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Items: 1 to 20 of 95

1.

PKNOX1, a gene encoding PREP1, a new regulator of Pbx activity, maps on human chromosome 21q22.3 and murine chromosome 17B/C.

Berthelsen J, Viggiano L, Schulz H, Ferretti E, Consalez GG, Rocchi M, Blasi F.

Genomics. 1998 Jan 15;47(2):323-4. No abstract available.

PMID:
9479508
2.

Prep1, a novel functional partner of Pbx proteins.

Berthelsen J, Zappavigna V, Mavilio F, Blasi F.

EMBO J. 1998 Mar 2;17(5):1423-33.

3.

Cloning of a novel homeobox-containing gene, PKNOX1, and mapping to human chromosome 21q22.3.

Chen H, Rossier C, Nakamura Y, Lynn A, Chakravarti A, Antonarakis SE.

Genomics. 1997 Apr 15;41(2):193-200.

PMID:
9143494
5.

The PBX-regulating protein PREP1 is present in different PBX-complexed forms in mouse.

Ferretti E, Schulz H, Talarico D, Blasi F, Berthelsen J.

Mech Dev. 1999 May;83(1-2):53-64.

6.

Meis1 and pKnox1 bind DNA cooperatively with Pbx1 utilizing an interaction surface disrupted in oncoprotein E2a-Pbx1.

Knoepfler PS, Calvo KR, Chen H, Antonarakis SE, Kamps MP.

Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14553-8.

7.

The novel homeoprotein Prep1 modulates Pbx-Hox protein cooperativity.

Berthelsen J, Zappavigna V, Ferretti E, Mavilio F, Blasi F.

EMBO J. 1998 Mar 2;17(5):1434-45.

8.

Meis1, a PBX1-related homeobox gene involved in myeloid leukemia in BXH-2 mice.

Moskow JJ, Bullrich F, Huebner K, Daar IO, Buchberg AM.

Mol Cell Biol. 1995 Oct;15(10):5434-43.

9.

Bfl-1, a Bcl-2-related gene, is the human homolog of the murine A1, and maps to chromosome 15q24.3.

Choi SS, Park SH, Kim UJ, Shin HS.

Mamm Genome. 1997 Oct;8(10):781-2. No abstract available.

PMID:
9321477
10.
11.
12.

Genetic instability of chromosome 3 in HPV-immortalized and tumorigenic human keratinocytes.

Montgomery KD, Tedford KL, McDougall JK.

Genes Chromosomes Cancer. 1995 Oct;14(2):97-105.

PMID:
8527399
13.

Overexpression of FABP7 in Down syndrome fetal brains is associated with PKNOX1 gene-dosage imbalance.

Sánchez-Font MF, Bosch-Comas A, Gonzàlez-Duarte R, Marfany G.

Nucleic Acids Res. 2003 Jun 1;31(11):2769-77.

14.

Isolation of human and murine homologues of the Drosophila minibrain gene: human homologue maps to 21q22.2 in the Down syndrome "critical region".

Song WJ, Sternberg LR, Kasten-Sportès C, Keuren ML, Chung SH, Slack AC, Miller DE, Glover TW, Chiang PW, Lou L, Kurnit DM.

Genomics. 1996 Dec 15;38(3):331-9.

PMID:
8975710
16.
17.

A conserved motif N-terminal to the DNA-binding domains of myogenic bHLH transcription factors mediates cooperative DNA binding with pbx-Meis1/Prep1.

Knoepfler PS, Bergstrom DA, Uetsuki T, Dac-Korytko I, Sun YH, Wright WE, Tapscott SJ, Kamps MP.

Nucleic Acids Res. 1999 Sep 15;27(18):3752-61.

18.
19.

Minibrain (MNBH) is a single copy gene mapping to human chromosome 21q22.2.

Guimera J, Pritchard M, Nadal M, Estivill X.

Cytogenet Cell Genet. 1997;77(3-4):182-4.

PMID:
9284911
20.

Cloning and gene mapping of the mouse homologue of the CBFA2T1 gene associated with human acute myeloid leukemia.

Niwa-Kawakita M, Miyoshi H, Gotoh O, Matsushima Y, Nishimura M, Shisa H, Ohki M.

Genomics. 1995 Oct 10;29(3):755-9.

PMID:
8575770
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