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1.

Structural basis for regulation of the nucleo-cytoplasmic distribution of Bag6 by TRC35.
by Mock, Jee-Young

Proceedings of the National Academy of Sciences of the United States of America, October 31, 2017, Vol.114(44), pp.11679-11684

2.

Rapid metabolic evolution in human prefrontal cortex.
by Fu, Xing

Proceedings of the National Academy of Sciences of the United States of America, April 12, 2011, Vol.108(15), pp.6181-6186

3.

Z-DNA-forming silencer in the first exon regulates human ADAM-12 gene expression.
by Ray, Bimal K

Proceedings of the National Academy of Sciences of the United States of America, January 4, 2011, Vol.108(1), pp.103-108

4.

Variable motif utilization in homeotic selector (Hox)-cofactor complex formation controls specificity.
by Lelli, Katherine M

Proceedings of the National Academy of Sciences of the United States of America, December 27, 2011, Vol.108(52), pp.21122-21127

5.

C5orf30 is a negative regulator of tissue damage in rheumatoid arthritis.
by Muthana, Munitta

Proceedings of the National Academy of Sciences of the United States of America, September 15, 2015, Vol.112(37), pp.11618-11623

7.

Human cytomegalovirus tegument protein pp150 acts as a cyclin A2-CDK-dependent sensor of the host cell cycle and differentiation state.
by Bogdanow, Boris

Proceedings of the National Academy of Sciences of the United States of America, October 22, 2013, Vol.110(43), pp.17510-17515

9.

An RNA virus hijacks an incognito function of a DNA repair enzyme.
by Virgen-Slane, Richard

Proceedings of the National Academy of Sciences of the United States of America, September 4, 2012, Vol.109(36), pp.14634-14639

10.

CHD3 protein recognizes and regulates methylated histone H3 lysines 4 and 27 over a subset of targets in the rice genome.
by Hu, Yongfeng

Proceedings of the National Academy of Sciences of the United States of America, April 10, 2012, Vol.109(15), pp.5773-5778

11.

Eukaryotic-type plastid nucleoid protein pTAC3 is essential for transcription by the bacterial-type plastid RNA polymerase.
by Yagi, Yusuke

Proceedings of the National Academy of Sciences of the United States of America, May 8, 2012, Vol.109(19), pp.7541-7546

12.

Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures
by Myrick, Leila K

Proceedings of the National Academy of Sciences of the United States of America, 27 January 2015, Vol.112(4), pp.949-56

13.

Promoter-mediated diversification of transcriptional bursting dynamics following gene duplication.
by Tunnacliffe, Edward

Proceedings of the National Academy of Sciences of the United States of America, August 14, 2018, Vol.115(33), pp.8364-8369

14.

Identification of a de novo thymidylate biosynthesis pathway in mammalian mitochondria
by Anderson, Donald D

Proceedings of the National Academy of Sciences of the United States of America, 13 September 2011, Vol.108(37), pp.15163-8

15.

Sensing nerve injury at the axonal ER: activated Luman/CREB3 serves as a novel axonally synthesized retrograde regeneration signal
by Ying, Zhengxin

Proceedings of the National Academy of Sciences of the United States of America, 11 November 2014, Vol.111(45), pp.16142-7

16.

Two apextrin-like proteins mediate extracellular and intracellular bacterial recognition in amphioxus.
by Huang, Guangrui

Proceedings of the National Academy of Sciences of the United States of America, September 16, 2014, Vol.111(37), pp.13469-13474

17.

NLR family member NLRC5 is a transcriptional regulator of MHC class I genes.
by Meissner, Torsten B

Proceedings of the National Academy of Sciences of the United States of America, August 3, 2010, Vol.107(31), pp.13794-13799

18.

Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function
by Tao, Jifang

Proceedings of the National Academy of Sciences of the United States of America, 24 March 2009, Vol.106(12), pp.4882-7

19.

Groucho corepressor functions as a cofactor for the Knirps short-range transcriptional repressor.
by Payankaulam, Sandhya

Proceedings of the National Academy of Sciences of the United States of America, October 13, 2009, Vol.106(41), pp.17314-17319

20.

Familial hypercatabolic hypoproteinemia caused by deficiency of the neonatal Fc receptor, FcRn, due to a mutant β2-microglobulin gene
by Manzoor A. Wani

Proceedings of the National Academy of Sciences of the United States of America, 28 March 2006, Vol.103(13), p.5084

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