Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 230,286,099 papers from all fields of science
Search
Sign In
Create Free Account
FNDC3A gene
Known as:
bA203I16.5
, fibronectin type III domain containing 3A
, FNDC3A
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
1 relation
Fibronectins
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Identification of Region-Specific Myocardial Gene Expression Patterns in a Chronic Swine Model of Repaired Tetralogy of Fallot
S. Charron
,
F. Roubertie
,
+11 authors
C. Rooryck
PLoS ONE
2015
Corpus ID: 197183
Surgical repair of Tetralogy of Fallot (TOF) is highly successful but may be complicated in adulthood by arrhythmias, sudden…
Expand
Review
2011
Review
2011
Identification of Close Relatives in the HUGO Pan-Asian SNP Database
Xiong Yang
,
Shuhua Xu
PLoS ONE
2011
Corpus ID: 14738192
The HUGO Pan-Asian SNP Consortium has recently released a genome-wide dataset, which consists of 1,719 DNA samples collected from…
Expand
2009
2009
Hyperlink Management System and ID Converter System: enabling maintenance-free hyperlinks among major biological databases
T. Imanishi
,
H. Nakaoka
Nucleic Acids Res.
2009
Corpus ID: 101608
Hyperlink Management System (HMS) is a system for automatically updating and maintaining hyperlinks among major public databases…
Expand
2008
2008
HUGO (FNDC3A): a New Gene Overexpressed in Human Odontoblasts
F. Carrouel
,
M. Couble
,
C. Vanbelle
,
M. Staquet
,
H. Magloire
,
F. Bleicher
Journal of dentistry research
2008
Corpus ID: 27513925
Previously, we established a subtractive cDNA library enriched in odontoblast-specific genes and hypothesized that new…
Expand
2006
2006
On the elucidation of a tumour suppressor role of 3p in lung cancer
A. Elst
2006
Corpus ID: 25579422
Bij longkanker is het nog onduidelijk welke genen of regulerende stukjes DNA (‘regelsequenties’) verantwoordelijk zijn voor het…
Expand
2003
2003
Cytogenetic and comparative genomic hybridization findings in four cases of breast cancer after neoadjuvant chemotherapy.
B. Fazeny-Dörner
,
M. Piribauer
,
+8 authors
C. Marosi
Cancer Genetics and Cytogenetics
2003
Corpus ID: 25862043
1999
1999
Identification of four novel mutations of the XLRS1 gene in Japanese patients with X‐linked juvenile retinoschisis
Y. Mashima
,
K. Shinoda
,
+5 authors
N. Shimizu
Human Mutation
1999
Corpus ID: 19136839
The XLRS1 gene (HUGO‐approved symbol, RS1) has been found to cause X‐linked recessive retinoschisis (RS) which is characterized…
Expand
1998
1998
Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family
K. Kirschhofer
,
J. Kenyon
,
+4 authors
W. Kimberling
Cytogenetic and Genome Research
1998
Corpus ID: 46792102
A four-generation family suffering from an autosomal-dominant, congenital, nonprogressive, nonsyndromic hearing loss was found in…
Expand
Review
1992
Review
1992
Genome sequence analysis: scientific objectives and practical strategies.
J. Craig Venter
,
M. Adams
,
A. Martin-Gallardo
,
W. Richard McCombie
,
Chris Fields
Trends in Biotechnology
1992
Corpus ID: 46226394
1992
1992
They Could See Stars from their Beds: The Plight of the Rural Poor in the Aftermath of Hurricane Hugo
Catherine M. Simile
,
Kristen S. Miller
1992
Corpus ID: 131456088
Charles Fritz (1961) once noted that disasters are natural laboratories for studying underlying social processes. In September…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE