Documents (400) JSON TSV

source DB	source ID	text	size	updated at	# proj.	updated_at
PubMed	10788334	Founder mutations in the BRCA1 gene in Polish families with breast-ovarian cancer. We have undertake	1.53 KB	2015-11-15	35	2021-12-23
PubMed	1353340	Late-onset metachromatic leukodystrophy: molecular pathology in two siblings. We report on a new all	716 Bytes	2015-11-18	42	2021-12-23
PubMed	9294109	Myotonic dystrophy protein kinase is involved in the modulation of the Ca2+ homeostasis in skeletal	1.33 KB	2015-12-08	46	2021-12-23
PubMed	2491010	Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the	1.55 KB	2016-01-17	33	2021-12-23
PubMed	7668252	Cloning of human very-long-chain acyl-coenzyme A dehydrogenase and molecular characterization of its	1.43 KB	2015-03-12	30	2021-12-23
PubMed	1671881	Two distinct mutations at a single BamHI site in phenylketonuria. Classical phenylketonuria is an au	701 Bytes	2015-11-23	49	2021-12-23
PubMed	8755918	Mutations associated with variant phenotypes in ataxia-telangiectasia. We have identified 14 familie	1.31 KB	2015-11-27	49	2021-12-23
PubMed	2422478	Midline B3 serotonin nerves in rat medulla are involved in hypotensive effect of methyldopa. Previou	1.64 KB	2016-01-15	49	2021-12-23
PubMed	1848636	Debrisoquine phenotype and the pharmacokinetics and beta-2 receptor pharmacodynamics of metoprolol a	1.78 KB	2015-12-07	32	2021-12-23
PubMed	19048115	Neurofibromin 1 (NF1) defects are common in human ovarian serous carcinomas and co-occur with TP53 m	1.67 KB	2015-11-24	28	2021-12-23