PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
33218491-9	2020	Via binding with a different pair of PA and PB, this suspension sensor array has successfully typed and quantified cancer-associated miRNAs of miR-21, miR-155, miR-335, and miR-122 in buffer and serum conditions.	Protactinium	37-39	microRNA 21	Homo sapiens	143-149	
34406744-6	2021	The probe demonstrated a ratiometric PA limit of detection of 148 pM miR-21, sequence specificity against one- and two-base mutations, and selectivity over other microRNAs.	Protactinium	37-39	microRNA 21	Homo sapiens	69-75	
34406744-7	2021	It was further tested in live human ovarian cancer (SKOV3) and noncancerous (HEK 293T) cells to exemplify in situ PA activation based on differences in endogenous miR-21 regulation (p = 0.0002).	Protactinium	114-116	microRNA 21	Homo sapiens	163-169	
34406744-9	2021	The probe"s miR-21-specific activation and its ability to maintain contrast in biologically relevant absorbing and scattering media support its consideration for live-cell PA microscopy and potential cancer diagnostics.	Protactinium	172-174	microRNA 21	Homo sapiens	12-18	
32717421-10	2020	Furthermore, overexpression of miR-21 improved the impaired mitochondrial biogenesis and decreased the cardiomyocyte apoptosis induced by HG/PA, while inhibition of miR-21 exerted the opposite effects.	Protactinium	141-143	microRNA 21	Homo sapiens	31-37	
30109002-3	2018	Here, we report the design, synthesis and binding of a peptidic-aminoglycoside (PA) based chemical library against pre-miR21 that led to the identification of a group of small molecules that bind to pre-miR21 with high affinities and antagonize miR-21 maturation and function, thereby reversing EMT.	Protactinium	80-82	microRNA 21	Homo sapiens	119-124	
30109002-3	2018	Here, we report the design, synthesis and binding of a peptidic-aminoglycoside (PA) based chemical library against pre-miR21 that led to the identification of a group of small molecules that bind to pre-miR21 with high affinities and antagonize miR-21 maturation and function, thereby reversing EMT.	Protactinium	80-82	microRNA 21	Homo sapiens	203-208	
30109002-3	2018	Here, we report the design, synthesis and binding of a peptidic-aminoglycoside (PA) based chemical library against pre-miR21 that led to the identification of a group of small molecules that bind to pre-miR21 with high affinities and antagonize miR-21 maturation and function, thereby reversing EMT.	Protactinium	80-82	microRNA 21	Homo sapiens	245-251