PubMed for id: 4507369

Year	Number of Results
1986	1
1987	1
1990	1
1992	2
2017	1
2019	1
2020	2
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

Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.

Haenig C, Atias N, Taylor AK, Mazza A, Schaefer MH, Russ J, Riechers SP, Jain S, Coughlin M, Fontaine JF, Freibaum BD, Brusendorf L, Zenkner M, Porras P, Stroedicke M, Schnoegl S, Arnsburg K, Boeddrich A, Pigazzini L, Heutink P, Taylor JP, Kirstein J, Andrade-Navarro MA, Sharan R, Wanker EE. Haenig C, et al. Cell Rep. 2020 Aug 18;32(7):108050. doi: 10.1016/j.celrep.2020.108050. Cell Rep. 2020. PMID: 32814053 Free article.

3

A reference map of the human binary protein interactome.

Luck K, Kim DK, Lambourne L, Spirohn K, Begg BE, Bian W, Brignall R, Cafarelli T, Campos-Laborie FJ, Charloteaux B, Choi D, Coté AG, Daley M, Deimling S, Desbuleux A, Dricot A, Gebbia M, Hardy MF, Kishore N, Knapp JJ, Kovács IA, Lemmens I, Mee MW, Mellor JC, Pollis C, Pons C, Richardson AD, Schlabach S, Teeking B, Yadav A, Babor M, Balcha D, Basha O, Bowman-Colin C, Chin SF, Choi SG, Colabella C, Coppin G, D'Amata C, De Ridder D, De Rouck S, Duran-Frigola M, Ennajdaoui H, Goebels F, Goehring L, Gopal A, Haddad G, Hatchi E, Helmy M, Jacob Y, Kassa Y, Landini S, Li R, van Lieshout N, MacWilliams A, Markey D, Paulson JN, Rangarajan S, Rasla J, Rayhan A, Rolland T, San-Miguel A, Shen Y, Sheykhkarimli D, Sheynkman GM, Simonovsky E, Taşan M, Tejeda A, Tropepe V, Twizere JC, Wang Y, Weatheritt RJ, Weile J, Xia Y, Yang X, Yeger-Lotem E, Zhong Q, Aloy P, Bader GD, De Las Rivas J, Gaudet S, Hao T, Rak J, Tavernier J, Hill DE, Vidal M, Roth FP, Calderwood MA. Luck K, et al. Nature. 2020 Apr;580(7803):402-408. doi: 10.1038/s41586-020-2188-x. Epub 2020 Apr 8. Nature. 2020. PMID: 32296183 Free PMC article.

4

Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.

Fragoza R, Das J, Wierbowski SD, Liang J, Tran TN, Liang S, Beltran JF, Rivera-Erick CA, Ye K, Wang TY, Yao L, Mort M, Stenson PD, Cooper DN, Wei X, Keinan A, Schimenti JC, Clark AG, Yu H. Fragoza R, et al. Nat Commun. 2019 Sep 12;10(1):4141. doi: 10.1038/s41467-019-11959-3. Nat Commun. 2019. PMID: 31515488 Free PMC article.

5

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

6

Inherited and de novo deletion of the tyrosine aminotransferase gene locus at 16q22.1----q22.3 in a patient with tyrosinemia type II.

Natt E, Westphal EM, Toth-Fejel SE, Magenis RE, Buist NR, Rettenmeier R, Scherer G. Natt E, et al. Hum Genet. 1987 Dec;77(4):352-8. doi: 10.1007/BF00291426. Hum Genet. 1987. PMID: 2891604

7

Assignment of the human tyrosine aminotransferase gene to chromosome 16.

Natt E, Kao FT, Rettenmeier R, Scherer G. Natt E, et al. Hum Genet. 1986 Mar;72(3):225-8. doi: 10.1007/BF00291882. Hum Genet. 1986. PMID: 2870018

8

Isolation and characterization of the human tyrosine aminotransferase gene.

Rettenmeier R, Natt E, Zentgraf H, Scherer G. Rettenmeier R, et al. Nucleic Acids Res. 1990 Jul 11;18(13):3853-61. doi: 10.1093/nar/18.13.3853. Nucleic Acids Res. 1990. PMID: 1973834 Free PMC article.

9

Point mutations in the tyrosine aminotransferase gene in tyrosinemia type II.

Natt E, Kida K, Odievre M, Di Rocco M, Scherer G. Natt E, et al. Proc Natl Acad Sci U S A. 1992 Oct 1;89(19):9297-301. doi: 10.1073/pnas.89.19.9297. Proc Natl Acad Sci U S A. 1992. PMID: 1357662 Free PMC article.

10

Hereditary tyrosinaemia type II in a consanguineous Ashkenazi Jewish family: intrafamilial variation in phenotype; absence of parental phenotype effects on the fetus.

Chitayat D, Balbul A, Hani V, Mamer OA, Clow C, Scriver CR. Chitayat D, et al. J Inherit Metab Dis. 1992;15(2):198-203. doi: 10.1007/BF01799631. J Inherit Metab Dis. 1992. PMID: 1356171

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