PubMed for id: 6898

Year	Number of Results
1969	1
1982	1
1986	1
1987	1
1990	1
1992	2
1994	1
1995	1
1998	1
2002	2
2003	1
2004	1
2006	3
2008	1
2009	2
2010	1
2011	2
2012	2
2013	1
2014	3
2015	2
2016	1
2017	2
2019	1
2020	2
2021	1
2023	1
2024	0

1

Most synonymous allelic variants in HIV tat are not silent.

Giacoletto CJ, Benjamin R, Deng HW, Rotter JI, Schiller MR. Giacoletto CJ, et al. Genomics. 2023 May;115(3):110603. doi: 10.1016/j.ygeno.2023.110603. Epub 2023 Mar 7. Genomics. 2023. PMID: 36893872 Free PMC article.

2

Tyrosinemia type II: Mutation update, 11 novel mutations and description of 5 independent subjects with a novel founder mutation.

Peña-Quintana L, Scherer G, Curbelo-Estévez ML, Jiménez-Acosta F, Hartmann B, La Roche F, Meavilla-Olivas S, Pérez-Cerdá C, García-Segarra N, Giguère Y, Huppke P, Mitchell GA, Mönch E, Trump D, Vianey-Saban C, Trimble ER, Vitoria-Miñana I, Reyes-Suárez D, Ramírez-Lorenzo T, Tugores A. Peña-Quintana L, et al. Clin Genet. 2017 Sep;92(3):306-317. doi: 10.1111/cge.13003. Epub 2017 May 18. Clin Genet. 2017. PMID: 28255985

3

Tyrosinemia type II: Novel mutations in TAT in a boy with unusual presentation.

Gokay S, Kendirci M, Ustkoyuncu PS, Kardas F, Bayram AK, Per H, Poyrazoğlu HG. Gokay S, et al. Pediatr Int. 2016 Oct;58(10):1069-1072. doi: 10.1111/ped.13062. Epub 2016 Sep 4. Pediatr Int. 2016. PMID: 27285949

4

Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner-Hanhart syndrome.

Bouyacoub Y, Zribi H, Azzouz H, Nasrallah F, Abdelaziz RB, Kacem M, Rekaya B, Messaoud O, Romdhane L, Charfeddine C, Bouziri M, Bouziri S, Tebib N, Mokni M, Kaabachi N, Boubaker S, Abdelhak S. Bouyacoub Y, et al. Gene. 2013 Oct 15;529(1):45-9. doi: 10.1016/j.gene.2013.07.066. Epub 2013 Aug 13. Gene. 2013. PMID: 23954227

5

A large TAT deletion in a tyrosinaemia type II patient.

Legarda M, Wlodarczyk K, Lage S, Andrade F, Kim GJ, Bausch E, Scherer G, Aldamiz-Echevarria LJ. Legarda M, et al. Mol Genet Metab. 2011 Nov;104(3):407-9. doi: 10.1016/j.ymgme.2011.05.009. Epub 2011 May 16. Mol Genet Metab. 2011. PMID: 21636300

6

Down-regulation of tyrosine aminotransferase at a frequently deleted region 16q22 contributes to the pathogenesis of hepatocellular carcinoma.

Fu L, Dong SS, Xie YW, Tai LS, Chen L, Kong KL, Man K, Xie D, Li Y, Cheng Y, Tao Q, Guan XY. Fu L, et al. Hepatology. 2010 May;51(5):1624-34. doi: 10.1002/hep.23540. Hepatology. 2010. PMID: 20209601

7

Identification of two new mutations in the TAT gene in a Danish family with tyrosinaemia type II.

Pasternack SM, Betz RC, Brandrup F, Gade EF, Clemmensen O, Lund AM, Christensen E, Bygum A. Pasternack SM, et al. Br J Dermatol. 2009 Mar;160(3):704-6. doi: 10.1111/j.1365-2133.2008.08888.x. Epub 2008 Oct 13. Br J Dermatol. 2009. PMID: 18945316 No abstract available.

8

Genetically modified adenoviral vector with the protein transduction domain of Tat improves gene transfer to CAR-deficient cells.

Liu S, Mao Q, Zhang W, Zheng X, Bian Y, Wang D, Li H, Chai L, Zhao J, Xia H. Liu S, et al. Biosci Rep. 2009 Apr;29(2):103-9. doi: 10.1042/BSR20080023. Biosci Rep. 2009. PMID: 18721127 Free PMC article.

9

Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutations.

Charfeddine C, Monastiri K, Mokni M, Laadjimi A, Kaabachi N, Perin O, Nilges M, Kassar S, Keirallah M, Guediche MN, Kamoun MR, Tebib N, Ben Dridi MF, Boubaker S, Ben Osman A, Abdelhak S. Charfeddine C, et al. Mol Genet Metab. 2006 Jun;88(2):184-91. doi: 10.1016/j.ymgme.2006.02.006. Epub 2006 Mar 30. Mol Genet Metab. 2006. PMID: 16574453

10

Tyrosine aminotransferase and gamma-glutamyl transferase activity in human fetal hepatocyte primary cultures under proliferative conditions.

Rehman KK, Ayesha Q, Khan AA, Ahmed N, Habibullah CM. Rehman KK, et al. Cell Biochem Funct. 2004 Mar-Apr;22(2):89-96. doi: 10.1002/cbf.1061. Cell Biochem Funct. 2004. PMID: 15027097

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