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Genetic Disorders
Fragile X syndrome is an inherited intellectual disability caused by a mutation in the FMR1 gene.
… intellectual disability caused by a mutation in the FMR1 gene. … Fragile X syndrome is the most common form of … are caused by an alteration (mutation) in the FMR1 gene where a DNA segment, known as the CGG triplet repeat, is … findings include short-term memory loss, executive function deficits, cognitive decline, parkinsonism, …
Educational Resources
Genomics refers to the study of the entire genome of an organism whereas genetics refers to the study of a particular gene.
… whereas genetics refers to the study of a particular gene. … Genomics, Genes, Gene Expression, Human Genome Project … Genomics is a field … whereas genetics refers to the study of a particular gene. … Educational Resources …
Educational Resources
Transcription is the process of making an RNA copy of a gene sequence.
… … Transcription is the process of making an RNA copy of a gene sequence. … Cell, Cytoplasm, Deoxyribonucleic Acid (DNA), Gene, Gene Expression, Messenger RNA (mRNA), Nuclear Membrane, …
Educational Resources
Codominance is a relationship between two versions of a gene.
… … Codominance is a relationship between two versions of a gene. … Genes, Alleles, Recessive, Dominant, Family Health … of inheritance in which two versions (alleles) of the same gene are expressed separately to yield different traits in an … … Codominance is a relationship between two versions of a gene. … Educational Resources …
Educational Resources
An oncogene is a mutated gene that contributes to the development of a cancer.
… Oncogene … An oncogene is a mutated gene that contributes to the development of a cancer. … … Mutagen, Cancer, Cell, Mutation, Tumor Suppressor Gene … An oncogene is a mutated gene that has the potential to cause cancer. Before an …
Educational Resources
An exon is the portion of a gene that codes for amino acids.
… Exon … An exon is the portion of a gene that codes for amino acids. … Intron, DNA Sequence, DNA … of exons and introns. … An exon is the portion of a gene that codes for amino acids. … Educational Resources …
Research Funding
NHGRI solicits grant applications that relate to its scientific priorities and research interests
… the latest updates and revisions to these documents. Most grants require the submission of form number  PHS-398 , the  … 398 to the SF424 form AND electronic submission through Grants.gov! To do business with the NIH in the future, grantees MUST register with both Grants.gov AND the NIH eRA Commons. See detailed info at:  …
Research Funding
A list of current and previous Centers of Excellence in Genomic Science (CEGS) grant awards.
… of these variants do we understand how the expression or function of the encoded product is affected. As a … for making dramatic, coordinated changes to extensive gene loci in the form of Big DNAs of 50-1000 kb, which enable … will require accurate manipulation of DNA sequences and gene expression as well as interrogation of the functional …
Educational Resources
Sex linked is a trait in which a gene is located on a sex chromosome.
… Sex Linked … Sex linked is a trait in which a gene is located on a sex chromosome. … Cell, Mutation, Gene, Sex Chromosome … Sex-linked, as related to genetics, … a sex-linked disorder. … Sex linked is a trait in which a gene is located on a sex chromosome. … Educational Resources …
Fact Sheets
Epigenomics is a field in which researchers chart the locations and understand the functions of all the chemical tags that mark the genome.
… epigenomic compounds attach to DNA and modify its function, they are said to have "marked" the genome. These … DNA and DNA-associated proteins in the cell, which alter gene expression, and are heritable (via meiosis and mitosis). … … The human genome contains two copies of every gene-one copy inherited from the mother and one from the …