(Q36612555)

English

Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas

scientific article published on 31 October 2006

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas (English)

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

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E Bonora

1

0 references

Giovanni Tallini

object named as

G Tallini

4

0 references

author name string

C Evangelisti

2

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

F Bonichon

3

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

G Romeo

5

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

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publication date

31 October 2006

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

British Journal of Cancer

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

95

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

11

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

1529-1536

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360750

30 September 2017

Familial nonmedullary thyroid carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360750

30 September 2017

Prognostic factors of recurrence in encapsulated Hurthle cell carcinoma of the thyroid gland: a clinicopathologic study of 50 cases.

1 reference

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30 September 2017

How to define follicular thyroid carcinoma?

1 reference

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30 September 2017

Determinants of exon 7 splicing in the spinal muscular atrophy genes, SMN1 and SMN2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360750

30 September 2017

Somatic and germline mutation in GRIM-19, a dual function gene involved in mitochondrial metabolism and cell death, is linked to mitochondrion-rich (Hurthle cell) tumours of the thyroid.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360750

30 September 2017

Hürthle (oncocytic) cell tumors of thyroid: etiopathogenesis, diagnosis and clinical significance.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360750

30 September 2017

Regulated interactions of mtHsp70 with Tim44 at the translocon in the mitochondrial inner membrane

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360750

30 September 2017

Angiopoietins in tumours: the angiogenic switch

1 reference

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30 September 2017

Pin1 links the activities of c-Abl and p300 in regulating p73 function.

1 reference

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30 September 2017

Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360750

30 September 2017

J protein cochaperone of the mitochondrial inner membrane required for protein import into the mitochondrial matrix

1 reference

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30 September 2017

Two mammalian longevity assurance gene (LAG1) family members, trh1 and trh4, regulate dihydroceramide synthesis using different fatty acyl-CoA donors

1 reference

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30 September 2017

A role for mitochondrial enzymes in inherited neoplasia and beyond

1 reference

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30 September 2017

The sodium/iodide Symporter (NIS): characterization, regulation, and medical significance

1 reference

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30 September 2017

BRCA2 T2722R is a deleterious allele that causes exon skipping

1 reference

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30 September 2017

Hürthle cell carcinoma: a 60-year experience.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360750

30 September 2017

Mutations of CD40 gene cause an autosomal recessive form of immunodeficiency with hyper IgM.

1 reference

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30 September 2017

Identification and characterization of a family of Rab11-interacting proteins

1 reference

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30 September 2017

Hürthle cell carcinoma: a critical histopathologic appraisal.

1 reference

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30 September 2017

Mitochondrial activity in XTC.UC1 cells derived from thyroid oncocytoma

1 reference

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30 September 2017

Isolation of a ubiquitin-like (UBL5) gene from a screen identifying highly expressed and conserved iris genes

1 reference

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30 September 2017

Hürthle cell tumours of the thyroid. A review with emphasis on mitochondrial abnormalities with clinical relevance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2360750

30 September 2017

Mitochondrial protein import motor: the ATPase domain of matrix Hsp70 is crucial for binding to Tim44, while the peptide binding domain and the carboxy-terminal segment play a stimulatory role

1 reference

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30 September 2017

Analysis of the 5' end of the mouse Elavl1 (mHuA) gene reveals a transcriptional regulatory element and evidence for conserved genomic organization.

1 reference

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30 September 2017

Characterization of single-nucleotide polymorphisms in coding regions of human genes

1 reference

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30 September 2017

Genetic and structural characterization of the human mitochondrial inner membrane translocase

1 reference

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30 September 2017

A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2.

1 reference

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30 September 2017

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

1 reference

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30 September 2017

Increased expression of the sodium/iodide symporter in papillary thyroid carcinomas

1 reference

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Excessive formation of hydroxyl radicals and aldehydic lipid peroxidation products in cultured skin fibroblasts from patients with complex I deficiency

1 reference

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The future of genetic studies of complex human diseases

1 reference

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30 September 2017

Mitochondrial complex I deficiency leads to increased production of superoxide radicals and induction of superoxide dismutase

1 reference

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Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

1 reference

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30 September 2017

Mitochondrial Hsp70/MIM44 complex facilitates protein import

1 reference

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30 September 2017

MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells.

1 reference

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A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes

1 reference

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Gene delivery of Tim44 reduces mitochondrial superoxide production and ameliorates neointimal proliferation of injured carotid artery in diabetic rats

1 reference

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Antioxidant defences in cybrids harboring mtDNA mutations associated with Leber's hereditary optic neuropathy

1 reference

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1 reference

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1 reference

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Defective mitochondrial ATP synthesis in oxyphilic thyroid tumors.

1 reference

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20 September 2018

Genetic heterogeneity in familial nonmedullary thyroid carcinoma: exclusion of linkage to RET, MNG1, and TCO in 56 families. NMTC Consortium.

1 reference

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20 September 2018

Expression of the Na+/I- symporter gene in human thyroid tumors: a comparison study with other thyroid-specific genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17088905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of sodium/iodide symporter gene mutations in differentiated human thyroid carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/17088905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oncocytic tumours

1 reference

https://pubmed.ncbi.nlm.nih.gov/17088905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abstracts of the joint meeting of the Pathological Society of Great Britain and Ireland and the Dutch Pathological Society, 186th meeting of the Pathological Society of Great Britain and Ireland. 6-9 July 2004, Amsterdam, The Netherlands

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6603455

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.BJC.6603455

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

ResearchGate publication ID

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