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Gene Expression Image Detail
HESX1 protein (human) - STRING interaction network
Septooptic Dysplasia | Hereditary Ocular Diseases
Genetic Deletion of Hesx1 Promotes Exit from the Pluripotent State and Impairs Developmental Diapause - ScienceDirect
Development Of The Pituitary | Clinical Gate
Novel mutations associated with combined pituitary hormone deficiency in: Journal of Molecular Endocrinology Volume 46 Issue 3 (2011)
HESX1 antibody (17927-1-AP) | Proteintech
HESX1 Antibody (G-10) | SCBT - Santa Cruz Biotechnology
Descendants of Hesx1 -expressing cells in the anterior NP colonise... | Download Scientific Diagram
Model of mutant HESX1 effects on the PROP1-dependent program during... | Download Scientific Diagram
What is HESX1 Gene Septooptic dysplasia NGS Genetic DNA Test ?
HESX1 Gene - GeneCards | HESX1 Protein | HESX1 Antibody
HESX1 antibody | Anti-HESX1 | stjohnslabs
Anti-HESX1 antibody produced in mouse purified immunoglobulin, buffered aqueous solution
Recombinant Mouse HESX Homeobox 1 protein (ABIN3123032)
Generation of the Hesx1-Cre targeted allele | Download Scientific Diagram
Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse | Nature Genetics
JCI - A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction
Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse | Nature Genetics
Hesx1 protein (mouse) - STRING interaction network
HESX1 Antibody (NBP1-89090): Novus Biologicals
Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse | Nature Genetics
HESX1 Antibody (NBP1-89090): Novus Biologicals
Anti-HESX1 항체의, Biotin (PACO40949)
DNMT1 interacts with the developmental transcriptional repressor HESX1 - ScienceDirect
Characterization of a novel HESX1 mutation in a pediatric case of septo‐optic dysplasia - Pozzi - 2017 - Clinical Case Reports - Wiley Online Library
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