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34 in total

1. Molecular mechanism in the formation of a human ring chromosome 21.

Authors: C Wong; H H Kazazian; G Stetten; W C Earnshaw; M L Van Keuren; S E Antonarakis
Journal: Proc Natl Acad Sci U S A Date: 1989-03 Impact factor: 11.205

2. DNA sequence of a class I pseudogene from the Tla region of the murine MHC: recombination at a B2 alu repetitive sequence.

Authors: D A Fisher; M Pecht; L Hood
Journal: J Mol Evol Date: 1989-04 Impact factor: 2.395

3. Evolution of Alu family repeats since the divergence of human and chimpanzee.

Authors: I Sawada; C Willard; C K Shen; B Chapman; A C Wilson; C W Schmid
Journal: J Mol Evol Date: 1985 Impact factor: 2.395

4. Concerted deletions and inversions are caused by mitotic recombination between delta sequences in Saccharomyces cerevisiae.

Authors: R Rothstein; C Helms; N Rosenberg
Journal: Mol Cell Biol Date: 1987-03 Impact factor: 4.272

5. Characterization of the rearranged tpr-met oncogene breakpoint.

Authors: M Dean; M Park; G F Vande Woude
Journal: Mol Cell Biol Date: 1987-02 Impact factor: 4.272

6. Globin genes are useful markers to identify genetic similarities between Fijians and Pacific Islanders from Polynesia and Melanesia.

Authors: R J Trent; J G Buchanan; A Webb; R P Goundar; L M Seruvatu; K N Mickleson
Journal: Am J Hum Genet Date: 1988-04 Impact factor: 11.025

7. Activation of RNA polymerase III transcription of human Alu repetitive elements by adenovirus type 5: requirement for the E1b 58-kilodalton protein and the products of E4 open reading frames 3 and 6.

Authors: B Panning; J R Smiley
Journal: Mol Cell Biol Date: 1993-06 Impact factor: 4.272

8. Ruminant globin gene structures suggest an evolutionary role for Alu-type repeats.

Authors: J C Schimenti; C H Duncan
Journal: Nucleic Acids Res Date: 1984-02-10 Impact factor: 16.971

9. Homozygous hereditary C3 deficiency due to a partial gene deletion.

Authors: M Botto; K Y Fong; A K So; R Barlow; R Routier; B J Morley; M J Walport
Journal: Proc Natl Acad Sci U S A Date: 1992-06-01 Impact factor: 11.205

10. Severe combined immune deficiency due to a homozygous 3.2-kb deletion spanning the promoter and first exon of the adenosine deaminase gene.

Authors: T M Berkvens; E J Gerritsen; M Oldenburg; C Breukel; J T Wijnen; H van Ormondt; J M Vossen; A J van der Eb; P Meera Khan
Journal: Nucleic Acids Res Date: 1987-11-25 Impact factor: 16.971