(Q67295036)

English

Folic acid sensitive fragile sites are not limited to the human karyotype. Demonstration of nonrandom gaps and breaks in the Persian vole Ellobius lutescens Th. inducible by methotrexate, fluorodeoxyuridine, and aphidicolin

scientific article published on 01 January 1985

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3159643%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

Folic acid sensitive fragile sites are not limited to the human karyotype. Demonstration of nonrandom gaps and breaks in the Persian vole Ellobius lutescens Th. inducible by methotrexate, fluorodeoxyuridine, and aphidicolin (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3159643%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

M Djalali

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3159643%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

G Barbi

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3159643%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

P Steinbach

3

1 reference

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11 September 2019

publication date

1 January 1985

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11 September 2019

1 reference

Europe PubMed Central

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11 September 2019

70

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11 September 2019

183-185

1 reference

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11 September 2019

2

1 reference

Europe PubMed Central

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11 September 2019

https://scigraph.springernature.com/pub.10.1007/bf00273080

0 references

DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3159643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Coincidence between fragile site expression and interstitial deletion of chromosome 11 in a case of myelofibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3159643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An in vitro and in vivo study of a BrdU-sensitive fragile site in the Chinese hamster

1 reference

https://pubmed.ncbi.nlm.nih.gov/3159643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further delineation of X-linked mental retardation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3159643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enhancement of a fra(16)(q22) with distamycin A: A family ascertained through an abnormal proposita

1 reference

https://pubmed.ncbi.nlm.nih.gov/3159643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonrandom distribution of methotrexate-induced aberrations on human chromosomes. Detection of further folic acid sensitive fragile sites

1 reference

https://pubmed.ncbi.nlm.nih.gov/3159643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ellobius lutescens Th. (Rhodentia, Microtinae): Q-, R-, and replication banding patterns. Chromosome 1 polymorphism in the male and presumptive heterogamety in the female

1 reference

https://pubmed.ncbi.nlm.nih.gov/3159643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fragile X chromosome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3159643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00273080

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3159643%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3159643%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

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