117 related articles for article (PubMed ID: 22323337)
1. KMD: Korean Mutation Database for genes related to diseases.
Park MH; Koo SK; Lee JS; Yoo HW; Kim JW; Cheong HI; Park HY
Hum Mutat; 2012 Apr; 33(4):E2332-40. PubMed ID: 22323337
[TBL] [Abstract][Full Text] [Related]
2. The Needs and Priorities for Government Grants for Traditional Korean Medicine: Comparing the Public and Traditional Korean Medicine Doctors.
Hyun MK
Evid Based Complement Alternat Med; 2016; 2016():2625079. PubMed ID: 27994629
[TBL] [Abstract][Full Text] [Related]
3. The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies.
Stenson PD; Mort M; Ball EV; Evans K; Hayden M; Heywood S; Hussain M; Phillips AD; Cooper DN
Hum Genet; 2017 Jun; 136(6):665-677. PubMed ID: 28349240
[TBL] [Abstract][Full Text] [Related]
4. An integrated Korean biodiversity and genetic information retrieval system.
Lim J; Bhak J; Oh HM; Kim CB; Park YH; Paek WK
BMC Bioinformatics; 2008 Dec; 9 Suppl 12(Suppl 12):S24. PubMed ID: 19091024
[TBL] [Abstract][Full Text] [Related]
5. Singapore Human Mutation/Polymorphism Database: a country-specific database for mutations and polymorphisms in inherited disorders and candidate gene association studies.
Tan EC; Loh M; Chuon D; Lim YP
Hum Mutat; 2006 Mar; 27(3):232-5. PubMed ID: 16429432
[TBL] [Abstract][Full Text] [Related]
6. KRGDB: the large-scale variant database of 1722 Koreans based on whole genome sequencing.
Jung KS; Hong KW; Jo HY; Choi J; Ban HJ; Cho SB; Chung M
Database (Oxford); 2020 Jan; 2020():. PubMed ID: 32133509
[TBL] [Abstract][Full Text] [Related]
7. Characterization of 458 single nucleotide polymorphisms of disease candidate genes in the Korean population.
Lee JK; Kim HT; Cho SM; Kim KH; Jin HJ; Ryu GM; Oh B; Park C; Kimm K; Jo SA; Jung SC; Kim S; In SM; Lee JE; Jo I
J Hum Genet; 2003; 48(5):213-216. PubMed ID: 12768436
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 23860041
[TBL] [Abstract][Full Text] [Related]
9. Characteristics and spectrum of BRCA1 and BRCA2 mutations in 3,922 Korean patients with breast and ovarian cancer.
Kim H; Cho DY; Choi DH; Choi SY; Shin I; Park W; Huh SJ; Han SH; Lee MH; Ahn SH; Son BH; Kim SW; ; Haffty BG
Breast Cancer Res Treat; 2012 Aug; 134(3):1315-26. PubMed ID: 22798144
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 18484585
[TBL] [Abstract][Full Text] [Related]
11. PHKA2 mutation spectrum in Korean patients with glycogen storage disease type IX: prevalence of deletion mutations.
Choi R; Park HD; Kang B; Choi SY; Ki CS; Lee SY; Kim JW; Song J; Choe YH
BMC Med Genet; 2016 Apr; 17():33. PubMed ID: 27103379
[TBL] [Abstract][Full Text] [Related]
12. A genetic screen of the mutations in the Korean patients with early-onset Alzheimer's disease.
An SS; Park SA; Bagyinszky E; Bae SO; Kim YJ; Im JY; Park KW; Park KH; Kim EJ; Jeong JH; Kim JH; Han HJ; Choi SH; Kim S
Clin Interv Aging; 2016; 11():1817-1822. PubMed ID: 28008242
[TBL] [Abstract][Full Text] [Related]
13. Clinical features and mutations in the ENG, ACVRL1, and SMAD4 genes in Korean patients with hereditary hemorrhagic telangiectasia.
Lee ST; Kim JA; Jang SY; Kim DK; Do YS; Suh GY; Kim JW; Ki CS
J Korean Med Sci; 2009 Feb; 24(1):69-76. PubMed ID: 19270816
[TBL] [Abstract][Full Text] [Related]
14. The first Malay database toward the ethnic-specific target molecular variation.
Halim-Fikri H; Etemad A; Abdul Latif AZ; Merican AF; Baig AA; Annuar AA; Ismail E; Salahshourifar I; Liza-Sharmini AT; Ramli M; Shah MI; Johan MF; Hassan NN; Abdul-Aziz NM; Mohd Noor NH; Nur-Shafawati AR; Hassan R; Bahar R; Zain RB; Yusoff SM; Yusoff S; Tan SG; Thong MK; Wan-Isa H; Abdullah WZ; Mohamed Z; Abdul Latiff Z; Zilfalil BA;
BMC Res Notes; 2015 Apr; 8():176. PubMed ID: 25925844
[TBL] [Abstract][Full Text] [Related]
15. EvoSNP-DB: A database of genetic diversity in East Asian populations.
Kim YU; Kim YJ; Lee JY; Park K
BMB Rep; 2013 Aug; 46(8):416-21. PubMed ID: 23977990
[TBL] [Abstract][Full Text] [Related]
16. Korean Variant Archive (KOVA): a reference database of genetic variations in the Korean population.
Lee S; Seo J; Park J; Nam JY; Choi A; Ignatius JS; Bjornson RD; Chae JH; Jang IJ; Lee S; Park WY; Baek D; Choi M
Sci Rep; 2017 Jun; 7(1):4287. PubMed ID: 28655895
[TBL] [Abstract][Full Text] [Related]
17. General mutation databases: analysis and review.
George RA; Smith TD; Callaghan S; Hardman L; Pierides C; Horaitis O; Wouters MA; Cotton RG
J Med Genet; 2008 Feb; 45(2):65-70. PubMed ID: 17893115
[TBL] [Abstract][Full Text] [Related]
18. KGVDB: a population-based genomic map of CNVs tagged by SNPs in Koreans.
Moon S; Jung KS; Kim YJ; Hwang MY; Han K; Lee JY; Park K; Kim BJ
Bioinformatics; 2013 Jun; 29(11):1481-3. PubMed ID: 23626002
[TBL] [Abstract][Full Text] [Related]
19. Report of 5 novel mutations of the α-L-iduronidase gene and comparison of Korean mutations in relation with those of Japan or China in patients with mucopolysaccharidosis I.
Kwak MJ; Huh R; Kim J; Park HD; Cho SY; Jin DK
BMC Med Genet; 2016 Aug; 17(1):58. PubMed ID: 27520059
[TBL] [Abstract][Full Text] [Related]
20. 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. PubMed ID: 15300845
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
