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INSR Gene - GeneCards | INSR Protein | INSR Antibody GeneCards Summary for INSR Gene INSR (Insulin Receptor) is a Protein Coding gene Diseases associated with INSR include Donohue Syndrome and Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, And Somatic Abnormalities Among its related pathways are GPCR Pathway and ERK Signaling
INSR gene: MedlinePlus Genetics The INSR gene provides instructions for making a protein called an insulin receptor, which is found in many types of cells Learn about this gene and related health conditions
Orphanet: INSR-insulin receptor Listado de enfermedades Mutaciones germinales causantes de enfermedad en Hiperinsulinismo por deficiencia de INSR ORPHA:263458 Mutaciones germinales causantes de enfermedad en Síndrome de resistencia a la insulina tipo A ORPHA:2297 Mutaciones germinales causantes de enfermedad en Síndrome de Donohue ORPHA:508
Transcriptional Regulation of INSR, the Insulin Receptor Gene The human INSR gene is likely to contain a similar level of transcriptional complexity; here, we summarize over three decades of molecular biology and genetic research that points to a still incompletely understood regulatory control system
Receptor de insulina - Wikiwand El receptor de insulina es una proteína codificada por el gen INSR localizado en el cromosoma 19 (humano), brazo corto, banda p13 3-13 2 [12] Codifica una cadena de 1382 aminoácidos, que es clivada en 2 cadenas: la Insulin receptor subunidad alfa α y la Insulin receptor subunidad beta β
Gene - INSR Click the + buttons to view associations for INSR from the datasets below If available, associations are ranked by standardized value
INSR -Related Severe Insulin Resistance Syndrome - PubMed Clinical characteristics: INSR -related severe insulin resistance syndrome (INSR -SIRS) comprises a phenotypic spectrum that is a continuum from the severe phenotype of Donohue syndrome to the milder phenotype of Rabson-Mendenhall syndrome (RMS)