miles Imboden, 1878-1951. Med Radiogr Photogr. 1953;29(4):Cover 2; passim, 110
SPILLMAN, R. (1953). Harry Miles Imboden, 1878-1951. Medical radiography and photography, 29(4), Cover 2; passim, 110.
SPILLMAN, R. "Harry Miles Imboden, 1878-1951." Medical radiography and photography vol. 29,4 (1953): Cover 2; passim, 110.
SPILLMAN R. Harry Miles Imboden, 1878-1951. Med Radiogr Photogr. 1953 Nov 04;29(4):Cover 2; passim, 110. PMID: 13119051.
Copy Download .nbib Format: NLM
Isocitritase in Escherichia coli.

Nature

WONG DT, AJL SJ.
PMID: 13272728
Nature. 1955 Nov 19;176(4490):970-1. doi: 10.1038/176970a0.

No abstract available.

Cite
WONG DT, AJL SJ. Isocitritase in Escherichia coli. Nature. 1955;176(4490):970-1doi: 10.1038/176970a0.
WONG, D. T., & AJL, S. J. (1955). Isocitritase in Escherichia coli. Nature, 176(4490), 970-1. https://doi.org/10.1038/176970a0
WONG, D T, and AJL, S J. "Isocitritase in Escherichia coli." Nature vol. 176,4490 (1955): 970-1. doi: https://doi.org/10.1038/176970a0
WONG DT, AJL SJ. Isocitritase in Escherichia coli. Nature. 1955 Nov 19;176(4490):970-1. doi: 10.1038/176970a0. PMID: 13272728.
Copy Download .nbib Format: NLM
An analysis of the acid-soluble fraction of normal and T2r-infected cells of Escherichia coli, strain B.

The Journal of biological chemistry

O'DONNELL JF, MACKAL RP, EVANS EA.
PMID: 13610867
J Biol Chem. 1958 Dec;233(6):1523-7.

No abstract available.

Cite
O'DONNELL JF, MACKAL RP, EVANS EA. An analysis of the acid-soluble fraction of normal and T2r-infected cells of Escherichia coli, strain B. J Biol Chem. 1958;233(6):1523-7
O'DONNELL, J. F., MACKAL, R. P., & EVANS, E. A. (1958). An analysis of the acid-soluble fraction of normal and T2r-infected cells of Escherichia coli, strain B. The Journal of biological chemistry, 233(6), 1523-7.
O'DONNELL, J F, et al. "An analysis of the acid-soluble fraction of normal and T2r-infected cells of Escherichia coli, strain B." The Journal of biological chemistry vol. 233,6 (1958): 1523-7.
O'DONNELL JF, MACKAL RP, EVANS EA. An analysis of the acid-soluble fraction of normal and T2r-infected cells of Escherichia coli, strain B. J Biol Chem. 1958 Dec;233(6):1523-7. PMID: 13610867.
Copy Download .nbib Format: NLM
Showing 25 to 36 of 56 entries