This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Neonatal Maladjustment Syndrome
Information about Neonatal Maladjustment Syndrome: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Neonatal Maladjustment Syndrome
Most recent studies have shown that Neonatal Maladjustment Syndrome shares some biological mechanisms with agitation, autonomic-nervous-system-imbalance, bipolar-disorder, catatonia, confusion, dementia, depressive-disorder, malignant-hyperpyrexia-due-to-anesthesia, malignant-paraganglionic-neoplasm, mental-disorders, muscle-rigidity, nervousness, neurally-mediated-syncope, neuroleptic-malignant-syndrome, pain, parkinson-disease, psychotic-disorders, schizophrenia, syncope.
Among the many pathways, these few ones have gauged particular interests from scientists studying Neonatal Maladjustment Syndrome, and have been seen in publications frequently: Aging, Cell Proliferation, Coagulation, Cognition, Hypersensitivity, Immune Response, Lactation, Localization, Locomotion, Mating, Muscle Contraction, Pathogenesis, Reflex, Regeneration, Response To Hypoxia, Secretion, Sensitization, Swimming, Transport, Vasoconstriction
Quite a number of genes have been found to play important roles in Neonatal Maladjustment Syndrome, such as ACHE, ASRGL1, C3, CHKA, CHKB, CHRM1, CHRM2, CSF2, LAMC2, NMS, NMU, NMUR1, NMUR2, PIK3C2A, POMC. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.