Cloning of the T gene required in mesoderm formation in the mouse.

PubWeight™: 4.20‹?› | Rank: Top 1%

🔗 View Article (PMID 2154694)

Published in Nature on February 15, 1990

Authors

B G Herrmann1, S Labeit, A Poustka, T R King, H Lehrach

Author Affiliations

1: Laboratory of Molecular Embryology, National Institute for Medical Research, London, UK.

Articles citing this

(truncated to the top 100)

The polycomb-group gene Ezh2 is required for early mouse development. Mol Cell Biol (2001) 7.20

Hematopoietic commitment during embryonic stem cell differentiation in culture. Mol Cell Biol (1993) 6.33

Functional redundancy of GSK-3alpha and GSK-3beta in Wnt/beta-catenin signaling shown by using an allelic series of embryonic stem cell lines. Dev Cell (2007) 4.39

Severe global DNA hypomethylation blocks differentiation and induces histone hyperacetylation in embryonic stem cells. Mol Cell Biol (2004) 3.76

Development of the hemangioblast defines the onset of hematopoiesis in human ES cell differentiation cultures. Blood (2007) 3.71

T (Brachyury) is a direct target of Wnt3a during paraxial mesoderm specification. Genes Dev (1999) 3.13

Aberrant transcription caused by the insertion of an early transposable element in an intron of the Fas antigen gene of lpr mice. Proc Natl Acad Sci U S A (1993) 2.81

T-box genes in early embryogenesis. Dev Dyn (2004) 2.45

Structure and expression of mobile ETnII retroelements and their coding-competent MusD relatives in the mouse. J Virol (2003) 2.33

The delta-crystallin enhancer-binding protein delta EF1 is a repressor of E2-box-mediated gene activation. Mol Cell Biol (1994) 2.27

Forward and reverse genetic approaches to behavior in the mouse. Science (1994) 2.20

Evidence for involvement of activin A and bone morphogenetic protein 4 in mammalian mesoderm and hematopoietic development. Mol Cell Biol (1995) 2.12

Nanog binds to Smad1 and blocks bone morphogenetic protein-induced differentiation of embryonic stem cells. Proc Natl Acad Sci U S A (2006) 2.10

The T-box transcription factor Brachyury promotes epithelial-mesenchymal transition in human tumor cells. J Clin Invest (2010) 1.98

The Brachyury gene encodes a novel DNA binding protein. EMBO J (1993) 1.94

The T protein encoded by Brachyury is a tissue-specific transcription factor. EMBO J (1995) 1.89

FGF4, a direct target of LEF1 and Wnt signaling, can rescue the arrest of tooth organogenesis in Lef1(-/-) mice. Genes Dev (2002) 1.88

Two dominant mutations in the mouse fused gene are the result of transposon insertions. Genetics (1997) 1.76

WNT signaling, in synergy with T/TBX6, controls Notch signaling by regulating Dll1 expression in the presomitic mesoderm of mouse embryos. Genes Dev (2004) 1.74

The T-box family. Genome Biol (2002) 1.69

The Xenopus Brachyury promoter is activated by FGF and low concentrations of activin and suppressed by high concentrations of activin and by paired-type homeodomain proteins. Genes Dev (1997) 1.66

UTF1, a novel transcriptional coactivator expressed in pluripotent embryonic stem cells and extra-embryonic cells. EMBO J (1998) 1.65

Glutathione synthesis is essential for mouse development but not for cell growth in culture. Proc Natl Acad Sci U S A (2000) 1.54

eFGF regulates Xbra expression during Xenopus gastrulation. EMBO J (1994) 1.51

The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome. Am J Hum Genet (1999) 1.41

Novel ENU-Induced Mutation in Tbx6 Causes Dominant Spondylocostal Dysostosis-Like Vertebral Malformations in the Rat. PLoS One (2015) 1.40

A dominant negative mutation of the alpha retinoic acid receptor gene in a retinoic acid-nonresponsive embryonal carcinoma cell. Mol Cell Biol (1990) 1.37

