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Klaus Schmitz‐Abe

harvard university medical affiliates
H指数:39
被引数:4,389
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Notch3+regulatory T cells drive autoimmune neuroinflammation in multiple sclerosis

Notch3调节性T细胞在多发性硬化症中驱动自身免疫性神经炎症

2025-11-010
PRE
Notch3 destabilizes regulatory T cells to drive autoimmune neuroinflammation in multiple sclerosis

Notch3破坏调节性T细胞,以驱动多发性硬化中的自身免疫性神经炎症。

Immunity
IF26.3
2025-10-020
PRE
Relationship between placental oxygen transport, fetal birth weight, and umbilical cord transcriptome in monochorionic twins

单绒毛膜双胎中胎盘氧转运、胎儿出生体重与脐带转录组之间的关系

2025-10-010
PRE
The solute carrier family 26 member 9 modifies rapidly progressing cystic fibrosis associated with homozygous F508del CFTR mutation
2024-07-011
PRE
Integrated multi-omics approach reveals the role of striated muscle preferentially expressed protein kinase in skeletal muscle including its relationship with myospryn complex
2024-05-090
OA
Atypical Localization of Eczema Discriminates DOCK8 or STAT3 Deficiencies from Atopic Dermatitis
2023-07-290
OA
Severe allergic dysregulation due to a gain of function mutation in the transcription factor STAT6

由于转录因子STAT6的功能突变而导致的严重过敏性失调

2023-07-0131
PRE
Reanalysis of clinical exome identifies the second variant in two individuals with recessive disorders
2023-01-235
OA
The Notch1/CD22 signaling axis disrupts Treg function in SARS-CoV-2-associated multisystem inflammatory syndrome in children
2023-01-0315
OAAI
A Stk4-Foxp3-NF-κB p65 transcriptional complex promotes Treg cell activation and homeostasis
2022-09-3011
OA
Reanalysis of Exome Data Identifies Novel SLC25A46 Variants Associated with Leigh Syndrome

外显子组数据的再分析确定了与Leigh综合征相关的新型SLC25A46变异

2021-12-025
OAAI
Congenital X-linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6
2021-11-032
OA
Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders
2021-08-0123
OAAI
Evolution and long-term outcomes of combined immunodeficiency due to CARMIL2 deficiency

CARMIL2缺陷引起的联合免疫缺陷的演变和长期结果

2021-07-3030
OAAI
A homozygous stop-gain variant in ARHGAP42 is associated with childhood interstitial lung disease, systemic hypertension, and immunological findings
2021-07-073
OAAI
A data-driven architecture using natural language processing to improve phenotyping efficiency and accelerate genetic diagnoses of rare disorders
2021-07-012
OAAI
Notch4 signaling limits regulatory T-cell-mediated tissue repair and promotes severe lung inflammation in viral infections
IMMUNITY
IF26.3
2021-06-0180
OAAI
A regulatory T cell Notch4-GDF15 axis licenses tissue inflammation in asthma (vol 21, pg 1359, 2020)
2021-04-261
OAAI
A regulatory T cell Notch4-GDF15 axis licenses tissue inflammation in asthma (vol 21, pg 1359, 2020)
2020-11-190
OAAI
A regulatory T cell Notch4-GDF15 axis licenses tissue inflammation in asthma
2020-09-1486
OAAI