机译:偶发性淋巴水肿,树突状细胞,单核细胞,B细胞和NK细胞(DCML)缺乏以及骨髓增生异常病例的GATA-2异常和临床表型
Department of Pediatrics and Blood and Marrow transplantation, Matsushita Memorial Hospital, 5-55, Sotojima-cho, Moriguchi, 570-8540, Japan;
Department of Pediatrics, Tokyo Medical and Dental University, 5-45 Yushima 1-Chome, Bunkyo-Ku, Tokyo, 113-8510, Japan;
Department of Pediatrics, National Defense Medical College, 3-2 Namiki, Tokorozawa, 359-8513, Japan;
Department of Pediatrics and Blood and Marrow transplantation, Matsushita Memorial Hospital, 5-55, Sotojima-cho, Moriguchi, 570-8540, Japan;
Department of Pediatrics, Kyoto Prefectural University of Medicine, 465 Kajii-Cho, Kawaramachi-Hirokoji, Kamigyo-Ku, Kyoto, 602-8566, Japan;
Department of Pathology, Japanese Red Cross Nagoya First Hospital, 3-35 Michishita-cho, Nakamura-ku, Nagoya, 453-0046, Japan;
Department of Pediatrics, National Defense Medical College, 3-2 Namiki, Tokorozawa, 359-8513, Japan;
Emberger syndrome; MonoMAC; Monocytopenia; B- and NK-cell lymphopenia; Immunodeficiency; Myelodysplasia;
机译:偶发性淋巴水肿,树突状细胞,单核细胞,B细胞和NK细胞(DCML)缺乏以及骨髓增生异常病例的GATA-2异常和临床表型。
机译:外显子组测序确定GATA-2突变为树突状细胞,单核细胞,B和NK淋巴缺乏的原因。
机译:树突状细胞,单核细胞,B和NK淋巴样缺陷定义了新的GATA-2依赖性骨髓增生异常综合症的丢失谱系|血液学
机译:PLGA微粒联合疗法在人单核细胞衍生的树突状细胞中诱导耐受性表型
机译:树突状细胞单核细胞B和NK淋巴样缺陷定义了新的GATA-2依赖性骨髓增生异常综合症的丢失谱系
机译:树突状细胞,单核细胞,B和NK淋巴样缺陷定义了新的GATA-2依赖性骨髓增生异常综合症的丢失谱系