The human MyoD1 (MYF3) gene maps on the short arm of chromosome 11 but is not associated with the WAGR locus or the region for the Beckwith-Wiedemann syndrome

Expression of a single transfected cDNA converts fibroblasts to myoblasts

1987 • 3,373 citations

A new DNA binding and dimerization motif in immunoglobulin enhancer binding, daughterless, MyoD, and myc proteins

1989 • 2,706 citations

Soft-Tissue Sarcomas, Breast Cancer, and Other Neoplasms

1969 • 1,437 citations

A novel human muscle factor related to but distinct from MyoD1 induces myogenic conversion in 10T1/2 fibroblasts.

1989 • 919 citations

MyoD1: A Nuclear Phosphoprotein Requiring a Myc Homology Region to Convert Fibroblasts to Myoblasts

1988 • 839 citations

Chromosomal Imbalance in the Aniridia-Wilms' Tumor Association: 11p Interstitial Deletion

1978 • 726 citations

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

1985 • 555 citations

Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour

1984 • 538 citations

Myf-6, a new member of the human gene family of myogenic determination factors: evidence for a gene cluster on chromosome 12.

1990 • 508 citations

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

1989 • 448 citations

daughterless, a Drosophila gene essential for both neurogenesis and sex determination, has sequence similarities to myc and the achaete-scute complex

1988 • 442 citations

Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13

1979 • 404 citations

Differential expression of myogenic determination genes in muscle cells: possible autoactivation by the Myf gene products.

1989 • 349 citations

DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome

1985 • 313 citations

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

1989 • 306 citations

Abnormality of chromosome 11 in patients withfeatures of Beckwith-Wiedemann syndrome

1983 • 236 citations

Molecular differential pathology of rhabdomyosarcoma

1989 • 225 citations

Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma.

1989 • 147 citations

Cancer in survivors of childhood soft tissue sarcoma and their relatives.

1987 • 143 citations

Interstitial deletion of short arm of chromosome 11 limited to Wilms' tumor cells in a patient without aniridia.

1981 • 117 citations

DNA replication patterns of human chromosomes from fibroblasts and amniotic fluid cells revealed by a Giemsa staining technique

1975 • 110 citations

Neoplasms associated with the Beckwith-Wiedemann syndrome.

1976 • 108 citations

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma

1989 • 97 citations

Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11

1988 • 91 citations

HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.

1987 • 72 citations

A deletion map of the WAGR region on chromosome 11.

1989 • 59 citations

A physical map around the WAGR complex on the short arm of chromosome 11

1989 • 55 citations

Cloning of Breakpoints of a Chromosome Translocation Identifies the AN2 Locus

1989 • 53 citations

Rhabdomyosarcoma-associated locus and MYOD1 are syntenic but separate loci on the short arm of human chromosome 11.

1990 • 50 citations

Expression of the MyoD1 muscle determination gene defines differentiation capability but not tumorigenicity of human rhabdomyosarcomas.

1989 • 34 citations

Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13

1989 • 26 citations

Expression of the MyoD1 Muscle Determination Gene Defines Differentiation Capability but Not Tumorigenicity of Human Rhabdomyosarcomas

1989 • 10 citations