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Search Results to Stephen Scherer

This is a "connection" page, showing the details of why an item matched the keywords from your search.

                     
                     

One or more keywords matched the following items that are connected to Scherer, Stephen

Item TypeName
Concept DNA-Binding Proteins
Academic Article Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia.
Academic Article A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome.
Academic Article Failure of a medulloblastoma-derived mutant of SUFU to suppress WNT signaling.
Academic Article 2q23 de novo microdeletion involving the MBD5 gene in a patient with developmental delay, postnatal microcephaly and distinct facial features.
Academic Article Severe intellectual disability and autistic features associated with microduplication 2q23.1.
Academic Article A CGG-repeat expansion mutation in ZNF713 causes FRA7A: association with autistic spectrum disorder in two families.
Academic Article Ankrd11 is a chromatin regulator involved in autism that is essential for neural development.
Academic Article CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping Conditions.
Academic Article The Ikaros gene encodes a family of lymphocyte-restricted zinc finger DNA binding proteins, highly conserved in human and mouse.
Academic Article Identification and purification of a family of dimeric major cold shock protein homologs from the psychrotrophic Bacillus cereus WSBC 10201.
Academic Article MADR2 maps to 18q21 and encodes a TGFbeta-regulated MAD-related protein that is functionally mutated in colorectal carcinoma.
Academic Article Evidence that the homeodomain protein Gtx is involved in the regulation of oligodendrocyte myelination.
Academic Article Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome.
Academic Article PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7.
Academic Article Chromosomal localization of phospholipase A2 activating protein, an Ets2 target gene, to 9p21.
Academic Article Localization of the human SP3 gene to chromosome 7p14-p15.2. The lack of expression in multiple sclerosis does not reflect abnormal gene organization.
Academic Article t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia.
Academic Article Mutation analysis of the origin recognition complex subunit 5 (ORC5L) gene in adult patients with myeloid leukemias exhibiting deletions of chromosome band 7q22.
Academic Article Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia.
Academic Article GATA1 mutations in transient leukemia and acute megakaryoblastic leukemia of Down syndrome.
Academic Article Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity.
Academic Article Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.

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  • DNA Binding Proteins