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Items: 1 to 20 of 31

1.

Analysis of the murine Hoxa-9 cDNA: an alternatively spliced transcript encodes a truncated protein lacking the homeodomain.

Fujimoto S, Araki K, Chisaka O, Araki M, Takagi K, Yamamura K.

Gene. 1998 Mar 16;209(1-2):77-85.

PMID:
9524228
2.

Genetic interactions of Hox genes in limb development: learning from compound mutants.

Rijli FM, Chambon P.

Curr Opin Genet Dev. 1997 Aug;7(4):481-7.

PMID:
9309178
3.

Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract.

Goodman FR, Mundlos S, Muragaki Y, Donnai D, Giovannucci-Uzielli ML, Lapi E, Majewski F, McGaughran J, McKeown C, Reardon W, Upton J, Winter RM, Olsen BR, Scambler PJ.

Proc Natl Acad Sci U S A. 1997 Jul 8;94(14):7458-63.

4.

RET in human development and oncogenesis.

Edery P, Eng C, Munnich A, Lyonnet S.

Bioessays. 1997 May;19(5):389-95. Review.

PMID:
9174404
6.

Mutation of HOXA13 in hand-foot-genital syndrome.

Mortlock DP, Innis JW.

Nat Genet. 1997 Feb;15(2):179-80.

PMID:
9020844
7.

Long-range disruption of gene expression by a selectable marker cassette.

Pham CT, MacIvor DM, Hug BA, Heusel JW, Ley TJ.

Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13090-5.

8.

Synpolydactyly in mice with a targeted deficiency in the HoxD complex.

Zákány J, Duboule D.

Nature. 1996 Nov 7;384(6604):69-71.

PMID:
8900279
9.
10.

Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families.

Akarsu AN, Stoilov I, Yilmaz E, Sayli BS, Sarfarazi M.

Hum Mol Genet. 1996 Jul;5(7):945-52.

PMID:
8817328
11.

Interrelationships of the pathways of mRNA decay and translation in eukaryotic cells.

Jacobson A, Peltz SW.

Annu Rev Biochem. 1996;65:693-739. Review.

PMID:
8811193
12.
13.

Protein degradation: de-ubiquitinate to decide your fate.

Kalderon D.

Curr Biol. 1996 Jun 1;6(6):662-5. Review.

14.

Analysis of Hox gene expression in the chick limb bud.

Nelson CE, Morgan BA, Burke AC, Laufer E, DiMambro E, Murtaugh LC, Gonzales E, Tessarollo L, Parada LF, Tabin C.

Development. 1996 May;122(5):1449-66.

15.
16.

Know your neighbors: three phenotypes in null mutants of the myogenic bHLH gene MRF4.

Olson EN, Arnold HH, Rigby PW, Wold BJ.

Cell. 1996 Apr 5;85(1):1-4. Review. No abstract available.

17.

Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13.

Muragaki Y, Mundlos S, Upton J, Olsen BR.

Science. 1996 Apr 26;272(5261):548-51.

PMID:
8614804
18.

The mutational spectrum in Waardenburg syndrome.

Tassabehji M, Newton VE, Liu XZ, Brady A, Donnai D, Krajewska-Walasek M, Murday V, Norman A, Obersztyn E, Reardon W, et al.

Hum Mol Genet. 1995 Nov;4(11):2131-7.

PMID:
8589691
19.

Patterning of the Drosophila embryo by a homeodomain-deleted Ftz polypeptide.

Copeland JW, Nasiadka A, Dietrich BH, Krause HM.

Nature. 1996 Jan 11;379(6561):162-5.

PMID:
8538765
20.

PAX6 mutations in aniridia.

Hanson IM, Seawright A, Hardman K, Hodgson S, Zaletayev D, Fekete G, van Heyningen V.

Hum Mol Genet. 1993 Jul;2(7):915-20.

PMID:
8364574

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