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1
Low soluble FcRIII receptor demonstrates reduced neutrophil reserves in preterm neonates.低溶性FcRIII受体表明早产儿中性粒细胞储备减少。
Arch Dis Child Fetal Neonatal Ed. 2000 Sep;83(2):F160. doi: 10.1136/fn.83.2.f160.
2
Changes in plasma FcRIII demonstrate increasing receptor production during late pregnancy and after preterm birth.
Pediatr Res. 1992 Nov;32(5):505-8. doi: 10.1203/00006450-199211000-00001.
3
Abnormal FcRIII expression by neutrophils from very preterm neonates.极早产儿中性粒细胞的异常FcRIII表达。
Blood. 1990 Aug 1;76(3):607-11.
4
Cell-surface expression of immunoglobulin G receptors on the polymorphonuclear leukocytes and monocytes of extremely premature infants.
Pediatr Res. 1993 May;33(5):452-7. doi: 10.1203/00006450-199305000-00007.
5
Impaired neutrophil phagocytosis in preterm neonates: lack of correlation with expression of immunoglobulin or complement receptors.早产儿中性粒细胞吞噬功能受损:与免疫球蛋白或补体受体表达缺乏相关性。
Biol Neonate. 1995;68(4):264-9. doi: 10.1159/000244245.
6
Neutrophils from term and preterm newborn infants express the high affinity Fcgamma-receptor I (CD64) during bacterial infections.足月和早产新生儿的中性粒细胞在细菌感染期间表达高亲和力Fcγ受体I(CD64)。
Pediatr Res. 1999 Jun;45(6):871-6. doi: 10.1203/00006450-199906000-00016.
7
The PI-linked receptor FcRIII is released on stimulation of neutrophils.磷脂酰肌醇连接受体FcRIII在中性粒细胞受到刺激时释放。
Nature. 1988 Jun 16;333(6174):667-9. doi: 10.1038/333667a0.
8
Neutrophil chemotaxis and adhesion in preterm babies.早产儿中性粒细胞趋化性与黏附性
Arch Dis Child. 1993 Jan;68(1 Spec No):68. doi: 10.1136/adc.68.1_spec_no.68.
9
Soluble Fc gamma receptor III in human plasma originates from release by neutrophils.人血浆中的可溶性Fcγ受体III源自中性粒细胞的释放。
J Clin Invest. 1990 Aug;86(2):416-23. doi: 10.1172/JCI114727.
10
The 40-kDa Fc gamma receptor (FcRII) on human neutrophils is essential for the IgG-induced respiratory burst and IgG-induced phagocytosis.人类中性粒细胞上的40 kDa Fcγ受体(FcRII)对于IgG诱导的呼吸爆发和IgG诱导的吞噬作用至关重要。
J Immunol. 1989 Apr 1;142(7):2365-9.

引用本文的文献

1
An IL-10/DEL-1 axis supports granulopoiesis and survival from sepsis in early life.IL-10/DEL-1 轴支持生命早期脓毒症中的粒细胞生成和存活。
Nat Commun. 2024 Jan 23;15(1):680. doi: 10.1038/s41467-023-44178-y.
2
Neonatal sepsis and transient immunodeficiency: Potential for novel immunoglobulin therapies?新生儿败血症和短暂性免疫缺陷:新型免疫球蛋白治疗的潜力?
Front Immunol. 2022 Oct 18;13:1016877. doi: 10.3389/fimmu.2022.1016877. eCollection 2022.
3
Defective Leukocyte β2 Integrin Expression and Reactive Oxygen Species Production in Neonates.新生儿白细胞β2整合素表达缺陷与活性氧生成
Children (Basel). 2022 Apr 1;9(4):494. doi: 10.3390/children9040494.
4
Vaccination in preterm and low birth weight infants in India.印度早产儿和低出生体重儿的疫苗接种。
Hum Vaccin Immunother. 2022 Dec 31;18(1):1-12. doi: 10.1080/21645515.2020.1866950. Epub 2021 Feb 18.
5
Dysregulated Mucosal Immunity and Associated Pathogeneses in Preterm Neonates.早产儿黏膜免疫失调及其相关发病机制。
Front Immunol. 2020 May 15;11:899. doi: 10.3389/fimmu.2020.00899. eCollection 2020.
6
Age-Appropriate Functions and Dysfunctions of the Neonatal Neutrophil.新生儿中性粒细胞的年龄相关功能与功能障碍
Front Pediatr. 2017 Feb 28;5:23. doi: 10.3389/fped.2017.00023. eCollection 2017.
7
Bench-to-bedside review: Developmental influences on the mechanisms, treatment and outcomes of cardiovascular dysfunction in neonatal versus adult sepsis.从实验台到病床旁的综述:发育对新生儿与成人脓毒症中心血管功能障碍的机制、治疗及结局的影响
Crit Care. 2007;11(5):228. doi: 10.1186/cc6091.
8
Interaction of neonatal phagocytes with group B streptococcus: recognition and response.新生儿吞噬细胞与B族链球菌的相互作用:识别与反应。
Infect Immun. 2006 Jun;74(6):3085-95. doi: 10.1128/IAI.01551-05.
9
G-CSF and GM-CSF for treating or preventing neonatal infections.用于治疗或预防新生儿感染的粒细胞集落刺激因子和粒细胞-巨噬细胞集落刺激因子。
Cochrane Database Syst Rev. 2003;2003(3):CD003066. doi: 10.1002/14651858.CD003066.

Low soluble FcRIII receptor demonstrates reduced neutrophil reserves in preterm neonates.

作者信息

Carr R, Huizinga T W

出版信息

Arch Dis Child Fetal Neonatal Ed. 2000 Sep;83(2):F160. doi: 10.1136/fn.83.2.f160.

DOI:10.1136/fn.83.2.f160
PMID:11012271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1721145/
Abstract
摘要