Lalouel JM - Search Results

1

Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript.

Dunn DM, Ishigami T, Pankow J, von Niederhausern A, Alder J, Hunt SC, Leppert MF, Lalouel JM, Weiss RB. Dunn DM, et al. Among authors: lalouel jm. J Hum Genet. 2002;47(12):665-76. doi: 10.1007/s100380200102. J Hum Genet. 2002. PMID: 12522688

2

Further evidence of a quantitative trait locus on chromosome 18 influencing postural change in systolic blood pressure: the Hypertension Genetic Epidemiology Network (HyperGEN) Study.

Pankow JS, Dunn DM, Hunt SC, Leppert MF, Miller MB, Rao DC, Heiss G, Oberman A, Lalouel JM, Weiss RB. Pankow JS, et al. Among authors: lalouel jm. Am J Hypertens. 2005 May;18(5 Pt 1):672-8. doi: 10.1016/j.amjhyper.2004.12.004. Am J Hypertens. 2005. PMID: 15882550

3

From genetics to mechanism of disease liability.

Rohrwasser A, Lott P, Weiss RB, Lalouel JM. Rohrwasser A, et al. Among authors: lalouel jm. Adv Genet. 2008;60:701-26. doi: 10.1016/S0065-2660(07)00424-5. Adv Genet. 2008. PMID: 18358337 Review.

4

A human polymorphism affects NEDD4L subcellular targeting by leading to two isoforms that contain or lack a C2 domain.

Garrone NF, Blazer-Yost BL, Weiss RB, Lalouel JM, Rohrwasser A. Garrone NF, et al. Among authors: lalouel jm. BMC Cell Biol. 2009 Apr 13;10:26. doi: 10.1186/1471-2121-10-26. BMC Cell Biol. 2009. PMID: 19364400 Free PMC article.

5

From linkage maps to quantitative trait loci: the history and science of the Utah genetic reference project.

Prescott SM, Lalouel JM, Leppert M. Prescott SM, et al. Among authors: lalouel jm. Annu Rev Genomics Hum Genet. 2008;9:347-58. doi: 10.1146/annurev.genom.9.081307.164441. Annu Rev Genomics Hum Genet. 2008. PMID: 18544033 Review.

6

Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).

Chance PF, Bird TD, O'Connell P, Lipe H, Lalouel JM, Leppert M. Chance PF, et al. Among authors: lalouel jm. Am J Hum Genet. 1990 Dec;47(6):915-25. Am J Hum Genet. 1990. PMID: 2239969 Free PMC article.

7

Evidence for single gene contributions to hypertension and lipid disturbances: definition, genetics, and clinical significance.

Williams RR, Hunt SC, Hopkins PN, Wu LL, Lalouel JM. Williams RR, et al. Among authors: lalouel jm. Clin Genet. 1994 Jul;46(1 Spec No):80-7. doi: 10.1111/j.1399-0004.1994.tb04207.x. Clin Genet. 1994. PMID: 7988084 Review.

8

Lack of linkage between the endothelial nitric oxide synthase gene and hypertension.

Hunt SC, Williams CS, Sharma AM, Inoue I, Williams RR, Lalouel JM. Hunt SC, et al. Among authors: lalouel jm. J Hum Hypertens. 1996 Jan;10(1):27-30. J Hum Hypertens. 1996. PMID: 8642187

9

Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension.

Jeunemaitre X, Lifton RP, Hunt SC, Williams RR, Lalouel JM. Jeunemaitre X, et al. Among authors: lalouel jm. Nat Genet. 1992 Apr;1(1):72-5. doi: 10.1038/ng0492-72. Nat Genet. 1992. PMID: 1338766

10

Transcriptional diversity and expression of NEDD4L gene in distal nephron.

Umemura M, Ishigami T, Tamura K, Sakai M, Miyagi Y, Nagahama K, Aoki I, Uchino K, Rohrwasser A, Lalouel JM, Umemura S. Umemura M, et al. Among authors: lalouel jm. Biochem Biophys Res Commun. 2006 Jan 27;339(4):1129-37. doi: 10.1016/j.bbrc.2005.11.120. Epub 2005 Dec 5. Biochem Biophys Res Commun. 2006. PMID: 16338225

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