Lee B - Search Results

1

Mutation analysis of LMX1B gene in nail-patella syndrome patients.

McIntosh I, Dreyer SD, Clough MV, Dunston JA, Eyaid W, Roig CM, Montgomery T, Ala-Mello S, Kaitila I, Winterpacht A, Zabel B, Frydman M, Cole WG, Francomano CA, Lee B. McIntosh I, et al. Among authors: lee b. Am J Hum Genet. 1998 Dec;63(6):1651-8. doi: 10.1086/302165. Am J Hum Genet. 1998. PMID: 9837817 Free PMC article.

2

The centromeric/nucleolar chromatin protein ZFP-37 may function to specify neuronal nuclear domains.

Payen E, Verkerk T, Michalovich D, Dreyer SD, Winterpacht A, Lee B, De Zeeuw CI, Grosveld F, Galjart N. Payen E, et al. Among authors: lee b. J Biol Chem. 1998 Apr 10;273(15):9099-109. doi: 10.1074/jbc.273.15.9099. J Biol Chem. 1998. PMID: 9535899 Free article.

3

Cloning, characterization, and chromosomal assignment of the human ortholog of murine Zfp-37, a candidate gene for Nager syndrome.

Dreyer SD, Zhou L, Machado MA, Horton WA, Zabel B, Winterpacht A, Lee B. Dreyer SD, et al. Among authors: lee b. Mamm Genome. 1998 Jun;9(6):458-62. doi: 10.1007/s003359900796. Mamm Genome. 1998. PMID: 9585434

4

Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome.

Dreyer SD, Zhou G, Baldini A, Winterpacht A, Zabel B, Cole W, Johnson RL, Lee B. Dreyer SD, et al. Among authors: lee b. Nat Genet. 1998 May;19(1):47-50. doi: 10.1038/ng0598-47. Nat Genet. 1998. PMID: 9590287

5

Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome.

Chen H, Lun Y, Ovchinnikov D, Kokubo H, Oberg KC, Pepicelli CV, Gan L, Lee B, Johnson RL. Chen H, et al. Among authors: lee b. Nat Genet. 1998 May;19(1):51-5. doi: 10.1038/ng0598-51. Nat Genet. 1998. PMID: 9590288

6

The long and the short of it: developmental genetics of the skeletal dysplasias.

Dreyer SD, Zhou G, Lee B. Dreyer SD, et al. Among authors: lee b. Clin Genet. 1998 Dec;54(6):464-73. doi: 10.1111/j.1399-0004.1998.tb03766.x. Clin Genet. 1998. PMID: 9894792 Review.

7

Identification of LMX1B gene point mutations in italian patients affected with Nail-Patella syndrome.

Seri M, Melchionda S, Dreyer S, Marini M, Carella M, Cusano R, Piemontese MR, Caroli F, Silengo M, Zelante L, Romeo G, Ravazzolo R, Gasparini P, Lee B. Seri M, et al. Among authors: lee b. Int J Mol Med. 1999 Sep;4(3):285-90. doi: 10.3892/ijmm.4.3.285. Int J Mol Med. 1999. PMID: 10425280

8

CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia.

Zhou G, Chen Y, Zhou L, Thirunavukkarasu K, Hecht J, Chitayat D, Gelb BD, Pirinen S, Berry SA, Greenberg CR, Karsenty G, Lee B. Zhou G, et al. Among authors: lee b. Hum Mol Genet. 1999 Nov;8(12):2311-6. doi: 10.1093/hmg/8.12.2311. Hum Mol Genet. 1999. PMID: 10545612

9

Isolation, characterization, and mapping of a zinc finger gene, ZFP95, containing both a SCAN box and an alternatively spliced KRAB A domain.

Dreyer SD, Zheng Q, Zabel B, Winterpacht A, Lee B. Dreyer SD, et al. Among authors: lee b. Genomics. 1999 Nov 15;62(1):119-22. doi: 10.1006/geno.1999.5981. Genomics. 1999. PMID: 10585779

10

LMX1B transactivation and expression in nail-patella syndrome.

Dreyer SD, Morello R, German MS, Zabel B, Winterpacht A, Lunstrum GP, Horton WA, Oberg KC, Lee B. Dreyer SD, et al. Among authors: lee b. Hum Mol Genet. 2000 Apr 12;9(7):1067-74. doi: 10.1093/hmg/9.7.1067. Hum Mol Genet. 2000. PMID: 10767331

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