Dong J - Search Results

1

Using gene carrier probability to select high risk families for identifying germline mutations in breast cancer susceptibility genes.

Chang-Claude J, Dong J, Schmidt S, Shayeghi M, Komitowski D, Becher H, Stratton MR, Royer-Pokora B. Chang-Claude J, et al. Among authors: dong j. J Med Genet. 1998 Feb;35(2):116-21. doi: 10.1136/jmg.35.2.116. J Med Genet. 1998. PMID: 9507390 Free PMC article.

2

A high proportion of mutations in the BRCA1 gene in German breast/ovarian cancer families with clustering of mutations in the 3' third of the gene.

Dong J, Chang-Claude J, Wu Y, Schumacher V, Debatin I, Tonin P, Royer-Pokora B. Dong J, et al. Hum Genet. 1998 Aug;103(2):154-61. doi: 10.1007/s004390050799. Hum Genet. 1998. PMID: 9760198

3

Positional cloning of the gene for X-linked retinitis pigmentosa 2.

Schwahn U, Lenzner S, Dong J, Feil S, Hinzmann B, van Duijnhoven G, Kirschner R, Hemberger M, Bergen AA, Rosenberg T, Pinckers AJ, Fundele R, Rosenthal A, Cremers FP, Ropers HH, Berger W. Schwahn U, et al. Among authors: dong j. Nat Genet. 1998 Aug;19(4):327-32. doi: 10.1038/1214. Nat Genet. 1998. PMID: 9697692

4

Familial dysautonomia: detection of the IKBKAP IVS20(+6T --> C) and R696P mutations and frequencies among Ashkenazi Jews.

Dong J, Edelmann L, Bajwa AM, Kornreich R, Desnick RJ. Dong J, et al. Am J Med Genet. 2002 Jul 1;110(3):253-7. doi: 10.1002/ajmg.10450. Am J Med Genet. 2002. PMID: 12116234

5

Carrier screening for mucolipidosis type IV in the American Ashkenazi Jewish population.

Edelmann L, Dong J, Desnick RJ, Kornreich R. Edelmann L, et al. Among authors: dong j. Am J Hum Genet. 2002 Apr;70(4):1023-7. doi: 10.1086/339519. Epub 2002 Feb 13. Am J Hum Genet. 2002. PMID: 11845410 Free PMC article.

6

Nonradioactive detection of the common Connexin 26 167delT and 35delG mutations and frequencies among Ashkenazi Jews.

Dong J, Katz DR, Eng CM, Kornreich R, Desnick RJ. Dong J, et al. Mol Genet Metab. 2001 Jun;73(2):160-3. doi: 10.1006/mgme.2001.3182. Mol Genet Metab. 2001. PMID: 11386851

7

Identification of PATCHED mutations in medulloblastomas by direct sequencing.

Dong J, Gailani MR, Pomeroy SL, Reardon D, Bale AE. Dong J, et al. Hum Mutat. 2000 Jul;16(1):89-90. doi: 10.1002/1098-1004(200007)16:1<89::AID-HUMU18>3.0.CO;2-7. Hum Mutat. 2000. PMID: 10874314

8

Therapeutic potential of microglial SMEK1 in regulating H3K9 lactylation in cerebral ischemia-reperfusion.

Si WY, Yang CL, Wei SL, Du T, Li LK, Dong J, Zhou Y, Li H, Zhang P, Liu QJ, Duan RS, Duan RN. Si WY, et al. Among authors: dong j. Commun Biol. 2024 Dec 26;7(1):1701. doi: 10.1038/s42003-024-07425-6. Commun Biol. 2024. PMID: 39725685

9

CRISPR/Cas12a regulated preassembled bulb-shaped G-quadruplex signal unit for FL/CM dual-mode ultrasensitive detection of miRNA-155.

Li X, Dong J, Deng L, Huo D, Yang M, Hou C. Li X, et al. Among authors: dong j. Talanta. 2024 Dec 25;286:127413. doi: 10.1016/j.talanta.2024.127413. Online ahead of print. Talanta. 2024. PMID: 39724854

10

The spatiotemporal and paradoxical roles of NRF2 in renal toxicity and kidney diseases.

Bian Y, Dong J, Zhou Z, Zhou H, Xu Y, Zhang Q, Chen C, Pi J. Bian Y, et al. Among authors: dong j. Redox Biol. 2024 Dec 19;79:103476. doi: 10.1016/j.redox.2024.103476. Online ahead of print. Redox Biol. 2024. PMID: 39724848 Review.

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