Results
|
581.
|
|
|
582.
|
|
|
583.
|
Molecular and functional characterization of Arabidopsis Cullin 3A. [electronic resource] by
- Dieterle, Monika
- Thomann, Alexis
- Renou, Jean-Pierre
- Parmentier, Yves
- Cognat, Valerie
- Lemonnier, Gaetan
- Müller, Rebecca
- Shen, Wen-Hui
- Kretsch, Thomas
- Genschik, Pascal
Producer: 20050603
In:
The Plant journal : for cell and molecular biology vol. 41
Availability: No items available.
|
|
584.
|
JFK, a Kelch domain-containing F-box protein, links the SCF complex to p53 regulation. [electronic resource] by
- Sun, Luyang
- Shi, Lei
- Li, Wenqian
- Yu, Wenhua
- Liang, Jing
- Zhang, Hua
- Yang, Xiaohan
- Wang, Yan
- Li, Ruifang
- Yao, Xingrong
- Yi, Xia
- Shang, Yongfeng
Producer: 20090717
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 106
Availability: No items available.
|
|
585.
|
Human X-linked Intellectual Disability Factor CUL4B Is Required for Post-meiotic Sperm Development and Male Fertility. [electronic resource] by
- Lin, Chien-Yu
- Chen, Chun-Yu
- Yu, Chih-Hsiang
- Yu, I-Shing
- Lin, Shu-Rung
- Wu, June-Tai
- Lin, Ying-Hung
- Kuo, Pao-Lin
- Wu, Jui-Ching
- Lin, Shu-Wha
Producer: 20170106
In:
Scientific reports vol. 6
Availability: No items available.
|
|
586.
|
|
|
587.
|
Dominant Noonan syndrome-causing LZTR1 mutations specifically affect the Kelch domain substrate-recognition surface and enhance RAS-MAPK signaling. [electronic resource] by
- Motta, Marialetizia
- Fidan, Miray
- Bellacchio, Emanuele
- Pantaleoni, Francesca
- Schneider-Heieck, Konstantin
- Coppola, Simona
- Borck, Guntram
- Salviati, Leonardo
- Zenker, Martin
- Cirstea, Ion C
- Tartaglia, Marco
Producer: 20200309
In:
Human molecular genetics vol. 28
Availability: No items available.
|
|
588.
|
|
|
589.
|
|
|
590.
|
An interaction network of the mammalian COP9 signalosome identifies Dda1 as a core subunit of multiple Cul4-based E3 ligases. [electronic resource] by
- Olma, Michael Hans
- Roy, Marcia
- Le Bihan, Thierry
- Sumara, Izabela
- Maerki, Sarah
- Larsen, Brett
- Quadroni, Manfredo
- Peter, Matthias
- Tyers, Mike
- Pintard, Lionel
Producer: 20090611
In:
Journal of cell science vol. 122
Availability: No items available.
|
|
591.
|
|
|
592.
|
|
|
593.
|
|
|
594.
|
|
|
595.
|
|
|
596.
|
Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth. [electronic resource] by
- Hanson, Dan
- Murray, Philip G
- O'Sullivan, James
- Urquhart, Jill
- Daly, Sarah
- Bhaskar, Sanjeev S
- Biesecker, Leslie G
- Skae, Mars
- Smith, Claire
- Cole, Trevor
- Kirk, Jeremy
- Chandler, Kate
- Kingston, Helen
- Donnai, Dian
- Clayton, Peter E
- Black, Graeme C M
Producer: 20110919
In:
American journal of human genetics vol. 89
Availability: No items available.
|
|
597.
|
|
|
598.
|
|
|
599.
|
|
|
600.
|
Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome). [electronic resource] by
- Glover, Mark
- Ware, James S
- Henry, Amanda
- Wolley, Martin
- Walsh, Roddy
- Wain, Louise V
- Xu, Shengxin
- Van't Hoff, William G
- Tobin, Martin D
- Hall, Ian P
- Cook, Stuart
- Gordon, Richard D
- Stowasser, Michael
- O'Shaughnessy, Kevin M
Producer: 20140402
In:
Clinical science (London, England : 1979) vol. 126
Availability: No items available.
|