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Many patients with arteriovenous malformations of the brain have somatic activating KRAS mutations

KRAS Mutations Linked to Brain Arteriovenous Malformations

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Most tissue samples of arteriovenous malformations of the brain had somatic activating KRAS mutations
Obstetrician-gynecologists should be aware of who is eligible for cascade testing

ACOG Advocates Cascade Testing for Hereditary Gene Mutations

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Ob-gyns should identify eligible patients, offer testing, and assist in decreasing barriers to testing
Neuroanatomic abnormalities are seen in cohorts at high risk for autism spectrum disorder

Neuroanatomic Abnormalities ID’d in Those at Risk for Autism

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Seen in carriers of deletion or duplication at 16p11.2, a common cause of autism spectrum disorder
Genetics may be a factor in the experience of chronic pain post surgery

Gene Polymorphisms Linked to Risk of Chronic Post-Op Pain

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Genetic variations, age, gender, history of chronic pain all associated with risk
The majority of both high-risk and intermediate-risk women prefer a non-invasive cell-free prenatal DNA screening as a secondary screening test for trisomy 21

Majority of Women Prefer Non-Invasive Testing for Trisomy 21

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Yet, roughly one-third still want an invasive secondary test plus chromosomal microarray
Amplification of the inflammation-responsive RNA editase adenosine deaminase acting on RNA (ADAR)1 gene is associated with reduced survival in multiple myeloma

Multiple Myeloma Survival Down With High ADAR1 RNA Expression

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ADAR1 knockdown reduces regeneration of high-risk multiple myeloma in patient-derived xenografts
SERPINA1 DNA sequencing can identify alpha-1 antitrypsin deficiency

DNA Sequencing Identifies Alpha-1 Antitrypsin Deficiency

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Six rare mutations identified in seven subjects that would not have been uncovered without sequencing
A new approach to gene therapy can restore immune cell types in infants with newly diagnosed X-linked severe combined immunodeficiency

ASH: New Approach to Gene Tx Restores Immune Cells in X-SCID

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Efficient vector marking in bone marrow CD34+ cells, myeloid cells, B cells in newly diagnosed SCID
For men with hemophilia B who have factor IX coagulant activity of 2 percent or less of normal value

Gene Therapy Shows Beneficial Effect in Men With Hemophilia B

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Reduction in annualized bleeding rate and in factor use with infusion of viral vector with transgene
Lipid-associated genetic risk correlates with the risk of abdominal aortic aneurysm

Lipid-Linked Genetic Risk Tied to Abdominal Aortic Aneurysm

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Genetic elevation of LDL-C linked to increased AAA risk; increase for HDL-C linked to lower risk of AAA