Pages that link to "Q48117869"

The following pages link to Mouse neurofibromatosis type 1 cDNA sequence reveals high degree of conservation of both coding and non-coding mRNA segments (Q48117869):

Displaying 27 items.

• Molecular genetics of neurofibromatosis type 1 (NF1) (Q24518449) (← links)
• Optic glioma and precocious puberty in a girl with neurofibromatosis type 1 carrying an R681X mutation of NF1: case report and review of the literature (Q26775950) (← links)
• Alternative splicing of the neurofibromatosis type I pre-mRNA (Q26865241) (← links)
• Molecular basis of neurofibromatosis type 1 (NF1): mutation analysis and polymorphisms in the NF1 gene (Q28241993) (← links)
• Tumour predisposition in mice heterozygous for a targeted mutation in Nf1 (Q28863951) (← links)
• The neurofibromatosis type I pre-mRNA is a novel target of CELF protein-mediated splicing regulation (Q33566390) (← links)
• Characterisation of germline mutations in the neurofibromatosis type 1 (NF1) gene (Q33682450) (← links)
• Neurofibromatosis type 1 alternative splicing is a key regulator of Ras signaling in neurons (Q33743618) (← links)
• Molecular and cellular mechanisms of cognitive function: implications for psychiatric disorders (Q33842573) (← links)
• A distinct set of Drosophila brain neurons required for neurofibromatosis type 1-dependent learning and memory. (Q34051144) (← links)
• Molecular and cellular mechanisms underlying the cognitive deficits associated with neurofibromatosis 1. (Q34156479) (← links)
• Cloning, chromosomal mapping and expression pattern of the mouse Brca2 gene (Q34419177) (← links)
• Mouse models of neurofibromatosis type I: bridging the GAP. (Q35043758) (← links)
• Neurofibromatosis type 1: new insights into neurocognitive issues (Q36415807) (← links)
• A randomized placebo-controlled lovastatin trial for neurobehavioral function in neurofibromatosis I. (Q36786365) (← links)
• The murine homolog of the human breast and ovarian cancer susceptibility gene Brca1 maps to mouse chromosome 11D. (Q36791553) (← links)
• Mice with missense and nonsense NF1 mutations display divergent phenotypes compared with human neurofibromatosis type I. (Q37120427) (← links)
• Molecular and cellular mechanisms of learning disabilities: a focus on NF1. (Q37719525) (← links)
• Neurofibromatosis type 1: pathology, clinical features and molecular genetics. (Q40479884) (← links)
• Screening in silico predicted remotely acting NF1 gene regulatory elements for mutations in patients with neurofibromatosis type 1. (Q42564119) (← links)
• GTPase stimulation in shrimp Ras(Q(61)K) with geranylgeranyl pyrophosphate but not mammalian GAP. (Q42822828) (← links)
• Genomic characterization of the Neurofibromatosis Type 1 gene of Fugu rubripes (Q45254653) (← links)
• Ultrastructural synaptic changes associated with neurofibromatosis type 1: A quantitative analysis of hippocampal region CA1 in a Nf1 /− mouse model (Q50980984) (← links)
• Molecular analysis of the 5′-flanking region of the neurofibromatosis type 1 (NF1) gene: identification of five sequence variants (Q57263857) (← links)
• Two NF1 mutations: frameshift in the GAP-related domain, and loss of two codons toward the 3' end of the gene (Q72176877) (← links)
• Evaluation of cancer risk through genetic analysis? (Q73812889) (← links)
• Neurofibromin and NF1 gene analysis in composite pheochromocytoma and tumors associated with von Recklinghausen's disease (Q77794222) (← links)