LitCoin-SeqVar

Documents (400) JSON TSV

source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
PubMed	15064320	Compound heterozygous mutations in the SRD5A2 gene exon 4 in a male pseudohermaphrodite patient of Chinese origin. The goal of this study was to perform 5-alpha-reductase type 2 gene (SRD5A2) analysis	1.45 KB	2015-11-18	29	3	2021-12-16
PubMed	19996135	High-dose tranexamic Acid is associated with nonischemic clinical seizures in cardiac surgical patients. BACKGROUND: In 2 separate centers, we observed a notable increase in the incidence of postopera	1.69 KB	2016-07-04	25	0	2021-12-16
PubMed	15630069	Glucose metabolism in patients with schizophrenia treated with atypical antipsychotic agents: a frequently sampled intravenous glucose tolerance test and minimal model analysis. BACKGROUND: While the	3.1 KB	2015-11-22	23	0	2021-12-16
PubMed	22808010	Defining an EPOR- regulated transcriptome for primary progenitors, including Tnfr-sf13c as a novel mediator of EPO- dependent erythroblast formation. Certain concepts concerning EPO/EPOR action modes	1.67 KB	2016-01-10	24	0	2021-12-16
PubMed	28650467	Genome-wide loss-of-function genetic screening identifies opioid receptor μ1 as a key regulator of L-asparaginase resistance in pediatric acute lymphoblastic leukemia. L-asparaginase is a critical che	2.15 KB	2017-08-29	24	1	2021-12-16
PubMed	15018851	Comparison of sequential cytomegalovirus isolates in a patient with lymphoma and failing antiviral therapy. BACKGROUND: Long-term anti-cytomegalovirus (CMV) treatments in immunocompromised patients ar	1.61 KB	2015-11-22	40	2	2021-12-16
PubMed	26615423	Upregulation of centrosomal protein 55 is associated with unfavorable prognosis and tumor invasion in epithelial ovarian carcinoma. Centrosomal protein 55 (CEP55) is a cell cycle regulator implicated	2.35 KB	2016-01-26	27	0	2021-12-16
PubMed	17671735	Coincidence of mutations in different connexin genes in Hungarian patients. Mutations in the GJB2 gene are the most common cause of hereditary prelingual sensorineural hearing impairment in Europe. Se	1.26 KB	2015-12-28	42	9	2021-12-16
PubMed	26684240	Identification of the BRAF V600E mutation in gastroenteropancreatic neuroendocrine tumors. Genomic profiles of gastroenteropancreatic neuroendocrine tumors (GEP-NETs) are still insufficiently understo	1.66 KB	2016-01-26	44	5	2021-12-16
PubMed	16541406	Distinct patterns of germ-line deletions in MLH1 and MSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC). A relatively high frequency of germ-line genomic	1.36 KB	2015-11-19	26	0	2021-12-16