PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
26497390-4	2015	In the present study, constructs expressing wild-type and poly-Q reduction mutants of FOXP2 were generated by polymerase chain reaction (PCR) using lentiviral vectors and transfected into the SH-SY5Y neuronal cell line.	polyglutamine	58-64	forkhead box P2	Homo sapiens	86-91	
29212017-5	2017	We note that Foxp2 encodes the longest polyglutamine repeat protein in the human reference genome, and we show that it can be sequestered into aggregates with polyglutamine-expanded mutant Huntingtin protein (mHTT).	polyglutamine	39-52	forkhead box P2	Homo sapiens	13-18	
27933109-6	2016	Finally, we analysed the functional significance of the polyglutamine tracts in FOXP2, since tract length variations have been reported in cases of neurodevelopmental disorder.	polyglutamine	56-69	forkhead box P2	Homo sapiens	80-85	
27933109-13	2016	Finally, we found that FOXP2 variants with reduced polyglutamine tracts did not exhibit altered behaviour in cellular assays, indicating that such tracts are non-essential for core aspects of FOXP2 function, and that tract variation is unlikely to be a highly penetrant cause of speech/language disorder.	polyglutamine	51-64	forkhead box P2	Homo sapiens	23-28	
26497390-6	2015	Using this cell model, the impact of FOXP2 on the expression of contactin-associated protein-like 2 (CNTNAP2) were investigated, and CNTNAP2 mRNA expression levels were observed to be significantly higher in cells expressing poly-Q-reduced FOXP2.	polyglutamine	225-231	forkhead box P2	Homo sapiens	37-42	
26497390-6	2015	Using this cell model, the impact of FOXP2 on the expression of contactin-associated protein-like 2 (CNTNAP2) were investigated, and CNTNAP2 mRNA expression levels were observed to be significantly higher in cells expressing poly-Q-reduced FOXP2.	polyglutamine	225-231	forkhead box P2	Homo sapiens	240-245	
15108192-2	2004	FOXP2, located on 7q31, is a putative transcription factor containing a polyglutamine tract and a forkhead DNA binding domain.	polyglutamine	72-85	forkhead box P2	Homo sapiens	0-5	
15737702-1	2005	We analyzed the FOXP2 gene, which encodes a putative transcription factor containing a polyglutamine tract and a forkhead DNA-binding domain, for a possible causative mutation in autism.	polyglutamine	87-100	forkhead box P2	Homo sapiens	16-21	
11894222-1	2002	The FOXP2 gene, located on human 7q31 (at the SPCH1 locus), encodes a transcription factor containing a polyglutamine tract and a forkhead domain.	polyglutamine	104-117	forkhead box P2	Homo sapiens	4-9	
11894222-1	2002	The FOXP2 gene, located on human 7q31 (at the SPCH1 locus), encodes a transcription factor containing a polyglutamine tract and a forkhead domain.	polyglutamine	104-117	forkhead box P2	Homo sapiens	46-51	
10880297-9	2000	This clone contains the CAGH44 gene, which encodes a brain-expressed protein containing a large polyglutamine stretch.	polyglutamine	96-109	forkhead box P2	Homo sapiens	24-30