(Q34557916)

English

Human PMS2 gene family: origin, molecular evolution, and biological implications

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Human PMS2 gene family: origin, molecular evolution, and biological implications (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

author name string

D G Shpakovskii

1

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

E K Shematorova

2

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

G V Shpakovskii

3

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

publication date

1 May 2006

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Doklady. Biochemistry and biophysics

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

408

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

175-179

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Structure and function of the N-terminal 40 kDa fragment of human PMS2: a monomeric GHL ATPase

1 reference

https://pubmed.ncbi.nlm.nih.gov/16913423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning, characterization and chromosomal assignment of the human genes homologous to yeast PMS1, a member of mismatch repair genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16913423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16913423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A human RNA polymerase II subunit is encoded by a recently generated multigene family

1 reference

https://pubmed.ncbi.nlm.nih.gov/16913423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution of human mlh1 and pms2 ATPase activities to DNA mismatch repair

1 reference

https://pubmed.ncbi.nlm.nih.gov/16913423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mammalian DNA mismatch repair

1 reference

https://pubmed.ncbi.nlm.nih.gov/16913423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural basis for the control of translation initiation during stress

1 reference

https://pubmed.ncbi.nlm.nih.gov/16913423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human PMS2L proteins do not interact with hMLH1, a major DNA mismatch repair protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/16913423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic organization of the human PMS2 gene family.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16913423

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/16913423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16913423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16913423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations within the hMLH1 and hPMS2 subunits of the human MutLalpha mismatch repair factor affect its ATPase activity, but not its ability to interact with hMutSalpha

1 reference

https://pubmed.ncbi.nlm.nih.gov/16913423

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1134/S1607672906030185

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

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