Search Results - "Inaba, Yoshimi"
-
1
Droplet dynamics affecting the shape of patterns formed spontaneously by transforming UV-curable emulsions
Published in Scientific reports (26-03-2024)“…Forming large pitch and depth patterns spontaneously based on a bottom–up approach is a challenging task but with great industrial value. It is possible to…”
Get full text
Journal Article -
2
Spontaneous patterning method utilizing transformation of UV-curable emulsion
Published in Scientific reports (04-03-2022)“…A self-organizing structure is important for imparting functions and simplifying the manufacturing process. The development of spontaneous structures with a…”
Get full text
Journal Article -
3
Defining the 3′Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X Syndrome
Published in International journal of molecular sciences (01-07-2023)“…This study characterizes the DNA methylation patterns specific to fragile X syndrome (FXS) with a full mutation (FM > 200 CGGs), premutation (PM 55–199 CGGs),…”
Get full text
Journal Article -
4
Normal DNA methylation dynamics in DICER1-deficient mouse embryonic stem cells
Published in PLoS genetics (01-09-2012)“…Reduced DNA methylation has been reported in DICER1-deficient mouse ES cells. Reductions seen at pericentric satellite repeats have suggested that siRNAs are…”
Get full text
Journal Article -
5
Expression of a feedback insensitive anthranilate synthase gene from tobacco increases free tryptophan in soybean plants
Published in Plant cell reports (01-10-2007)“…Soybean [Glycine max (L.) Merr.] embryogenic cultures were transformed by particle bombardment with the feedback-insensitive tobacco anthranilate synthase (AS)…”
Get full text
Journal Article -
6
Defining the 3#8242;Epigenetic Boundary of the IFMR1/I Promoter and Its Loss in Individuals with Fragile X Syndrome
Published in International journal of molecular sciences (01-06-2023)“…This study characterizes the DNA methylation patterns specific to fragile X syndrome (FXS) with a full mutation (FM > 200 CGGs), premutation (PM 55–199 CGGs),…”
Get full text
Journal Article -
7
Defining the 3′Epigenetic Boundary of the IFMR1/I Promoter and Its Loss in Individuals with Fragile X Syndrome
Published in International journal of molecular sciences (01-06-2023)Get full text
Journal Article -
8
Defining the 3'Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X Syndrome
Published in International journal of molecular sciences (27-06-2023)“…This study characterizes the DNA methylation patterns specific to fragile X syndrome (FXS) with a full mutation (FM > 200 CGGs), premutation (PM 55-199 CGGs),…”
Get full text
Journal Article -
9
Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spots
Published in Clinical chemistry (Baltimore, Md.) (01-07-2014)“…Standard fragile X syndrome (FXS) diagnostic tests that target methylation of the fragile X mental retardation 1 (FMR1) CpG island 5' of the CGG expansion can…”
Get full text
Journal Article -
10
Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women
Published in Neurology (21-04-2015)“…OBJECTIVE:To examine the epigenetic basis of psychiatric symptoms and dysexecutive impairments in FMR1 premutation (PM55 to 199 CGG repeats) women. METHODS:A…”
Get full text
Journal Article -
11
Fragile X Mental Retardation 1 (FMR1) Intron 1 Methylation in Blood Predicts Verbal Cognitive Impairment in Female Carriers of Expanded FMR1 Alleles: Evidence from a Pilot Study
Published in Clinical chemistry (Baltimore, Md.) (01-03-2012)“…Cognitive status in females with mutations in the FMR1 (fragile X mental retardation 1) gene is highly variable. A biomarker would be of value for predicting…”
Get full text
Journal Article -
12
The use of droplet digital PCR and high resolution melt for detection of low level mosaicism
Published in Pathology (01-02-2018)Get full text
Journal Article -
13
Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and puberty
Published in Human molecular genetics (15-04-2013)“…Methylation of the fragile X-related epigenetic element 2 (FREE2) located on the exon 1/intron 1 boundary of the FMR1 gene is related to FMRP expression and…”
Get full text
Journal Article -
14
Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysis
Published in Expert reviews in molecular medicine (01-07-2015)“…Methylation of the fragile X mental retardation 1 (FMR1) exon 1/intron 1 boundary positioned fragile X related epigenetic element 2 (FREE2), reveals skewed…”
Get more information
Journal Article -
15
Fragile X–related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study
Published in Genetics in medicine (01-04-2013)“…Purpose: We show that a novel fragile X–related epigenetic element 2 FMR1 methylation test can be used along with a test for sex-determining region Y ( SRY )…”
Get full text
Journal Article -
16
Specificity of expression of the GUS reporter gene ( uidA) driven by the tobacco ASA2 promoter in soybean plants and tissue cultures
Published in Journal of plant physiology (01-07-2007)“…Twelve independent lines were transformed by particle bombardment of soybean embryogenic suspension cultures with the tobacco anthranilate synthase (ASA2)…”
Get full text
Journal Article -
17
-
18