Jin W - Search Results

1

Lu L, Jin W, Wang LL. Lu L, et al. Among authors: jin w. Adv Exp Med Biol. 2020;1258:37-54. doi: 10.1007/978-3-030-43085-6_3. Adv Exp Med Biol. 2020. PMID: 32767233 Review.

2

Sensitivity of RECQL4-deficient fibroblasts from Rothmund-Thomson syndrome patients to genotoxic agents.

Jin W, Liu H, Zhang Y, Otta SK, Plon SE, Wang LL. Jin W, et al. Hum Genet. 2008 Jul;123(6):643-53. doi: 10.1007/s00439-008-0518-4. Epub 2008 May 27. Hum Genet. 2008. PMID: 18504617 Free PMC article.

3

Identification of a novel C16orf57 mutation in Athabaskan patients with Poikiloderma with Neutropenia.

Clericuzio C, Harutyunyan K, Jin W, Erickson RP, Irvine AD, McLean WH, Wen Y, Bagatell R, Griffin TA, Shwayder TA, Plon SE, Wang LL. Clericuzio C, et al. Among authors: jin w. Am J Med Genet A. 2011 Feb;155A(2):337-42. doi: 10.1002/ajmg.a.33807. Epub 2010 Dec 22. Am J Med Genet A. 2011. PMID: 21271650 Free PMC article.

4

Configuration and rearrangement of the human GAGE gene clusters.

Killen MW, Taylor TL, Stults DM, Jin W, Wang LL, Moscow JA, Pierce AJ. Killen MW, et al. Among authors: jin w. Am J Transl Res. 2011 May 15;3(3):234-42. Epub 2011 May 8. Am J Transl Res. 2011. PMID: 21654878 Free PMC article.

5

RECQ DNA helicases and osteosarcoma.

Lu L, Jin W, Liu H, Wang LL. Lu L, et al. Among authors: jin w. Adv Exp Med Biol. 2014;804:129-45. doi: 10.1007/978-3-319-04843-7_7. Adv Exp Med Biol. 2014. PMID: 24924172 Review.

6

RECQL4 Regulates p53 Function In Vivo During Skeletogenesis.

Lu L, Harutyunyan K, Jin W, Wu J, Yang T, Chen Y, Joeng KS, Bae Y, Tao J, Dawson BC, Jiang MM, Lee B, Wang LL. Lu L, et al. Among authors: jin w. J Bone Miner Res. 2015 Jun;30(6):1077-89. doi: 10.1002/jbmr.2436. J Bone Miner Res. 2015. PMID: 25556649 Free article.

7

Aging in Rothmund-Thomson syndrome and related RECQL4 genetic disorders.

Lu L, Jin W, Wang LL. Lu L, et al. Among authors: jin w. Ageing Res Rev. 2017 Jan;33:30-35. doi: 10.1016/j.arr.2016.06.002. Epub 2016 Jun 7. Ageing Res Rev. 2017. PMID: 27287744 Review.

8

Generalized metabolic bone disease and fracture risk in Rothmund-Thomson syndrome.

Cao F, Lu L, Abrams SA, Hawthorne KM, Tam A, Jin W, Dawson B, Shypailo R, Liu H, Lee B, Nagamani SCS, Wang LL. Cao F, et al. Among authors: jin w. Hum Mol Genet. 2017 Aug 15;26(16):3046-3055. doi: 10.1093/hmg/ddx178. Hum Mol Genet. 2017. PMID: 28486640 Free PMC article.

9

Generation of an induced pluripotent stem cell line from an individual with a heterozygous RECQL4 mutation.

Jewell BE, Liu M, Lu L, Zhou R, Tu J, Zhu D, Huo Z, Xu A, Wang D, Mata H, Jin W, Xia W, Rao PH, Zhao R, Hung MC, Wang LL, Lee DF. Jewell BE, et al. Among authors: jin w. Stem Cell Res. 2018 Dec;33:36-40. doi: 10.1016/j.scr.2018.10.003. Epub 2018 Oct 2. Stem Cell Res. 2018. PMID: 30312871 Free PMC article.

10

Mutations in ANAPC1, Encoding a Scaffold Subunit of the Anaphase-Promoting Complex, Cause Rothmund-Thomson Syndrome Type 1.

Ajeawung NF, Nguyen TTM, Lu L, Kucharski TJ, Rousseau J, Molidperee S, Atienza J, Gamache I, Jin W, Plon SE, Lee BH, Teodoro JG, Wang LL, Campeau PM. Ajeawung NF, et al. Among authors: jin w. Am J Hum Genet. 2019 Sep 5;105(3):625-630. doi: 10.1016/j.ajhg.2019.06.011. Epub 2019 Jul 11. Am J Hum Genet. 2019. PMID: 31303264 Free PMC article.

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