Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43.
about
Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North AmericaEtiology and pathogenesis of uterine leiomyomas: a reviewFamilial clustering of Leiomyomatosis peritonealis disseminata: an unknown genetic syndrome?Uterine smooth muscle tumors with features suggesting fumarate hydratase aberration: detailed morphologic analysis and correlation with S-(2-succino)-cysteine immunohistochemistry.Aerobic glycolysis: a novel target in kidney cancer.Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer.Multiple hits for the association of uterine fibroids on human chromosome 1q43.Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors.Adrenal nodular hyperplasia in hereditary leiomyomatosis and renal cell cancerThe TCA cycle and tumorigenesis: the examples of fumarate hydratase and succinate dehydrogenase.Reed's Syndrome: A Case of Multiple Cutaneous and Uterine Leiomyomas.Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathologyEvaluation of GWAS candidate susceptibility loci for uterine leiomyoma in the multi-ethnic NIEHS uterine fibroid study.Fine mapping of the uterine leiomyoma locus on 1q43 close to a lncRNA in the RGS7-FH intervalSignificance of gene expression analysis of renal cell carcinoma.Diffuse and segmental variants of cutaneous leiomyomatosis: novel mutations in the fumarate hydratase gene and review of the literature.Multiple cutaneous and uterine leiomyomatosis syndrome: a review.Cutaneous leiomyomatosis in a mother and daughter.Anetoderma arising in Reed syndrome: a case report and review of the literature.Familial multiple cutaneous and uterine leiomyomas associated with papillary renal cell cancer.Confounding by linkage disequilibrium.Crusted Piloleiomyoma with mental retardation: a rare association.Novel human, mouse and xenopus genes encoding a member of the RAS superfamily of low-molecular-weight GTP-binding proteins and its downregulation in W/WV mouse jejunum.Multiple linear leiomyomas of the forehead as the presenting sign of Reed syndrome.A twist on piloleiomyoma: segmental cutaneous leiomyomatosis.No germline FH mutations in familial breast cancer patients
P2860
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P2860
Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43.
description
2001 nî lūn-bûn
@nan
2001 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի մարտին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Localization of a gene (MCUL1) ...... oids to chromosome 1q42.3-q43.
@ast
Localization of a gene (MCUL1) ...... oids to chromosome 1q42.3-q43.
@en
Localization of a gene
@nl
type
label
Localization of a gene (MCUL1) ...... oids to chromosome 1q42.3-q43.
@ast
Localization of a gene (MCUL1) ...... oids to chromosome 1q42.3-q43.
@en
Localization of a gene
@nl
prefLabel
Localization of a gene (MCUL1) ...... oids to chromosome 1q42.3-q43.
@ast
Localization of a gene (MCUL1) ...... oids to chromosome 1q42.3-q43.
@en
Localization of a gene
@nl
P2093
P2860
P50
P356
P1476
Localization of a gene (MCUL1) ...... roids to chromosome 1q42.3-q43
@en
P2093
Anderson J
Churchman M
P2860
P304
P356
10.1086/320124
P407
P577
2001-03-14T00:00:00Z