Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
The protein encoded by LSAMP is a neuronal surface glycoprotein found in cortical and subcortical regions of the limbic system. Zusätzlich bieten wir Ihnen Limbic System-Associated Membrane Protein Proteine (10) und Limbic System-Associated Membrane Protein Kits (6) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 39 products:
We detected African-specific SNPs at ZNF649 (zeige ZNF649 Antikörper) and LSAMP, with associations of genome-wide significance for ulcerative colitis.
A novel genomic alteration of LSAMP associates with aggressive prostate cancer in African American men
The results showed significant allelic and haplotypic associations between LSAMP gene and schizophrenia.
The tumor suppressor function of LSAMP is most likely exerted by reducing the proliferation rate of the tumor cells, possibly by indirectly upregulating one or more of the genes HES1 (zeige HES1 Antikörper), CTAG2 (zeige CTAG2 Antikörper) or KLF10 (zeige KLF10 Antikörper).
This study presents the first evidence of a possible role of LSAMP gene in mood and anxiety disorders in humans.
proteomic assessments of membrane microdomains in prefrontal cortex and validation in two brain series, strongly implicates LAMP, STXBP1 (zeige STXBP1 Antikörper) and BASP1 (zeige BASP1 Antikörper) in schizophreina and supports the view of a neuritic and synaptic dysfunction in the neuropathology
Single nucleotide polymorphisms of LSAMP is associated with the pathogenesis of coronary artery disease.
LSAMP might play a role in pathoaetiology of suicidal behaviour but further studies are needed to understand its exact contribution
results show that LSAMP is a novel candidate tumor suppressor gene in osteosarcomas
Identification of chromosomal aberrations associated with disease progression and a novel 3q13.31 deletion involving LSAMP gene in osteosarcoma.
Limbic system-associated membrane protein is involved in emotional and social operating systems by complex regulation of two alternative promoters.
Lsamp(-/-) mice are a promising model to study the neurobiological mechanisms of deviant social behaviour and adaptation impairment observed in many psychiatric disorders.
Lsamp-deficient mice were less sensitive to isolation stress than their wild-type littermates.
lsamp knockout mice have a deficit in spatial memory acquisition and poorly sustained CA1 (zeige CA1 Antikörper) long-term potentiation.
genomic features of the Lsamp gene indicate an intricate mechanism of gene expression regulation that may be relevant in the context of human neuropsychiatric and neurological disorders, where LAMP expression may be altered
Genetic deletion of Lsamp causes exaggerated behavioral activation in novel environments.
The protein encoded by this gene is a neuronal surface glycoprotein found in cortical and subcortical regions of the limbic system. During development of the limbic system, this encoded protein is found on the surface of axonal membranes and growth cones, where it acts as a selective homophilic adhesion molecule, and guides the development of specific patterns of neuronal connections.
, E19S protein
, IgLON family member 3
, limbic system-associated membrane protein