Turnitin
降AI改写
早检测系统
早降重系统
Turnitin-UK版
万方检测-期刊版
维普编辑部版
Grammarly检测
Paperpass检测
checkpass检测
PaperYY检测
STAT3 hyper-IgE syndrome—an update and unanswered questions
C Tsilifis, AF Freeman, AR Gennery - Journal of clinical immunology, 2021 - Springer
The hyper-IgE syndromes (HIES) are a heterogeneous group of inborn errors of immunity
sharing manifestations including increased infection susceptibility, eczema, and raised …
sharing manifestations including increased infection susceptibility, eczema, and raised …
DOCK8 deficiency: insights into pathophysiology, clinical features and management
Abstract Dedicator of cytokinesis 8 (DOCK8) deficiency is a combined immunodeficiency
that exemplifies the broad clinical features of primary immunodeficiencies (PIDs), extending …
that exemplifies the broad clinical features of primary immunodeficiencies (PIDs), extending …
Signaling pathways involved in the T‐cell‐mediated immunity against Epstein‐Barr virus: Lessons from genetic diseases
S Latour, A Fischer - Immunological reviews, 2019 - Wiley Online Library
Primary immunodeficiencies (PIDs) provide researchers with unique models to understand
in vivo immune responses in general and immunity to infections in particular. In humans …
in vivo immune responses in general and immunity to infections in particular. In humans …
Hyper IgE syndromes: clinical and molecular characteristics
T Al‐Shaikhly, HD Ochs - Immunology and cell biology, 2019 - Wiley Online Library
Hyper IgE syndromes comprise a group of rare primary immunodeficiency disorders
characterized by a triad of atopic dermatitis, recurrent skin and lung infections along with …
characterized by a triad of atopic dermatitis, recurrent skin and lung infections along with …
Intrinsic and extrinsic causes of malignancies in patients with primary immunodeficiency disorders
F Hauck, R Voss, C Urban, MG Seidel - Journal of Allergy and Clinical …, 2018 - Elsevier
Malignancies occur with a higher incidence rate and manifest earlier in life in patients with
primary immunodeficiency disorders (PIDs) than in the general population. However, no …
primary immunodeficiency disorders (PIDs) than in the general population. However, no …
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
The total number of acquired melanocytic nevi on the skin is strongly correlated with
melanoma risk. Here we report a meta-analysis of 11 nevus GWAS from Australia …
melanoma risk. Here we report a meta-analysis of 11 nevus GWAS from Australia …
Inherited immunodeficiencies with high predisposition to Epstein–Barr virus-driven lymphoproliferative diseases
S Latour, S Winter - Frontiers in immunology, 2018 - frontiersin.org
Epstein–Barr Virus (EBV) is a gamma-herpes virus that infects 90% of humans without any
symptoms in most cases, but has an oncogenic potential, especially in immunocompromised …
symptoms in most cases, but has an oncogenic potential, especially in immunocompromised …
Human inborn errors of immunity to herpes viruses
Infections with any of the nine human herpes viruses (HHV) can be asymptomatic or life-
threatening. The study of patients with severe diseases caused by HHVs, in the absence of …
threatening. The study of patients with severe diseases caused by HHVs, in the absence of …
Personalized hematopoietic stem cell transplantation for inborn errors of immunity
M Slatter, SH Lum - Frontiers in Immunology, 2023 - frontiersin.org
Patients with inborn errors of immunity (IEI) have been transplanted for more than 50 years.
Many long-term survivors have ongoing medical issues showing the need for further …
Many long-term survivors have ongoing medical issues showing the need for further …
Dual T cell– and B cell–intrinsic deficiency in humans with biallelic RLTPR mutations
Combined immunodeficiency (CID) refers to inborn errors of human T cells that also affect B
cells because of the T cell deficit or an additional B cell–intrinsic deficit. In this study, we …
cells because of the T cell deficit or an additional B cell–intrinsic deficit. In this study, we …