P30HD27748/HD/NICHD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1992	3
1993	3
2001	1
2002	2
2003	1
2004	1
2024	0

1

Schutte BC, McCray PB Jr. Schutte BC, et al. Annu Rev Physiol. 2002;64:709-48. doi: 10.1146/annurev.physiol.64.081501.134340. Annu Rev Physiol. 2002. PMID: 11826286 Review.

2

Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13.

Stone EM, Kimura AE, Folk JC, Bennett SR, Nichols BE, Streb LM, Sheffield VC. Stone EM, et al. Hum Mol Genet. 1992 Dec;1(9):685-9. doi: 10.1093/hmg/1.9.685. Hum Mol Genet. 1992. PMID: 1284594

3

Deficiency of neuronal nitric oxide synthase (nNOS) worsens alcohol-induced microencephaly and neuronal loss in developing mice.

Bonthius DJ, Tzouras G, Karacay B, Mahoney J, Hutton A, McKim R, Pantazis NJ. Bonthius DJ, et al. Brain Res Dev Brain Res. 2002 Sep 20;138(1):45-59. doi: 10.1016/s0165-3806(02)00458-3. Brain Res Dev Brain Res. 2002. PMID: 12234657

4

FGF-2, NGF and IGF-1, but not BDNF, utilize a nitric oxide pathway to signal neurotrophic and neuroprotective effects against alcohol toxicity in cerebellar granule cell cultures.

Bonthius DJ, Karacay B, Dai D, Pantazis NJ. Bonthius DJ, et al. Brain Res Dev Brain Res. 2003 Jan 10;140(1):15-28. doi: 10.1016/s0165-3806(02)00549-7. Brain Res Dev Brain Res. 2003. PMID: 12524173

5

Procollagen II gene mutation in Stickler syndrome.

Brown DM, Nichols BE, Weingeist TA, Sheffield VC, Kimura AE, Stone EM. Brown DM, et al. Arch Ophthalmol. 1992 Nov;110(11):1589-93. doi: 10.1001/archopht.1992.01080230089027. Arch Ophthalmol. 1992. PMID: 1444917

6

Glutaric acidemia type II. Heterogeneity in beta-oxidation flux, polypeptide synthesis, and complementary DNA mutations in the alpha subunit of electron transfer flavoprotein in eight patients.

Freneaux E, Sheffield VC, Molin L, Shires A, Rhead WJ. Freneaux E, et al. J Clin Invest. 1992 Nov;90(5):1679-86. doi: 10.1172/JCI116040. J Clin Invest. 1992. PMID: 1430199 Free PMC article.

7

The sensitivity of single-strand conformation polymorphism analysis for the detection of single base substitutions.

Sheffield VC, Beck JS, Kwitek AE, Sandstrom DW, Stone EM. Sheffield VC, et al. Genomics. 1993 May;16(2):325-32. doi: 10.1006/geno.1993.1193. Genomics. 1993. PMID: 8314571

8

A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea.

Nichols BE, Drack AV, Vandenburgh K, Kimura AE, Sheffield VC, Stone EM. Nichols BE, et al. Hum Mol Genet. 1993 May;2(5):601-3. doi: 10.1093/hmg/2.5.601. Hum Mol Genet. 1993. PMID: 8251014 No abstract available.

9

A user-friendly Hypercard interface for human linkage analysis.

Nichols BE, Sheffield VC, Stone EM. Nichols BE, et al. Comput Appl Biosci. 1993 Dec;9(6):757-9. doi: 10.1093/bioinformatics/9.6.757. Comput Appl Biosci. 1993. PMID: 8143163

10

Ontogeny of the H19 gene in sheep and effect of maternal fasting on its expression in the fetus.

Naimeh LG, Schutte BC, Hamilton WS, Tsalikian E. Naimeh LG, et al. Endocr Res. 2001 Nov;27(4):417-31. doi: 10.1081/erc-100107866. Endocr Res. 2001. PMID: 11794466

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