Novel mouse type D endogenous proviruses and ETn elements share long terminal repeat and internal sequences. J Virol (2000) 1.36

Evolution of mouse T-box genes by tandem duplication and cluster dispersion. Genetics (1996) 1.35

Brachyury downstream notochord differentiation in the ascidian embryo. Genes Dev (1999) 1.32

A single morphogenetic field gives rise to two retina primordia under the influence of the prechordal plate. Development (1997) 1.32

The KH domain protein encoded by quaking functions as a dimer and is essential for notochord development in Xenopus embryos. Genes Dev (1997) 1.28

Brachyury-related transcription factor Tbx2 and repression of the melanocyte-specific TRP-1 promoter. Mol Cell Biol (1998) 1.28

Developmental control of segment numbers in vertebrates. J Exp Zool B Mol Dev Evol (2009) 1.28

Mesoderm-inducing factors in early vertebrate development. EMBO J (1993) 1.26

Influence of IL-8 on the epithelial-mesenchymal transition and the tumor microenvironment. Future Oncol (2012) 1.22

Diverse functional networks of Tbx3 in development and disease. Wiley Interdiscip Rev Syst Biol Med (2012) 1.21

RNA helicase A is essential for normal gastrulation. Proc Natl Acad Sci U S A (1998) 1.18

The mouse homeobox gene Not is required for caudal notochord development and affected by the truncate mutation. Genes Dev (2004) 1.17

The mouse lethal nonagouti (a(x)) mutation deletes the S-adenosylhomocysteine hydrolase (Ahcy) gene. EMBO J (1994) 1.17

Specification of germ cell fate in mice. Philos Trans R Soc Lond B Biol Sci (2003) 1.16

Selective disruption of genes transiently induced in differentiating mouse embryonic stem cells by using gene trap mutagenesis and site-specific recombination. Mol Cell Biol (1998) 1.15

Effects of thioredoxin reductase-1 deletion on embryogenesis and transcriptome. Free Radic Biol Med (2007) 1.13

Efficient high-resolution genetic mapping of mouse interspersed repetitive sequence PCR products, toward integrated genetic and physical mapping of the mouse genome. Proc Natl Acad Sci U S A (1995) 1.12

From notochord formation to hereditary chordoma: the many roles of Brachyury. Biomed Res Int (2013) 1.12

Loss of FGF-dependent mesoderm identity and rise of endogenous retinoid signalling determine cessation of body axis elongation. PLoS Biol (2012) 1.11

Specification of mesodermal pattern in Xenopus laevis by interactions between Brachyury, noggin and Xwnt-8. EMBO J (1994) 1.10

Transcription repression by Xenopus ET and its human ortholog TBX3, a gene involved in ulnar-mammary syndrome. Proc Natl Acad Sci U S A (1999) 1.09

Xwnt11 and the regulation of gastrulation in Xenopus. Philos Trans R Soc Lond B Biol Sci (2000) 1.08

Molecular cloning and analysis of the fragile X region in man. Nucleic Acids Res (1991) 1.08

Deletion mapping of the head tilt (het) gene in mice: a vestibular mutation causing specific absence of otoliths. Genetics (1998) 1.05

Identification of direct T-box target genes in the developing zebrafish mesoderm. Development (2009) 1.02

Characterization of NF-kappa B/I kappa B proteins in zebra fish and their involvement in notochord development. Mol Cell Biol (2004) 1.01

An autocrine loop between TGF-β1 and the transcription factor brachyury controls the transition of human carcinoma cells into a mesenchymal phenotype. Mol Cancer Ther (2013) 1.00

Isolation and characterization of two T-box genes from sponges, the phylogenetically oldest metazoan taxon. Dev Genes Evol (2003) 0.99

Immunological targeting of tumor cells undergoing an epithelial-mesenchymal transition via a recombinant brachyury-yeast vaccine. Oncotarget (2013) 0.98

