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source DB |
source ID
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text
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size
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updated at |
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# proj.
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# Ann.
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updated_at |
| PubMed |
28479159 |
Proteomic analysis of filaggrin deficiency identifies molecular signatures characteristic of atopic |
2.24 KB |
2019-09-23 |
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30 |
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22 |
-
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| PubMed |
28483841 |
TREM2 deficiency impairs chemotaxis and microglial responses to neuronal injury.
Sequence variations |
1.6 KB |
2019-09-23 |
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28 |
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37 |
-
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| PubMed |
28488085 |
Novel loss of function mutation in KRIT1/CCM1 is associated with distinctly progressive cerebral and |
1.75 KB |
2019-09-23 |
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28 |
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32 |
-
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| PubMed |
28507206 |
Real-World Data on Prognostic Factors for Overall Survival in EGFR Mutation-Positive Advanced Non-Sm |
2.53 KB |
2019-09-23 |
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21 |
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7 |
-
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| PubMed |
28512217 |
Loss of the homologous recombination gene rad51 leads to Fanconi anemia-like symptoms in zebrafish.
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1.52 KB |
2019-09-23 |
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30 |
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15 |
-
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| PubMed |
28525545 |
Gene Co-Expression Network Analysis for Identifying Modules and Functionally Enriched Pathways in SC |
1.36 KB |
2019-09-23 |
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28 |
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7 |
-
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| PubMed |
28525834 |
Exposure to phenols, parabens and UV filters: Associations with loss-of-function mutations in the fi |
1.93 KB |
2019-09-23 |
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28 |
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9 |
-
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| PubMed |
28533163 |
GRIN2B gain of function mutations are sensitive to radiprodil, a negative allosteric modulator of Gl |
1.81 KB |
2019-09-23 |
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28 |
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9 |
-
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| PubMed |
28543872 |
PAI-1 gain-of-function genotype, factors increasing PAI-1 levels, and airway obstruction: The GALA I |
2.12 KB |
2019-09-23 |
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29 |
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11 |
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| PubMed |
28548960 |
Severe hypertriglyceridemia due to two novel loss-of-function lipoprotein lipase gene mutations (C31 |
1.65 KB |
2019-09-23 |
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28 |
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36 |
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