Zou R - Search Results

1

Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.

Huang L, Chardon JW, Carter MT, Friend KL, Dudding TE, Schwartzentruber J, Zou R, Schofield PW, Douglas S, Bulman DE, Boycott KM. Huang L, et al. Among authors: zou r. Orphanet J Rare Dis. 2012 Sep 17;7:67. doi: 10.1186/1750-1172-7-67. Orphanet J Rare Dis. 2012. PMID: 22986007 Free PMC article.

2

Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.

Huang L, Warman-Chardon J, Carter MT, Friend KL, Dudding TE, Schwartzentruber J, Zou R, Schofield PW, Douglas S, Bulman DE, Boycott KM. Huang L, et al. Among authors: zou r. Orphanet J Rare Dis. 2022 Mar 29;17(1):143. doi: 10.1186/s13023-022-02297-7. Orphanet J Rare Dis. 2022. PMID: 35351177 Free PMC article. No abstract available.

3

Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome.

Hood RL, Lines MA, Nikkel SM, Schwartzentruber J, Beaulieu C, Nowaczyk MJ, Allanson J, Kim CA, Wieczorek D, Moilanen JS, Lacombe D, Gillessen-Kaesbach G, Whiteford ML, Quaio CR, Gomy I, Bertola DR, Albrecht B, Platzer K, McGillivray G, Zou R, McLeod DR, Chudley AE, Chodirker BN, Marcadier J; FORGE Canada Consortium; Majewski J, Bulman DE, White SM, Boycott KM. Hood RL, et al. Among authors: zou r. Am J Hum Genet. 2012 Feb 10;90(2):308-13. doi: 10.1016/j.ajhg.2011.12.001. Epub 2012 Jan 19. Am J Hum Genet. 2012. PMID: 22265015 Free PMC article.

4

Translated mutation in the Nurr1 gene as a cause for Parkinson's disease.

Grimes DA, Han F, Panisset M, Racacho L, Xiao F, Zou R, Westaff K, Bulman DE. Grimes DA, et al. Among authors: zou r. Mov Disord. 2006 Jul;21(7):906-9. doi: 10.1002/mds.20820. Mov Disord. 2006. PMID: 16532445

5

Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update.

Huang L, Vanstone MR, Hartley T, Osmond M, Barrowman N, Allanson J, Baker L, Dabir TA, Dipple KM, Dobyns WB, Estrella J, Faghfoury H, Favaro FP, Goel H, Gregersen PA, Gripp KW, Grix A, Guion-Almeida ML, Harr MH, Hudson C, Hunter AG, Johnson J, Joss SK, Kimball A, Kini U, Kline AD, Lauzon J, Lildballe DL, López-González V, Martinezmoles J, Meldrum C, Mirzaa GM, Morel CF, Morton JE, Pyle LC, Quintero-Rivera F, Richer J, Scheuerle AE, Schönewolf-Greulich B, Shears DJ, Silver J, Smith AC, Temple IK; UCLA Clinical Genomics Center; van de Kamp JM, van Dijk FS, Vandersteen AM, White SM, Zackai EH, Zou R; Care4Rare Canada Consortium; Bulman DE, Boycott KM, Lines MA. Huang L, et al. Among authors: zou r. Hum Mutat. 2016 Feb;37(2):148-54. doi: 10.1002/humu.22924. Epub 2015 Nov 19. Hum Mutat. 2016. PMID: 26507355 Free PMC article. Review.

6

Concordance between whole-exome sequencing and clinical Sanger sequencing: implications for patient care.

Hamilton A, Tétreault M, Dyment DA, Zou R, Kernohan K, Geraghty MT; FORGE Canada Consortium; Care4Rare Canada Consortium; Hartley T, Boycott KM. Hamilton A, et al. Among authors: zou r. Mol Genet Genomic Med. 2016 May 10;4(5):504-12. doi: 10.1002/mgg3.223. eCollection 2016 Sep. Mol Genet Genomic Med. 2016. PMID: 27652278 Free PMC article.

7

Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia.

Lemire G, Zheng B, Ediae GU, Zou R, Bhola PT, Chisholm C, de Nanassy J, Lo B, Wang C, Shril S, El Desoky S, Shalaby M, Kari JA, Wang X; Care4Rare Canada Consortium; Kernohan KD, Boycott KM, Hildebrandt F, Sawyer SL. Lemire G, et al. Among authors: zou r. Am J Med Genet A. 2021 Oct;185(10):3005-3011. doi: 10.1002/ajmg.a.62398. Epub 2021 Jun 19. Am J Med Genet A. 2021. PMID: 34145744 Free PMC article.

8

A circular network of adenosine-mediated mitochondrial dysfunction as coregulators of acute myocardial infarction.

Liu Y, Xiao T, Wang Z, Ou Y, Tan Y, Chen L, Zhou N, Zou R. Liu Y, et al. Among authors: zou r. Int J Med Sci. 2024 May 19;21(7):1353-1365. doi: 10.7150/ijms.97066. eCollection 2024. Int J Med Sci. 2024. PMID: 38818463 Free PMC article.

9

Effect of Jianpi Shengxue Tablet on Iron Metabolism and Nutritional Status in Patients with Renal Anemia: A Prospective, Randomized, Open, Parallel Controlled and Multicenter Clinical Study.

Yang J, Liang MY, Li Y, Zhang H, Li W, Lv J, Dong LP, Jin JS, Yang C, Zhang QH, Long L, Zou R, Gao Y, Song D, Pan CQ, Yao Y, Zhan XL, Wang XH. Yang J, et al. Among authors: zou r. Curr Med Sci. 2024 May 28. doi: 10.1007/s11596-024-2867-1. Online ahead of print. Curr Med Sci. 2024. PMID: 38802649

10

Role of radiation in chimeric antigen receptor T-cell therapy for patients with relapsed/refractory non-Hodgkin lymphoma: Current studies and future prospects.

Yu L, Zou R, He J, Qu C. Yu L, et al. Among authors: zou r. Crit Rev Oncol Hematol. 2024 May 22;199:104390. doi: 10.1016/j.critrevonc.2024.104390. Online ahead of print. Crit Rev Oncol Hematol. 2024. PMID: 38782146 Review.

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