Scienmag

AUGUST 12, 2020

12) — Columbia researchers have uncovered an array of new genes that cause stillbirth, significantly increasing the understanding of the condition’s genetic foundations. The findings suggest that genetic analysis could be used to counsel parents who have previously experienced stillbirth and to unlock new human biology.

Genetics 40

Genetics Genetic Analysis Gene Research 40

XTalks

DECEMBER 1, 2020

Over the past several years, personalized medicine has led the charge in medical innovation, leading drug development efforts as well as furthering the research community’s understanding of human disease states.

Clinical Trials 96

Clinical Trials Clinical Trials Trials Clinical Research 96

The Pharma Data

SEPTEMBER 3, 2020

Our new study offers an important basis from which to start developing new treatment strategies for a rare form of cancer, which starts in the hormone-producing cells of the pancreas,” noted Dr Anguraj Sadanandam, team leader in Systems and Precision Cancer Medicine at The ICR, London. “We

Research 52

Research Genetic Analysis Gene Scientist 52

pharmaphorum

APRIL 5, 2022

Genetic analysis of tumours can reveal mutations that are fuelling cancers growth, some of which can be targeted with treatment, they note. However, genomics alone is not able to reliably select drug combinations, and layering in their proteomics approach can improve the predictive power of this approach.

Protein 67

Protein Genomics Genome Genetic Analysis 67

Delveinsight

FEBRUARY 25, 2021

Beam Therapeutics has taken over a startup whose technology could proffer the biotech’s genetic medicines to more tissues in the body, widening the potential to approach more diseases. Cambridge, Massachusetts-based Beam aims to make more precise edits with genetic medicines, which employ base-editing.

DNA 52

DNA In-Vivo Genetics Medicine 52

The Pharma Data

DECEMBER 11, 2020

“There is significant work to be done and sizable gaps to bridge,” said Dr. Chancellor Donald, assistant professor of medicine, hematology and medical oncology at Tulane University School of Medicine in New Orleans, who led the briefing.

Genetics 52

Genetics Clinical Trials Clinical Trials Genetic Analysis 52

pharmaphorum

NOVEMBER 16, 2022

So, pegcetacoplan blocks an inflammatory pathway that appears to be central for geopathic genesis based on extensive genetic analysis,” Dr Wykoff concluded. “AMD is the most common cause of blindness by far, in the US, in Europe, in many parts around the world,” Dr Wykoff said. About the interviewee. Dr Charles C.

Genetics 105

Genetics Trials Clinical Trials Clinical Trials 105

The Pharma Data

JANUARY 7, 2021

. “The potential utility of this is that it can be used to define men who are at elevated risk of developing prostate cancer,” said lead author Christopher Haiman, professor of preventive medicine at Keck School of Medicine at the University of Southern California (USC) in Los Angeles.

Gene 52

Gene Genetics Genomics Genome 52

XTalks

JULY 29, 2024

Next-generation sequencing (NGS) allows for efficient analysis of known genetic mutations, enhancing diagnostic accuracy. Overall, the diagnostic process for LOPD typically involves a series of assessments, including clinical, laboratory and imaging tests, culminating in genetic analysis to confirm the diagnosis.

Clinical Trials 105

Clinical Trials Clinical Trials Trials Research 105

XTalks

JANUARY 6, 2025

Whether its the integration of nanotechnology in medicine, the evolution of point-of-care (POC) diagnostics or the transformative impact of CRISPR and regenerative medicine, these biotech trends are pushing scientific boundaries and creating new opportunities for businesses and researchers alike. billion by 2032, with a CAGR of 10.1

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Gene Therapy RNA Gene Editing Gene 111