Pages that link to "Q42487386"

The following pages link to Substance P immunoreactivity in Rett syndrome (Q42487386):

Displaying 29 items.

• Rett syndrome and MeCP2: linking epigenetics and neuronal function (Q24616417) (← links)
• Cardiac disease and Rett syndrome (Q24675541) (← links)
• Review article: breaking new ground with Rett syndrome (Q28187714) (← links)
• Rett syndrome: review of biological abnormalities. (Q30639662) (← links)
• Rett syndrome neuropathology review 2000. (Q30666805) (← links)
• Neurons and neuronal systems involved in the pathophysiologies of Rett syndrome (Q30666808) (← links)
• Neuropathology of Rett syndrome (Q30703376) (← links)
• Human biodistribution and radiation dosimetry of the tachykinin NK1 antagonist radioligand [18F]SPA-RQ: comparison of thin-slice, bisected, and 2-dimensional planar image analysis. (Q34055608) (← links)
• Substance P modulation of TRPC3/7 channels improves respiratory rhythm regularity and ICAN-dependent pacemaker activity (Q34106886) (← links)
• Alterations of Gene Expression and Glutamate Clearance in Astrocytes Derived from an MeCP2-Null Mouse Model of Rett Syndrome (Q34245079) (← links)
• Neurobiology and neurochemistry of Rett syndrome (Q34460547) (← links)
• Annotation: Rett syndrome: recent progress and implications for research and clinical practice (Q34863995) (← links)
• Rett syndrome: the complex nature of a monogenic disease (Q35128931) (← links)
• The molecular pathology of Rett syndrome: synopsis and update (Q36617701) (← links)
• Comparative DNA methylation among females with neurodevelopmental disorders and seizures identifies TAC1 as a MeCP2 target gene (Q36980707) (← links)
• Breathing dysfunction in Rett syndrome: understanding epigenetic regulation of the respiratory network (Q37148672) (← links)
• Neuromodulation and the orchestration of the respiratory rhythm. (Q37207464) (← links)
• A histologically derived stereotaxic atlas and substance P immunohistochemistry in the brain of the least shrew (Cryptotis parva) support its role as a model organism for behavioral and pharmacological research (Q37315620) (← links)
• Rett syndrome: The state of clinical and basic research, and future perspectives (Q37828281) (← links)
• Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes (Q38110760) (← links)
• Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome (Q41697077) (← links)
• Survey of MeCP2 in the Rett syndrome and the non-Rett syndrome brain (Q42453621) (← links)
• Neural development of methyl-CpG-binding protein 2 null embryonic stem cells: A system for studying Rett syndrome (Q42917795) (← links)
• Reduced expression of neuropeptides can be related to respiratory disturbances in Rett syndrome (Q43819366) (← links)
• Substance P immunoreactivity in the enteric nervous system in Rett syndrome (Q43819369) (← links)
• Substance P-mediated modulation of pacemaker properties in the mammalian respiratory network. (Q45030468) (← links)
• Deep sedation with propofol in patients with Rett syndrome (Q48659910) (← links)
• Long-term deprivation of substance P in PPT-A mutant mice alters the anoxic response of the isolated respiratory network (Q51712189) (← links)
• Glial Dysfunction in MeCP2 Deficiency Models: Implications for Rett Syndrome (Q92454378) (← links)