G. Landes

发表

Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH).

K. Klinger, G. Landes, D. Shook, 1992, American journal of human genetics.

G. Landes, A. Lash, K. Kinzler, 1999, Nature Genetics.

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

G. Landes, A. Moss, P. Schwartz, 1996, Nature Genetics.

Combining serial analysis of gene expression and array technologies to identify genes differentially expressed in breast cancer.

G. Landes, S. Sukumar, W. Zhang, 1999, Cancer research.

Tuberin-dependent membrane localization of polycystin-1: a functional link between polycystic kidney disease and the TSC2 tumor suppressor gene.

G. Landes, O. Ibraghimov-Beskrovnaya, C. Walker, 2001, Molecular cell.

A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region.

G. Landes, J. Carpten, D. Stephan, 2000, Genomics.

The NTN2L gene encoding a novel human netrin maps to the autosomal dominant polycystic kidney disease region on chromosome 16p13.3.

K. Klinger, G. Landes, T. Burn, 1997, Genomics.

Isolation and Characterization of Human Casein Kinase Iε (CKI), a Novel Member of the CKI Gene Family (*)

G. Landes, D. Virshup, A. Cegielska, 1995, The Journal of Biological Chemistry.

Isolation and characterization of human casein kinase I epsilon (CKI), a novel member of the CKI gene family.

G. Landes, D. Virshup, A. Cegielska, 1995, The Journal of biological chemistry.

Molecular analysis of human Chromosome 16 cosmid clones containing NotI sites

K. Klinger, G. Landes, D. Shook, 2004, Mammalian Genome.

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

A. Feinberg, G. Landes, M. Adams, 1999, Human molecular genetics.

Evidence for more than one mechanism of action of the glucocorticoid hormones.

G. Landes, B. Keller, P. Kitos, 1982, Biochimica et biophysica acta.

Isolation of polyadenylic acid-containing RNA using Ca(II).

G. Landes, P. Kitos, 1975, Biochemical and biophysical research communications.

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

K. Klinger, G. Landes, T. Houseal, 1993, American journal of human genetics.

The cloning of a human ABC gene (ABC3) mapping to chromosome 16p13.3.

K. Klinger, G. Landes, T. Burn, 1997, Genomics.

Increased exon-trapping efficiency through modifications to the pSPL3 splicing vector.

K. Klinger, G. Landes, T. Burn, 1995, Gene.

Generation of a transcriptional map for a 700-kb region surrounding the polycystic kidney disease type 1 (PKD1) and tuberous sclerosis type 2 (TSC2) disease genes on human chromosome 16p3.3.

K. Klinger, G. Landes, J. Millholland, 1996, Genome research.

A PCR-based linkage map of human chromosome 1.

J. Weber, L. Peltonen, T. Hudson, 1993, Genomics.

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

T. Matise, G. Landes, J. Vance, 1994, Cytogenetics and Cell Genetics.

Hemoglobin switching in chickens. Is the switch initiated post-transcriptionally?

G. Landes, H. Martinson, T. Pribyl, 1982, The Journal of biological chemistry.

Isolation of polymorphic DNA segments from human chromosome 21.

G. Landes, R. Eddy, R. Tanzi, 1985, Nucleic acids research.

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.

A. Feinberg, G. Landes, L. Johnson, 1997, Genomics.

A novel ribosomal protein L3-like gene (RPL3L) maps to the autosomal dominant polycystic kidney disease gene region.

K. Klinger, G. Landes, T. Burn, 1996, Genomics.

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

K. Klinger, G. Landes, M. L. Le Beau, 1992, Human molecular genetics.

Polycystin: in vitro synthesis, in vivo tissue expression, and subcellular localization identifies a large membrane-associated protein.

K. Klinger, G. Landes, O. Ibraghimov-Beskrovnaya, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Report of the first international workshop on human chomosome 1 mapping 1994

T. Matise, G. Landes, J. Vance, 1994 .

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).

G. Landes, N. Doggett, J. Millholland, 1995, Human molecular genetics.

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

K. Klinger, G. Landes, J. Carpten, 2001, Genomics.

Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1.

K. Klinger, G. Landes, O. Ibraghimov-Beskrovnaya, 2000, Human molecular genetics.

A 2.5 kb polypyrimidine tract in the PKD1 gene contains at least 23 H-DNA-forming sequences.

K. Klinger, G. Landes, G. Germino, 1996, Microbial & comparative genomics.

High resolution mapping of overlapping cosmids by fluorescence in situ hybridization.

K. Klinger, G. Landes, T. Houseal, 1994, Cytometry.

The chicken beta globin gene region. Delineation of transcription units and developmental regulation of interspersed DNA repeats.

G. Landes, M. Pankratz, H. Martinson, 1982, The Journal of biological chemistry.

Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cells.

K. Klinger, G. Landes, D. Ward, 1992, Human molecular genetics.

A modified two-step phage display selection for isolation of polycystin-1 ligands

K. Klinger, G. Landes, O. Ibraghimov-Beskrovnaya, 2000, Functional & Integrative Genomics.

Transcriptional properties of chick embryonic erythroid nuclei in vitro.

G. Landes, H. Martinson, 1982, The Journal of biological chemistry.

New insights into ADPKD molecular pathways using combination of SAGE and microarray technologies.

K. Klinger, G. Landes, O. Ibraghimov-Beskrovnaya, 2004, Genomics.

Beta-hydroxyaspartic acid in the first epidermal growth factor-like domain of protein C. Its role in Ca2+ binding and biological activity.

G. Landes, J. Stenflo, P. Bourdon, 1988, The Journal of biological chemistry.

Molecular cloning, characterization, and genomic localization of a human potassium channel gene.

G. Landes, M. Curran, M. Keating, 1992, Genomics.

Comparative genomic hybridization and its application to Wilms’ tumorigenesis

G. Landes, T. Houseal, J. Cowell, 1998, Cytogenetic and Genome Research.

Human ciliary neurotrophic factor: localization to the proximal region of the long arm of chromosome 11 and association with CA/GT dinucleotide repeat.

G. Landes, S. Hauser, D. Rosen, 1993, Genomics.

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

K. Klinger, G. Landes, G. Germino, 1998, Molecular cell.

The region surrounding the PKD1 gene: a 700-kb P1 contig from a YAC-deficient interval.

K. Klinger, G. Landes, D. Housman, 1996, Genome research.