Ames EG - Search Results

1

Rare disease therapeutics: The future of medical genetics in a changing landscape.

Connolly CD, Quinonez SC, Ames EG. Connolly CD, et al. Among authors: ames eg. Genet Med. 2023 Feb;25(2):100339. doi: 10.1016/j.gim.2022.11.007. Epub 2022 Dec 7. Genet Med. 2023. PMID: 36476402 Free article. No abstract available.

2

Sequencing of mRNA identifies re-expression of fetal splice variants in cardiac hypertrophy.

Ames EG, Lawson MJ, Mackey AJ, Holmes JW. Ames EG, et al. J Mol Cell Cardiol. 2013 Sep;62:99-107. doi: 10.1016/j.yjmcc.2013.05.004. Epub 2013 May 17. J Mol Cell Cardiol. 2013. PMID: 23688780 Free PMC article.

3

Mechanisms of Amplified Arteriogenesis in Collateral Artery Segments Exposed to Reversed Flow Direction.

Heuslein JL, Meisner JK, Li X, Song J, Vincentelli H, Leiphart RJ, Ames EG, Blackman BR, Blackman BR, Price RJ. Heuslein JL, et al. Among authors: ames eg. Arterioscler Thromb Vasc Biol. 2015 Nov;35(11):2354-65. doi: 10.1161/ATVBAHA.115.305775. Epub 2015 Sep 3. Arterioscler Thromb Vasc Biol. 2015. PMID: 26338297 Free PMC article.

4

Effects of stretch and shortening on gene expression in intact myocardium.

Haggart CR, Ames EG, Lee JK, Holmes JW. Haggart CR, et al. Among authors: ames eg. Physiol Genomics. 2014 Jan 15;46(2):57-65. doi: 10.1152/physiolgenomics.00103.2013. Epub 2013 Dec 3. Physiol Genomics. 2014. PMID: 24302644 Free PMC article.

5

A cautionary tale of pyridoxine toxicity in cystathionine beta-synthase deficiency detected by two-tier newborn screening highlights the need for clear pyridoxine dosing guidelines.

Ames EG, Scott AJ, Pappas KB, Moloney SM, Conway RL, Ahmad A. Ames EG, et al. Am J Med Genet A. 2020 Nov;182(11):2704-2708. doi: 10.1002/ajmg.a.61815. Epub 2020 Aug 20. Am J Med Genet A. 2020. PMID: 32820583 Free article.

6

Further description of two patients with biallelic variants in NADSYN1 in association with cardiac and vertebral anomalies.

Kortbawi H, Ames E, Pritchard A, Devine P, van Ziffle J, Slavotinek A. Kortbawi H, et al. Am J Med Genet A. 2022 Aug;188(8):2479-2484. doi: 10.1002/ajmg.a.62765. Epub 2022 May 2. Am J Med Genet A. 2022. PMID: 35491967

7

Multicenter appraisal of comorbid TANGO2 deficiency disorder in patients with 22q11.2 deletion syndrome.

Owlett LD, Zapanta B, Sandkuhler SE, Ames EG, Hickey SE, Mackenzie SJ, Meisner JK. Owlett LD, et al. Among authors: ames eg. Am J Med Genet A. 2024 Oct;194(10):e63778. doi: 10.1002/ajmg.a.63778. Epub 2024 Jun 3. Am J Med Genet A. 2024. PMID: 38829177

8

Differing Experiences with Breastfeeding in Residency Between Mothers and Coresidents.

Ames EG, Burrows HL. Ames EG, et al. Breastfeed Med. 2019 Oct;14(8):575-579. doi: 10.1089/bfm.2019.0001. Epub 2019 Jun 20. Breastfeed Med. 2019. PMID: 31219317

9

Evaluation for genetic disease in kidney transplant candidates: A practice resource.

Ames EG, Anand PM, Bekheirnia MR, Doshi MD, El Ters M, Freese ME, Gbadegesin RA, Guay-Woodford LM, Java A, Ranch D, Rodig NM, Wang X, Thomas CP. Ames EG, et al. Am J Transplant. 2024 Oct 31:S1600-6135(24)00679-8. doi: 10.1016/j.ajt.2024.10.019. Online ahead of print. Am J Transplant. 2024. PMID: 39488252 Review.

10

Programmed Cell Death in Cystinosis.

Ames EG, Thoene JG. Ames EG, et al. Cells. 2022 Feb 15;11(4):670. doi: 10.3390/cells11040670. Cells. 2022. PMID: 35203319 Free PMC article. Review.

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