Results 271 to 280 of about 190,232 (322)

Imprinting Disorders and Epigenetic Alterations in Children Conceived by Assisted Reproductive Technologies: Mechanisms, Clinical Outcomes, and Prenatal Diagnosis. [PDF]

open access: yesGenes (Basel)
Gambadauro A   +9 more
europepmc   +1 more source

Id gene expression during development and molecular cloning of the human Id-1 gene

Molecular Brain Research, 1995
Id genes encode helix-loop-helix proteins that inhibit transcription by forming inactive heterodimers with basic helix-loop-helix (bHLH) proteins. bHLH proteins normally form either homodimers or heterodimers with other bHLH proteins and bind to a DNA sequence element activating transcription. Id-containing heterodimers are inactive because Id proteins
W, Zhu   +8 more
openaire   +2 more sources

X-Linked ASDs and ID Gene Mutations

2016
Intellectual disability (ID) defines a group of disorders that cause impairment in intellectual performance. Autism spectrum disorders (ASDs) cause deficits in communication and social skills in addition to repetitive and stereotyped behaviors. We focus our attention on IDs and ASDs caused by mutations within the X chromosome on genes that exert their ...
Moretto E, Passafaro M, Bassani S
openaire   +3 more sources

Id genes and proteins as promising targets in cancer therapy

Trends in Molecular Medicine, 2004
Since the identification of Id proteins more than a decade ago, much work has demonstrated their regulatory roles in development, cell fate and lineage determination, proliferation, differentiation, angiogenesis, invasion and migration. Recent studies reveal not only that Id protein expression is significantly correlated both with cancer progression ...
Sylvia, Fong   +2 more
openaire   +2 more sources

Polymorphism of the murine inhibitor of differentiation-controlling gene, Id

Gene, 1995
The structure of Id was examined by Southern analysis in inbred mouse lines which included five subspecies of Mus musculus. No variation was detected within this species. The species Mus cookii shares the same form found in mice of M. musculus derivation, indicative of a long evolutionary history and a common origin.
S A, Marlow   +2 more
openaire   +2 more sources

Gene symbol: IDS. Disease: mucopolysaccharidosis type II (Hunter syndrome).

Human genetics, 2006
We report here the first exonic splicing mutation in a 8-year old intermediate Hunter patient. Genomic DNA sequencing identified a G to C transversion involving the last nucleotide of IDS exon VI (ExVI 1003G>C). The mutation leads to the disappearance of the normal exon VI/intron 6 splice donor site, resulting in the skipping of a 28 bp fragment of ...
Villani GR   +6 more
openaire   +4 more sources

Nucleos(t)ide analogues causes HBV S gene mutations and carcinogenesis

Hepatobiliary & Pancreatic Diseases International, 2016
The long-term use of nucleos(t)ide analogues causes drug resistance and mutations in the HBV reverse transcriptase (RT) region of the polymerase gene. The RT region overlaps the HBV surface gene (S gene) and therefore, the mutations in the RT region simultaneously modify S gene sequence.
Meng-Lan, Wang, Hong, Tang
openaire   +2 more sources

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