Výsledky vyhledávání - "Emiko Noguchi"

Akademický článek

Gut microbiota of one-and-a-half-year-old food-allergic and healthy children

Autor: Monami Hara, Hisato Suzuki, Daisuke Hayashi, Wataru Morii, Takako Nakamura, Kaori Kiyoki, Hideki Hara, Ryota Ishii, Emiko Noguchi, Hidetoshi Takada

Publikováno v: Allergology International, Vol 73, Iss 4, Pp 550-555 (2024)

Background: Intestinal bacteria may play a role in the development of food allergies. This study aimed to analyze and compare the gut microbiota of food-allergic children with that of healthy children of the same age. Methods: Stool samples were coll

Externí odkaz: https://doaj.org/article/96f2b12c233e40888c15ef40b8a99a7c

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Akademický článek

Influence of household pet ownership and filaggrin loss-of-function mutations on eczema prevalence in children: A birth cohort study

Publikováno v: Allergology International, Vol 73, Iss 3, Pp 422-427 (2024)

Background: The association between pet exposure in infancy, early childhood eczema, and FLG mutations remains unclear. Methods: This was a birth cohort study performed in Tokyo, Japan. The primary outcome was current eczema based on questionnaire re

Externí odkaz: https://doaj.org/article/be00c4123e42439abf3eff7e4126fab3

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Akademický článek

A genome-wide association study for allergen component sensitizations identifies allergen component–specific and allergen protein group–specific associations

Autor: Wataru Morii, PhD, Koki Kasai, BS, Takako Nakamura, MSc, Daisuke Hayashi, MD, Monami Hara, MD, Tatsuhiko Naito, MD, PhD, Kyuto Sonehara, MD, PhD, Tatsuki Fukuie, MD, PhD, Mayako Saito-Abe, MD, PhD, Limin Yang, MD, PhD, Kiwako Yamamoto-Hanada, MD, PhD, Masami Narita, MD, PhD, Kazushi Maruo, PhD, Yukinori Okada, MD, PhD, Emiko Noguchi, MD, PhD, Yukihiro Ohya, MD, PhD

Publikováno v: Journal of Allergy and Clinical Immunology: Global, Vol 2, Iss 2, Pp 100086- (2023)

Background: Allergic diseases are some of the most common diseases worldwide. Genome-wide association studies (GWASs) have been conducted to elucidate the genetic factors of allergic diseases. However, no GWASs for allergen component sensitization ha

Externí odkaz: https://doaj.org/article/058964c6d2e64335bbff19fe91a7e2b9

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Akademický článek

ORMDL3/GSDMB genotype as a risk factor for early-onset adult asthma is linked to total serum IgE levels but not to allergic sensitization

Autor: Haruna Kitazawa, Hironori Masuko, Jun Kanazawa, Rie Shigemasa, Kentaro Hyodo, Hideyasu Yamada, Yohei Yatagai, Yoshiko Kaneko, Hiroaki Iijima, Takashi Naito, Takefumi Saito, Emiko Noguchi, Satoshi Konno, Tomomitsu Hirota, Mayumi Tamari, Tohru Sakamoto, Nobuyuki Hizawa

Publikováno v: Allergology International, Vol 70, Iss 1, Pp 55-60 (2021)

Background: An orosomucoid-like 3 (ORMDL3)/gasdermin B (GSDMB) gene locus on chromosome 17q is consistently associated with childhood-onset asthma, which is highly atopic. As some evidence suggests the relationship between asthma and allergic sensiti

Externí odkaz: https://doaj.org/article/dc9be9a4d43e4fd5afaaa778667fc0ba

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Akademický článek

A Family with Gitelman Syndrome with Asymptomatic Phenotypes while Carrying Reported SLC12A3 Mutations

Autor: Moena Ishikawa, Yumi Tada, Hiromu Tanaka, Wataru Morii, Masako Inaba, Hidetoshi Takada, Takayasu Mori, Emiko Noguchi

Publikováno v: Case Reports in Nephrology and Dialysis, Vol 10, Iss 2, Pp 71-78 (2020)

Gitelman syndrome (GS) is an autosomal recessive disorder characterized by alkalosis, hypokalemia, and hypomagnesemia. Although hundreds of genetic variants associated with GS have been reported, many of them are categorized as of uncertain significa

Externí odkaz: https://doaj.org/article/d10e3bb601fd4cbcb524a7c61b66a087

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Akademický článek

Ovarian metastases from ileum cancer in a patient with germline EPCAM gene deletion successfully treated with surgical resection and CAPOX chemotherapy: a case report

Autor: Narushi Iwata, Ayumi Shikama, Wataru Takao, Yoshihiko Hosokawa, Hiroya Itagaki, Nobutaka Tasaka, Azusa Akiyama, Hiroyuki Ochi, Takeo Minaguchi, Miwa Arita, Emiko Noguchi, Toshikazu Moriwaki, Toyomi Satoh

Publikováno v: BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)

Abstract Background Despite recent findings that epithelial cell adhesion molecule (EPCAM) deletions can cause Lynch syndrome (LS), its clinical characteristics are still unknown. We present the first case of ileum cancer in a patient with germline E

Externí odkaz: https://doaj.org/article/9972b91304144c0998593b68f0b11c4c

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