Trusgnich MA - Search Results

1

Developmental and genetic regulation of human surfactant protein B in vivo.

Hamvas A, Heins HB, Guttentag SH, Wegner DJ, Trusgnich MA, Bennet KW, Yang P, Carlson CS, An P, Cole FS. Hamvas A, et al. Among authors: trusgnich ma. Neonatology. 2009;95(2):117-24. doi: 10.1159/000153095. Epub 2008 Sep 6. Neonatology. 2009. PMID: 18776725 Free PMC article.

2

Genetic variant characterization in intron 4 of the surfactant protein B gene.

Hamvas A, Wegner DJ, Trusgnich MA, Madden K, Heins H, Liu Y, Rice T, An P, Watkins-Torry J, Cole FS. Hamvas A, et al. Among authors: trusgnich ma. Hum Mutat. 2005 Nov;26(5):494-5. doi: 10.1002/humu.9378. Hum Mutat. 2005. PMID: 16211553

3

Comprehensive genetic variant discovery in the surfactant protein B gene.

Hamvas A, Wegner DJ, Carlson CS, Bergmann KR, Trusgnich MA, Fulton L, Kasai Y, An P, Mardis ER, Wilson RK, Cole FS. Hamvas A, et al. Among authors: trusgnich ma. Pediatr Res. 2007 Aug;62(2):170-5. doi: 10.1203/PDR.0b013e3180a03232. Pediatr Res. 2007. PMID: 17597650 Free PMC article.

4

Recombination as a mechanism for sporadic mutation in the surfactant protein-C gene.

McBee AD, Wegner DJ, Carlson CS, Wambach JA, Yang P, Heins HB, Saugstad OD, Trusgnich MA, Watkins-Torry J, Nogee LM, Henderson H, Cole FS, Hamvas A. McBee AD, et al. Among authors: trusgnich ma. Pediatr Pulmonol. 2008 May;43(5):443-50. doi: 10.1002/ppul.20782. Pediatr Pulmonol. 2008. PMID: 18383112 Free PMC article.

5

Informed consent for genetic research.

Hamvas A, Madden KK, Nogee LM, Trusgnich MA, Wegner DJ, Heins HB, Cole FS. Hamvas A, et al. Among authors: trusgnich ma. Arch Pediatr Adolesc Med. 2004 Jun;158(6):551-5. doi: 10.1001/archpedi.158.6.551. Arch Pediatr Adolesc Med. 2004. PMID: 15184218

6

Population-based estimates of surfactant protein B deficiency.

Cole FS, Hamvas A, Rubinstein P, King E, Trusgnich M, Nogee LM, deMello DE, Colten HR. Cole FS, et al. Pediatrics. 2000 Mar;105(3 Pt 1):538-41. doi: 10.1542/peds.105.3.538. Pediatrics. 2000. PMID: 10699106

7

Population-based screening for rare mutations: high-throughput DNA extraction and molecular amplification from Guthrie cards.

Hamvas A, Trusgnich M, Brice H, Baumgartner J, Hong Y, Nogee LM, Cole FS. Hamvas A, et al. Pediatr Res. 2001 Nov;50(5):666-8. doi: 10.1203/00006450-200111000-00021. Pediatr Res. 2001. PMID: 11641464

8

Mother's genome or maternally-inherited genes acting in the fetus influence gestational age in familial preterm birth.

Plunkett J, Feitosa MF, Trusgnich M, Wangler MF, Palomar L, Kistka ZA, DeFranco EA, Shen TT, Stormo AE, Puttonen H, Hallman M, Haataja R, Luukkonen A, Fellman V, Peltonen L, Palotie A, Daw EW, An P, Teramo K, Borecki I, Muglia LJ. Plunkett J, et al. Hum Hered. 2009;68(3):209-19. doi: 10.1159/000224641. Epub 2009 Jun 11. Hum Hered. 2009. PMID: 19521103 Free PMC article.

9

Characterization of four human YAC libraries for clone size, chimerism and X chromosome sequence representation.

Nagaraja R, Kere J, MacMillan S, Masisi MJ, Johnson D, Molini BJ, Halley GR, Wein K, Trusgnich M, Eble B, et al. Nagaraja R, et al. Nucleic Acids Res. 1994 Aug 25;22(16):3406-11. doi: 10.1093/nar/22.16.3406. Nucleic Acids Res. 1994. PMID: 8078777 Free PMC article.

10

YAC/STS map of 15Mb of Xp21.3-p11.3, at 100kb resolution, with refined comparisons of genetic distances and DMD structure.

Nagaraja R, Jermak C, Trusgnich M, Yoon J, MacMillan S, McCauley MB, Brownstein B, Schlessinger D. Nagaraja R, et al. Gene. 1998 Jul 30;215(2):259-67. doi: 10.1016/s0378-1119(98)00293-5. Gene. 1998. PMID: 9714824

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