(Q35897747)

11 August 2017

At-risk populations for osteosarcoma: the syndromes and beyond (English)

1 reference

11 August 2017

4

Lisa Cannon-Albright

0 references

author name string

George T Calvert

1

1 reference

11 August 2017

R Lor Randall

2

1 reference

11 August 2017

Kevin B Jones

3

1 reference

11 August 2017

Stephen Lessnick

5

1 reference

11 August 2017

Joshua D Schiffman

6

1 reference

11 August 2017

12 March 2012

1 reference

11 August 2017

1 reference

11 August 2017

2012

1 reference

11 August 2017

152382

1 reference

Creative Commons Attribution 3.0 Unported

11 August 2017

start time

1 January 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

Sarcomas in TP53 germline mutation carriers: a review of the IARC TP53 database

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Using epidemiology and genomics to understand osteosarcoma etiology

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Osteosarcomagenesis: modeling cancer initiation in the mouse

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Imaging of cancer predisposition syndromes in children

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Radio-induced malignancies after breast cancer postoperative radiotherapy in patients with Li-Fraumeni syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Retinoblastoma - current treatment and future direction

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Retinoblastoma management: advances in enucleation, intravenous chemoreduction, and intra-arterial chemotherapy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

The etiology of osteosarcoma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Ribosomal protein genes RPS10 and RPS26 are commonly mutated in Diamond-Blackfan anemia

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

The contribution of CHEK2 to the TP53-negative Li-Fraumeni phenotype

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

International osteosarcoma incidence patterns in children and adolescents, middle ages and elderly persons

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Rising from the RecQ-age: the role of human RecQ helicases in genome maintenance

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Survival with retinoblastoma in the USA: 1975-2004.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Osteosarcoma associated with diamond-blackfan anaemia: a case of a child receiving growth hormone therapy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Cancer screening practices of adult survivors of retinoblastoma at risk of second cancers

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Risk stratification in cancer predisposition syndromes: lessons learned from novel molecular developments in Li-Fraumeni syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Multiple cutaneous neoplasms in a patient with Rothmund-Thomson syndrome: case report and published work review

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

p53 and disease: when the guardian angel fails

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Improving clinical care and elucidating the pathophysiology of Diamond Blackfan anemia: an update from the Diamond Blackfan Anemia Registry

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Biochemical characterization of the RECQ4 protein, mutated in Rothmund-Thomson syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Biology of osteogenic sarcoma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Malignant transformation and new primary tumours after therapeutic radiation for benign disease: substantial risks in certain tumour prone syndromes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

The search for the retinoblastoma cell of origin

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Lifetime risks of common cancers among retinoblastoma survivors

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

American Society of Clinical Oncology Policy Statement Update: Genetic Testing for Cancer Susceptibility

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Sensitivity and predictive value of criteria for p53 germline mutation screening

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

The Ashkenazic Jewish Bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestry

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

CDKN2A gene deletions and loss of p16 expression occur in osteosarcomas that lack RB alterations

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Frequency of somatic and germ-line mosaicism in retinoblastoma: implications for genetic counseling.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Cancer incidence after retinoblastoma. Radiation dose and sarcoma risk

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Bloom's syndrome. XX. The first 100 cancers

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Excess of rare cancers in Werner syndrome (adult progeria)

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Positional cloning of the Werner's syndrome gene

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

The Bloom's syndrome gene product is homologous to RecQ helicases

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Mutation and cancer: statistical study of retinoblastoma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

A cancer family syndrome in twenty-four kindreds

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

RAPADILINO syndrome with radial and patellar aplasia/hypoplasia as main manifestations

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Follow-up study of twenty-four families with Li-Fraumeni syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Multiple primary malignancies in osteosarcoma patients. Incidence and predictive value of osteosarcoma subtype for cancer syndromes related with osteosarcoma

27 July 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

The molecular pathogenesis of osteosarcoma: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

Beyond Li Fraumeni Syndrome: clinical characteristics of families with p53 germline mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

The epidemiological challenge of the most frequent eye cancer: retinoblastoma, an issue of birth and death

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

Non-ocular tumours following retinoblastoma in Great Britain 1951 to 2004.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

Genetic and epigenetic alterations of the cell cycle regulators and tumor suppressor genes in pediatric osteosarcomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

Low penetrance hereditary retinoblastoma in a family: what should we consider in the genetic counselling process and follow up?

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

Screening for retinoblastoma: presenting signs as prognosticators of patient and ocular survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

Human RECQ helicases: roles in DNA metabolism, mutagenesis and cancer biology

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

Rothmund-Thomson syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

The mutation spectrum in RECQL4 diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

Atypical osteosarcomas in Werner Syndrome (adult progeria).

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

High incidence of malformation syndromes in a series of 1,073 children with cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

Li-Fraumeni and related syndromes: correlation between tumor type, family structure, and TP53 genotype

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Alteration of pRb/p16/cdk4 regulation in human osteosarcoma

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3329649

Is CHEK2 a cause of the Li Fraumeni syndrome?

22 October 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

In the Service of Power: The Global Political Economy of Citizenship and Human Rights

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F152382

Familial risk for histology-specific bone cancers: an updated study in Sweden

21 January 2018

1 reference

12 December 2020

Carrier frequency of the Bloom syndrome blmAsh mutation in the Ashkenazi Jewish population

1 reference

12 December 2020

Hierarchical deterioration of body systems in Werner's syndrome: implications for normal ageing

1 reference

12 December 2020

2009 Version of the Chompret Criteria for Li Fraumeni Syndrome

1 reference

12 December 2020

Homozygosity mapping of the Werner syndrome locus (WRN)

1 reference

12 December 2020

CDK4 gene amplification in osteosarcoma: reciprocal relationship with INK4A gene alterations and mapping of 12q13 amplicons

1 reference

12 December 2020

Identifiers

DOI

10.1155/2012/152382

1 reference

11 August 2017

1 reference

11 August 2017

PubMed publication ID

22550413

1 reference