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/vufind/Search/Results?lookfor=%22Momenilandi%2C+Mana%22&type=Person&sort=year
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PubPharm (26)
1
The immunopathological landscape of human pre-TCRα deficiency : From rare to common variants
enthalten in:
Science (New York, N.Y.)
| 2024
von
Materna, M.
|
Delmonte, O.
|
Bosticardo, M.
| +96
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2
Human germline gain-of-function in STAT6 : from severe allergic disease to lymphoma and beyond
enthalten in:
Trends in immunology
| 2024
von
STAT6 Gain-of-Function International Consortium. Electronic address: sturvey@bcchr.ca
|
STAT6 Gain-of-Function International Consortium
|
Sharma, M.
| +21
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3
Human inherited CCR2 deficiency underlies progressive polycystic lung disease
enthalten in:
Cell
| 2024
von
Neehus, A.
|
Carey, B.
|
Landekic, M.
| +69
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4
Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria
enthalten in:
Cell
| 2023
von
Bohlen, J.
|
Zhou, Q.
|
Philippot, Q.
| +55
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5
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency
enthalten in:
Nature
| 2023
von
Le Voyer, T.
|
Parent, A.
|
Liu, X.
| +98
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6
Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency : Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population
enthalten in:
Journal of clinical immunology
| 2023
von
Mousavi Khorshidi, M.
|
Seeleuthner, Y.
|
Chavoshzadeh, Z.
| +21
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7
Clinical, immunological, and genetic findings in Iranian patients with MHC-II deficiency: confirmation of c.121delG RFXANK founder mutation in the Iranian population
enthalten in:
ResearchSquare.com
| 2023
von
Khorshidi, M.
|
Seeleuthner, Y.
|
Chavoshzadeh, Z.
| +22
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8
Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population
enthalten in:
Journal of clinical immunology
| 2023
von
Mousavi Khorshidi, M.
|
Seeleuthner, Y.
|
Chavoshzadeh, Z.
| +21
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9
Human inherited complete STAT2 deficiency underlies inflammatory viral diseases
enthalten in:
The Journal of clinical investigation
| 2023
von
Bucciol, G.
|
Moens, L.
|
Ogishi, M.
| +34
CommentIn: J Clin Invest. 2023 Jun 15;133(12):. - PMID 37317971
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10
Inherited human ZNF341 deficiency
enthalten in:
Current opinion in immunology
| 2023
von
Béziat, V.
|
Fieschi, C.
|
Momenilandi, M.
| +4
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26
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24
E-Artikel
24
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2
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Zeitschriftentitel
8
Journal of clinical immunology
4
Cell
3
The Journal of experimental medicine
2
Pharmaceutical biology
1
Annals of Human Genetics
1
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Current opinion in immunology
1
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Thema
16
Journal Article
11
Research Support, Non-U.S. Gov't
8
Research Support, N.I.H., Extramural
3
Bare lymphocyte syndrome type 1 (BLS-1)
3
Necrotizing granulomata
3
TAP2 deficiency
3
Transporter associated with antigen processing ...
3
inborn error of immunity
2
37341-29-0
2
82115-62-6
2
CD28 Antigens
2
Case Reports
2
DNA-Binding Proteins
2
Founder effect
2
Hematopoietic stem cell transplantation
2
IL-23
2
Immunoglobulin E
2
Inborn error of immunity
2
Interferon Type I
2
Interferon-gamma
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Erscheinungszeitraum
23
2020-
3
2010-2019
Erscheinungsjahr(e)
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Sprache
25
Englisch
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