Human chromosome hot points. IV. Uridine-induced hot-point breaks at 3p14 and 16q23-24 and increased expression of fragile site Xq27 in folate-free medium (Q93660038)

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English	Human chromosome hot points. IV. Uridine-induced hot-point breaks at 3p14 and 16q23-24 and increased expression of fragile site Xq27 in folate-free medium	No description defined

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4077052%20AND%20SRC:MED&resulttype=core&format=json

9 May 2020

Human chromosome hot points. IV. Uridine-induced hot-point breaks at 3p14 and 16q23-24 and increased expression of fragile site Xq27 in folate-free medium (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4077052%20AND%20SRC:MED&resulttype=core&format=json

9 May 2020

author name string

N Li

1

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9 May 2020

X T Zhou

2

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9 May 2020

publication date

1 January 1985

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9 May 2020

1 reference

Europe PubMed Central

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9 May 2020

71

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9 May 2020

4

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9 May 2020

363-365

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PubMed publication ID

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9 May 2020

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/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new familial "fragile site" on chromosome 16 (q23-24). Cytogenetic and clinical considerations

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apparently spontaneous chromosome damage in human leukocytes and the nature of chromatid gaps.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Formation of Okazaki fragments in polyoma DNA synthesis caused by misincorporation of uracil

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distribution of spontaneous chromosome breaks in human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methotrexate-induced misincorporation of uracil into DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fragile X chromosome: Current methods

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

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/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accumulation of small fragments of DNA in isolated HeLa cell nuclei due to transient incorporation of dUMP

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome abnormalities in lymphocytes from normal human subjects. A study of 3,720 cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritable fragile sites on human chromosomes. X. New folate-sensitive fragile sites: 6p23, 9p21, 9q32, and 11q23

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methotrexate-induced increase in gap formation in human chromosome band 3p14

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome banding required for studies on X-linked mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human chromosome hot points. 1. Hot point at 3p14 in three populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distribution of spontaneous chromosome breaks in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/4077052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00388465

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4077052%20AND%20SRC:MED&resulttype=core&format=json

9 May 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4077052%20AND%20SRC:MED&resulttype=core&format=json

9 May 2020

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