PubMed (OMIM) for id: 4953

Year	Number of Results
1986	1
1987	3
1988	2
1989	1
1997	1
1998	1
2000	2
2003	1
2018	2
2024	0

1

Gain-of-function variants in the ODC1 gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities.

Rodan LH, Anyane-Yeboa K, Chong K, Klein Wassink-Ruiter JS, Wilson A, Smith L, Kothare SV, Rajabi F, Blaser S, Ni M, DeBerardinis RJ, Poduri A, Berry GT. Rodan LH, et al. Am J Med Genet A. 2018 Dec;176(12):2554-2560. doi: 10.1002/ajmg.a.60677. Epub 2018 Nov 26. Am J Med Genet A. 2018. PMID: 30475435

2

Novel de novo pathogenic variant in the ODC1 gene in a girl with developmental delay, alopecia, and dysmorphic features.

Bupp CP, Schultz CR, Uhl KL, Rajasekaran S, Bachmann AS. Bupp CP, et al. Am J Med Genet A. 2018 Dec;176(12):2548-2553. doi: 10.1002/ajmg.a.40523. Epub 2018 Sep 21. Am J Med Genet A. 2018. PMID: 30239107

3

Pronounced reduction in adenoma recurrence associated with aspirin use and a polymorphism in the ornithine decarboxylase gene.

Martinez ME, O'Brien TG, Fultz KE, Babbar N, Yerushalmi H, Qu N, Guo Y, Boorman D, Einspahr J, Alberts DS, Gerner EW. Martinez ME, et al. Proc Natl Acad Sci U S A. 2003 Jun 24;100(13):7859-64. doi: 10.1073/pnas.1332465100. Epub 2003 Jun 16. Proc Natl Acad Sci U S A. 2003. PMID: 12810952 Free PMC article.

4

Functional analysis of human ornithine decarboxylase alleles.

Guo Y, Harris RB, Rosson D, Boorman D, O'Brien TG. Guo Y, et al. Cancer Res. 2000 Nov 15;60(22):6314-7. Cancer Res. 2000. PMID: 11103791

5

A cell cycle-dependent internal ribosome entry site.

Pyronnet S, Pradayrol L, Sonenberg N. Pyronnet S, et al. Mol Cell. 2000 Apr;5(4):607-16. doi: 10.1016/s1097-2765(00)80240-3. Mol Cell. 2000. PMID: 10882097 Free article.

6

Transcription factor ZBP-89 regulates the activity of the ornithine decarboxylase promoter.

Law GL, Itoh H, Law DJ, Mize GJ, Merchant JL, Morris DR. Law GL, et al. J Biol Chem. 1998 Aug 7;273(32):19955-64. doi: 10.1074/jbc.273.32.19955. J Biol Chem. 1998. PMID: 9685330 Free article.

7

c-Myc/Max heterodimers bind cooperatively to the E-box sequences located in the first intron of the rat ornithine decarboxylase (ODC) gene.

Walhout AJ, Gubbels JM, Bernards R, van der Vliet PC, Timmers HT. Walhout AJ, et al. Nucleic Acids Res. 1997 Apr 15;25(8):1493-501. doi: 10.1093/nar/25.8.1493. Nucleic Acids Res. 1997. PMID: 9162900 Free PMC article.

8

Human ornithine decarboxylase sequences map to chromosome regions 2pter----p23 and 7cen----qter but are not coamplified with the NMYC oncogene.

Winqvist R, Mäkelä TP, Seppänen P, Jänne OA, Alhonen-Hongisto L, Jänne J, Grzeschik KH, Alitalo K. Winqvist R, et al. Cytogenet Cell Genet. 1986;42(3):133-40. doi: 10.1159/000132266. Cytogenet Cell Genet. 1986. PMID: 3755388

9

Complete amino acid sequence of human ornithine decarboxylase deduced from complementary DNA.

Hickok NJ, Seppänen PJ, Gunsalus GL, Jänne OA. Hickok NJ, et al. DNA. 1987 Jun;6(3):179-87. doi: 10.1089/dna.1987.6.179. DNA. 1987. PMID: 3595418

10

Mouse ornithine decarboxylase gene: cloning, structure, and expression.

Brabant M, McConlogue L, van Daalen Wetters T, Coffino P. Brabant M, et al. Proc Natl Acad Sci U S A. 1988 Apr;85(7):2200-4. doi: 10.1073/pnas.85.7.2200. Proc Natl Acad Sci U S A. 1988. PMID: 3353375 Free PMC article.

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