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Microhydranencephaly: Disease Bioinformatics

Research of Microhydranencephaly has been linked to Microcephaly, Hydranencephaly, Congenital Abnormality, Hereditary Diseases, Fetal Diseases. The study of Microhydranencephaly has been mentioned in research publications which can be found using our bioinformatics tool below. Browse our catalog of research reagents for Microhydranencephaly including antibodies and ELISA kits against NDE1.

Microhydranencephaly Bioinformatics Tool

Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Microhydranencephaly below! For more information on how to use Laverne, please read the How to Guide.
Vizit™, under license from BioVista Inc.

Top Research Reagents

We have 29 products for the study of Microhydranencephaly that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

Western Blot: NDE1 Antibody [NBP1-83671] - Lane 1: NIH-3T3 cell lysate (Mouse embryonic fibroblast cells)<br/>Lane 2: NBT-II cell lysate (Rat Wistar bladder tumour cells)Immunohistochemistry-Paraffin: NDE1 Antibody [NBP1-83671] - Staining of human cerebral cortex shows moderate nucleolar positivity in neuronal cells.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB, IHC, IHC-P

Related Genes

Microhydranencephaly has been researched against:

Related Pathways

Related PTMs

Alternate Names

Microhydranencephaly is also known as Hydranencephaly And Microcephaly.