Renbaum P - Search Results

1

(TA)n UGT 1A1 promoter polymorphism: a crucial factor in the pathophysiology of jaundice in G-6-PD deficient neonates.

Kaplan M, Renbaum P, Vreman HJ, Wong RJ, Levy-Lahad E, Hammerman C, Stevenson DK. Kaplan M, et al. Among authors: renbaum p. Pediatr Res. 2007 Jun;61(6):727-31. doi: 10.1203/pdr.0b013e31805365c5. Pediatr Res. 2007. PMID: 17426648

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. Among authors: renbaum p. 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

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. Among authors: renbaum p. Reprod Biomed Online. 2007 Jul;15(1):83-8. doi: 10.1016/s1472-6483(10)60696-7. Reprod Biomed Online. 2007. PMID: 17623543

5

(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. Among authors: renbaum p. Pediatr Res. 2008 Jan;63(1):109-11. doi: 10.1203/PDR.0b013e31815b8e7e. Pediatr Res. 2008. PMID: 18043502

6

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. Among authors: renbaum p. Prenat Diagn. 2008 Oct;28(10):929-33. doi: 10.1002/pd.2070. Prenat Diagn. 2008. PMID: 18792920

7

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. Among authors: renbaum p. Gene. 2009 Oct 15;446(2):81-9. doi: 10.1016/j.gene.2009.06.015. Epub 2009 Jun 30. Gene. 2009. PMID: 19573580

8

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.

9

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. Among authors: renbaum p. Hum Reprod. 2009 Dec;24(12):3225-9. doi: 10.1093/humrep/dep293. Epub 2009 Aug 17. Hum Reprod. 2009. PMID: 19687056

10

Preimplantation genetic diagnosis (PGD) for nonsyndromic deafness by polar body and blastomere biopsy.

Altarescu G, Eldar-Geva T, Brooks B, Zylber-Haran E, Varshaver I, Margalioth EJ, Levy-Lahad E, Renbaum P. Altarescu G, et al. Among authors: renbaum p. J Assist Reprod Genet. 2009 Jul;26(7):391-7. doi: 10.1007/s10815-009-9335-5. J Assist Reprod Genet. 2009. PMID: 19728075 Free PMC article.

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