PubMed (OMIM) for id: 4385

Year	Number of Results
1977	1
1982	1
1983	1
1985	1
1987	2
1989	3
1990	2
1991	5
1992	4
1993	2
1994	2
1995	1
1996	1
1997	2
1998	1
2000	1
2001	3
2002	5
2003	4
2004	1
2005	1
2024	0

1

An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes.

O'Doherty A, Ruf S, Mulligan C, Hildreth V, Errington ML, Cooke S, Sesay A, Modino S, Vanes L, Hernandez D, Linehan JM, Sharpe PT, Brandner S, Bliss TV, Henderson DJ, Nizetic D, Tybulewicz VL, Fisher EM. O'Doherty A, et al. Science. 2005 Sep 23;309(5743):2033-7. doi: 10.1126/science.1114535. Science. 2005. PMID: 16179473 Free PMC article.

2

A chromosome 21 critical region does not cause specific Down syndrome phenotypes.

Olson LE, Richtsmeier JT, Leszl J, Reeves RH. Olson LE, et al. Science. 2004 Oct 22;306(5696):687-90. doi: 10.1126/science.1098992. Science. 2004. PMID: 15499018 Free PMC article.

3

Global disruption of the cerebellar transcriptome in a Down syndrome mouse model.

Saran NG, Pletcher MT, Natale JE, Cheng Y, Reeves RH. Saran NG, et al. Hum Mol Genet. 2003 Aug 15;12(16):2013-9. doi: 10.1093/hmg/ddg217. Hum Mol Genet. 2003. PMID: 12913072

4

Lower neonatal screening thyroxine concentrations in down syndrome newborns.

van Trotsenburg AS, Vulsma T, van Santen HM, Cheung W, de Vijlder JJ. van Trotsenburg AS, et al. J Clin Endocrinol Metab. 2003 Apr;88(4):1512-5. doi: 10.1210/jc.2002-021303. J Clin Endocrinol Metab. 2003. PMID: 12679431

5

GATA1 mutations in transient leukemia and acute megakaryoblastic leukemia of Down syndrome.

Hitzler JK, Cheung J, Li Y, Scherer SW, Zipursky A. Hitzler JK, et al. Blood. 2003 Jun 1;101(11):4301-4. doi: 10.1182/blood-2003-01-0013. Epub 2003 Feb 13. Blood. 2003. PMID: 12586620 Free article.

6

Mutagenesis of GATA1 is an initiating event in Down syndrome leukemogenesis.

Mundschau G, Gurbuxani S, Gamis AS, Greene ME, Arceci RJ, Crispino JD. Mundschau G, et al. Blood. 2003 Jun 1;101(11):4298-300. doi: 10.1182/blood-2002-12-3904. Epub 2003 Jan 30. Blood. 2003. PMID: 12560215 Free article.

7

Mutation of the AML1/RUNX1 gene in a transient myeloproliferative disorder patient with Down syndrome.

Taketani T, Taki T, Takita J, Ono R, Horikoshi Y, Kaneko Y, Sako M, Hanada R, Hongo T, Hayashi Y. Taketani T, et al. Leukemia. 2002 Sep;16(9):1866-7. doi: 10.1038/sj.leu.2402612. Leukemia. 2002. PMID: 12200707 No abstract available.

8

A leukemogenic twist for GATA1.

Look AT. Look AT. Nat Genet. 2002 Sep;32(1):83-4. doi: 10.1038/ng960. Epub 2002 Aug 12. Nat Genet. 2002. PMID: 12172549 No abstract available.

9

Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome.

Wechsler J, Greene M, McDevitt MA, Anastasi J, Karp JE, Le Beau MM, Crispino JD. Wechsler J, et al. Nat Genet. 2002 Sep;32(1):148-52. doi: 10.1038/ng955. Epub 2002 Aug 12. Nat Genet. 2002. PMID: 12172547

10

Altered metabolism of the amyloid beta precursor protein is associated with mitochondrial dysfunction in Down's syndrome.

Busciglio J, Pelsman A, Wong C, Pigino G, Yuan M, Mori H, Yankner BA. Busciglio J, et al. Neuron. 2002 Feb 28;33(5):677-88. doi: 10.1016/s0896-6273(02)00604-9. Neuron. 2002. PMID: 11879646 Free article.

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