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Items: 1 to 20 of 141

1.

Thailand mutation and variation database (ThaiMUT).

Ruangrit U, Srikummool M, Assawamakin A, Ngamphiw C, Chuechote S, Thaiprasarnsup V, Agavatpanitch G, Pasomsab E, Yenchitsomanus PT, Mahasirimongkol S, Chantratita W, Palittapongarnpim P, Uyyanonvara B, Limwongse C, Tongsima S.

Hum Mutat. 2008 Aug;29(8):E68-75. doi: 10.1002/humu.20787.

PMID:
18484585
3.

Hellenic National Mutation database: a prototype database for mutations leading to inherited disorders in the Hellenic population.

Patrinos GP, van Baal S, Petersen MB, Papadakis MN.

Hum Mutat. 2005 Apr;25(4):327-33.

PMID:
15776445
5.

The human FOXL2 mutation database.

Beysen D, Vandesompele J, Messiaen L, De Paepe A, De Baere E.

Hum Mutat. 2004 Sep;24(3):189-93.

PMID:
15300845
6.

An integrated database-pipeline system for studying single nucleotide polymorphisms and diseases.

Yang JO, Hwang S, Oh J, Bhak J, Sohn TK.

BMC Bioinformatics. 2008 Dec 12;9 Suppl 12:S19. doi: 10.1186/1471-2105-9-S12-S19.

8.

UMD-USHbases: a comprehensive set of databases to record and analyse pathogenic mutations and unclassified variants in seven Usher syndrome causing genes.

Baux D, Faugère V, Larrieu L, Le Guédard-Méreuze S, Hamroun D, Béroud C, Malcolm S, Claustres M, Roux AF.

Hum Mutat. 2008 Aug;29(8):E76-87. doi: 10.1002/humu.20780.

PMID:
18484607
9.

The novel human SHOX allelic variant database.

Niesler B, Röth R, Wilke S, Fujimura F, Fischer C, Rappold G.

Hum Mutat. 2007 Oct;28(10):933-8.

PMID:
17726696
10.

Gene Prospector: an evidence gateway for evaluating potential susceptibility genes and interacting risk factors for human diseases.

Yu W, Wulf A, Liu T, Khoury MJ, Gwinn M.

BMC Bioinformatics. 2008 Dec 8;9:528. doi: 10.1186/1471-2105-9-528.

11.

FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide.

van Baal S, Kaimakis P, Phommarinh M, Koumbi D, Cuppens H, Riccardino F, Macek M Jr, Scriver CR, Patrinos GP.

Nucleic Acids Res. 2007 Jan;35(Database issue):D690-5.

12.

The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility.

Charoute H, Nahili H, Abidi O, Gabi K, Rouba H, Fakiri M, Barakat A.

Eur J Hum Genet. 2014 Mar;22(3):322-6. doi: 10.1038/ejhg.2013.151.

13.

RAMEDIS: a comprehensive information system for variations and corresponding phenotypes of rare metabolic diseases.

Töpel T, Scheible D, Trefz F, Hofestädt R.

Hum Mutat. 2010 Jan;31(1):E1081-8. doi: 10.1002/humu.21169.

PMID:
19953641
14.

SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes.

Packer BR, Yeager M, Staats B, Welch R, Crenshaw A, Kiley M, Eckert A, Beerman M, Miller E, Bergen A, Rothman N, Strausberg R, Chanock SJ.

Nucleic Acids Res. 2004 Jan 1;32(Database issue):D528-32.

15.

Time for a unified system of mutation description and reporting: a review of locus-specific mutation databases.

Claustres M, Horaitis O, Vanevski M, Cotton RG.

Genome Res. 2002 May;12(5):680-8.

16.

MitBASE: a comprehensive and integrated mitochondrial DNA database.

Attimonelli M, Altamura N, Benne R, Boyen C, Brennicke A, Carone A, Cooper JM, D'Elia D, de Montalvo A, de Pinto B, De Robertis M, Golik P, Grienenberger JM, Knoop V, Lanave C, Lazowska J, Lemagnen A, Malladi BS, Memeo F, Monnerot M, Pilbout S, Schapira AH, Sloof P, Slonimski P, Saccone C, et al.

Nucleic Acids Res. 1999 Jan 1;27(1):128-33.

17.

A1ATVar: a relational database of human SERPINA1 gene variants leading to alpha1-antitrypsin deficiency and application of the VariVis software.

Zaimidou S, van Baal S, Smith TD, Mitropoulos K, Ljujic M, Radojkovic D, Cotton RG, Patrinos GP.

Hum Mutat. 2009 Mar;30(3):308-13. doi: 10.1002/humu.20857.

PMID:
19021233
18.

CTGA: the database for genetic disorders in Arab populations.

Tadmouri GO, Al Ali MT, Al-Haj Ali S, Al Khaja N.

Nucleic Acids Res. 2006 Jan 1;34(Database issue):D602-6.

19.

The Pain Genes Database: An interactive web browser of pain-related transgenic knockout studies.

Lacroix-Fralish ML, Ledoux JB, Mogil JS.

Pain. 2007 Sep;131(1-2):3.e1-4. Review.

PMID:
17574758
20.

The IARC TP53 database: new online mutation analysis and recommendations to users.

Olivier M, Eeles R, Hollstein M, Khan MA, Harris CC, Hainaut P.

Hum Mutat. 2002 Jun;19(6):607-14.

PMID:
12007217
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