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FNIP1 gene

Known as: KIAA1961, FNIP1, folliculin interacting protein 1 
 
National Institutes of Health

Papers overview

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2020
2020
AMPK (adenosine monophosphate-activated protein kinase) is phosphorylated (AMPK-P) in response to low energy through allosteric… Expand
2020
2020
ABSTRACT Embryonic and neonatal skeletal muscles grow via the proliferation and fusion of myogenic cells, whereas adult skeletal… Expand
2019
2019
Key Points Fnip1 is required for pre–B cell development/survival independent of p53 and Bcl-xL. Fnip1 is required for optimal… Expand
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2018
2018
Birt-Hogg-Dube’ Syndrome (BHDS) is a rare genetic disorder in humans characterized by skin hamartomas, lung cysts, pneumothorax… Expand
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2017
2017
Obesity is often accompanied by decreases in the proportion of skeletal muscle slow-twitch fibers and insulin sensitivity… Expand
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2016
2016
Defining the full complement of substrates for each ubiquitin ligase remains an important challenge. Improvements in mass… Expand
Highly Cited
2015
Highly Cited
2015
Significance The role of FLCN as a tumor suppressor in kidney cancer has been well documented, whereas the functional roles of… Expand
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Highly Cited
2008
Highly Cited
2008
Birt-Hogg-Dube' syndrome characterized by increased risk for renal neoplasia is caused by germline mutations in the BHD/FLCN gene… Expand
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Highly Cited
2006
Highly Cited
2006
Birt–Hogg–Dubé syndrome, a hamartoma disorder characterized by benign tumors of the hair follicle, lung cysts, and renal… Expand
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