Elimination of glutamatergic transmission from Hb9 interneurons does not impact treadmill locomotion | Scientific Reports
MNX1 Protein Overview: Sequence, Structure, Function and Protein Interaction | Sino Biological
Mnx1 Gene Expression Results - GXD
Gene: MNX1 (ENSPTRG00000019918) - Summary - Pan_troglodytes - Ensembl genome browser 108
Novel MNX1 mutations and genotype–phenotype analysis of patients with Currarino syndrome | Orphanet Journal of Rare Diseases | Full Text
Gene: MNX1 (ENSG00000130675) - Summary - Homo_sapiens - Ensembl genome browser 108
Cells | Free Full-Text | Pan-Cancer Analysis Identifies MNX1 and Associated Antisense Transcripts as Biomarkers for Cancer
LncRNA MNX1-AS1 promotes progression of intrahepatic cholangiocarcinoma through the MNX1/Hippo axis | Cell Death & Disease
MNX1 Gene - GeneCards | MNX1 Protein | MNX1 Antibody
Homeobox transcription factor MNX1 is crucial for restraining the expression of pan-neuronal genes in motor neurons | bioRxiv
Cells | Free Full-Text | Pan-Cancer Analysis Identifies MNX1 and Associated Antisense Transcripts as Biomarkers for Cancer
Expression, Clinical Significance, and Functional Prediction of MNX1 in Breast Cancer: Molecular Therapy - Nucleic Acids
Expression, Clinical Significance, and Functional Prediction of MNX1 in Breast Cancer: Molecular Therapy - Nucleic Acids
MNX1-ETV6 fusion gene in an acute megakaryoblastic leukemia and expression of the MNX1 gene in leukemia and normal B cell lines. | Semantic Scholar
MNX1 Gene - GeneCards | MNX1 Protein | MNX1 Antibody
MNX1 Gene - GeneCards | MNX1 Protein | MNX1 Antibody
An induced pluripotent stem cell t(7;12)(q36;p13) acute myeloid leukemia model shows high expression of MNX1 and a block in differentiation of the erythroid and megakaryocytic lineages - Nilsson - 2022 - International
MNX1 directly upregulates CCNE1 and CCNE2 promoter activity in bladder... | Download Scientific Diagram
Novel MNX1 mutations and genotype–phenotype analysis of patients with Currarino syndrome
Novel MNX1 mutations and genotype–phenotype analysis of patients with Currarino syndrome | Orphanet Journal of Rare Diseases | Full Text
Gene: Mnx1 (ENSMUSG00000001566) - Summary - Mus_musculus - Ensembl genome browser 109
Homeobox transcription factor MNX1 is crucial for restraining the expression of pan-neuronal genes in motor neurons | bioRxiv
MNX1 reduces sensitivity to anoikis by activating TrkB in human glioma cells