The T-box factor MLS-1 acts as a molecular switch during specification of nonstriated muscle in C. elegans. Genes Dev (2002) 0.98

The T-box gene family: emerging roles in development, stem cells and cancer. Development (2014) 0.96

Transcriptomic and phenotypic analysis of murine embryonic stem cell derived BMP2+ lineage cells: an insight into mesodermal patterning. Genome Biol (2007) 0.96

Genomic targets of Brachyury (T) in differentiating mouse embryonic stem cells. PLoS One (2012) 0.96

Eya1 interacts with Six2 and Myc to regulate expansion of the nephron progenitor pool during nephrogenesis. Dev Cell (2014) 0.95

LMP4 regulates Tbx5 protein subcellular localization and activity. J Cell Biol (2006) 0.95

The T-box transcription factor Brachyury regulates epithelial-mesenchymal transition in association with cancer stem-like cells in adenoid cystic carcinoma cells. BMC Cancer (2012) 0.95

Overlapping deletions spanning the proximal two-thirds of the mouse t complex. Mamm Genome (2003) 0.94

Nuclear Brachyury Expression Is Consistent in Chordoma, Common in Germ Cell Tumors and Small Cell Carcinomas, and Rare in Other Carcinomas and Sarcomas: An Immunohistochemical Study of 5229 Cases. Am J Surg Pathol (2015) 0.93

The caenorhabditis elegans fate-determining gene mab-9 encodes a T-box protein required to pattern the posterior hindgut. Genes Dev (2000) 0.93

Genome-wide association identifies the T gene as a novel asthma pharmacogenetic locus. Am J Respir Crit Care Med (2012) 0.93

Activator-to-repressor conversion of T-box transcription factors by the Ripply family of Groucho/TLE-associated mediators. Mol Cell Biol (2008) 0.92

The retinoblastoma protein modulates Tbx2 functional specificity. Mol Biol Cell (2010) 0.92

Foxa1 and Foxa2 are required for formation of the intervertebral discs. PLoS One (2013) 0.92

Brachyury and SMAD signalling collaboratively orchestrate distinct mesoderm and endoderm gene regulatory networks in differentiating human embryonic stem cells. Development (2015) 0.91

Bridging the Gap: Understanding Embryonic Intervertebral Disc Development. Cell Dev Biol (2012) 0.91

The embryonic RNA helicase gene (ERH): a new member of the DEAD box family of RNA helicases. Biochem J (1995) 0.90

Concordia discors: duality in the origin of the vertebrate tail. J Anat (2003) 0.90

Current Bioengineering Methods for Whole Kidney Regeneration. Stem Cells Int (2015) 0.89

A ribozyme-mediated, gene "knockdown" strategy for the identification of gene function in zebrafish. Proc Natl Acad Sci U S A (1997) 0.89

Caudal regression in adrenocortical dysplasia (acd) mice is caused by telomere dysfunction with subsequent p53-dependent apoptosis. Dev Biol (2009) 0.89

Functional analysis of mutations of murine chromosome 17 with the use of tertiary trisomy. Genetics (1991) 0.87

Single cell lineage analysis of mouse embryonic stem cells at the exit from pluripotency. Biol Open (2013) 0.86

Direct selection of cDNAs using whole chromosomes. Nucleic Acids Res (1995) 0.86

Sequence at insertion site of E.Tn retrotransposon into an immunoglobulin switch region suggests a role for switch recombinase. Nucleic Acids Res (1991) 0.85

Identification and linkage mapping of Hst7, a new M. spretus/M. m. domesticus chromosome 17 hybrid sterility locus. Mamm Genome (1997) 0.84

Mutation watch: mouse brachyury (T), the T-box gene family, and human disease. Mamm Genome (1997) 0.84

Tbx2/3 is an essential mediator within the Brachyury gene network during Ciona notochord development. Development (2013) 0.84

An SP1-like transcription factor Spr2 acts downstream of Fgf signaling to mediate mesoderm induction. EMBO J (2003) 0.84

