Identification and characterization of transcripts from the neurofibromatosis 1 region: the sequence and genomic structure of EVI2 and mapping of other transcripts
about
Targeted disruption of the ubiquitous CNC-bZIP transcription factor, Nrf-1, results in anemia and embryonic lethality in mice.Molecular genetics of neurofibromatosis type 1 (NF1)The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 geneTranscriptional and epigenetic regulation of the integrin collagen receptor locus ITGA1-PELO-ITGA2The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulationLinkage disequilibrium in the neurofibromatosis 1 (NF1) region: implications for gene mappingThe RASopathiesExpansion of the RASopathiesDeletions of NF1 gene and exons detected by multiplex ligation-dependent probe amplificationMolecular biology of neurological diseases.Drosophila arginase is produced from a nonvital gene that contains the elav locus within its third intron.High level multiplex genotyping by MALDI-TOF mass spectrometry.The alcohol dehydrogenase gene is nested in the outspread locus of Drosophila melanogaster.Ras in cancer and developmental diseasesThe silence RNA keeps: cis mechanisms of RNA mediated epigenetic silencing in mammals.Perioperative management of neurofibromatosis type 1.The NF1 translocation breakpoint region.Mouse models of glioblastoma: lessons learned and questions to be answered.Modeling RASopathies with Genetically Modified Mouse Models.Pulmonary Hypertension and Cancer: Etiology, Diagnosis, and Management.Aurora-A phosphorylates, activates, and relocalizes the small GTPase RalANeurofibromatosis type 1: pathology, clinical features and molecular genetics.A BamHI polymorphism in the human EVI2A gene (human homolog of the murine gene Evi-2).Neurofibromatosis and related tumors. Natural occurrence and animal models.Neurocristopathy: its growth and development in 20 years.A 90 kb DNA deletion associated with neurofibromatosis type 1.A highly sensitive genetic protocol to detect NF1 mutations.Variation in a range of mTOR-related genes associates with intracranial volume and intellectual disability.Quantification of NF1 transcripts reveals novel highly expressed splice variants.The investigation for potential modifier genes in patients with neurofibromatosis type 1 based on next-generation sequencing.The neurofibromatosis type 1 (NF1) gene: identification and partial characterization of a putative tumor suppressor gene.
P2860
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P2860
Identification and characterization of transcripts from the neurofibromatosis 1 region: the sequence and genomic structure of EVI2 and mapping of other transcripts
description
1990 nî lūn-bûn
@nan
1990 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Identification and characteriz ...... d mapping of other transcripts
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Identification and characteriz ...... d mapping of other transcripts
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Identification and characteriz ...... d mapping of other transcripts
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Identification and characteriz ...... d mapping of other transcripts
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type
label
Identification and characteriz ...... d mapping of other transcripts
@ast
Identification and characteriz ...... d mapping of other transcripts
@en
Identification and characteriz ...... d mapping of other transcripts
@en-gb
Identification and characteriz ...... d mapping of other transcripts
@nl
prefLabel
Identification and characteriz ...... d mapping of other transcripts
@ast
Identification and characteriz ...... d mapping of other transcripts
@en
Identification and characteriz ...... d mapping of other transcripts
@en-gb
Identification and characteriz ...... d mapping of other transcripts
@nl
P2093
P1433
P1476
Identification and characteriz ...... d mapping of other transcripts
@en
P2093
A M Buchberg
D Viskochil
N A Jenkins
N G Copeland
P O'Connell
R M Cawthon
P304
P356
10.1016/0888-7543(90)90199-5
P407
P577
1990-08-01T00:00:00Z