Isolated diffuse mesangial sclerosis and Wilms tumor suppressor gene

Journal of Pediatrics

Volumn 138, Issue 3, 2001, Pages 425-427

  Ito, Shu ichi ^a,b   Takata, Ayako ^a,b   Hataya, Hiroshi ^a,b   Ikeda, Masahiro ^a,b   Kikuchi, Haruhito ^a,b   Hata, Jun ichi ^a,b   Honda, Masataka ^a,b  

^a TOKYO METROPOLITAN CHILDREN'S MEDICAL CENTER   (Japan)

^b KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; CHILD; CLINICAL ARTICLE; DENYS DRASH SYNDROME; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GLOMERULOSCLEROSIS; HISTOLOGY; HUMAN; HUMAN TISSUE; INFANT; KIDNEY BIOPSY; KIDNEY DISEASE; MALE; NEPHROBLASTOMA; NEWBORN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

EID: 0035092225     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1067/mpd.2001.111317     Document Type: Article

References (13)

1. Congenital and infantile nephrotic syndrome
2. Association d'un syndrome anatomopathologique de pseudohermaphrodisme masculin, d'une tumeur de Wilm's, d'une nephropahtie parenchymateuse et d'un mosaicisme XX/XY
3. A syndrome of pseudohermaphroditism, Wilm's tumor, hypertension and degenerative renal disease
4. Germline mutations in the Wilms tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
5. Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database
6. Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations
7. Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome?
8. Nephrotic syndrome in the 1st year of life
9. Isolation and characterization of zinc finger polypeptide gene at the human chromosome 11 Wilms tumor locus
10. Homozygous deletion in Wilms tumors of a zinc finger gene identified by chromosome jumping
11. Donor splice-site mutations in WT1 are responsible for Frasier syndrome
12. The same mutation affecting the splicing of WT1 gene is present on. Frasier syndrome patients with or without Wilms tumor
13. Children at increased risk for Wilms tumor: Monitoring issues