Documents (11) JSON TSV

source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
@dpavot	29901133	No pathogenic mutations were detected in PAX6, FOXC1 or PITX2 in the only patient with a sporadic fo	197 Bytes	2020-02-26	1	5	-
@dpavot	22744456	MESP2, HES7 and DUSP6 genes may not be involved in the etiopathogenesis of sporadic and non-syndromi	131 Bytes	2020-02-21	1	3	-
@dpavot	24888247	In conclusion, CPS1 4217C>A polymorphism may not be associated with the development of hyperammon	128 Bytes	2020-02-21	1	3	-
@dpavot	28145425	As previously observed in the mutant mouse carrying a disrupted KCNC1 gene, these findings reveal th	218 Bytes	2020-02-21	1	3	-
@dpavot	26683626	While control subjects with high PGC-1α expression exhibited high PV and Nefh expression, schizophre	235 Bytes	2020-02-21	1	3	-
@dpavot	26399219	Prior studies that explored the hypothesis that EMT gene variants contribute to epithelial ovarian c	220 Bytes	2020-02-21	1	3	-
@dpavot	16960806	To date, CRYBA4 was the only gene in this cluster not associated with either human or murine catarac	103 Bytes	2020-02-21	1	3	-
@dpavot	28663096	Our data suggest that mutations of the SRD5A2 gene are the main causes of posterior hypospadias and	233 Bytes	2020-02-21	1	3	-
@dpavot	25142535	Previously there have been no reports of SCA31 associated with dystonia.	72 Bytes	2020-02-21	1	3	-
@dpavot	28792508	Our results suggested that variants in DCTN1 are not common risk factors for Chinese sporadic ALS an	187 Bytes	2020-02-21	1	3	-