137 related articles for article (PubMed ID: 25469862)
1. Positive selection with diversity in oculocutaneous albinisms type 2 gene (OCA2) among Japanese.
Shimanuki M; Abe Y; Tamiya G; Ueki M; Hozumi Y; Suzuki T
Pigment Cell Melanoma Res; 2015 Mar; 28(2):233-5. PubMed ID: 25469862
[No Abstract] [Full Text] [Related]
2. Distribution of OCA2∗481Thr and OCA2∗615Arg, associated with hypopigmentation, in several additional populations.
Yuasa I; Harihara S; Jin F; Nishimukai H; Fujihara J; Fukumori Y; Takeshita H; Umetsu K; Saitou N
Leg Med (Tokyo); 2011 Jul; 13(4):215-7. PubMed ID: 21565543
[TBL] [Abstract][Full Text] [Related]
3. Novel compound heterozygous mutations in OCA2 gene associated with non-syndromic oculocutaneous albinism in a Chinese Han patient: a case report.
Wang H; Wan Y; Yang Y; Li H; Mao L; Gao S; Xu J; Wang J
BMC Med Genet; 2019 Jul; 20(1):130. PubMed ID: 31345173
[TBL] [Abstract][Full Text] [Related]
4. Mutational Analysis of the TYR and OCA2 Genes in Four Chinese Families with Oculocutaneous Albinism.
Wang Y; Wang Z; Chen M; Fan N; Yang J; Liu L; Wang Y; Liu X
PLoS One; 2015; 10(4):e0125651. PubMed ID: 25919014
[TBL] [Abstract][Full Text] [Related]
5. Genetic analyses of oculocutaneous albinism types 1 and 2 with four novel mutations.
Yang Q; Yi S; Li M; Xie B; Luo J; Wang J; Rong X; Zhang Q; Qin Z; Hang L; Feng S; Fan X
BMC Med Genet; 2019 Jun; 20(1):106. PubMed ID: 31196117
[TBL] [Abstract][Full Text] [Related]
6. Genetic analyses of oculocutaneous albinism types 2 and 4 with eight novel mutations.
Okamura K; Araki Y; Abe Y; Shigyou A; Fujiyama T; Baba A; Kanekura T; Chinen Y; Kono M; Niizeki H; Tsubota A; Konno T; Hozumi Y; Suzuki T
J Dermatol Sci; 2016 Feb; 81(2):140-2. PubMed ID: 26573111
[No Abstract] [Full Text] [Related]
7. Recent advances in genetic analyses of oculocutaneous albinism types 2 and 4.
Suzuki T; Tomita Y
J Dermatol Sci; 2008 Jul; 51(1):1-9. PubMed ID: 18407468
[TBL] [Abstract][Full Text] [Related]
8. Two novel mutations detected in Japanese patients with oculocutaneous albinism.
Ito S; Suzuki T; Inagaki K; Suzuki N; Kono M; Tomita Y; Iwamoto T; Mochizuki N
J Dermatol Sci; 2006 Nov; 44(2):116-8. PubMed ID: 17008060
[No Abstract] [Full Text] [Related]
9. Oculocutaneous albinism (OCA) in Japanese patients: five novel mutations.
Okamura K; Yoshizawa J; Abe Y; Hanaoka K; Higashi N; Togawa Y; Nakagawa S; Kambe N; Funasaka Y; Ohko K; Hozumi Y; Suzuki T
J Dermatol Sci; 2014 May; 74(2):173-4. PubMed ID: 24461674
[No Abstract] [Full Text] [Related]
10. A novel P gene missense mutation in a Japanese patient with oculocutaneous albinism type II (OCA2).
Kato A; Fukai K; Oiso N; Hosomi N; Saitoh S; Wada T; Shimizu H; Ishii M
J Dermatol Sci; 2003 May; 31(3):189-92. PubMed ID: 12727022
[TBL] [Abstract][Full Text] [Related]
11. P gene mutations associated with oculocutaneous albinism type II (OCA2).
Oetting WS; Garrett SS; Brott M; King RA
Hum Mutat; 2005 Mar; 25(3):323. PubMed ID: 15712365
[TBL] [Abstract][Full Text] [Related]
12. A patient with subclinical oculocutaneous albinism type 2 diagnosed on getting severely sunburned.
Kawai M; Suzuki T; Ito S; Inagaki K; Suzuki N; Tomita Y
Dermatology; 2005; 210(4):322-3. PubMed ID: 15942220
[TBL] [Abstract][Full Text] [Related]
13. SLC45A2 variations in Indian oculocutaneous albinism patients.
Sengupta M; Chaki M; Arti N; Ray K
Mol Vis; 2007 Aug; 13():1406-11. PubMed ID: 17768386
[TBL] [Abstract][Full Text] [Related]
14. A comprehensive analysis reveals mutational spectra and common alleles in Chinese patients with oculocutaneous albinism.
Wei A; Wang Y; Long Y; Wang Y; Guo X; Zhou Z; Zhu W; Liu J; Bian X; Lian S; Li W
J Invest Dermatol; 2010 Mar; 130(3):716-24. PubMed ID: 19865097
[TBL] [Abstract][Full Text] [Related]
15. NGS-based targeted sequencing identified two novel variants in Southwestern Chinese families with oculocutaneous albinism.
Xiao Y; Zhou C; Xie H; Huang S; Wang J; Liu S
BMC Genomics; 2022 Apr; 23(1):332. PubMed ID: 35488210
[TBL] [Abstract][Full Text] [Related]
16. Six novel P gene mutations and oculocutaneous albinism type 2 frequency in Japanese albino patients.
Suzuki T; Miyamura Y; Matsunaga J; Shimizu H; Kawachi Y; Ohyama N; Ishikawa O; Ishikawa T; Terao H; Tomita Y
J Invest Dermatol; 2003 May; 120(5):781-3. PubMed ID: 12713581
[TBL] [Abstract][Full Text] [Related]
17. Oculocutaneous albinism spectrum.
Chiang PW; Spector E; Tsai AC
Am J Med Genet A; 2009 Jul; 149A(7):1590-1. PubMed ID: 19533789
[No Abstract] [Full Text] [Related]
18. Identification of P gene mutations in individuals with oculocutaneous albinism in sub-Saharan Africa.
Kerr R; Stevens G; Manga P; Salm S; John P; Haw T; Ramsay M
Hum Mutat; 2000; 15(2):166-72. PubMed ID: 10649493
[TBL] [Abstract][Full Text] [Related]
19. SLC45A2 mutation frequency in Oculocutaneous Albinism Italian patients doesn't differ from other European studies.
Mauri L; Barone L; Al Oum M; Del Longo A; Piozzi E; Manfredini E; Stanzial F; Benedicenti F; Penco S; Patrosso MC
Gene; 2014 Jan; 533(1):398-402. PubMed ID: 24096233
[TBL] [Abstract][Full Text] [Related]
20. A Korean case of oculocutaneous albinism type IV caused by a D157N mutation in the MATP gene.
Suzuki T; Inagaki K; Fukai K; Obana A; Lee ST; Tomita Y
Br J Dermatol; 2005 Jan; 152(1):174-5. PubMed ID: 15656822
[No Abstract] [Full Text] [Related]
[Next] [New Search]