Epigeneetika (Estonian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Epigeneetika" in Estonian language version.

refsWebsite

Global rank Estonian rank

5nih.gov

4^th place

14^th place

2nature.com

234^th place

88^th place

2wiley.com

222^nd place

147^th place

2sciencedirect.com

149^th place

130^th place

1oxforddictionaries.com

710^th place

1,274^th place

1cshlp.org

low place

3,673^rd place

1the-scientist.com

7,827^th place

6,885^th place

1sciencemag.org

857^th place

269^th place

1springer.com

274^th place

191^st place

1plosgenetics.org

low place

1discoverymedicine.com

low place

1omim.org

4,380^th place

low place

cshlp.org

cshperspectives.cshlp.org

Gary Felsenfeld (15. juuni 2014). "A Brief History of Epigenetics". Cold Spring Harbor Perspectives in Biology.

discoverymedicine.com

Richard Chahwan,Sandeep N Wontakal & Sergio Roa (17. märts 2011). "The multidimensional nature of epigenetic information and its role in disease". Discovery Medicine.

nature.com

Gerda Egger, Gangning Liang, Ana Aparicio & Peter A. Jones (27. mai 2004). "Epigenetics in human disease and prospects for epigenetic therapy". 429 (inglise). Nature.{{netiviide}}: CS1 hooldus: mitu nime: autorite loend (link)
Gerda Egger, Gangning Liang, Ana Aparicio & Peter A. Jones (27. mai 2004). "Epigenetics in human disease and prospects for epigenetic therapy" (PDF) (inglise keeles). Nature. Vaadatud 04.10.2014.{{netiviide}}: CS1 hooldus: mitu nime: autorite loend (link) CS1 hooldus: tundmatu keel (link)

nih.gov

ncbi.nlm.nih.gov

Tronick, Ed; Hunter, Richard G. "Waddington, Dynamic Systems, and Epigenetics". Frontiers in Behavioral Neuroscience. 10.
Alhamwe, Bilal Alaskhar; Khalaila, Razi; Wolf, Johanna; et al. "Histone modifications and their role in epigenetics of atopy and allergic diseases". Allergy, Asthma & Clinical Immunology. 14.
Benjamin P. Howden,corresponding authora, Marie Beaume, Paul F. Harrison, David Hernandez, Jacques Schrenzel, Torsten Seemann, Patrice Francois & Timothy P. Stinear (august 2013). "Analysis of the Small RNA Transcriptional Response in Multidrug-Resistant Staphylococcus aureus after Antimicrobial Exposure". Antimicrob Agents Chemother.{{netiviide}}: CS1 hooldus: mitu nime: autorite loend (link)
Michael Lynch (2007). "The frailty of adaptive hypotheses for the origins of organismal complexity". Proceedings of the National Academy of Sciences of the United States of America.
Andrew J Wood & Rebecca J Oakey (november 2007). "Genomic Imprinting in Mammals: Emerging Themes and Established Theories". PLOS genetics.

omim.org

Richard Chahwan. "ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED; ANCR, INCLUDED".

oxforddictionaries.com

Epigenetics – Oxford Dictionary^{[alaline kõdulink]}

plosgenetics.org

Cortland K. Griswold & Joanna Masel (12. juuni 2009). "Complex Adaptations Can Drive the Evolution of the Capacitor (PSI+), Even with Realistic Rates of Yeast Sex". PLOS genetics.

sciencedirect.com

Wang Z, Yao H, Lin S, Zhu X, Shen Z, Lu G, Poon WS, Xie D, Lin MC & Kung HF (30. aprill 2013). "Transcriptional and epigenetic regulation of human microRNAs". Cancer Letters.{{netiviide}}: CS1 hooldus: mitu nime: autorite loend (link)
Silvia Costa & Peter Shawemail (2006). "'Open minded' cells: how cells can change fate". Trends in Cell Biology.

sciencemag.org

Randal Halfmann & Susan Lindquist (29. oktoober 2010). "Epigenetics in the Extreme: Prions and the Inheritance of Environmentally Acquired Traits". Science.

springer.com

link.springer.com

James Griesemer,Matthew H. Haber, Grant Yamashita & Lisa Gannett (2005). "Critical Notice: Cycles of Contingency – Developmental Systems and Evolution". Biology and Philosophy.{{netiviide}}: CS1 hooldus: mitu nime: autorite loend (link)

the-scientist.com

Charles Q. Choi (25. mai 2006). "RNA can be hereditary molecule". The scientist.

wiley.com

onlinelibrary.wiley.com

John S. Mattick, Paulo P. Amaral, Marcel E. Dinger, Tim R. Mercer & Mark F. Mehler (jaanuar 2009). "RNA regulation of epigenetic processes". BioEssays.{{netiviide}}: CS1 hooldus: mitu nime: autorite loend (link)
J. H. M. Knoll1, R. D. Nicholls, R. E. Magenis, J. M. Graham Jr., M. Lalande, S. A. Latt, John M. Opitz Editor & James F. Reynolds (veebruar 1989). "Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion". American Journal of Medical Genetics. {{netiviide}}: parameetris |autor= on üldnimi (juhend)CS1 hooldus: mitu nime: autorite loend (link)