Jennings LJ - Search Results

1

Comparison of PHOX2B testing methods in the diagnosis of congenital central hypoventilation syndrome and mosaic carriers.

Jennings LJ, Yu M, Zhou L, Rand CM, Berry-Kravis EM, Weese-Mayer DE. Jennings LJ, et al. Diagn Mol Pathol. 2010 Dec;19(4):224-31. doi: 10.1097/PDM.0b013e3181eb92ff. Diagn Mol Pathol. 2010. PMID: 21051998

2

Congenital central hypoventilation syndrome from past to future: model for translational and transitional autonomic medicine.

Weese-Mayer DE, Rand CM, Berry-Kravis EM, Jennings LJ, Loghmanee DA, Patwari PP, Ceccherini I. Weese-Mayer DE, et al. Among authors: jennings lj. Pediatr Pulmonol. 2009 Jun;44(6):521-35. doi: 10.1002/ppul.21045. Pediatr Pulmonol. 2009. PMID: 19422034 Review.

3

A novel HLA-A*03 allele, HLA-A*03:71.

Yu M, Hall JE, Hartman K, Czech J, Jennings L. Yu M, et al. Tissue Antigens. 2010 Oct;76(4):331. doi: 10.1111/j.1399-0039.2010.01532.x. Tissue Antigens. 2010. PMID: 20630036

4

Validation of multiplex ligation-dependent probe amplification for confirmation of array comparative genomic hybridization.

Jennings LJ, Yu M, Fitzpatrick C, Smith FA. Jennings LJ, et al. Diagn Mol Pathol. 2011 Sep;20(3):166-74. doi: 10.1097/PDM.0b013e31820b2517. Diagn Mol Pathol. 2011. PMID: 21817904

5

Variable human phenotype associated with novel deletions of the PHOX2B gene.

Jennings LJ, Yu M, Rand CM, Kravis N, Berry-Kravis EM, Patwari PP, Weese-Mayer DE. Jennings LJ, et al. Pediatr Pulmonol. 2012 Feb;47(2):153-61. doi: 10.1002/ppul.21527. Epub 2011 Aug 9. Pediatr Pulmonol. 2012. PMID: 21830319

6

A novel HLA-A*30 allele, HLA-A*30:36.

Jennings L, Hall JE, Caparelli E, Silva M, Yu M. Jennings L, et al. Tissue Antigens. 2012 Feb;79(2):132-4. doi: 10.1111/j.1399-0039.2011.01782.x. Epub 2011 Oct 31. Tissue Antigens. 2012. PMID: 22035629

7

Pilot study of the association of the DDAH2 -449G polymorphism with asymmetric dimethylarginine and hemodynamic shock in pediatric sepsis.

Weiss SL, Yu M, Jennings L, Haymond S, Zhang G, Wainwright MS. Weiss SL, et al. PLoS One. 2012;7(3):e33355. doi: 10.1371/journal.pone.0033355. Epub 2012 Mar 12. PLoS One. 2012. PMID: 22428028 Free PMC article.

8

Developmental alterations of the respiratory human retrotrapezoid nucleus in sudden unexplained fetal and infant death.

Lavezzi AM, Weese-Mayer DE, Yu MY, Jennings LJ, Corna MF, Casale V, Oneda R, Matturri L. Lavezzi AM, et al. Among authors: jennings lj. Auton Neurosci. 2012 Sep 25;170(1-2):12-9. doi: 10.1016/j.autneu.2012.06.005. Epub 2012 Jul 15. Auton Neurosci. 2012. PMID: 22796552

9

Germline mosaicism of PHOX2B mutation accounts for familial recurrence of congenital central hypoventilation syndrome (CCHS).

Rand CM, Yu M, Jennings LJ, Panesar K, Berry-Kravis EM, Zhou L, Weese-Mayer DE. Rand CM, et al. Among authors: jennings lj. Am J Med Genet A. 2012 Sep;158A(9):2297-301. doi: 10.1002/ajmg.a.35499. Epub 2012 Jul 20. Am J Med Genet A. 2012. PMID: 22821709

10

Detection and quantification of chimerism by droplet digital PCR.

George D, Czech J, John B, Yu M, Jennings LJ. George D, et al. Among authors: jennings lj. Chimerism. 2013 Jul-Sep;4(3):102-8. doi: 10.4161/chim.25400. Epub 2013 Jun 20. Chimerism. 2013. PMID: 23974275 Free PMC article.

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