Inhibited gastrulation in mouse embryos overexpressing the leukemia inhibitory factor. Proc Natl Acad Sci U S A (1992) 0.83

Escape from genomic imprinting at the mouse T-associated maternal effect (Tme) locus. Genetics (1991) 0.83

A new spontaneous deletion on chromosome 17 including brachyury. Mamm Genome (1997) 0.82

Anteroposterior neural tissue specification by activin-induced mesoderm. Proc Natl Acad Sci U S A (1997) 0.82

Genome-wide association mapping and identification of candidate genes for the rumpless and ear-tufted traits of the Araucana chicken. PLoS One (2012) 0.82

Mixl1 localizes to putative axial stem cell reservoirs and their posterior descendants in the mouse embryo. Gene Expr Patterns (2014) 0.81

Activin A promotes hematopoietic fated mesoderm development through upregulation of brachyury in human embryonic stem cells. Stem Cells Dev (2012) 0.81

Expression, function and regulation of Brachyenteron in the short germband insect Tribolium castaneum. Dev Genes Evol (2008) 0.81

Notochordal cell-derived therapeutic strategies for discogenic back pain. Global Spine J (2013) 0.81

Nature and extent of left/right axis defects in T(Wis) /T(Wis) mutant mouse embryos. Dev Dyn (2014) 0.80

Knockdown of the T-box transcription factor Brachyury increases sensitivity of adenoid cystic carcinoma cells to chemotherapy and radiation in vitro: implications for a new therapeutic principle. Int J Oncol (2014) 0.80

Molecular specification of germ layers in vertebrate embryos. Cell Mol Life Sci (2015) 0.80

Tbx15 controls skeletal muscle fibre-type determination and muscle metabolism. Nat Commun (2015) 0.80

Sex-specific modifiers of tail development in mice heterozygous for the brachyury (T) mutation. Mamm Genome (1998) 0.80

Eleven densely clustered genes, six of them novel, in 176 kb of mouse t-complex DNA. Genome Res (2000) 0.79

Articles by these authors

Initial sequencing and analysis of the human genome. Nature (2001) 212.86

RNA molecular weight determinations by gel electrophoresis under denaturing conditions, a critical reexamination. Biochemistry (1977) 38.82

Lambda replacement vectors carrying polylinker sequences. J Mol Biol (1983) 32.76

The genome sequence of Schizosaccharomyces pombe. Nature (2002) 14.26

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice. Cell (1996) 12.59

A physical map of the human genome. Nature (2001) 12.39

The DNA sequence of human chromosome 21. Nature (2000) 10.66

Nucleotide sequence of cdna coding for Semliki Forest virus membrane glycoproteins. Nature (1980) 8.07

Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo. Cell (1997) 7.59

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions. Nat Genet (1998) 6.82

Rapid restriction mapping of DNA cloned in lambda phage vectors. Gene (1984) 6.25

An integrated and simplified approach to cloning into plasmids and single-stranded phages. Methods Enzymol (1983) 5.81

RNomics: an experimental approach that identifies 201 candidates for novel, small, non-messenger RNAs in mouse. EMBO J (2001) 5.70

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping. Nature (1990) 5.13

Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing. EMBO Rep (2000) 5.06

Normalization strategies for cDNA microarrays. Nucleic Acids Res (2000) 4.61

Self-assembly of polyglutamine-containing huntingtin fragments into amyloid-like fibrils: implications for Huntington's disease pathology. Proc Natl Acad Sci U S A (1999) 4.58

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene. Nat Genet (1996) 4.36

DNA sequence and comparative analysis of chimpanzee chromosome 22. Nature (2004) 4.12

Selective isolation of cosmid clones by homologous recombination in Escherichia coli. Proc Natl Acad Sci U S A (1984) 4.11

A subcloning strategy for DNA sequence analysis. Nucleic Acids Res (1980) 4.06

Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs. Genome Res (2001) 3.97

The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system. Circ Res (2001) 3.68

