Sun Y - Search Results

1

No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.

Schumacher J, Otte AC, Becker T, Sun Y, Wienker TF, Wirth B, Franke P, Abou Jamra R, Propping P, Deckert J, Nöthen MM, Cichon S. Schumacher J, et al. Among authors: sun y. Hum Genet. 2003 Dec;114(1):115-7. doi: 10.1007/s00439-003-1022-5. Epub 2003 Sep 25. Hum Genet. 2003. PMID: 14513359

2

Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy.

Sun Y, Grimmler M, Schwarzer V, Schoenen F, Fischer U, Wirth B. Sun Y, et al. Hum Mutat. 2005 Jan;25(1):64-71. doi: 10.1002/humu.20111. Hum Mutat. 2005. PMID: 15580564

3

Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.

Aretz S, Uhlhaas S, Sun Y, Pagenstecher C, Mangold E, Caspari R, Möslein G, Schulmann K, Propping P, Friedl W. Aretz S, et al. Among authors: sun y. Hum Mutat. 2004 Nov;24(5):370-80. doi: 10.1002/humu.20087. Hum Mutat. 2004. PMID: 15459959

4

Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient.

Sun Y, Nicholls RD, Butler MG, Saitoh S, Hainline BE, Palmer CG. Sun Y, et al. Hum Mol Genet. 1996 Apr;5(4):517-24. doi: 10.1093/hmg/5.4.517. Hum Mol Genet. 1996. PMID: 8845846 Free PMC article.

5

Marker chromosome 21 identified by microdissection and FISH.

Sun Y, Rubinstein J, Soukup S, Palmer CG. Sun Y, et al. Am J Med Genet. 1995 Mar 27;56(2):151-4. doi: 10.1002/ajmg.1320560207. Am J Med Genet. 1995. PMID: 7542834

6

G2 phase cell cycle disturbance as a manifestation of genetic cell damage.

Seyschab H, Sun Y, Friedl R, Schindler D, Hoehn H. Seyschab H, et al. Among authors: sun y. Hum Genet. 1993 Aug;92(1):61-8. doi: 10.1007/BF00216146. Hum Genet. 1993. PMID: 8365728

7

Complex chromosomal mechanisms lead to APRT loss of heterozygosity in heteroploid cells.

Shao C, Gupta PK, Sun Y, Sahota A, Tischfield JA. Shao C, et al. Among authors: sun y. Cytogenet Cell Genet. 1996;75(4):216-21. doi: 10.1159/000134486. Cytogenet Cell Genet. 1996. PMID: 9067427

8

Comparative evaluation of diepoxybutane sensitivity and cell cycle blockage in the diagnosis of Fanconi anemia.

Seyschab H, Friedl R, Sun Y, Schindler D, Hoehn H, Hentze S, Schroeder-Kurth T. Seyschab H, et al. Among authors: sun y. Blood. 1995 Apr 15;85(8):2233-7. Blood. 1995. PMID: 7718895 Free article.

9

Modulation of the spontaneous G2 phase blockage in Fanconi anemia cells by caffeine: differences from cells arrested by X-irradiation.

Seyschab H, Bretzel G, Friedl R, Schindler D, Sun Y, Hoehn H. Seyschab H, et al. Among authors: sun y. Mutat Res. 1994 Jul 16;308(2):149-57. doi: 10.1016/0027-5107(94)90150-3. Mutat Res. 1994. PMID: 7518042

10

Preimplantation genetic diagnosis for spinal muscular atrophy type I.

Fallon L, Harton GL, Sisson ME, Rodriguez E, Field LK, Fugger EF, Geltinger M, Sun Y, Dorfmann A, Schoener C, Bick D, Schulman J, Levinson G, Black SH. Fallon L, et al. Among authors: sun y. Neurology. 1999 Sep 22;53(5):1087-90. doi: 10.1212/wnl.53.5.1087. Neurology. 1999. PMID: 10496271

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