(Q36338216)

English

Syndrome of early onset colon cancers, hematologic malignancies & features of neurofibromatosis in HNPCC families with homozygous mismatch repair gene mutations

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

1 reference

Europe PubMed Central

Syndrome of early onset colon cancers, hematologic malignancies & features of neurofibromatosis in HNPCC families with homozygous mismatch repair gene mutations (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

1 reference

based on heuristic

inferred from title

DNA mismatch repair

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Prathap Bandipalliam

1

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

publication date

1 January 2005

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

Familial Cancer

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

323-333

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

https://scigraph.springernature.com/pub.10.1007/s10689-005-8351-6

0 references

Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibromatosis type 1 gene as a mutational target in a mismatch repair-deficient cell type.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mlh1 deficiency accelerates myeloid leukemogenesis in neurofibromatosis 1 (Nf1) heterozygous mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Café-au-lait spots and early onset colorectal neoplasia: a variant of HNPCC?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The muir-torre syndrome: a rare variant of hereditary nonpolyposis colorectal cancer associated with hmsh2 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extensive somatic microsatellite mutations in normal human tissue.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transgenic expression of human MGMT blocks the hypersensitivity of PMS2-deficient mice to low dose MNU thymic lymphomagenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A homozygous MSH6 mutation in a child with café-au-lait spots, oligodendroglioma and rectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary nonpolyposis colorectal cancer: a call for attention

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mice defective in the DNA mismatch gene PMS2 are hypersensitive to MNU induced thymic lymphoma and are partially protected by transgenic expression of human MGMT.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis of Turcot's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early onset brain tumor and lymphoma in MSH2-deficient children

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AGA technical review on hereditary colorectal cancer and genetic testing.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary nonpolyposis colorectal cancer: the syndrome, the genes, and historical perspectives.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). I. Clinical description of resource

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibromatosis and early onset of cancers in hMLH1-deficient children

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The hPMS2 exon 5 mutation and malignant glioma. Case report.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficient detection of hereditary nonpolyposis colorectal cancer gene carriers by screening for tumor microsatellite instability before germline genetic testing.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Muir-Torre syndrome in kindreds with hereditary nonpolyposis colorectal cancer (Lynch syndrome): A classic obligation in preventive medicine

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DNA mismatch repair

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in the mismatch repair gene Msh6 causes cancer susceptibility

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features and pathobiology of neurofibromatosis 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting Highlights and Bethesda Guidelines

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Drastic genetic instability of tumors and normal tissues in Turcot syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous intestinal carcinomas and skin neoplasms in Msh2-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HNPCC mutation MLH1 P648S makes the functional protein unstable, and homozygosity predisposes to mild neurofibromatosis type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical diagnosis and management of hereditary colorectal cancer syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16341812

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10689-005-8351-6

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

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