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2021
1 Caiella, Alessia.
The effect of N-terminal acetylation on α-Synuclein’s pathogenicity in Parkinson’s disease. : Institutt for biomedisin, Universitetet i Bergen 2021
UiB Untitled
 
2 Dutta, Ravi Kumar; Larsson, Malin; Arnesen, Thomas; Heie, Anette; Walz, Martin K.; Alesina, Piero; Gimm, Oliver; Söderkvist, Peter.
X-chromosome variants are associated with aldosterone producing adenomas. Scientific Reports 2021 ;Volum 11.(1) s. -
UiB HAUKELAND Untitled
 
3 Krogstad, Liv Svenningsson.
Uncovering NAA60’s Role in the Nervous System -Primary familial brain disease and beyond. : Institutt for biomedisin, Universitetet i Bergen 2021
UiB Untitled
 
4 Kweon, Hyae Yon; Lee, Mi-Ni; Dörfel, Max J; Seo, Seungwoon; Gottlieb, Leah; PaPazyan, Thomas; Tiernan, Nina Mc; Ree, Rasmus Moen; Bolton, David; Garcia, Andrew; Flory, Michael; Crain, Jonathan; Sebold, Alison; Lyons, Scott; Ismail, Ahmed; Marchi, Elaine; Sonn, Seong-Keun; Jeong, Se-Jin; Jeon, Sejin; Ju, Shinyeong; Conway, Simon; Kim, Taesoo; Kim, Hyun-Seok; Lee, Cheolju; Roh, Tae-Young; Arnesen, Thomas; Marmorstein, Ronen; Oh, Goo Taeg; Lyon, Gholson J.
Naa12 compensates for Naa10 in mice in the amino-terminal acetylation pathway. eLIFE 2021 ;Volum 10.
HAUKELAND UiB Untitled
 
5 Morrison, Jennifer; Altuwaijri, Norah; Brønstad, Kirsten Marie; Aksnes, Henriette; Alsaif, Hessa; Evans, Anthony; Hashem, Mais; Wheeler, Patricia; Webb, Bryn D; Alkuraya, Fowzan S.; Arnesen, Thomas.
Missense NAA20 variants impairing the NatB protein N-terminal acetyltransferase cause autosomal recessive developmental delay, intellectual disability, and microcephaly. Genetics in Medicine 2021 s. 1-6
HAUKELAND UiB Untitled
 
6 Ward, Tarsha; Tai, Warren; Morton, Sarah; Impens, Francis; Van Damme, Petra; Van Haver, Delphi; Timmerman, Evy; Venturini, Gabriela; Zhang, Kehan; Jang, Min Young; Willcox, Jonathan A.; Haghighi, Alireza; Gelb, Bruce D.; Chung, Wendy K.; Goldmuntz, Elizabeth; Porter, George; Lifton, Richard P; Brueckner, Martina; Yost, Joseph; Bruneau, Benoit; Gorham, Joshua; Kim, Yuri; Pereira, Alexandre; Homsy, Jason; Benson, Craig; DePalma, Steven R.; Varland, Sylvia; Chen, Christopher; Arnesen, Thomas; Gevaert, Kris; Seidman, Christine E.; Seidman, Jonathan G..
Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency. Circulation Research 2021 ;Volum 128. s. 1156-1169
UiB Untitled