Results 21 to 30 of about 227,914 (337)

A new and versatile method for the successful conversion of AFLP-TM markers into simple single locus markers [PDF]

open access: yes, 2003
Genetic markers can efficiently be obtained by using amplified fragment length polymorphism (AFLP) fingerprinting because no prior information on DNA sequence is required.
Brugmans, B.W.   +4 more
core   +2 more sources

Characteristics of Glucose Oxidase Gene (GGOx) from Aspergillus niger IPBCC 08.610

open access: yesJurnal Kimia Valensi, 2020
Glucose oxidase is used in various industries for the development of enzymatic fuel cell. Based on prior studies, this compound is sourced from the local isolates of Aspergillus niger IPBCC 08.610, although investigations on the encoding gene have not ...
Popi Asri Kurniatin   +5 more
doaj   +1 more source

A red/far-red light-responsive bi-stable toggle switch to control gene expression in mammalian cells [PDF]

open access: yes, 2013
Growth and differentiation of multicellular systems is orchestrated by spatially restricted gene expression programs in specialized subpopulations. The targeted manipulation of such processes by synthetic tools with high-spatiotemporal resolution could ...
Busacker, Moritz   +5 more
core   +1 more source

The Investigation of Haplotype Phasing Efficiency at the PAH Gene Region in Iranian Family Trios [PDF]

open access: yesIranian Journal of Public Health, 2009
Background: The haplotype phasing is more useful than genotyping markers independently at carrier detection and prena­tal diagnosis of diseases. The PAH gene region contains several markers used in detection of PKU disease.
Z Fazeli, S Vallian
doaj   +1 more source

An EcoRI polymorphism for the PLAUR gene [PDF]

open access: yesNucleic Acids Research, 1991
Udgivelsesdato: 1991-Dec ...
A. D. Børglum   +3 more
openaire   +4 more sources

Joining of Immunoglobulin Heavy Chain Gene Segments: Implications from a Chromosome with Evidence of Three D-JH Fusions [PDF]

open access: yes, 1982
A chromosomal segment with a unique structure around the immunoglobulin heavy chain joining region (JH) has been molecularly cloned from an Abelson murine leukemia virus-transformed cell line.
Alt, Frederick W., Baltimore, David
core   +1 more source

EcoRI analysis of bacteriophage P22 DNA packaging [PDF]

open access: yesJournal of Molecular Biology, 1978
Abstract Bacteriophage P22 linear DNA molecules are a set of circularly permuted sequences with ends located in a limited region of the physical map. This mature form of the viral chromosome is cut in headful lengths from a concatemeric precursor during DNA encapsulation.
Jackson, Ethel Noland   +2 more
openaire   +3 more sources

Facilitated diffusion during catalysis by EcoRI endonuclease. Nonspecific interactions in EcoRI catalysis.

open access: yesJournal of Biological Chemistry, 1985
The potential for processive EcoRI endonuclease hydrolysis has been examined on several DNA substrates containing two EcoRI sites which were embedded in identical sequence environments. With a 388-base pair circular DNA, in which the two recognition sites are separated by 51 base pairs (shorter distance) or 337 base pairs (longer distance), 77 and 34 ...
B J, Terry, W E, Jack, P, Modrich
openaire   +2 more sources

The N-terminal intrinsically disordered domain of mgm101p is localized to the mitochondrial nucleoid. [PDF]

open access: yes, 2013
The mitochondrial genome maintenance gene, MGM101, is essential for yeasts that depend on mitochondrial DNA replication. Previously, in Saccharomyces cerevisiae, it has been found that the carboxy-terminal two-thirds of Mgm101p has a functional core ...
A Moya   +48 more
core   +9 more sources

Organization and sequence of the gene encoding the human acrosin-trypsin inhibitor (HUSI-II) [PDF]

open access: yes, 1993
A complete cDNA encoding the acrosin-trypsin inhibitor, HUSI-II, was used as a probe to isolate genomic clones from a human placenta library. Three clones which cover the entire HUSI-II gene were isolated and characterized.
Abelson   +28 more
core   +1 more source

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