Brown WT - Search Results

1

Mutations in the gene DNAJC5 cause autosomal dominant Kufs disease in a proportion of cases: study of the Parry family and 8 other families.

Velinov M, Dolzhanskaya N, Gonzalez M, Powell E, Konidari I, Hulme W, Staropoli JF, Xin W, Wen GY, Barone R, Coppel SH, Sims K, Brown WT, Züchner S. Velinov M, et al. Among authors: brown wt. PLoS One. 2012;7(1):e29729. doi: 10.1371/journal.pone.0029729. Epub 2012 Jan 3. PLoS One. 2012. PMID: 22235333 Free PMC article.

2

Substrate Reduction Therapy in Four Patients with Milder CLN1 Mutations and Juvenile-Onset Batten Disease Using Cysteamine Bitartrate.

Gavin M, Wen GY, Messing J, Adelman S, Logush A, Jenkins EC, Brown WT, Velinov M. Gavin M, et al. Among authors: brown wt. JIMD Rep. 2013;11:87-92. doi: 10.1007/8904_2013_226. Epub 2013 Apr 16. JIMD Rep. 2013. PMID: 23588842 Free PMC article.

3

Psychotic manifestations in a patient with mental retardation and a 6.2 megabase deletion at the distal short arm of chromosome 12.

Velinov M, Beldia G, Gu H, Tsiouris JA, Jenkins EC, Brown WT. Velinov M, et al. Among authors: brown wt. CNS Spectr. 2008 Jun;13(6):515-9. doi: 10.1017/s1092852900016758. CNS Spectr. 2008. PMID: 18567976

4

De-novo 2.15 Mb terminal Xq duplication involving MECP2 but not L1CAM gene in a male patient with mental retardation.

Velinov M, Novelli A, Gu H, Fenko M, Dolzhanskaya N, Bernardini L, Capalbo A, Dallapiccola B, Jenkins EC, Brown WT. Velinov M, et al. Among authors: brown wt. Clin Dysmorphol. 2009 Jan;18(1):9-12. doi: 10.1097/MCD.0b013e3283157cad. Clin Dysmorphol. 2009. PMID: 19090026

5

Transmission electron microscopy of chromosomes by longitudinal section preparation: application to fragile X chromosome analysis.

Wen GY, Jenkins EC, Yao XL, Yoon D, Brown WT, Wisniewski HM. Wen GY, et al. Among authors: brown wt. Am J Med Genet. 1997 Feb 11;68(4):445-9. doi: 10.1002/(sici)1096-8628(19970211)68:4<445::aid-ajmg14>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9021019

6

Expression of inflammatory cytokines, Bcl2 and cathepsin D are altered in lymphoblasts of autistic subjects.

Malik M, Sheikh AM, Wen G, Spivack W, Brown WT, Li X. Malik M, et al. Among authors: brown wt. Immunobiology. 2011 Jan-Feb;216(1-2):80-5. doi: 10.1016/j.imbio.2010.03.001. Epub 2010 Mar 12. Immunobiology. 2011. PMID: 20399529

7

Folate receptor autoantibodies are prevalent in children diagnosed with autism spectrum disorder, their normal siblings and parents.

Quadros EV, Sequeira JM, Brown WT, Mevs C, Marchi E, Flory M, Jenkins EC, Velinov MT, Cohen IL. Quadros EV, et al. Among authors: brown wt. Autism Res. 2018 May;11(5):707-712. doi: 10.1002/aur.1934. Epub 2018 Feb 2. Autism Res. 2018. PMID: 29394471

8

Reduced telomere length in older men with premutation alleles of the fragile X mental retardation 1 gene.

Jenkins EC, Tassone F, Ye L, Gu H, Xi M, Velinov M, Brown WT, Hagerman RJ, Hagerman PJ. Jenkins EC, et al. Among authors: brown wt. Am J Med Genet A. 2008 Jun 15;146A(12):1543-6. doi: 10.1002/ajmg.a.32342. Am J Med Genet A. 2008. PMID: 18478592 Free PMC article.

9

Ultrastructure of the fragile X chromosome: new observations on the fragile site.

Wen GY, Jenkins EC, Goldberg EM, Genovese M, Brown WT, Wisniewski HM. Wen GY, et al. Among authors: brown wt. Am J Med Genet. 1999 Apr 2;83(4):331-3. Am J Med Genet. 1999. PMID: 10208174

10

BDNF-Akt-Bcl2 antiapoptotic signaling pathway is compromised in the brain of autistic subjects.

Sheikh AM, Malik M, Wen G, Chauhan A, Chauhan V, Gong CX, Liu F, Brown WT, Li X. Sheikh AM, et al. Among authors: brown wt. J Neurosci Res. 2010 Sep;88(12):2641-7. doi: 10.1002/jnr.22416. J Neurosci Res. 2010. PMID: 20648653

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