A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast. Nat Genet (1996) 3.67

Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium. Nature (2000) 3.61

High resolution cosmid and P1 maps spanning the 14 Mb genome of the fission yeast S. pombe. Cell (1993) 3.56

Accumulation of mutant huntingtin fragments in aggresome-like inclusion bodies as a result of insufficient protein degradation. Mol Biol Cell (2001) 3.41

Field gradients improve resolution on DNA sequencing gels. J Biochem Biophys Methods (1984) 3.37

Phosphorylation switches specific for the cardiac isoform of myosin binding protein-C: a modulator of cardiac contraction? EMBO J (1995) 3.28

Construction and characterization of a 2.5-kilobase procollagen clone. Proc Natl Acad Sci U S A (1978) 3.26

The capsid protein of Semliki Forest virus has clusters of basic amino acids and prolines in its amino-terminal region. Proc Natl Acad Sci U S A (1980) 3.26

Derivation of clones close to met by preparative field inversion gel electrophoresis. Science (1987) 3.21

Analysis of cosmids using linearization by phage lambda terminase. Gene (1985) 2.98

Yeast artificial chromosome libraries containing large inserts from mouse and human DNA. Proc Natl Acad Sci U S A (1991) 2.89

A large inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal t complex inversion. Cell (1987) 2.88

Membrane filter assay for detection of amyloid-like polyglutamine-containing protein aggregates. Methods Enzymol (1999) 2.65

Construction and use of human chromosome jumping libraries from NotI-digested DNA. Nature (1987) 2.58

Molecular clones of the mouse t complex derived from microdissected metaphase chromosomes. Cell (1984) 2.55

Changes in titin and collagen underlie diastolic stiffness diversity of cardiac muscle. J Mol Cell Cardiol (2000) 2.54

Sequence interpretation. Functional annotation of mouse genome sequences. Science (2001) 2.54

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy. Nat Genet (1995) 2.52

A complete BAC-based physical map of the Arabidopsis thaliana genome. Nat Genet (1999) 2.47

Genetic analysis of the proximal portion of the mouse t complex: evidence for a second inversion within t haplotypes. Cell (1986) 2.40

Series of exon-skipping events in the elastic spring region of titin as the structural basis for myofibrillar elastic diversity. Circ Res (2000) 2.39

Procollagen complementary DNA, a probe for messenger RNA purification and the number of type I collagen genes. Biochemistry (1978) 2.37

Dickkopf genes are co-ordinately expressed in mesodermal lineages. Mech Dev (1999) 2.36

Deletions in immunoglobulin mu chains. EMBO J (1982) 2.35

Primer design for large scale sequencing. Nucleic Acids Res (1998) 2.31

Geldanamycin activates a heat shock response and inhibits huntingtin aggregation in a cell culture model of Huntington's disease. Hum Mol Genet (2001) 2.29

Differential expression of cardiac titin isoforms and modulation of cellular stiffness. Circ Res (2000) 2.28

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy. Proc Natl Acad Sci U S A (1999) 2.27

Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy. Circ Res (1997) 2.25

Clustering of multiallele DNA markers near the Huntington's disease gene. J Clin Invest (1989) 2.25

Identification and classification of differentially expressed genes in renal cell carcinoma by expression profiling on a global human 31,500-element cDNA array. Genome Res (2001) 2.25

Huntington disease-linked locus D4S111 exposed as the alpha-L-iduronidase gene. Somat Cell Mol Genet (1991) 2.23

Establishment of a gene-trap sequence tag library to generate mutant mice from embryonic stem cells. Nat Genet (2000) 2.22

Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries. Proc Natl Acad Sci U S A (1991) 2.21

Genetic and cytogenetic localisation of the homeo box containing genes on mouse chromosome 6 and human chromosome 7. EMBO J (1986) 2.19

DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumours. Nat Genet (1997) 2.18

Construction of recombinant plasmids containing rat muscle actin and myosin light chain DNA sequences. Proc Natl Acad Sci U S A (1980) 2.17

