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GARDASIL [Quadrivalent Human Papillomavirus (Types 6,11,16,18) Recombinant Vaccine] — Description, Dosage, Side Effects | PillsCard
OTC
GARDASIL [Quadrivalent Human Papillomavirus (Types 6,11,16,18) Recombinant Vaccine]
滅菌懸液注射劑
INN: TYPE 6 L1 PROTEIN
Data updated: 2026-04-11
Available in:
🇩🇪🇬🇧🇷🇴🇹🇷
Form
滅菌懸液注射劑
Dosage
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Route
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Storage
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About This Product
User Reviews
Reviews reflect personal experiences and are not medical advice. Always consult your doctor.
Manufacturer
MERCK SHARP & DOHME B.V. (TW)
Source
TFDA
right hemisphere of cerebellumspinal gangliatrigeminal ganglioncerebellar vermissural nerveparaflocculus of cerebellumolfactory bulbBrodmann area 10right frontal lobesuperior frontal gyrus
medial dorsal nucleussuperior cervical ganglionsubiculumlateral geniculate nucleusbarrel cortexmedial geniculate nucleusventromedial nucleusparaventricular nucleus of hypothalamusdorsomedial hypothalamic nucleusnucleus accumbens
protein bindingprotein domain specific bindingaxon guidance receptor activity
cell projectiongrowth conemembranefocal adhesioncell surfaceintegral component of membraneaxonal growth coneplasma membraneaxondendritesomaextracellular matrixcollagen-containing extracellular matrix
multicellular organism developmentnervous system developmentpositive regulation of axon extensioncell differentiationleukocyte migrationcell adhesionchemotaxiscell-matrix adhesionaxon guidancecell migrationneuron projection developmentsynapse organizationaxon developmenthomophilic cell adhesion via plasma membrane adhesion molecules
3897
16728
ENSG00000198910
ENSMUSG00000031391
P32004
P11627
NM_024003NM_000425NM_001143963NM_001278116
NM_008478NM_001374694
NP_000416NP_001137435NP_001265045NP_076493
n/a
L1, also known asL1CAM, is atransmembrane proteinmember of theL1 protein family, encoded by theL1CAMgene. This protein, of 200 to 220 kDa, is a neuronalcell adhesion moleculewith a strong implication in cell migration, adhesion, neurite outgrowth, myelination and neuronal differentiation.It also plays a key role in treatment-resistant cancers due to its function. It was first identified in 1984 by M. Schachner who found the protein in post-mitotic miceneurons.
Mutations in the L1 protein are the cause ofL1 syndrome, sometimes known by the acronym CRASH(corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia and hydrocephalus).