Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
Mais filtros

Base de dados
Tipo de documento
Intervalo de ano de publicação
1.
Prog Earth Planet Sci ; 9(1): 11, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35127336

RESUMO

The exact occurrence frequency of noctilucent clouds (NLCs) in middle latitudes is significant information because it is thought to be sensitive to long-term atmospheric change. We conducted NLC observation from airline jets in the Northern Hemisphere during the summer 2019 to evaluate the effectiveness of NLC observation from airborne platforms. By cooperating with the Japanese airline All Nippon Airways (ANA), imaging observations of NLCs were conducted on 13 flights from Jun 8 to Jul 12. As a result of careful analysis, 8 of these 13 flights were found to successfully detect NLCs from middle latitudes (lower than 55° N) during their cruising phase. Based on the results of these test observations, it is shown that an airline jet is a powerful tool to continuously monitor the occurrence frequency of NLCs at midlatitudes which is generally difficult with a polar orbiting satellite due to sparse sampling in both temporal and spatial domain. The advantages and merits of NLC observation from jets over satellite observation from a point of view of imaging geometry are also presented.

2.
Biol Pharm Bull ; 45(1): 118-123, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-34980773

RESUMO

Medication wastage is a global issue; however, there are few reports in Japanese hospitals. The purpose of this study was to clarify the situation of medication wastage at our university hospital. We investigated the numbers, costs, reasons, occurrence departments, and involvement of high-priced medications of medication wastage for two years. We analyzed 6730 cases and the total cost was 22782027 Japanese yen (JPY). The most common reasons for medication wastage were change or discontinuation of medication after preparation and breakage or contamination due to dropping. The highest cost was expired medications. The department with the highest number of cases was the hospital wards; however, the hospital pharmacy department accounted for the majority of the costs and most of the reasons were expired medications. Medication wastage of 50000 JPY or more per case was only 1.3% of the total but accounted for 70.7% of the cost and medication wastage of 100000 JPY or more per case was only 0.7% of the total but accounted for 58.6% of the cost. These findings indicate that expired medications in the hospital pharmacy department have the largest impact on medication wastage from the viewpoint of economic loss, and suggest the need for efforts on medication management focusing on high-priced medications. The challenge of minimizing medication wastage should be addressed from the perspectives of both hospital management and the effective use of resources.


Assuntos
Assistência Farmacêutica , Hospitais Universitários , Humanos , Japão
3.
Orphanet J Rare Dis ; 16(1): 443, 2021 10 21.
Artigo em Inglês | MEDLINE | ID: mdl-34674729

RESUMO

BACKGROUND: Basal cell carcinoma (BCC) is the most commonly occurring neoplasm in patients with Gorlin syndrome. It is widely accepted that multiple basal cell carcinomas simultaneously develop in middle-aged patients with this syndrome. However, the presence of driver genes other than the PTCH1 in Gorlin syndrome has not been explored. This study aimed to identify common gene mutations other than PTCH1 in simultaneously occurring basal cell carcinomas in patients with Gorlin syndrome via exome sequencing analysis. METHODS: Next-generation sequencing analysis was performed using four basal cell carcinoma samples, one dental keratinocyte sample, and two epidermoid cyst samples, which were surgically resected from one patient with Gorlin syndrome on the same day. RESULTS: Overall, 282 somatic mutations were identified in the neoplasms. No additional somatic mutations in PTCH1, PTCH2, TP53, and SMO were identified. However, enrichment analysis showed that multiple genes, such as IFT172 and KIFAP3, could regulate ciliary functions important for Hedgehog signaling. CONCLUSION: The development of BCCs in patients with Gorlin syndrome may be triggered by mutations that cause substantial dysfunction of cilia.


Assuntos
Síndrome do Nevo Basocelular , Carcinoma Basocelular , Neoplasias Cutâneas , Proteínas Adaptadoras de Transdução de Sinal , Síndrome do Nevo Basocelular/genética , Carcinoma Basocelular/genética , Proteínas do Citoesqueleto , Proteínas Hedgehog/metabolismo , Humanos , Pessoa de Meia-Idade , Receptor Patched-1/genética , Neoplasias Cutâneas/genética
4.
Bull Tokyo Dent Coll ; 62(1): 41-47, 2021 Mar 13.
Artigo em Inglês | MEDLINE | ID: mdl-33583876

RESUMO

Many cases of immunoglobulin G4-related disease (IgG4-RD) involve swelling of the salivary glands, often affecting the parotid and submandibular glands in the head and neck region, in addition to the lacrimal glands. Cases of IgG4-RD characterized by swelling of the palatal glands, however, are extremely rare. Here, we describe a case of IgG4-RD involving bilateral swelling of the palatal glands. An 83-year-old man presented at our hospital with bilateral swelling of the lacrimal and submandibular glands. A solid bilateral swelling of normal colour and unclear boundaries was observed in the hard palate. The lesion was diagnosed as IgG4-RD and steroid therapy initiated. A subsequent decrease in swelling of the palatal, lacrimal, and submandibular glands was confirmed by magnetic resonance imaging. These results indicate that dentists should suspect IgG4-RD in patients presenting with bilateral swelling of the palatal glands.


