Genetic News and Research

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Genomic analysis of uncultured bacteria from patients identifies more than thirty new species

Unknown germs are a common occurrence in hospitals. Researchers at the University of Basel have spent many years collecting and analyzing them.

8 Jan 2024

Gut microbiota: the new frontier in Alzheimer’s disease research and therapy

The current evidence of the role of gut microbiota in Alzheimer’s disease (AD) pathogenesis.

8 Jan 2024

Does SARS-CoV-2's ability to infect humans stem from its evolutionary past?

Study challenges the hypothesis of genetic recombination in SARS-CoV-2's evolution, suggesting its ancestral virus already possessed human-infecting traits, based on analyses of over 100 viral genomes.

7 Jan 2024

Genetic keys to COVID-19 vaccine response unlocked

A genome-wide association study in the U.K. Biobank reveals genetic factors influencing IgG serostatus against SARS-CoV-2, highlighting the role of HLA class II genes in variable immune responses to COVID-19 vaccines.

7 Jan 2024

Gut enzyme discovery sheds light on bilirubin balance in humans

Researchers study identified BilR, a gut microbiota-derived enzyme, crucial for converting bilirubin to urobilinogen, impacting bilirubin homeostasis in humans.

7 Jan 2024

Discovery on housekeeping genetic elements reveals a novel avenue in cancer therapy

Technological advancements have enabled scientists to comprehensively explore genetic control elements, unraveling the complexities of gene activation mechanisms in our genetic code.

5 Jan 2024

Study identifies 9 novel genes linked to gestational diabetes

The largest genetic study of gestational diabetes to date has led to a discovery of nine novel genetic regions linked to this severe and common pregnancy complication.

5 Jan 2024

Epilepsy drug may alleviate joint degeneration associated with osteoarthritis

A new study in Nature described Nav1.7 as a key regulatory molecule in cartilage cells and reported the effectiveness of Nav1.7 blockade in reducing pain and slowing progression in OA.

5 Jan 2024

YAP and TAZ proteins guide bone development in the womb

A pair of proteins, YAP and TAZ, has been identified as conductors of bone development in the womb and could provide insight into genetic diseases such as osteogenesis imperfecta, known commonly as "brittle bone disease."

4 Jan 2024

Study: Two-thirds of babies with sickle cell disease are born to mothers living in disadvantaged areas

As if starting life with a potentially disabling genetic blood disease wasn't enough, a study shows that almost two-thirds of babies born with sickle cell disease are born to mothers who live in disadvantaged areas.

4 Jan 2024

Bipolar disorder cuts lives short more than smoking

Having bipolar disorder – a serious mental illness that can cause both manic and depressed moods – can make life more challenging.

4 Jan 2024

Researchers discover PPFIA3 gene as a cause of previously unknown syndromic neurodevelopmental disorder

An international collaborative study led by postdoctoral scientist, Dr. Maimuna Paul, and child neurologist, Dr. Hsiao-Tuan Chao, an assistant professor at Baylor College, a faculty member with the Cain Pediatric Neurology Research Foundation Laboratories at the Jan and Dan Duncan Neurological Research Institute (Duncan NRI) at Texas Children's Hospital, and an investigator at the McNair Medical Institute with The Robert and Janice McNair Foundation, recently discovered that variants in the PPFIA3 gene cause a previously unknown syndromic neurodevelopmental disorder.

4 Jan 2024

New study highlights the work of biobank at the Colorado Center for Personalized Medicine

A new peer-reviewed study in the American Journal of Human Genetics highlights the work of the biobank at the Colorado Center for Personalized Medicine (CCPM), a world-class site for precision medicine in research and clinical care created in partnership with the University of Colorado Anschutz Medical Campus and UCHealth.

4 Jan 2024

HPV infection linked to doubled risk of thyroid cancer

Study finds previously unidentified genetic mutation in a small protein provides significant protection against Parkinson’s disease

Researchers explored the effects of a small humanin-like peptide 2 (SHLP2) variant on mitochondrial function.

4 Jan 2024

Genetic News and Research

Genomic analysis of uncultured bacteria from patients identifies more than thirty new species

Gut microbiota: the new frontier in Alzheimer’s disease research and therapy

Does SARS-CoV-2's ability to infect humans stem from its evolutionary past?

Genetic keys to COVID-19 vaccine response unlocked

Gut enzyme discovery sheds light on bilirubin balance in humans

Discovery on housekeeping genetic elements reveals a novel avenue in cancer therapy

Study identifies 9 novel genes linked to gestational diabetes

Epilepsy drug may alleviate joint degeneration associated with osteoarthritis

YAP and TAZ proteins guide bone development in the womb

Study: Two-thirds of babies with sickle cell disease are born to mothers living in disadvantaged areas

Bipolar disorder cuts lives short more than smoking

Researchers discover PPFIA3 gene as a cause of previously unknown syndromic neurodevelopmental disorder

New study highlights the work of biobank at the Colorado Center for Personalized Medicine

HPV infection linked to doubled risk of thyroid cancer

AI model predicts future spread of SARS-CoV-2 variants using genomic data

Research identifies genetic connection between anorexia and morning chronotype

Researchers develop peptide to target "chaotic" MYC protein in 75% of cancers

Stanford Medicine researchers demonstrate new way to temporarily heighten hypnotizablity

IDO2 deficiency in mice leads to behavioral abnormalities resembling autism spectrum disorder

Study finds previously unidentified genetic mutation in a small protein provides significant protection against Parkinson’s disease

Sequencing & Genomics: Elevating Science and Healthcare eBook

Lab Matters host Harriet Gould on building a more connected lab community

The Critical Role of Sample Storage in Drug Discovery and Development

Advancing Neuroscience Research Through Collaboration and Patient-Centered Innovation

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