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UnknownArachnid Fauna (Araneae and Opiliones) from the Castro Verde Special Protection Area, southern Portugal.
Not available
S-EPMC10719938 | biostudies-literature
UnknownThe putative flavin carrier family FlcA-C is important for Aspergillus fumigatus virulence.
Not available
S-EPMC5626198 | biostudies-literature
UnknownInternal Disequilibria and Phenotypic Diversification during Replication of Hepatitis C Virus in a Noncoevolving Cellular Environment.
Not available
S-EPMC5411618 | biostudies-literature
UnknownAuditory capacities in Middle Pleistocene humans from the Sierra de Atapuerca in Spain.
Not available
S-EPMC454200 | biostudies-literature
UnknownHints of the existence of C-rich massive evolved stars.
Not available
S-EPMC6520254 | biostudies-literature
ProteomicsArsenic response of three altiplanic Exiguobacterium strains with different tolerance levels against the metalloid species: a proteomics study
In this work we compare the protein expression patterns of the three strains in response to arsenic by proteomic approach, strains were grown in absence of the metalloid and in presence of As(III) and As(V) sublethal concentrations and the protein separation was carried out in 2D electrophoresis gel...
ORGANISM(S): Exiguobacterium sp. SH31 
2019-10-23 | PXD014701 | Pride
Resistance Exiguobacterium 2-de Arsenic 
ProteomicsCRISPR targeting of FOXL2 c.402C>G mutation reduces malignant phenotype in granulosa tumor cells and identifies anti-tumoral compounds
FOXL2 is a transcription factor that plays a key role in sex determination, ovary development and maintenance. Mutations related to this gene have been described in syndromes involving premature ovarian failure and granulosa cell tumors. This kind of rare cancer (less than 5% of diagnosed ovarian ca...
ORGANISM(S): Homo sapiens (Human) 
2025-03-15 | PXD053682 | Pride
Tmt Rare cancer Crispr Granulosa cell tumor Proteomics Foxl2 
UnknownCitrus Leprosis Virus C Encodes Three Proteins With Gene Silencing Suppression Activity.
Not available
S-EPMC7325951 | biostudies-literature
Unknownc.1103T>C (p.Ile368Th) de novo Variant in Synaptotagmin 1 (SYT1) Gene is Pathogenic, Leading to an Ultra-Rare Neurodevelopmental Disorder: The Baker-Gordon Syndrome.
Not available
S-EPMC10822096 | biostudies-literature
Unknownc-Abl Activation Linked to Autophagy-Lysosomal Dysfunction Contributes to Neurological Impairment in Niemann-Pick Type A Disease.
Not available
S-EPMC8985125 | biostudies-literature
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