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Aadh Syndrome: Disease Bioinformatics

Research of Aadh Syndrome has been linked to Hypogonadism, Conductive Hearing Loss, Olfaction Disorders, Neurocutaneous Syndromes, Hypogonadotropic Hypogonadism. The study of Aadh Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Aadh Syndrome has been researched in relation to the Ovulation Pathway. This pathway complements our catalog of research reagents for the study of Aadh Syndrome including antibodies and ELISA kits against TCOF1.

Aadh Syndrome 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 Aadh Syndrome 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 8 products for the study of Aadh Syndrome that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NBP1-86908
Western Blot: Treacher Collins syndrome protein Antibody [NBP1-86908] - Analysis in human cell line CACO-2.Immunocytochemistry/Immunofluorescence: Treacher Collins syndrome protein Antibody [NBP1-86908] - Staining of human cell line U-2 OS shows localization to nucleoli fibrillar center. Antibody staining is shown in green.

Rabbit Polyclonal
Species Human
Applications WB, ICC/IF, IHC

1 Publication

Related Genes

Aadh Syndrome has been researched against:

Related Pathways

Aadh Syndrome has been linked to:

Alternate Names

Aadh Syndrome is also known as Alopecia-anosmia-deafness-hypogonadism Syndrome, Johnson-mcmillin Syndrome.