Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Connie E. Kim"'
Autor:
Mariana Santos, Sandra Rebelo, Paula J M Van Kleeff, Connie E Kim, William T Dauer, Margarida Fardilha, Odete A da Cruz E Silva, Edgar F da Cruz E Silva
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e76788 (2013)
Protein phosphatase 1 (PP1) binding proteins are quintessential regulators, determining substrate specificity and defining subcellular localization and activity of the latter. Here, we describe a novel PP1 binding protein, the nuclear membrane protei
Externí odkaz:
https://doaj.org/article/aa03d26da1d141e18470d8003e4c191a
Publikováno v:
Nature Reviews Neurology. 5:598-609
Primary dystonia is characterized by involuntary twisting and turning movements that occur in the absence of overt brain lesions or evidence of neurodegeneration. As Tanabe et al. discuss in this article, advances in structural and functional imaging
Publikováno v:
D78. PATHWAYS AND MODELS OF LUNG ONCOGENESIS.
Publikováno v:
Cancers
Cancers, Vol 3, Iss 3, Pp 2975-2989 (2011)
Cancers, Vol 3, Iss 3, Pp 2975-2989 (2011)
Lung cancer is the leading cause of cancer deaths, with an overall survival of 15% at five years. Biomarkers that can sensitively and specifically detect lung cancer at early stage are crucial for improving this poor survival rate. Sputum has been th
Publikováno v:
C69. LUNG CANCER BIOMARKERS.
A striking but poorly understood feature of many diseases is the unique involvement of neural tissue. One example is the CNS-specific disorder DYT1 dystonia, caused by a 3-bp deletion (“ΔE”) in the widely expressed gene TOR1A . Disease mutant kn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::458fe8dab70abf9b04ef47ff7fe68d0a
https://europepmc.org/articles/PMC2906867/
https://europepmc.org/articles/PMC2906867/
Publikováno v:
Neuron. 48(6)
Summary An enigmatic feature of many genetic diseases is that mutations in widely expressed genes cause tissue-specific illness. One example is DYT1 dystonia, a neurodevelopmental disease caused by an in-frame deletion (Δgag) in the gene encoding to
Autor:
Vivette D. D'Agati, Jonathan D. Licht, Benjamin Tycko, Connie E. Kim, Vundavalli V. Murty, Chi Ming Li, Jacqueline M. Mason, Paul E. Grundy, Eric R. Fearon, Adam A. Margolin, Terrence Hensle, Meirong Guo, Jimmy Zhu
Gain-of-function mutations in exon 3 of beta-catenin (CTNNB1) are specific for Wilms' tumors that have lost WT1, but 50% of WT1-mutant cases lack such "hot spot" mutations. To ask whether stabilization of beta-catenin might be essential after WT1 los
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daa9c30faf34b803fa02d7ac2d808d00
https://europepmc.org/articles/PMC1618727/
https://europepmc.org/articles/PMC1618727/
Autor:
Paula J. M. van Kleeff, Sandra Rebelo, Connie E. Kim, Margarida Fardilha, Edgar F. da Cruz e Silva, William T. Dauer, Mariana Santos, Odete A. da Cruz e Silva
Publikováno v:
research@ua; Vol 4 (2013); 30
research@ua; vol. 4 (2013); 30
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
PLoS ONE
PLoS ONE, Vol 8, Iss 10, p e76788 (2013)
research@ua; vol. 4 (2013); 30
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
PLoS ONE
PLoS ONE, Vol 8, Iss 10, p e76788 (2013)
Protein phosphatase 1 (PP1) binding proteins are quintessential regulators, determining substrate specificity and defining subcellular localization and activity of the latter. Here, we describe a novel PP1 binding protein, the nuclear membrane protei
Autor:
Connie E. Kim
Publikováno v:
Clinical Nuclear Medicine; Sep2003, Vol. 28 Issue 9, p782, 2p