Search Results - "Matsuda, Chie"
-
1
Obstetrical outcomes of labor with and without analgesia in Robson classification groups 1 and 2a: a single-center retrospective study
Published in Journal of anesthesia (01-02-2023)“…Purpose This study aimed to elucidate the effects of neuraxial analgesia on labor in women classified based on the Robson classification system. Methods We…”
Get full text
Journal Article -
2
Structural instability of lamin A tail domain modulates its assembly and higher order function in Emery–Dreifuss muscular dystrophy
Published in Biochemical and biophysical research communications (23-04-2019)“…The C-terminal Ig-domain of lamin A plays critical roles in cell function via interaction with proteins, DNA, and chromatin. Mutations in this domain are known…”
Get full text
Journal Article -
3
Upregulated expression of FGF13/FHF2 mediates resistance to platinum drugs in cervical cancer cells
Published in Scientific reports (11-10-2013)“…Cancer cells often develop drug resistance. In cisplatin-resistant HeLa cisR cells, fibroblast growth factor 13 (FGF13/FHF2) gene and protein expression was…”
Get full text
Journal Article -
4
Effects of microgravity exposure and fructo-oligosaccharide ingestion on the proteome of soleus and extensor digitorum longus muscles in developing mice
Published in NPJ microgravity (17-09-2021)“…Short-chain fatty acids produced by the gut bacterial fermentation of non-digestible carbohydrates, e.g., fructo-oligosaccharide (FOS), contribute to the…”
Get full text
Journal Article -
5
Augmented autocrine bone morphogenic protein (BMP) 7 signaling increases the metastatic potential of mouse breast cancer cells
Published in Clinical & experimental metastasis (01-04-2012)“…As malignant breast cancers progress, they acquire the ability to spread to other regions of the body, including bone and lung, but the molecular mechanism…”
Get full text
Journal Article -
6
Contribution of dysferlin deficiency to skeletal muscle pathology in asymptomatic and severe dystroglycanopathy models: generation of a new model for Fukuyama congenital muscular dystrophy
Published in PloS one (08-09-2014)“…Defects in dystroglycan glycosylation are associated with a group of muscular dystrophies, termed dystroglycanopathies, that include Fukuyama congenital…”
Get full text
Journal Article -
7
Successful pulmonary embolectomy for massive pulmonary embolism during pregnancy: a case report
Published in JA clinical reports (25-08-2017)“…Background Pulmonary embolism (PE) resulting from venous thromboembolism is a leading cause of maternal mortality in pregnancy. In patients with massive PE and…”
Get full text
Journal Article -
8
Dietary intervention of mice using an improved Multiple Artificial-gravity Research System (MARS) under artificial 1 g
Published in NPJ microgravity (08-07-2019)“…Japan Aerospace Exploration Agency (JAXA) has developed mouse habitat cage units equipped with an artificial gravity-producing centrifuge, called the Multiple…”
Get full text
Journal Article -
9
Incidence and Cause of Headache after Cesarean Section
Published in THE JOURNAL OF JAPAN SOCIETY FOR CLINICAL ANESTHESIA (15-11-2020)“…We analyzed a series of 657 parturients that had cesarean sections between January 2016 and April 2019 using data from electronic patient records. Of the 118…”
Get full text
Journal Article -
10
Distal anterior compartment myopathy: A dysferlin mutation causing a new muscular dystrophy phenotype
Published in Annals of neurology (01-01-2001)“…We report a family with a new phenotype of autosomal recessive muscle dystrophy caused by a dysferlin mutation. The onset of the illness is distal, in the…”
Get full text
Journal Article -
11
Defective Myotilin Homodimerization Caused by a Novel Mutation in MYOT Exon 9 in the First Japanese Limb Girdle Muscular Dystrophy 1A Patient
Published in Journal of neuropathology and experimental neurology (01-06-2009)“…Myotilin is a muscle-specific Z disk protein. Several missense mutations in the myotilin gene (MYOT) have been identified in limb girdle muscular dystrophy…”
Get full text
Journal Article -
12
Mutations in the integrin α7 gene cause congenital myopathy
Published in Nature genetics (01-05-1998)Get full text
Journal Article -
13
Ultrasound guided nerve block in infants undergoing pyloromyotomy
Published in Masui. The Japanese journal of anesthesiology (01-04-2013)“…Ultrasound guided nerve block has become popular in pediatric practice. We applied this technique to infants undergoing pyloromyotomy. We retrospectively…”
Get more information
Journal Article -
14
The effect of nitroglycerin 200 microg on uterine relaxation during cesarean delivery
Published in Masui. The Japanese journal of anesthesiology (01-04-2013)“…Rapid and transient uterine relaxation is sometimes required for fetal distress or difficult delivery due to uterine hyperactivity during cesarean section. For…”
Get more information
Journal Article -
15
Ultrasound guided transversus abdominis plane block in early infancy
Published in Masui. The Japanese journal of anesthesiology (01-08-2013)“…We retrospectively examined the transversus abdominis plane (TAP) block performed in 8 infants (range, 1-115 days) from July 2010 to March 2011. Ultrasound…”
Get more information
Journal Article -
16
-
17
Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy
Published in The Journal of clinical investigation (01-09-2009)“…Caveolae are invaginations of the plasma membrane involved in many cellular processes, including clathrin-independent endocytosis, cholesterol transport, and…”
Get full text
Journal Article -
18
Two endoplasmic reticulum-associated degradation (ERAD) systems for the novel variant of the mutant dysferlin: ubiquitin/proteasome ERAD(I) and autophagy/lysosome ERAD(II)
Published in Human molecular genetics (15-03-2007)“…Dysferlin is a type-II transmembrane protein and the causative gene of limb girdle muscular dystrophy type 2B and Miyoshi myopathy (LGMD2B/MM), in which…”
Get full text
Journal Article -
19
Incidence and Cause of Headache after Cesarean Section
Published in Nihon Rinshō Masui Gakkai shi (15-11-2020)Get full text
Journal Article -
20
Specific phosphorylation of Ser458 of A-type lamins in LMNA-associated myopathy patients
Published in Journal of cell science (15-11-2010)“…Mutations in LMNA, which encodes A-type nuclear lamins, cause various human diseases, including myopathy, cardiomyopathy, lipodystrophy and progeria syndrome…”
Get full text
Journal Article