Rearrangement of the HumanCDC5LGene by a t(6;19)(p21;q13.1) in a Patient with Multicystic Renal Dysplasia

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1970 • 253,849 citations

Basic local alignment search tool

1990 • 87,358 citations

DNA sequencing with chain-terminating inhibitors

1977 • 69,181 citations

Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector.

1992 • 1,651 citations

The evolutionary dynamics of repetitive DNA in eukaryotes

1994 • 1,584 citations

Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumours

1995 • 575 citations

Solution structure of a specific DNA complex of the Myb DNA-binding domain with cooperative recognition helices

1994 • 484 citations

Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction.

1990 • 454 citations

Censor—a program for identification and elimination of repetitive elements from DNA sequences

1996 • 411 citations

Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents.

1990 • 408 citations

Continuum of overlapping clones spanning the entire human chromosome 21q

1992 • 393 citations

One billion years of Myb.

1996 • 310 citations

The cavity in the hydrophobic core of Myb DNA-binding domain is reserved for DNA recognition and trans-activation

1996 • 285 citations

Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21–cen

1994 • 256 citations

Isolation of human cDNA clones ofmyb-related genes, A-myband B-myb

1988 • 222 citations

GAL4 fusion vectors for expression in yeast or mammalian cells

1992 • 213 citations

The molecular basis of embryonic kidney development

1997 • 191 citations

Familial Nature of Congenital Absence and Severe Dysgenesis of Both Kidneys

1984 • 183 citations

Human c-myb protooncogene: nucleotide sequence of cDNA and organization of the genomic locus.

1986 • 174 citations

Comparison of the free and DNA-complexed forms of the DMA-binding domain from c-Myb

1995 • 157 citations

Fetal Renal Defects: Associated Malformations and Chromosomal Defects

1992 • 107 citations

Glucose-dependent Liver Gene Expression in Upstream Stimulatory Factor 2 −/− Mice

1997 • 102 citations

MYB: An old oncoprotein with new roles

1995 • 97 citations

The Schizosaccharomyces pombe cdc5+ gene encodes an essential protein with homology to c-Myb.

1994 • 94 citations

A cdc5 ⁺ homolog of a higher plant, Arabidopsis thaliana

1996 • 79 citations

Fetal Uropathy

1990 • 76 citations

Physical Mapping of Chromosome 12q Breakpoints in Lipoma, Pleomorphic Salivary Gland Adenoma, Uterine Leiomyoma, and Myxoid Liposarcoma

1994 • 66 citations

Pombe Cdc5-related Protein

1997 • 56 citations

Evidence for genetic heterogeneity in hereditary hydronephrosis caused by pelvi-ureteric junction obstruction, with one locus assigned to chromosome 6p

1992 • 51 citations

Structure, Sequence, and Chromosome 19 Localization of HumanUSF2and Its Rearrangement in a Patient with Multicystic Renal Dysplasia

1996 • 39 citations

A 6-Mb Yeast Artificial Chromosome Contig and Long-Range Physical Map Encompassing the Region on Chromosome 12q15 Frequently Rearranged in a Variety of Benign Solid Tumors

1995 • 37 citations

Hereditary Renal Adysplasia: New Observations and Hypotheses

1994 • 35 citations

Cardiac Tachyarrhythmia in the Fetus: Diagnosis, Treatment and Prognosis

1987 • 30 citations

Structure of the B‐Myb DNA‐binding Domain in Solution and Evidence for Multiple Conformations in the Region of Repeat‐2 Involved in DNA Binding

1996 • 28 citations

Familial Urinary Tract Anomalies: Association with the Major Histocompatibility Complex in Man

1979 • 27 citations

HLA linkage with familial vesicoureteral reflux and familial pelvi‐ureteric junction obstruction

1989 • 25 citations

Familial urinary tract anomalies.

1970 • 22 citations

Increased Expression of Platelet-Derived Growth Factor A and Collagenous Matrix Proteins in Congenital Multicystic Renal Dysplasia

1997 • 13 citations

Isolation of cosmids corresponding to the chromosome breakpoints of a de novo autosomal translocation, t(6;19)(p21;q13.1), in a patient with multicystic renal dysplasia

1996 • 6 citations

Hereditary renal diseases

1993 • 5 citations

MCDK, UPJO, and VUR: A common genetic cause

1995 • 3 citations