LitCoin_Mondo

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source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
PubMed	20651814	Lack of association between ADRA2B-4825 gene insertion/deletion polymorphism and migraine in Chinese Han population. OBJECTIVE: The present study aimed to estimate the association between susceptibili	1.02 KB	2015-11-25	27	0	2021-12-16
PubMed	20534762	Two novel mutations of the TSH-beta subunit gene underlying congenital central hypothyroidism undetectable in neonatal TSH screening. CONTEXT: Patients with TSH-beta subunit defects and congenital hyp	1.82 KB	2016-01-02	33	12	2021-12-16
PubMed	20523265	Association study of complement factor H, C2, CFB, and C3 and age-related macular degeneration in a Han Chinese population. PURPOSE: Genes in the complement pathway, including complement factor H (CFH	2.3 KB	2025-10-02	32	4	2021-12-16
PubMed	20126413	U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line. U87MG is a commonly studied grade IV glioma cell line that has been analyzed in at least 1,700 publications ov	2.07 KB	2016-01-01	42	5	2021-12-16
PubMed	20005218	A potential regulatory single nucleotide polymorphism in the promoter of the Klotho gene may be associated with essential hypertension in the Chinese Han population. BACKGROUND: Mice with defects in t	1.67 KB	2015-11-25	28	2	2021-12-16
PubMed	19394258	The first founder DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome. Deoxyguanosine kinase (dGK) deficiency is a frequent cause of mitochondrial DNA depletion associat	1.57 KB	2015-11-25	29	1	2021-12-16
PubMed	19365571	Macular corneal dystrophy in a Chinese family related with novel mutations of CHST6. PURPOSE: To identify mutations in the carbohydrate sulfotransferase gene (CHST6) for a Chinese family with macular	1.85 KB	2015-11-25	29	4	2021-12-16
PubMed	19101703	Study of a Taiwanese family with oculopharyngeal muscular dystrophy. BACKGROUND: Oculopharyngeal muscular dystrophy (OPMD) is a late onset autosomal dominant muscle disorder. OPMD is caused by a short	1.2 KB	2015-11-24	26	4	2021-12-16
PubMed	19082493	Combination of polymorphisms within 5' and 3' untranslated regions of thymidylate synthase gene modulates survival in 5 fluorouracil-treated colorectal cancer patients. In the present study we explore	2.15 KB	2015-08-06	25	6	2021-12-16
PubMed	19037252	Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosis. Diffuse mesangial sclerosis occurs as an isolated abnormality or as a part of a syndrome. Recently, muta	1.06 KB	2015-11-24	29	2	2021-12-16