HD34059/HD/NICHD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1997	1
1998	1
1999	2
2000	3
2001	1
2002	2
2025	0

1

Severe limb defects in Hypodactyly mice result from the expression of a novel, mutant HOXA13 protein.

Post LC, Margulies EH, Kuo A, Innis JW. Post LC, et al. Dev Biol. 2000 Jan 15;217(2):290-300. doi: 10.1006/dbio.1999.9550. Dev Biol. 2000. PMID: 10625554 Free article.

2

Altered Hox expression and increased cell death distinguish Hypodactyly from Hoxa13 null mice.

Post LC, Innis JW. Post LC, et al. Int J Dev Biol. 1999 Jul;43(4):287-94. Int J Dev Biol. 1999. PMID: 10470645

3

Mutation of HOXA13 in hand-foot-genital syndrome.

Mortlock DP, Innis JW. Mortlock DP, et al. Nat Genet. 1997 Feb;15(2):179-80. doi: 10.1038/ng0297-179. Nat Genet. 1997. PMID: 9020844

4

Infertility in adult hypodactyly mice is associated with hypoplasia of distal reproductive structures.

Post LC, Innis JW. Post LC, et al. Biol Reprod. 1999 Dec;61(6):1402-8. doi: 10.1095/biolreprod61.6.1402. Biol Reprod. 1999. PMID: 10569982

5

Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.

Goodman FR, Bacchelli C, Brady AF, Brueton LA, Fryns JP, Mortlock DP, Innis JW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ. Goodman FR, et al. Am J Hum Genet. 2000 Jul;67(1):197-202. doi: 10.1086/302961. Epub 2000 Jun 5. Am J Hum Genet. 2000. PMID: 10839976 Free PMC article.

6

Limb development: molecular dysmorphology is at hand!

Innis JW, Mortlock DP. Innis JW, et al. Clin Genet. 1998 May;53(5):337-48. doi: 10.1111/j.1399-0004.1998.tb02744.x. Clin Genet. 1998. PMID: 9660051 Free article. Review.

7

A comparative molecular analysis of developing mouse forelimbs and hindlimbs using serial analysis of gene expression (SAGE).

Margulies EH, Kardia SL, Innis JW. Margulies EH, et al. Genome Res. 2001 Oct;11(10):1686-98. doi: 10.1101/gr.192601. Genome Res. 2001. PMID: 11591645 Free PMC article.

8

A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome.

Innis JW, Goodman FR, Bacchelli C, Williams TM, Mortlock DP, Sateesh P, Scambler PJ, McKinnon W, Guttmacher AE. Innis JW, et al. Hum Mutat. 2002 May;19(5):573-4. doi: 10.1002/humu.9036. Hum Mutat. 2002. PMID: 11968094 Free article.

9

Integrative biology and the developing limb bud.

Innis JW, Margulies EH, Kardia S. Innis JW, et al. Evol Dev. 2002 Sep-Oct;4(5):378-89. doi: 10.1046/j.1525-142x.2002.02025.x. Evol Dev. 2002. PMID: 12356268 Free article.

10

eSAGE: managing and analysing data generated with serial analysis of gene expression (SAGE).

Margulies EH, Innis JW. Margulies EH, et al. Bioinformatics. 2000 Jul;16(7):650-1. doi: 10.1093/bioinformatics/16.7.650. Bioinformatics. 2000. PMID: 11038335

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