Towards a molecular understanding of the elasticity of titin. J Mol Biol (1996) 2.12

Construction and characterization of pro alpha 1 collagen complementary deoxyribonucleic acid clones. Biochemistry (1979) 2.08

Protein kinase A phosphorylates titin's cardiac-specific N2B domain and reduces passive tension in rat cardiac myocytes. Circ Res (2002) 2.07

Muscle assembly: a titanic achievement? Curr Opin Cell Biol (1999) 2.07

Identification of muscle specific ring finger proteins as potential regulators of the titin kinase domain. J Mol Biol (2001) 2.05

A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene. Genomics (1988) 2.04

A method for global protein expression and antibody screening on high-density filters of an arrayed cDNA library. Nucleic Acids Res (1998) 2.01

Olfactory receptor gene cluster on human chromosome 17: possible duplication of an ancestral receptor repertoire. Hum Mol Genet (1994) 2.00

Hybridization fingerprinting of high-density cDNA-library arrays with cDNA pools derived from whole tissues. Mamm Genome (1992) 1.99

Molecular approaches to mammalian genetics. Cold Spring Harb Symp Quant Biol (1986) 1.99

Myopalladin, a novel 145-kilodalton sarcomeric protein with multiple roles in Z-disc and I-band protein assemblies. J Cell Biol (2001) 1.97

Complete coverage of the Schizosaccharomyces pombe genome in yeast artificial chromosomes. Nat Genet (1992) 1.93

Titin extensibility in situ: entropic elasticity of permanently folded and permanently unfolded molecular segments. J Cell Biol (1998) 1.93

Fragile X syndrome without CCG amplification has an FMR1 deletion. Nat Genet (1992) 1.91

HIP-I: a huntingtin interacting protein isolated by the yeast two-hybrid system. Hum Mol Genet (1997) 1.90

Inhibition of huntingtin fibrillogenesis by specific antibodies and small molecules: implications for Huntington's disease therapy. Proc Natl Acad Sci U S A (2000) 1.88

I-band titin in cardiac muscle is a three-element molecular spring and is critical for maintaining thin filament structure. J Cell Biol (1999) 1.88

Processing and quality control of DNA array hybridization data. Bioinformatics (2000) 1.86

Unexplained aplastic anaemia, immunodeficiency, and cerebellar hypoplasia (Hoyeraal-Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene, DKC1. Br J Haematol (1999) 1.84

Complex patterns of linkage disequilibrium in the Huntington disease region. Am J Hum Genet (1991) 1.84

X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene. Am J Hum Genet (1999) 1.80

Fluorescence quenching: A tool for single-molecule protein-folding study. Proc Natl Acad Sci U S A (2000) 1.79

The NH2 terminus of titin spans the Z-disc: its interaction with a novel 19-kD ligand (T-cap) is required for sarcomeric integrity. J Cell Biol (1998) 1.78

Mechanically driven contour-length adjustment in rat cardiac titin's unique N2B sequence: titin is an adjustable spring. Circ Res (1999) 1.75

Overlap of dyskeratosis congenita with the Hoyeraal-Hreidarsson syndrome. J Pediatr (2000) 1.74

A microdeletion of less than 250 kb, including the proximal part of the FMR-I gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome. Am J Hum Genet (1992) 1.73

Tissue-specific expression and alpha-actinin binding properties of the Z-disc titin: implications for the nature of vertebrate Z-discs. J Mol Biol (1997) 1.70

A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3"-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression. Hum Mol Genet (1999) 1.70

Cloning of gp-340, a putative opsonin receptor for lung surfactant protein D. Proc Natl Acad Sci U S A (1999) 1.69

Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemia. Hum Mol Genet (1997) 1.69

Identifying splits with clear separation: a new class discovery method for gene expression data. Bioinformatics (2001) 1.67

Hybridization analyses of arrayed cDNA libraries. Trends Genet (1991) 1.66

Automated image analysis for array hybridization experiments. Bioinformatics (2001) 1.66