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

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

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Kristiina Aittomäki

6

object named as

Kristiina Aittomäki

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Jukka-Pekka Mecklin

14

object named as

Jukka-Pekka Mecklin

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object named as

Lauri A Aaltonen

21

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Heikki Järvinen

12

object named as

Heikki Järvinen

1 reference

Europe PubMed Central

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6 August 2017

Kirsti Husgafvel-Pursiainen

10

object named as

Kirsti Husgafvel-Pursiainen

1 reference

Europe PubMed Central

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6 August 2017

Pasi A. Koivisto

13

object named as

Pasi Koivisto

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

9

object named as

Charis Eng

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Europe PubMed Central

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6 August 2017

author name string

Rainer Lehtonen

1

1 reference

Europe PubMed Central

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6 August 2017

Maija Kiuru

2

1 reference

Europe PubMed Central

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6 August 2017

Sakari Vanharanta

3

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6 August 2017

Jari Sjöberg

4

1 reference

Europe PubMed Central

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6 August 2017

Leena-Maija Aaltonen

5

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Europe PubMed Central

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6 August 2017

Johanna Arola

7

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Europe PubMed Central

PubMed publication ID

6 August 2017

Ralf Butzow

8

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6 August 2017

Jorma Isola

11

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Europe PubMed Central

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6 August 2017

Päivi Peltomäki

15

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Europe PubMed Central

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6 August 2017

Reijo Salovaara

16

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Europe PubMed Central

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6 August 2017

Veli-Matti Wasenius

17

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6 August 2017

Auli Karhu

18

1 reference

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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

0 references

publication date

1 January 2004

1 reference

Europe PubMed Central

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6 August 2017

The American Journal of Pathology

1 reference

Europe PubMed Central

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6 August 2017

164

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Europe PubMed Central

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6 August 2017

1

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6 August 2017

17-22

1 reference

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PubMed publication ID

6 August 2017

A role for mitochondrial enzymes in inherited neoplasia and beyond

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

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

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

Two genetic hits (more or less) to cancer

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

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

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

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

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

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

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

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

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

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

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

Denaturing high-performance liquid chromatography: A review

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

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

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

Inherited susceptibility to uterine leiomyomas and renal cell cancer

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

Uterine fibroids.

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

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

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

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

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

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

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

Mitochondrial diseases in man and mouse

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

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

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

A genetic register for von Hippel-Lindau disease

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

No fumarate hydratase (FH) mutations in hereditary prostate cancer

1 reference

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

27 September 2018

Gene fusion involving HMGIC is a frequent aberration in uterine leiomyomas

1 reference

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

27 September 2018

Germline SDHD mutation in familial phaeochromocytoma

1 reference

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

27 September 2018

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

1 reference

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

27 September 2018

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

1 reference

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

27 September 2018

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

1 reference

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

7 January 2021

Chromosome analysis of 96 uterine leiomyomas

1 reference

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

7 January 2021

Molecular and cytogenetic analysis of chromosome 7 in uterine leiomyomas

1 reference

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

7 January 2021

Allelotype of uterine leiomyomas

1 reference

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

7 January 2021

Complex chromosome rearrangements involving 12q14 in two uterine leiomyomas

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/14695314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High incidence of somatic mitochondrial DNA mutations in human ovarian carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/14695314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/14695314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/14695314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/S0002-9440(10)63091-X

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

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