Assuntos
Dacriocistite , Sialadenite , Idoso de 80 Anos ou mais , Dacriocistite/diagnóstico , Dacriocistite/tratamento farmacológico , Humanos , Imunoglobulina G , Masculino , Glândulas Salivares , Sialadenite/diagnóstico , Glândula Submandibular/diagnóstico por imagem
5.
Med Mol Morphol ; 54(2): 69-78, 2021 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-32816116

RESUMO

Gorlin syndrome (GS) is an autosomal dominant genetic disorder involving Patched 1 (PTCH1) mutations. The PTCH1 is a receptor as well as an inhibitor of hedgehog (Hh) to sequester downstream Hh pathway molecules called Smoothened (SMO). PTCH1 mutations causes a variety of GS conditions including falx calcification, odontogenic keratocytes and basal cell carcinomas (BCC). Because PTCH1 is a major driver gene of sporadic BCC, GS patients are characteristically prone to BCC. In order to elucidate the pathological mechanism of BCC-prone GS patients, we investigated keratinocytes derived from GS patient specific iPS cells (G-OFiPSCs) which were generated and reported previously. We found that keratinocytes derived from G-OFiPSCs (GKCs) have increased expression of Hh target molecules. GKCs were irradiated and those cells showed high resistance to UV induced apoptosis. BCL2, known as anti-apoptotic molecule as well as Hh target, significantly increased in GKCs. Several molecules involved in DNA repair, cell cycle control, senescence, and genotoxic stress such as TP53, BRCA1 and GADD45A increased only in GKCs. GKCs are indicated to be resistant to UV irradiation by upregulating molecules which control DNA repair and genotoxic even under DNA damage caused by UV. The anti-apoptotic properties of GKCs may contribute BCC.


Assuntos
Síndrome do Nevo Basocelular/metabolismo , Ciclo Celular , Reparo do DNA , Queratinócitos/metabolismo , Receptor Patched-1/genética , Raios Ultravioleta , Apoptose , Povo Asiático , Proteína BRCA1/genética , Proteína BRCA1/metabolismo , Síndrome do Nevo Basocelular/genética , Síndrome do Nevo Basocelular/fisiopatologia , Carcinoma Basocelular , Proteínas de Ciclo Celular/genética , Proteínas de Ciclo Celular/metabolismo , Regulação da Expressão Gênica , Proteínas Hedgehog/metabolismo , Humanos , Células-Tronco Pluripotentes Induzidas , Queratinócitos/fisiologia , Queratinócitos/efeitos da radiação , Mutação , Transdução de Sinais , Receptor Smoothened/genética , Proteína Supressora de Tumor p53/genética , Proteína Supressora de Tumor p53/metabolismo
6.
Int J Mol Sci ; 21(20)2020 Oct 13.
Artigo em Inglês | MEDLINE | ID: mdl-33066274

RESUMO

Gorlin syndrome is a skeletal disorder caused by a gain of function mutation in Hedgehog (Hh) signaling. The Hh family comprises of many signaling mediators, which, through complex mechanisms, play several important roles in various stages of development. The Hh information pathway is essential for bone tissue development. It is also the major driver gene in the development of basal cell carcinoma and medulloblastoma. In this review, we first present the recent advances in Gorlin syndrome research, in particular, the signaling mediators of the Hh pathway and their functions at the genetic level. Then, we discuss the phenotypes of mutant mice and Hh signaling-related molecules in humans revealed by studies using induced pluripotent stem cells.


Assuntos
Síndrome do Nevo Basocelular/genética , Testes Genéticos/métodos , Animais , Síndrome do Nevo Basocelular/diagnóstico , Síndrome do Nevo Basocelular/metabolismo , Osso e Ossos/metabolismo , Osso e Ossos/patologia , Instabilidade Genômica , Proteínas Hedgehog/genética , Proteínas Hedgehog/metabolismo , Humanos , Receptores Patched/genética , Receptores Patched/metabolismo
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA