Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors (Q35083362)

6 August 2017

title

Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors (English)

1 reference

6 August 2017

6

Kristiina Aittomäki

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Jukka-Pekka Mecklin

14

Jukka-Pekka Mecklin

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Lauri Aaltonen

Lauri A Aaltonen

21

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Heikki Järvinen

12

Heikki Järvinen

1 reference

Kirsti Husgafvel-Pursiainen

6 August 2017

10

Kirsti Husgafvel-Pursiainen

1 reference

6 August 2017

13

Pasi Koivisto

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6 August 2017

9

Charis Eng

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6 August 2017

Rainer Lehtonen

1

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6 August 2017

Maija Kiuru

2

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6 August 2017

Sakari Vanharanta

3

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6 August 2017

Jari Sjöberg

4

1 reference

6 August 2017

Leena-Maija Aaltonen

5

1 reference

6 August 2017

Johanna Arola

7

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6 August 2017

Ralf Butzow

8

1 reference

6 August 2017

Jorma Isola

11

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6 August 2017

Päivi Peltomäki

15

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6 August 2017

Reijo Salovaara

16

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6 August 2017

Veli-Matti Wasenius

17

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6 August 2017

Auli Karhu

18

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6 August 2017

Virpi Launonen

19

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6 August 2017

Nina N Nupponen

20

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6 August 2017

language of work or name

English

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publication date

1 January 2004

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The American Journal of Pathology

6 August 2017

published in

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6 August 2017

volume

164

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6 August 2017

issue

1

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6 August 2017

page(s)

17-22

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A role for mitochondrial enzymes in inherited neoplasia and beyond

6 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Low frequency of somatic mutations in the FH/multiple cutaneous leiomyomatosis gene in sporadic leiomyosarcomas and uterine leiomyomas

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Two genetic hits (more or less) to cancer

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathology

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Denaturing high-performance liquid chromatography: A review

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Inherited susceptibility to uterine leiomyomas and renal cell cancer

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Advances in uterine leiomyoma research: conference overview, summary, and future research recommendations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

HMGI(Y) and HMGI-C dysregulation: a common occurrence in human tumors

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Mitochondrial diseases in man and mouse

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

HMGI(Y) expression in human uterine leiomyomata. Involvement of another high-mobility group architectural factor in a benign neoplasm

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

A genetic register for von Hippel-Lindau disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

No fumarate hydratase (FH) mutations in hereditary prostate cancer

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Gene fusion involving HMGIC is a frequent aberration in uterine leiomyomas

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Germline SDHD mutation in familial phaeochromocytoma

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumours

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1602244

Analysis of Ki-ras, p53, and MDM2 genes in uterine leiomyomas and leiomyosarcomas

27 September 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963091-X

Chromosome analysis of 96 uterine leiomyomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963091-X

Molecular and cytogenetic analysis of chromosome 7 in uterine leiomyomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963091-X

Allelotype of uterine leiomyomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963091-X

Complex chromosome rearrangements involving 12q14 in two uterine leiomyomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963091-X

Evidence for RAD51L1/HMGIC fusion in the pathogenesis of uterine leiomyoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963091-X

Expression of HMGIY in three uterine leiomyomata with complex rearrangements of chromosome 6

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963091-X

Molecular cytogenetic analysis of uterine leiomyoma and leiomyosarcoma by comparative genomic hybridization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963091-X

Fusion transcripts involving HMGA2 are not a common molecular mechanism in uterine leiomyomata with rearrangements in 12q15

7 January 2021

1 reference

12 December 2020

High incidence of somatic mitochondrial DNA mutations in human ovarian carcinomas

1 reference

12 December 2020

Detection of mitochondrial DNA mutations in primary breast cancer and fine-needle aspirates

1 reference

12 December 2020

Few FH mutations in sporadic counterparts of tumor types observed in hereditary leiomyomatosis and renal cell cancer families

1 reference

12 December 2020

10.1016/S0002-9440(10)63091-X

Identifiers

DOI

1 reference

6 August 2017

1 reference

6 August 2017

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