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/vufind/Search/Results?lookfor=%22Cardinale%2C+Christopher+J%22&type=Person&sort=year
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PubPharm (26)
1
Elevated Levels of the Cytokine LIGHT in Pediatric Crohn's Disease
enthalten in:
Journal of immunology (Baltimore, Md. : 1950)
| 2023
von
Cardinale, C.
|
Abrams, D.
|
Mentch, F.
| +5
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2
Genome-wide association study of the age of onset of type 1 diabetes reveals HTATIP2 as a novel T cell regulator
enthalten in:
Frontiers in immunology
| 2023
von
Cardinale, C.
|
Chang, X.
|
Wei, Z.
| +4
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3
A novel MBTPS2 variant associated with BRESHECK syndrome impairs sterol-regulated transcription and the endoplasmic reticulum stress response
enthalten in:
American journal of medical genetics. Part A
| 2022
von
Strong, A.
|
March, M.
|
Cardinale, C.
| +13
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4
A novel MBTPS2 variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
enthalten in:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
| 2022
von
Strong, A.
|
March, M.
|
Cardinale, C.
| +13
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5
Elevated levels of the cytokine LIGHT in Crohn’s disease
enthalten in:
bioRxiv.org
| 2021
von
Cardinale, C.
|
Abrams, D.
|
Mentch, F.
| +4
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6
Regulation of Janus Kinase 2 by an Inflammatory Bowel Disease Causal Non-coding Single Nucleotide Polymorphism
enthalten in:
Journal of Crohn's & colitis
| 2020
von
Cardinale, C.
|
March, M.
|
Lin, X.
| +7
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7
Multiple Epistasis Interactions Within MHC Are Associated With Ulcerative Colitis
enthalten in:
Frontiers in genetics
| 2019
von
Zhang, J.
|
Wei, Z.
|
Cardinale, C.
| +5
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8
Association of a rare NOTCH4 coding variant with systemic sclerosis : a family-based whole exome sequencing study
enthalten in:
BMC musculoskeletal disorders
| 2016
von
Cardinale, C.
|
Li, D.
|
Tian, L.
| +10
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9
Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study
enthalten in:
BMC musculoskeletal disorders
| 2016
von
Cardinale, C.
|
Li, D.
|
Tian, L.
| +10
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10
Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study
enthalten in:
BMC musculoskeletal disorders
| 2016
von
Cardinale, C.
|
Li, D.
|
Tian, L.
| +10
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BMC musculoskeletal disorders
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American Journal of Medical Genetics Part C: Se...
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Journal of Crohn's & colitis
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Thema
16
Journal Article
10
Research Support, Non-U.S. Gov't
6
Research Support, N.I.H., Extramural
4
Transcription Factors
3
Mendelian genetics
3
NOTCH4
3
Scleroderma
3
Systemic sclerosis
3
Whole exome sequencing
2
Cytokines
2
EC 2.3.1.48
2
Genetics
2
Meta-Analysis
2
T cells
1
62229-50-9
1
63231-63-0
1
AKNAD1 protein, human
1
ARNTL Transcription Factors
1
Acetyltransferases
1
Adaptor Proteins, Signal Transducing
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Erscheinungszeitraum
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2020-
14
2010-2019
6
2000-2009
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