Levy-Lahad E - Search Results

1

Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population.

Shaag A, Walsh T, Renbaum P, Kirchhoff T, Nafa K, Shiovitz S, Mandell JB, Welcsh P, Lee MK, Ellis N, Offit K, Levy-Lahad E, King MC. Shaag A, et al. Hum Mol Genet. 2005 Feb 15;14(4):555-63. doi: 10.1093/hmg/ddi052. Epub 2005 Jan 13. Hum Mol Genet. 2005. PMID: 15649950

2

Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism.

Kaplan M, Hammerman C, Rubaltelli FF, Vilei MT, Levy-Lahad E, Renbaum P, Vreman HJ, Stevenson DK, Muraca M. Kaplan M, et al. Hepatology. 2002 Apr;35(4):905-11. doi: 10.1053/jhep.2002.32526. Hepatology. 2002. PMID: 11915038

3

Egr-1 upregulates the Alzheimer's disease presenilin-2 gene in neuronal cells.

Renbaum P, Beeri R, Gabai E, Amiel M, Gal M, Ehrengruber MU, Levy-Lahad E. Renbaum P, et al. Gene. 2003 Oct 30;318:113-24. doi: 10.1016/s0378-1119(03)00766-2. Gene. 2003. PMID: 14585504

4

Familial clustering of site-specific cancer risks associated with BRCA1 and BRCA2 mutations in the Ashkenazi Jewish population.

Simchoni S, Friedman E, Kaufman B, Gershoni-Baruch R, Orr-Urtreger A, Kedar-Barnes I, Shiri-Sverdlov R, Dagan E, Tsabari S, Shohat M, Catane R, King MC, Lahad A, Levy-Lahad E. Simchoni S, et al. Proc Natl Acad Sci U S A. 2006 Mar 7;103(10):3770-4. doi: 10.1073/pnas.0511301103. Epub 2006 Feb 28. Proc Natl Acad Sci U S A. 2006. PMID: 16537453 Free PMC article.

5

Simultaneous preimplantation genetic diagnosis for Tay-Sachs and Gaucher disease.

Altarescu G, Brooks B, Margalioth E, Eldar Geva T, Levy-Lahad E, Renbaum P. Altarescu G, et al. Reprod Biomed Online. 2007 Jul;15(1):83-8. doi: 10.1016/s1472-6483(10)60696-7. Reprod Biomed Online. 2007. PMID: 17623543

6

(TA)n UDP-glucuronosyltransferase 1A1 promoter polymorphism in Nigerian neonates.

Kaplan M, Slusher T, Renbaum P, Essiet DF, Pam S, Levy-Lahad E, Hammerman C. Kaplan M, et al. Pediatr Res. 2008 Jan;63(1):109-11. doi: 10.1203/PDR.0b013e31815b8e7e. Pediatr Res. 2008. PMID: 18043502

7

PGD on a recombinant allele: crossover between the TSC2 gene and 'linked' markers impairs accurate diagnosis.

Altarescu G, Eldar Geva T, Brooks B, Margalioth E, Levy-Lahad E, Renbaum P. Altarescu G, et al. Prenat Diagn. 2008 Oct;28(10):929-33. doi: 10.1002/pd.2070. Prenat Diagn. 2008. PMID: 18792920

8

Transcriptional regulation of the murine Presenilin-2 gene reveals similarities and differences to its human orthologue.

Ounallah-Saad H, Beeri R, Goshen I, Yirmiya R, Renbaum P, Levy-Lahad E. Ounallah-Saad H, et al. Gene. 2009 Oct 15;446(2):81-9. doi: 10.1016/j.gene.2009.06.015. Epub 2009 Jun 30. Gene. 2009. PMID: 19573580

9

Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 gene.

Renbaum P, Kellerman E, Jaron R, Geiger D, Segel R, Lee M, King MC, Levy-Lahad E. Renbaum P, et al. Am J Hum Genet. 2009 Aug;85(2):281-9. doi: 10.1016/j.ajhg.2009.07.006. Epub 2009 Jul 30. Am J Hum Genet. 2009. PMID: 19646678 Free PMC article.

10

Real-time reverse linkage using polar body analysis for preimplantation genetic diagnosis in female carriers of de novo mutations.

Altarescu G, Eldar-Geva T, Varshower I, Brooks B, Haran EZ, Margalioth EJ, Levy-Lahad E, Renbaum P. Altarescu G, et al. Hum Reprod. 2009 Dec;24(12):3225-9. doi: 10.1093/humrep/dep293. Epub 2009 Aug 17. Hum Reprod. 2009. PMID: 19687056

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