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UnknownTwelve Chinese patent medicines combined with conventional medicine for the treatment of functional dyspepsia: a network meta-analysis.
Not available
S-EPMC12741128 | biostudies-literature
TranscriptomicsDissecting the developmental transcriptomes of rice
Transcriptional programs are important for the development of complex eukaryotic organisms. Suites of genes expressed with temporal and spatial controls by regulatory networks in response to environmental cues are the cornerstone for achieving the specification of morphology and physiology of the ti...
ORGANISM(S): Oryza sativa Indica Group 
2010-01-20 | E-GEOD-19024 | biostudies-arrayexpress
UnknownA splicing variant of Merlin promotes metastasis in hepatocellular carcinoma.
Not available
S-EPMC4633634 | biostudies-literature
UnknownEarly-life exposure to polypropylene nanoplastics induces neurodevelopmental toxicity in mice and human iPSC-derived cerebral organoids.
Not available
S-EPMC12210689 | biostudies-literature
UnknownBiallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella.
Not available
S-EPMC5473723 | biostudies-literature
ProteomicsIdentification of candidate microRNA biomarkers of endometriosis in different bodily fluids
Endometriosis is a common gynecological condition that affects approximately 10% of women of reproductive age and up to half of those experiencing infertility. However, there is a lack of reliable noninvasive diagnostic tools for diagnosing endometriosis. This study aims to identify novel biomarkers...
ORGANISM(S): Homo Sapiens 
2025-11-17 | PXD070868 |
ProteomicsRegulation of the PKD2 channel function and associated disease phenotypes by RASSF4
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common monogenic genetic disorders, caused by mutations in receptor PKD1 or ion channel PKD2, and is characterized by progressive renal cyst development with additional hepatic and extrarenal manifestations. As effective treatme...
ORGANISM(S): Homo Sapiens 
2026-02-13 | PXD074819 |
UnknownLarge-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defects.
Not available
S-EPMC10080761 | biostudies-literature
ProteomicsFLAG-TCF21 interactome in HCT116 and TPCs by IP-MS
This project presents the proteomic profiling of protein complexes associated with the transcription factor TCF21, achieved through affinity purification coupled with mass spectrometry (AP-MS). The study aimed to comprehensively map the TCF21 interactome in two distinct cellular models: the human co...
ORGANISM(S): Homo Sapiens 
2025-12-12 | PXD071976 |
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