A step-by-step model of TBP/TATA box binding allows predicting human hereditary diseases by single nucleotide polymorphism (Q58003364)

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8 January 2020

title

A step-by-step model of TBP/TATA box binding allows predicting human hereditary diseases by single nucleotide polymorphism (English)

1 reference

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single-nucleotide polymorphism

8 January 2020

main subject

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7

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8 January 2020

author name string

P M Ponomarenko

1

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8 January 2020

L K Savinkova

2

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8 January 2020

I A Drachkova

3

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8 January 2020

M V Lysova

4

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8 January 2020

T V Arshinova

5

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8 January 2020

M P Ponomarenko

6

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8 January 2020

publication date

1 March 2008

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Doklady. Biochemistry and biophysics

8 January 2020

published in

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volume

419

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8 January 2020

issue

1

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page(s)

88-92

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https://scigraph.springernature.com/pub.10.1134/s1607672908020117

8 January 2020

exact match

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Analysis of a genetic defect in the TATA box of the SOD1 gene in a patient with familial amyotrophic lateral sclerosis

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Angiotensinogen promoter B-haplotype associated with cerebral small vessel disease enhances basal transcriptional activity

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A point mutation in the putative TATA box, detected in nondiseased individuals and patients with hereditary breast cancer, decreases promoter activity of the 17 beta-hydroxysteroid dehydrogenase type 1 gene 2 (EDH17B2) in vitro

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Activation of the gamma E-crystallin pseudogene in the human hereditary Coppock-like cataract.

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Polymorphisms in the transferrin 5' flanking region associated with differences in total iron binding capacity: possible implications in iron homeostasis

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12 December 2020

Polymorphisms of the interleukin-1 beta gene are associated with increased risk of non-small cell lung cancer.

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12 December 2020