FRAS1 gene

Known as: Fraser extracellular matrix complex subunit 1, FRAS1, FLJ22031 
 

Topic mentions per year

Topic mentions per year

2003-2017
02420032017

Papers overview

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2015
2015
Developmental mutations that inhibit normal formation of extracellular matrix (ECM) in fetal diaphragms have been identified in… (More)
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2014
2014
Congenital anomalies of the kidney and urinary tract (CAKUT) account for approximately 40% of children with ESRD in the United… (More)
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2014
2014
Distal metastasis is the major cause of death for the vast majority of lung cancer patients. Many extracellular matrix (ECM… (More)
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2013
2013
Fraser syndrome (FS) and microphthalmia syndromic 9 (MCOPS9) are autosomal recessive conditions with distinct, and some… (More)
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2013
2013
Congenital High Airway Obstruction Syndrome (CHAOS) is a potential lethal condition. We describe a case report of CHAOS, with… (More)
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2012
2012
Lesions in the epithelially expressed human gene FRAS1 cause Fraser syndrome, a complex disease with variable symptoms, including… (More)
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2012
2012
Congenital abnormalities of the kidney and urinary tract (CAKUT) are the most frequent cause of chronic kidney disease in… (More)
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2012
2012
Fraser syndrome (FS) is an autosomal recessive disease characterized by skin lesions and kidney and upper airway malformations… (More)
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2008
2008
FRAS1 is mutated in some individuals with Fraser syndrome (FS) and the encoded protein is expressed in embryonic epidermal cells… (More)
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2008
2008
Mouse studies have highlighted the requirement of the extracellular matrix Fras and Frem proteins for embryonic epidermal… (More)
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