The RET receptor: function in development and dysfunction in congenital malformation.
about
Multiple endocrine neoplasia type 2Rap1GAP interacts with RET and suppresses GDNF-induced neurite outgrowthInteraction of SH2-Bbeta with RET is involved in signaling of GDNF-induced neurite outgrowthThe RET/PTC-RAS-BRAF linear signaling cascade mediates the motile and mitogenic phenotype of thyroid cancer cellsCharacterization of gene expression induced by RET with MEN2A or MEN2B mutationNeutralizing aptamers from whole-cell SELEX inhibit the RET receptor tyrosine kinaseOn the Origin of Cells and Derivation of Thyroid Cancer: C Cell Story RevisitedFamilial syndromes associated with neuroendocrine tumoursGenerating human intestinal tissues from pluripotent stem cells to study development and diseaseMultiple endocrine neoplasia type 2: an overviewProtein kinase Czeta and glycogen synthase kinase-3beta control neuronal polarity in developing rodent enteric neurons, whereas SMAD specific E3 ubiquitin protein ligase 1 promotes neurite growth but does not influence polarityIdentification of a novel glial cell line-derived neurotrophic factor-inducible gene required for renal branching morphogenesisRET gene abnormalities and thyroid disease: who should be screened and whenParacrine regulation of pancreatic cancer cell invasion by peripheral nerves.Medullary sponge kidney and testicular dysgenesis syndrome: a rare association.Dependence receptors: between life and death.Distinct turnover of alternatively spliced isoforms of the RET kinase receptor mediated by differential recruitment of the Cbl ubiquitin ligase.Cell-specific aptamers for targeted therapies.Medullary thyroid carcinoma: targeted therapies and future directionsPhenotype-genotype correlation in Hirschsprung disease is illuminated by comparative analysis of the RET protein sequence.Effects of IKAP/hELP1 deficiency on gene expression in differentiating neuroblastoma cells: implications for familial dysautonomia.Identification of GDNF gene sequence variations in patients with medullary sponge kidney disease.RET mutational spectrum in Hirschsprung disease: evaluation of 601 Chinese patients.RET PLCγ phosphotyrosine binding domain regulates Ca2+ signaling and neocortical neuronal migration.Src-dependent autophagic degradation of Ret in FAK-signalling-defective cancer cells.Polymerase chain reaction-single strand conformational polymorphism analysis of rearranged during transfection proto-oncogene in Chinese familial Hirschsprung's disease.Identifying candidate Hirschsprung disease-associated RET variantsAdvances in ontogeny of the enteric nervous system.Induction of RET dependent and independent pro-inflammatory programs in human peripheral blood mononuclear cells from Hirschsprung patients.Focal adhesion kinase (FAK) binds RET kinase via its FERM domain, priming a direct and reciprocal RET-FAK transactivation mechanism.Predominant RET Germline Mutations in Exons 10, 11, and 16 in Iranian Patients with Hereditary Medullary Thyroid Carcinoma.The oncogenic activity of RET point mutants for follicular thyroid cells may account for the occurrence of papillary thyroid carcinoma in patients affected by familial medullary thyroid carcinoma.Activated RET and ROS: two new driver mutations in lung adenocarcinoma.Identification of rare germline copy number variations over-represented in five human cancer types.Alimentary tract innervation deficits and dysfunction in mice lacking GDNF family receptor alpha2.The influence of Hox genes and three intercellular signalling pathways on enteric neuromuscular development.Mammalian kidney development: principles, progress, and projectionsThe hamartomatous polyposis syndromes: a clinical and molecular review.Pediatric Medullary Thyroid CarcinomaA targeting mutation of tyrosine 1062 in Ret causes a marked decrease of enteric neurons and renal hypoplasia
P2860
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P2860
The RET receptor: function in development and dysfunction in congenital malformation.
description
2001 nî lūn-bûn
@nan
2001 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
The RET receptor: function in development and dysfunction in congenital malformation.
@ast
The RET receptor: function in development and dysfunction in congenital malformation.
@en
The RET receptor: function in development and dysfunction in congenital malformation.
@nl
type
label
The RET receptor: function in development and dysfunction in congenital malformation.
@ast
The RET receptor: function in development and dysfunction in congenital malformation.
@en
The RET receptor: function in development and dysfunction in congenital malformation.
@nl
prefLabel
The RET receptor: function in development and dysfunction in congenital malformation.
@ast
The RET receptor: function in development and dysfunction in congenital malformation.
@en
The RET receptor: function in development and dysfunction in congenital malformation.
@nl
P2093
P1433
P1476
The RET receptor: function in development and dysfunction in congenital malformation.
@en
P2093
P304
P356
10.1016/S0168-9525(01)02420-9
P577
2001-10-01T00:00:00Z