Tutulan-Cunita AC - Search Results

1

Autism and severe clinical phenotype in a patient with 8p21.2p11.21 deletion: Case report and literature review.

Arghir A, Papuc SM, Tutulan-Cunita AC, Erbescu A, Loddo S, Genovese S, Ciocca L, Goldoni M, Piscopo C, Bernardini L, Novelli A, Budisteanu M. Arghir A, et al. Among authors: tutulan cunita ac. Clin Case Rep. 2020 Nov 12;9(1):314-321. doi: 10.1002/ccr3.3523. eCollection 2021 Jan. Clin Case Rep. 2020. PMID: 33505690 Free PMC article.

2

3p interstitial deletion: novel case report and review.

Ţuţulan-Cunită AC, Papuc SM, Arghir A, Rötzer KM, Deshpande C, Lungeanu A, Budişteanu M. Ţuţulan-Cunită AC, et al. J Child Neurol. 2012 Aug;27(8):1062-6. doi: 10.1177/0883073811431016. Epub 2012 Jan 30. J Child Neurol. 2012. PMID: 22290856 Review.

3

Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architecture.

Tuţulan-Cuniţă AC, Budişteanu M, Papuc SM, Dupont JM, Blancho D, Lebbar A, Viot G, Lungeanu A, Arghir A. Tuţulan-Cuniţă AC, et al. Psychiatry Res. 2012 May 30;197(3):356-7. doi: 10.1016/j.psychres.2011.11.016. Epub 2012 Feb 22. Psychiatry Res. 2012. PMID: 22365273

4

Phenotypic Variability of 17q12 Microdeletion Syndrome - Three Cases and Review of Literature.

Țuțulan-Cuniță A, Pavel AG, Dimos L, Nedelea M, Ursuleanu A, Neacșu AT, Budișteanu M, Stambouli D. Țuțulan-Cuniță A, et al. Balkan J Med Genet. 2022 Jun 5;24(2):71-82. doi: 10.2478/bjmg-2021-0025. eCollection 2021 Nov. Balkan J Med Genet. 2022. PMID: 36249519 Free PMC article.

5

Variant e19a2 BCR-ABL1 fusion transcript in typical chronic myeloid leukemia.

Tutulan-Cunita AC, Chirieac SM, Mocanu G, Luca C, Costache M, Lungeanu A, Arghir A. Tutulan-Cunita AC, et al. Clin Lab. 2011;57(9-10):785-8. Clin Lab. 2011. PMID: 22029197

6

De-novo Williams-Beuren and inherited Marfan syndromes in a patient with developmental delay and lens dislocation.

Budisteanu M, Papuc SM, Tutulan-Cunita AC, Budisteanu B, Weis E, Arghir A, Zechner U, Bartsch O. Budisteanu M, et al. Among authors: tutulan cunita ac. Clin Dysmorphol. 2017 Jul;26(3):187-189. doi: 10.1097/MCD.0000000000000180. Clin Dysmorphol. 2017. PMID: 28277377 No abstract available.

7

Haploinsufficiency of BAZ1B contributes to Williams syndrome through transcriptional dysregulation of neurodevelopmental pathways.

Lalli MA, Jang J, Park JH, Wang Y, Guzman E, Zhou H, Audouard M, Bridges D, Tovar KR, Papuc SM, Tutulan-Cunita AC, Huang Y, Budisteanu M, Arghir A, Kosik KS. Lalli MA, et al. Among authors: tutulan cunita ac. Hum Mol Genet. 2016 Apr 1;25(7):1294-306. doi: 10.1093/hmg/ddw010. Epub 2016 Jan 10. Hum Mol Genet. 2016. PMID: 26755828

8

Microduplications of 3p26.3p26.2 containing CRBN gene in patients with intellectual disability and behavior abnormalities.

Papuc SM, Hackmann K, Andrieux J, Vincent-Delorme C, Budişteanu M, Arghir A, Schrock E, Ţuţulan-Cuniţă AC, Di Donato N. Papuc SM, et al. Among authors: tutulan cunita ac. Eur J Med Genet. 2015 May;58(5):319-23. doi: 10.1016/j.ejmg.2015.03.005. Epub 2015 Apr 6. Eur J Med Genet. 2015. PMID: 25858704

9

Involvement of Saccharomyces cerevisiae Pdr5p ATP-binding cassette transporter in calcium homeostasis.

Tutulan-Cunita AC, Ohnishi T, Mizunuma M, Hirata D, Miyakawa T. Tutulan-Cunita AC, et al. Biosci Biotechnol Biochem. 2005 Apr;69(4):857-60. doi: 10.1271/bbb.69.857. Biosci Biotechnol Biochem. 2005. PMID: 15849433 Free article.

10

Mutational analysis of the yeast multidrug resistance ABC transporter Pdr5p with altered drug specificity.

Tutulan-Cunita AC, Mikoshi M, Mizunuma M, Hirata D, Miyakawa T. Tutulan-Cunita AC, et al. Genes Cells. 2005 May;10(5):409-20. doi: 10.1111/j.1365-2443.2005.00847.x. Genes Cells. 2005. PMID: 15836770 Free article.

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