W. Dackowski

发表

The gene for protein S maps near the centromere of human chromosome 3.

R. Eddy, T. Shows, Y. Fukushima, 1988 .

Canine PKD1 is a single-copy gene: genomic organization and comparative analysis.

K. Klinger, O. Ibraghimov-Beskrovnaya, P. Manavalan, 2002, Genomics.

Somatically generated mouse myeloma variants synthesizing IgA half- molecules

D. Zack, S. Morrison, M. Scharff, 1981, The Journal of experimental medicine.

Molecular analysis of human Chromosome 16 cosmid clones containing NotI sites

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

The gene for protein S maps near the centromere of human chromosome 3.

E. H. Cohen, R. Eddy, T. Shows, 1988, Blood.

Chromosomal localization of glutamate receptor genes: relationship to familial amyotrophic lateral sclerosis and other neurological disorders of mice and humans.

J. Haines, G. Uhl, E. Jabs, 1993, Proceedings of the National Academy of Sciences of the United States of America.

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.

Expression of completely γ‐carboxylated and β‐hydroxylated recombinant human vitamin‐K‐dependent protein S with full biological activity

B. Dahlbäck, J. Malm, E. Cohen, 1990 .

Identification of a putative isoform of the Na,K-ATPase beta subunit. Primary structure and tissue-specific expression.

J. Emanuel, R. Levenson, P. Martín-Vasallo, 1989, The Journal of biological chemistry.

Inhibition of glucosylceramide accumulation results in effective blockade of polycystic kidney disease in mouse models

Laurie A. Smith, O. Ibraghimov-Beskrovnaya, B. Wang, 2010, Nature Medicine.

Expression of active human uterine tissue plasminogen activator in yeast.

J. Lemontt, C. Wei, W. Dackowski, 1985, DNA.

Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimens.

K. Klinger, B. Ward, K W Klinger, 1993, American journal of human 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.

Pkd1 and Nek8 mutations affect cell-cell adhesion and cilia in cysts formed in kidney organ cultures.

Laurie A. Smith, O. Ibraghimov-Beskrovnaya, H. Husson, 2008, American journal of physiology. Renal physiology.

Isolation and sequence of the cDNA for human protein S, a regulator of blood coagulation.

B. Dahlbäck, E. Cohen, J. Stenflo, 1986, Proceedings of the National Academy of Sciences of the United States of America.

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.

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.

Two alpha heavy chain disease proteins with different genomic deletions demonstrate that nonexpressed alpha heavy chain genes contain methylated bases.

S. Morrison, W. Dackowski, 1981, Proceedings of the National Academy of Sciences of the United States of America.

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

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

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.

Functional polycystin-1 expression is developmentally regulated during epithelial morphogenesis in vitro: downregulation and loss of membrane localization during cystogenesis.

K. Klinger, O. Ibraghimov-Beskrovnaya, H. Husson, 2002, Human molecular genetics.

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.

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.