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FNDC3A gene

Known as: bA203I16.5, fibronectin type III domain containing 3A, FNDC3A 
National Institutes of Health

Related topics

Related topics

1 relation
Fibronectins

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2011
Review
2011
Identification of Close Relatives in the HUGO Pan-Asian SNP Database
The HUGO Pan-Asian SNP Consortium has recently released a genome-wide dataset, which consists of 1,719 DNA samples collected from… 
2010
2010
Mutations of NFKBIA in biopsy specimens from Hodgkin lymphoma.
2009
2009
Hyperlink Management System and ID Converter System: enabling maintenance-free hyperlinks among major biological databases
Hyperlink Management System (HMS) is a system for automatically updating and maintaining hyperlinks among major public databases… 
2009
2009
HUGO BOSS：大班雍容
  • 兰若
  • 2009
  • Corpus ID: 170157298
喜欢山东烟台蓬莱的葡萄园区，这里与法国勃朗艮葡萄种植园维度相仿。窗外草地上，紫红粉白的紫薇花正当盛开，燕子低掠翻飞。栏杆下，一丛修竹，清雅文秀，随风摇曳。坐在屋外长长的回廊下，清晰可眺不远处宁静的湖泊，水后是起伏徐缓的山丘，深浅交错青绿色的山坡上略薇点缀着几处红瓦砖房。微风轻扬，鸟语婉啭，阳光温熏，此地几有法国乡村宁静秀美的韵致。 
2008
2008
HUGO (FNDC3A): a New Gene Overexpressed in Human Odontoblasts
Previously, we established a subtractive cDNA library enriched in odontoblast-specific genes and hypothesized that new… 
Highly Cited
2007
Highly Cited
2007
Women heterozygous for NALP7/NLRP7 mutations are at risk for reproductive wastage: report of two novel mutations
Familial recurrent hydatidiform moles are a rare recessive condition in which molar tissues have biparental contribution to their… 
2006
2006
On the elucidation of a tumour suppressor role of 3p in lung cancer
Bij longkanker is het nog onduidelijk welke genen of regulerende stukjes DNA (‘regelsequenties’) verantwoordelijk zijn voor het… 
2003
2003
Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene
Hereditary spastic paraplegia (HSP) is a heterogeneous condition characterised in its pure form by progressive lower limb… 
1999
1999
Identification of four novel mutations of the XLRS1 gene in Japanese patients with X‐linked juvenile retinoschisis
The XLRS1 gene (HUGO‐approved symbol, RS1) has been found to cause X‐linked recessive retinoschisis (RS) which is characterized… 
1998
1998
Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family
A four-generation family suffering from an autosomal-dominant, congenital, nonprogressive, nonsyndromic hearing loss was found in… 
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