A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease
about
Energy metabolism in neuroblastoma and Wilms tumorGenetic causes of focal segmental glomerulosclerosis: implications for clinical practiceA novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46,XY patient with Denys-Drash syndromeThe Denys-Drash syndromeIs There a Predisposition Gene for Ewing's Sarcoma?Frasier and Denys-Drash syndromes: different disorders or part of a spectrum?Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways.Tumour suppressor gene mutations in humans and mice: parallels and contrastsFrasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?Denys-Drash syndrome, septated vagina and low level of anti-Mullerian hormone in male neonate.Wilms tumor genetics.Angiogenesis and chronic kidney disease.Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutationsIdentification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation databaseDonor splice-site mutations in WT1 are responsible for Frasier syndrome.Identifying genes for male sex determination in humans.Analysis of wilms tumors using SNP mapping array-based comparative genomic hybridization.Estrogen receptor-negative breast ductal carcinoma: clinicopathological features and MIB-1 (Ki-67) proliferative index associationA novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1.Insights into the physiological role of WT1 from studies of genetically modified mice.WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis.Direct production of XY(DMY-) sex reversal female medaka (Oryzias latipes) by embryo microinjection of TALENsNPHS2 mutations account for only 15% of nephrotic syndrome cases.Bilateral Wilms' tumors in an infant with Denys-Drash syndrome and rarely seen truncation mutation in the WT1 gene-exon 6Screening of WT1 mutations in exon 8 and 9 in children with steroid resistant nephrotic syndrome from a single centre and establishment of a rapid screening assay using high-resolution melting analysis in a clinical setting.Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour.Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.Wilms' tumour 1 gene mutations in south Indian children with steroid-resistant nephrotic syndromeThe Wt1+/R394W mouse displays glomerulosclerosis and early-onset renal failure characteristic of human Denys-Drash syndrome.The podocyte as a target: cyclosporin A in the management of the nephrotic syndrome caused by WT1 mutations.PAX2 in human kidney malformations and disease.Gene mutations associated with anomalies of human gonad formation.Perspectives in Pediatric Pathology, Chapter 5. Gonadal Dysgenesis.Sequence and expression analysis of WT1 and Sox9 in the red-eared slider turtle, Trachemys scripta.The Battle of the Sexes: Human Sex Development and Its Disorders.The association of Wilms' tumor, male pseudohermaphroditism and diffuse glomerular disease (Drash syndrome): report of eight cases with clinical and morphologic findings and review of the literature.Diagnosis of congenital and infantile nephrotic syndromes in renal biopsies in Minas Gerais, Brazil: Six case reports.WT1 mutants reveal SRPK1 to be a downstream angiogenesis target by altering VEGF splicing.New look at mesoblastic nephroma.
P2860
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P2860
A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease
description
1970 nî lūn-bûn
@nan
1970 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1970 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1970年の論文
@ja
1970年論文
@yue
1970年論文
@zh-hant
1970年論文
@zh-hk
1970年論文
@zh-mo
1970年論文
@zh-tw
1970年论文
@wuu
name
A syndrome of pseudohermaphrod ...... and degenerative renal disease
@ast
A syndrome of pseudohermaphrod ...... and degenerative renal disease
@en
A syndrome of pseudohermaphrod ...... and degenerative renal disease
@nl
type
label
A syndrome of pseudohermaphrod ...... and degenerative renal disease
@ast
A syndrome of pseudohermaphrod ...... and degenerative renal disease
@en
A syndrome of pseudohermaphrod ...... and degenerative renal disease
@nl
prefLabel
A syndrome of pseudohermaphrod ...... and degenerative renal disease
@ast
A syndrome of pseudohermaphrod ...... and degenerative renal disease
@en
A syndrome of pseudohermaphrod ...... and degenerative renal disease
@nl
P2093
P3181
P1476
A syndrome of pseudohermaphrod ...... and degenerative renal disease
@en
P2093
R M Blizzard
W H Hartmann
P304
P3181
P356
10.1016/S0022-3476(70)80409-7
P407
P577
1970-04-01T00:00:00Z