HD is an autosomal dominantly inherited neurodegenerative disorder caused by a CAG repeat expansion in the gene
encoding huntingtin.
HD is caused by an unstable expansion of CAG repeats in the gene
encoding huntingtin protein.
Huntington's disease is an inherited genetic disorder caused by mutations in the gene that
encodes huntingtin protein.
Not exact matches
The
huntingtin gene
encodes a large scaffold protein, with many interaction partners, which is thought to be involved in intracellular trafficking.
In humans, Huntington's is an inherited disease caused by a gene
encoding a toxic protein, called mutant
huntingtin, which causes brain cells to die.
Huntington's disease is caused by a gene
encoding a toxic protein (mutant
huntingtin) that causes brain cells to die.
In a nonhuman primate model geneticist Anthony Chan DVM, PhD, and his colleagues at Yerkes developed, rhesus macaques carry a gene
encoding a fragment of mutant human
huntingtin.
That means a healthy parent whose
huntingtin gene
encodes proteins with 35 repeats may produce a child with 36 repeats.
Huntington's disease is caused by a gene
encoding a toxic protein (mutant
huntingtin or mHTT).
These three monkeys carried a gene
encoding a fragment of mutant human
huntingtin.
Huntington's is an inherited disease caused by a gene
encoding a toxic protein (mutant
huntingtin) that causes brain cells to die.
Huntington's disease is caused by a gene
encoding a toxic protein (mutant
huntingtin or mHTT) that causes brain cells to die.
Huntington's disease (HD) is a progressive neurodegenerative disorder caused by a CAG: CTG repeat expansion in exon 1 of the gene that
encodes the polyglutamine - containing protein
Huntingtin.
Huntingtin null neurons exhibit a significant reduction in transcripts
encoding proteins destined for the extracellular space, many of which are components of the extracellular matrix or involved in cellular adhesion, receptor binding and hormone activity.