The objective of this study was to identify potential transcription factor binding sites in the human NF1 gene through phylogenetic footprinting. The 5 upstream region (5UR) and Exon 1- Intron 1 of the NF1 gene from human, mouse, rat, and pufferfish were compared and analyzed using various bioinformatic tools. Three regions that have equal or higher homology than the coding regions were discovered in the NF1 5UR, and four more very highly homologous regions were found in intron 1. Five of these highly homologous regions had transcription factor binding site predictions that were similar for the two binding site detection programs used in this study. One of the highly homologous regions within intron 1 had no shared predictions between the t...
Von Recklinghausen neurofibromatosis, or type 1 neurofibromatosis (NF1), is a common autosomal domin...
Neurofibromatosis type 1 (NF1) is one of the most common inherited neurological disorders with a wid...
Neurofibromatosis type 1 (NF1) is caused by inactivating mutations in NF1. Due to the size, complexi...
The gene for type 1 neurofibromatosis (NF1) is most highly expressed in brain and spinal cord, altho...
The regulatory regions of the neurofibromatosis type 1 (NF1) gene have scarcely been screened either...
Dideoxy fingerprinting was used to analyse the 5' flanking region of the neurofibromin (NF1) gene in...
Abstract Neurofibromatosis type 1 (NF1), a neuroectodermal disorder, is caused by germline mutations...
Neurofibromatosis type 1 (NF1), a neuroectodermal disorder, is caused by germline mutations in the N...
Review on Neurofibromatosis type 1 (NF1), with data on clinics, and the genes involved
* These authors contributed equally to this work. Neurofibromatosis type 1 (NF1) is one of the most ...
Review on NF1 (neurofibromin 1), with data on DNA, on the protein encoded, and where the gene is imp...
Von Recklinghausen neurofibromatosis (NF1) is a common autosomal dominant disorder of humans. Linkag...
We describe 94 pathogenic NF1 gene alterations in a cohort of 97 Austrian neurofibromatosis type I p...
Neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant disorders. NF1 is clinic...
Transcription factors (TF) regulate expression by binding to specific DNA sequences. A binding event...
Von Recklinghausen neurofibromatosis, or type 1 neurofibromatosis (NF1), is a common autosomal domin...
Neurofibromatosis type 1 (NF1) is one of the most common inherited neurological disorders with a wid...
Neurofibromatosis type 1 (NF1) is caused by inactivating mutations in NF1. Due to the size, complexi...
The gene for type 1 neurofibromatosis (NF1) is most highly expressed in brain and spinal cord, altho...
The regulatory regions of the neurofibromatosis type 1 (NF1) gene have scarcely been screened either...
Dideoxy fingerprinting was used to analyse the 5' flanking region of the neurofibromin (NF1) gene in...
Abstract Neurofibromatosis type 1 (NF1), a neuroectodermal disorder, is caused by germline mutations...
Neurofibromatosis type 1 (NF1), a neuroectodermal disorder, is caused by germline mutations in the N...
Review on Neurofibromatosis type 1 (NF1), with data on clinics, and the genes involved
* These authors contributed equally to this work. Neurofibromatosis type 1 (NF1) is one of the most ...
Review on NF1 (neurofibromin 1), with data on DNA, on the protein encoded, and where the gene is imp...
Von Recklinghausen neurofibromatosis (NF1) is a common autosomal dominant disorder of humans. Linkag...
We describe 94 pathogenic NF1 gene alterations in a cohort of 97 Austrian neurofibromatosis type I p...
Neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant disorders. NF1 is clinic...
Transcription factors (TF) regulate expression by binding to specific DNA sequences. A binding event...
Von Recklinghausen neurofibromatosis, or type 1 neurofibromatosis (NF1), is a common autosomal domin...
Neurofibromatosis type 1 (NF1) is one of the most common inherited neurological disorders with a wid...
Neurofibromatosis type 1 (NF1) is caused by inactivating mutations in NF1. Due to the size, complexi...