Landes GM - Search Results

1

Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting.

Lee MP, Brandenburg S, Landes GM, Adams M, Miller G, Feinberg AP. Lee MP, et al. Among authors: landes gm. Hum Mol Genet. 1999 Apr;8(4):683-90. doi: 10.1093/hmg/8.4.683. Hum Mol Genet. 1999. PMID: 10072438

2

A 2.5-Mb transcript map of a tumor-suppressing subchromosomal transferable fragment from 11p15.5, and isolation and sequence analysis of three novel genes.

Hu RJ, Lee MP, Connors TD, Johnson LA, Burn TC, Su K, Landes GM, Feinberg AP. Hu RJ, et al. Among authors: landes gm. Genomics. 1997 Nov 15;46(1):9-17. doi: 10.1006/geno.1997.4981. Genomics. 1997. PMID: 9403053 Free article.

3

Analysis of the genomic sequence for the autosomal dominant polycystic kidney disease (PKD1) gene predicts the presence of a leucine-rich repeat. The American PKD1 Consortium (APKD1 Consortium).

Burn TC, Connors TD, Dackowski WR, Petry LR, Van Raay TJ, Millholland JM, Venet M, Miller G, Hakim RM, Landes GM, et al. Burn TC, et al. Among authors: landes gm. Hum Mol Genet. 1995 Apr;4(4):575-82. doi: 10.1093/hmg/4.4.575. Hum Mol Genet. 1995. PMID: 7633406

4

Comparative genomic hybridization and its application to Wilms' tumorigenesis.

Getman ME, Houseal TW, Miller GA, Grundy PE, Cowell JK, Landes GM. Getman ME, et al. Among authors: landes gm. Cytogenet Cell Genet. 1998;82(3-4):284-90. doi: 10.1159/000015120. Cytogenet Cell Genet. 1998. PMID: 9858837

5

Somatic mutation in individual liver cysts supports a two-hit model of cystogenesis in autosomal dominant polycystic kidney disease.

Watnick TJ, Torres VE, Gandolph MA, Qian F, Onuchic LF, Klinger KW, Landes G, Germino GG. Watnick TJ, et al. Mol Cell. 1998 Aug;2(2):247-51. doi: 10.1016/s1097-2765(00)80135-5. Mol Cell. 1998. PMID: 9734362 Free article.

6

Report and abstracts of the First International Workshop on Human Chromosome 1 Mapping 1994. Bethesda, Maryland, March 25-27, 1994.

Dracopoli NC, Bruns GA, Brodeur GM, Landes GM, Matise TC, Seldin MF, Vance JM, Weith A. Dracopoli NC, et al. Among authors: landes gm. Cytogenet Cell Genet. 1994;67(3):144-65. Cytogenet Cell Genet. 1994. PMID: 8062592 No abstract available.

7

Probe D16S273 detects a PstI RFLP with 8 alleles.

Lerner T, Wright G, Landes G. Lerner T, et al. Hum Mol Genet. 1992 May;1(2):142. doi: 10.1093/hmg/1.2.142. Hum Mol Genet. 1992. PMID: 1363781 No abstract available.

8

Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1.

Dixon MJ, Dixon J, Houseal T, Bhatt M, Ward DC, Klinger K, Landes GM. Dixon MJ, et al. Among authors: landes gm. Am J Hum Genet. 1993 May;52(5):907-14. Am J Hum Genet. 1993. PMID: 8488840 Free PMC article.

9

Cloning and characterization of 13 novel transcripts and the human RGS8 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locus.

Sood R, Bonner TI, Makalowska I, Stephan DA, Robbins CM, Connors TD, Morgenbesser SD, Su K, Faruque MU, Pinkett H, Graham C, Baxevanis AD, Klinger KW, Landes GM, Trent JM, Carpten JD. Sood R, et al. Among authors: landes gm. Genomics. 2001 Apr 15;73(2):211-22. doi: 10.1006/geno.2001.6500. Genomics. 2001. PMID: 11318611

10

Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2.

Dixon MJ, Dixon J, Raskova D, Le Beau MM, Williamson R, Klinger K, Landes GM. Dixon MJ, et al. Among authors: landes gm. Hum Mol Genet. 1992 Jul;1(4):249-53. doi: 10.1093/hmg/1.4.249. Hum Mol Genet. 1992. PMID: 1303194

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