Results 91 to 100 of about 3,079 (276)
Introducción: la creación de centros para el desarrollo de la Genética comunitaria, en todos los municipios del país, ha hecho posible el incremento de la cobertura de atención de los servicios de genética médica en la atención primaria.
Yanet Hernández Triguero +3 more
doaj
SPROUTS_DB: An Implemented Database of Contaminants for Extracellular Vesicle Proteomics Studies
ABSTRACT Current proteomics techniques allow rapid identification and quantification of proteins within any given biological source. However, LC–MS/MS proteomics is vulnerable to laboratory and sample‐associated contaminants. Therefore, accurate identification and annotation of such contaminants is crucial for development of reliable databases ...
Maria Gaetana Giovanna Pittalà +10 more
wiley +1 more source
Thrombocytopenia is common in hepatocellular carcinoma and may increase bleeding risk during antiangiogenic therapy, yet the clinically relevant platelet threshold remains uncertain. We found that a baseline platelet count < 50 × 109/L was associated with bleeding; patients below this cutoff had a substantially higher bleeding rate than those with ...
Jun Tie +8 more
wiley +1 more source
Se realizó un estudio descriptivo transversal en el Hospital Pediátrico "Dr. Eduardo Agramonte Piña" de Camagüey, con el objetivo de evaluar el Programa de diagnóstico prenatal de las malformaciones congénitas, a través de la cuantificación de la ...
Elisa Dyce Gordon +3 more
doaj
Current Cell/Organoid and Animal Models for Primary Sclerosing Cholangitis
Primary sclerosing cholangitis (PSC) is a chronic cholestatic liver disease with limited therapeutic options and a marked risk of progression to biliary fibrosis, cirrhosis, and malignancy. Progress in PSC research has been hindered by the lack of models that faithfully recapitulate the complex biliary microenvironment and disease heterogeneity ...
Qigu Yao +4 more
wiley +1 more source
Introducción: En los últimos años ha aumentado la importancia de las anomalías congénitas y enfermedades hereditarias como causa de muerte en el primer año de vida.
Pedro Antonio Ramírez Sosa +3 more
doaj
ヒト肝細胞癌の発癌機序:病理組織像と細胞動態細胞形質像.遺伝子学的性常との対比 [PDF]
金沢大学医学部癌遺伝子、癌抑制遺伝子の解析:ras癌遺伝子産物とp53癌抑制遺伝子産物を免疫組織化学的に検討した。p53はAHでは全く発現がなく、肝細胞癌の2%位に発現がみられた。従って、肝発癌ではp53の関与は、発癌後期に関与すると考えられた。ras遺伝子産物は、異型型AHと癌内包型AHの一部の症例で弱く発現されており、肝細胞癌で中等度に発現されていた。以上、rasの発現は、肝発癌の初期におこると思われた。AHのヌードマウスへの移植:最近外科切除AHがなく、実験できなかった。臨床追跡調査 ...
Terada Tadashi, 寺田 忠史
core +1 more source
Abstract Background Para‐testicular rhabdomyosarcoma (RMS) is a rare and aggressive malignancy primarily affecting children and adolescents, with peak incidence between ages 2 and 5 years. Of the histological variants of RMS, the spindle cell type of RMS is particularly uncommon, accounting for approximately 5% of cases.
Kholoud Alabassi +5 more
wiley +1 more source
Orthesenversorgung in Anlehnung an das Ferrari-Konzept bei Kindern und Erwachsenen mit Meningomyelozele [PDF]
BACKGROUND: Even today, myelomeningocele (MMC) is still encountered in clinical medicine and its incidence has not decreased over the last 20 years despite a known reduction in risk due to the use of folic acid supplements.
Schmid, Tim
core +1 more source

