Morris M - Search Results

1

A t(2;8) balanced translocation with breakpoints near the human HOXD complex causes mesomelic dysplasia and vertebral defects.

Spitz F, Montavon T, Monso-Hinard C, Morris M, Ventruto ML, Antonarakis S, Ventruto V, Duboule D. Spitz F, et al. Among authors: morris m. Genomics. 2002 Apr;79(4):493-8. doi: 10.1006/geno.2002.6735. Genomics. 2002. PMID: 11944980

2

Mapping of the human transcription factor GABPA (E4TF1-60) gene to chromosome 21.

Chrast R, Chen H, Morris MA, Antonarakis SE. Chrast R, et al. Among authors: morris ma. Genomics. 1995 Jul 1;28(1):119-22. doi: 10.1006/geno.1995.1117. Genomics. 1995. PMID: 7590737

3

Inversion-induced disruption of the Hoxd cluster leads to the partition of regulatory landscapes.

Spitz F, Herkenne C, Morris MA, Duboule D. Spitz F, et al. Nat Genet. 2005 Aug;37(8):889-93. doi: 10.1038/ng1597. Epub 2005 Jul 3. Nat Genet. 2005. PMID: 15995706 Free article.

4

Mapping of the gene for the p60 subunit of the human chromatin assembly factor (CAF1A) to the Down syndrome region of chromosome 21.

Blouin JL, Duriaux-Sail G, Chen H, Gos A, Morris MA, Rossier C, Antonarakis SE. Blouin JL, et al. Among authors: morris ma. Genomics. 1996 Apr 15;33(2):309-12. doi: 10.1006/geno.1996.0199. Genomics. 1996. PMID: 8660983

5

Localization of a human homolog of the mouse pericentrin gene (PCNT) to chromosome 21qter.

Chen H, Gos A, Morris MA, Antonarakis SE. Chen H, et al. Among authors: morris ma. Genomics. 1996 Aug 1;35(3):620-4. doi: 10.1006/geno.1996.0411. Genomics. 1996. PMID: 8812505

6

Cloning of the cDNA for the human ATP synthase OSCP subunit (ATP5O) by exon trapping and mapping to chromosome 21q22.1-q22.2.

Chen H, Morris MA, Rossier C, Blouin JL, Antonarakis SE. Chen H, et al. Among authors: morris ma. Genomics. 1995 Aug 10;28(3):470-6. doi: 10.1006/geno.1995.1176. Genomics. 1995. PMID: 7490082

7

The gene for human U2 snRNP auxiliary factor small 35-kDa subunit (U2AF1) maps to the progressive myoclonus epilepsy (EPM1) critical region on chromosome 21q22.3.

Lalioti MD, Gos A, Green MR, Rossier C, Morris MA, Antonarakis SE. Lalioti MD, et al. Among authors: morris ma. Genomics. 1996 Apr 15;33(2):298-300. doi: 10.1006/geno.1996.0196. Genomics. 1996. PMID: 8660980

8

Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping.

Chen H, Chrast R, Rossier C, Morris MA, Lalioti MD, Antonarakis SE. Chen H, et al. Among authors: morris ma. Genome Res. 1996 Aug;6(8):747-60. doi: 10.1101/gr.6.8.747. Genome Res. 1996. PMID: 8858350 Free article.

9

Deletion of the fibrinogen [correction of fibrogen] alpha-chain gene (FGA) causes congenital afibrogenemia.

Neerman-Arbez M, Honsberger A, Antonarakis SE, Morris MA. Neerman-Arbez M, et al. Among authors: morris ma. J Clin Invest. 1999 Jan;103(2):215-8. doi: 10.1172/JCI5471. J Clin Invest. 1999. PMID: 9916133 Free PMC article.

10

Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency.

Villard J, Reith W, Barras E, Gos A, Morris MA, Antonarakis SE, Van den Elsen PJ, Mach B. Villard J, et al. Among authors: morris ma. Hum Mutat. 1997;10(6):430-5. doi: 10.1002/(SICI)1098-1004(1997)10:6<430::AID-HUMU3>3.0.CO;2-H. Hum Mutat. 1997. PMID: 9401005

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