نتایج جستجو برای: upstream region analysis

تعداد نتایج: 3254422  

2012
Anna Ogrocká Eva Sýkorová Jiří Fajkus Miloslava Fojtová

Telomerase, an enzyme responsible for the maintenance of linear chromosome ends, is precisely regulated during plant development. In animals, involvement of the epigenetic state of the telomerase reverse transcriptase (TERT) gene in the complex regulation of telomerase activity has been reported. To reveal whether epigenetic mechanisms participate in the regulation of plant telomerase, the rela...

Journal: :Infection and immunity 1994
D L Kiska F L Macrina

Streptococcus mutans possesses several extracellular sucrose-metabolizing enzymes which have been implicated as important virulence factors in dental caries. This study was initiated to investigate the genetic regulation of one of these enzymes, the extracellular fructosyltransferase (Ftf). Fusions were constructed with the region upstream of the S. mutans GS5 Ftf gene (ftf) and a promoterless ...

Journal: :Molecular and cellular biology 1997
K D Tremblay K L Duran M S Bartolomei

The imprinted mouse H19 gene is hypermethylated on the inactive paternal allele in somatic tissues and sperm. Previous observations from a limited analysis have suggested that methylation of a few CpG dinucleotides in the region upstream from the start of transcription may be the mark that confers parental identity to the H19 alleles. Here we exploit bisulfite mutagenesis coupled with genomic s...

This study investigated the effect of the installation of flood dams on the morphological variation of Alburnoides samiii Mousavi-Sabet, Vatandoust & Doadrio, 2015, in Toolkhone River, origin from Somam Mountain, the South Caspian Sea basin, north of Iran. Multivariate analysis (MANOVA) was employed for morphometric characteristics of the fish inhabit upstream and downstream of the dams. Signif...

Journal: :Nucleic acids research 1991
G P van Wezel E Vijgenboom L Bosch

S. coelicolor A3(2) contains six ribosomal RNA operons. Here we describe the cloning of rrnA, rrnC and rrnE, thereby completing the cloning of all operons. Southern hybridisation of genomic DNA with a heterologous probe from the E.coli rrnB 16S rRNA gene showed differences in hybridisation among the six rRNA operon-containing bands. The nucleotide sequence of the 16S rRNA gene and the upstream ...

Journal: :Journal of bacteriology 1993
K L Brown

The two predominant polypeptides of the Bacillus thuringiensis subsp. thompsoni crystal are encoded by the cry40 and cry34 genes. These crystal protein genes are located in an operon. Western analysis (immunoblotting) demonstrated that the operon promoter activity was located in the region upstream of the cry40 gene. The Cry34 protein was expressed only when the upstream promoter region was pre...

2009
F J Higuera A Linan

An analysis is presented of the viscous-inviscid interaction region around the tip of a flame spreading over the surface of a solid fuel in a forced laminar high Reynolds number air stream that opposes the flame propagation. Through the interaction. the vaporization of the solid and the thermal expansion of the gas originate an adverse pressure gradient upstream of the flame tip. which leads to...

Journal: :Journal of medical genetics 2015
Gwang-Jin Kim Elisabeth Sock Astrid Buchberger Walter Just Friederike Denzer Wolfgang Hoepffner James German Trevor Cole Jillian Mann John H Seguin William Zipf Colm Costigan Hardi Schmiady Moritz Rostásy Mildred Kramer Simon Kaltenbach Bernd Rösler Ina Georg Elke Troppmann Anne-Christin Teichmann Anika Salfelder Sebastian A Widholz Peter Wieacker Olaf Hiort Giovanna Camerino Orietta Radi Michael Wegner Hans-Henning Arnold Gerd Scherer

BACKGROUND SOX9 mutations cause the skeletal malformation syndrome campomelic dysplasia in combination with XY sex reversal. Studies in mice indicate that SOX9 acts as a testis-inducing transcription factor downstream of SRY, triggering Sertoli cell and testis differentiation. An SRY-dependent testis-specific enhancer for Sox9 has been identified only in mice. A previous study has implicated co...

Journal: :Blood 1992
F Fernandez-Rachubinski R A Rachubinski M A Blajchman

This report details the precise mapping of a partially deleted human antithrombin III (AT-III) allele, found in a kindred with an inherited type 1 AT-III deficiency. Using truncated AT-III probes generated by polymerase chain reaction (PCR) amplification from a full-length AT-III cDNA, as well as other genomic probes specific for the 5' upstream region of the AT-III gene, we were able to charac...

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