Curry SM - Search Results

1

Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy-Walker malformation.

McCormack WM Jr, Shen JJ, Curry SM, Berend SA, Kashork C, Pinar H, Potocki L, Bejjani BA. McCormack WM Jr, et al. Among authors: curry sm. Am J Med Genet. 2002 Nov 1;112(4):384-9. doi: 10.1002/ajmg.10659. Am J Med Genet. 2002. Corrected and republished in: Am J Med Genet A. 2003 Apr 15;118A(2):384-9. PMID: 12376941 Corrected and republished.

2

Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy-Walker malformation.

McCormack WM Jr, Shen JJ, Curry SM, Berend SA, Kashork C, Pinar H, Potocki L, Bejjani BA. McCormack WM Jr, et al. Among authors: curry sm. Am J Med Genet A. 2003 Apr 15;118A(2):384-9. Am J Med Genet A. 2003. PMID: 12698964

3

Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in Ecuador.

Curry SM, Daou AG, Hermanns P, Molinari A, Lewis RA, Bejjani BA. Curry SM, et al. Ophthalmic Genet. 2004 Mar;25(1):3-9. doi: 10.1076/opge.25.1.3.28999. Ophthalmic Genet. 2004. PMID: 15255109

4

Molecular basis of Peters anomaly in Saudi Arabia.

Edward D, Al Rajhi A, Lewis RA, Curry S, Wang Z, Bejjani B. Edward D, et al. Ophthalmic Genet. 2004 Dec;25(4):257-70. doi: 10.1080/13816810490902648. Ophthalmic Genet. 2004. PMID: 15621878

5

Are the betaine-homocysteine methyltransferase (BHMT and BHMT2) genes risk factors for spina bifida and orofacial clefts?

Zhu H, Curry S, Wen S, Wicker NJ, Shaw GM, Lammer EJ, Yang W, Jafarov T, Finnell RH. Zhu H, et al. Am J Med Genet A. 2005 Jun 15;135(3):274-7. doi: 10.1002/ajmg.a.30739. Am J Med Genet A. 2005. PMID: 15887275

6

Cerebral folate deficiency with developmental delay, autism, and response to folinic acid.

Moretti P, Sahoo T, Hyland K, Bottiglieri T, Peters S, del Gaudio D, Roa B, Curry S, Zhu H, Finnell RH, Neul JL, Ramaekers VT, Blau N, Bacino CA, Miller G, Scaglia F. Moretti P, et al. Neurology. 2005 Mar 22;64(6):1088-90. doi: 10.1212/01.WNL.0000154641.08211.B7. Neurology. 2005. PMID: 15781839

7

Closed magnetic topology in the Venusian magnetotail and ion escape at Venus.

Xu S, Mitchell DL, Whittlesey P, Rahmati A, Livi R, Larson D, Luhmann JG, Halekas JS, Hara T, McFadden JP, Pulupa M, Bale SD, Curry SM, Persson M. Xu S, et al. Among authors: curry sm. Nat Commun. 2024 Jul 18;15(1):6065. doi: 10.1038/s41467-024-50480-0. Nat Commun. 2024. PMID: 39025884 Free PMC article.

8

The ex vivo human translaminar autonomous system to study spaceflight associated neuro-ocular syndrome pathogenesis.

Peng M, Curry SM, Liu Y, Lohawala H, Sharma G, Sharma TP. Peng M, et al. Among authors: curry sm. NPJ Microgravity. 2022 Oct 28;8(1):44. doi: 10.1038/s41526-022-00232-5. NPJ Microgravity. 2022. PMID: 36307487 Free PMC article.

9

A Statistical Investigation of Factors Influencing the Magnetotail Twist at Mars.

DiBraccio GA, Romanelli N, Bowers CF, Gruesbeck JR, Halekas JS, Ruhunusiri S, Weber T, Espley JR, Xu S, Luhmann JG, Harada Y, Dubinin E, Poh GK, Brain DA, Curry SM. DiBraccio GA, et al. Among authors: curry sm. Geophys Res Lett. 2022 Jun 28;49(12):e2022GL098007. doi: 10.1029/2022GL098007. Epub 2022 Jun 16. Geophys Res Lett. 2022. PMID: 35865912 Free PMC article.

10

The Role of Salmonella Genomic Island 4 in Metal Tolerance of Salmonella enterica Serovar I 4,[5],12:i:- Pork Outbreak Isolate USDA15WA-1.

Bearson BL, Trachsel JM, Shippy DC, Sivasankaran SK, Kerr BJ, Loving CL, Brunelle BW, Curry SM, Gabler NK, Bearson SMD. Bearson BL, et al. Among authors: curry sm. Genes (Basel). 2020 Oct 30;11(11):1291. doi: 10.3390/genes11111291. Genes (Basel). 2020. PMID: 33142960 Free PMC article.

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