Test-merged-2

Documents (100) JSON TSV

source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
PubMed	16904497	Cauda equina syndrome after epidural steroid injection: a case report. OBJECTIVE: Conventional treatment methods of lumbusacral radiculopathy are physical therapy, epidural steroid injections, oral me	1.65 KB	2017-09-04	10	18	2021-12-23
PubMed	16970763	Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity. BACKGROUND: To examine the contribution of mutations within the Norrie d	1.89 KB	2015-11-20	11	56	2021-12-23
PubMed	17000021	No independent role of the -1123 G>C and+2740 A>G variants in the association of PTPN22 with type 1 diabetes and juvenile idiopathic arthritis in two Caucasian populations. INTRODUCTION: The PTPN22 is	2.11 KB	2025-10-02	15	34	2021-12-23
PubMed	17033974	Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy. Retinal signal transmission depends on the activity of high voltage-gated l-type calcium channels	1.16 KB	2015-11-23	34	29	2021-12-23
PubMed	1711760	Delayed institution of hypertension during focal cerebral ischemia: effect on brain edema. The effect of induced hypertension instituted after a 2-h delay following middle cerebral artery occlusion (M	1.61 KB	2015-12-23	16	35	2021-12-23
PubMed	17273972	Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions. Deletion 22q11.2 syndrome is the most frequent known microdeletion syndrome and is associated	1.11 KB	2015-11-23	18	13	2021-12-23
PubMed	17286451	Retinoblastoma in India : microsatellite analysis and its application in genetic counseling. OBJECTIVES: This study was conducted with two objectives. The first was to estimate the frequency of loss o	1.73 KB	2015-12-24	9	34	2021-12-23
PubMed	17318851	Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis. Phenotypic characteristics expressed in syndromes give clues to the factors in	1.5 KB	2015-12-26	10	23	2021-12-23
PubMed	17327131	Molecular analysis of the CYP2F1 gene: identification of a frequent non-functional allelic variant. The CYP2F1 is a human cytochrome P450 that is selectively expressed in lung tissue and involved in t	1.71 KB	2015-12-28	11	20	2021-12-23
PubMed	17384765	Succimer chelation improves learning, attention, and arousal regulation in lead-exposed rats but produces lasting cognitive impairment in the absence of lead exposure. BACKGROUND: There is growing pre	1.79 KB	2021-12-23	24	17	2021-12-23