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New genetic sequencing lab creates 'tipping point' for personalised cancer ...
Science of genome-sequencing has rocketed forward in 10 years Milwaukee Journal Sentinel To a degree few had expected in the 1990s, the speed of genome sequencing has increased and the cost has dropped.
Medical School Establishes Biomarker Discovery Center Newswise (press release) Newswise — STRATFORD, NJ – Following recent discoveries by its researchers that could significantly change the diagnosis and treatment of a number of diseases, the...
CHARLES BANKHEAD: I'm Charles Bankhead of MedPage Today, and this is Expert Commentary, Non-Small Cell Lung Cancer. My guest is Dr. Lecia Sequist of the Massachusetts General Hospital. She is a thoracic medical oncologist at the MGH Cancer Center and is also assistant professor of medicine at Harvard. Thank you for joining us...
MRI scans of migraine sufferers have revealed that the intense, throbbing headaches they suffer are related to brain abnormalities, some of which are present at birth and others that develop over time, according to a study published online March 26...
Fifty years ago, oncologists relied upon the clinical exam to follow breast cancer patients with metastatic disease. Patients were treated with chemotherapy, and then the physicians waited for symptoms to return before deciding on the next treatment course. Some patients could go months or even years without symptoms, but during this time they played a waiting game. Technology did not yet exist to allow physicians to detect cancer progression in the absence of overt clinical clues.
THE first publication on the use of WA’s Lotterywest Next-Gen sequencing platform in a human context has been released, revealing two novel genetic aberrations that lead to the onset of a devastating neuromuscular disease in utero. Equally significant is proof that the latest sequencing technology can be used successfully and cost-effectively in gene discovery and diagnosis of rare disease cases. Neuromuscular disease experts, Dr Gina Ravenscroft and Professor Nigel Laing from the Western Australian Institute for Medical Research (WAIMR), and clinicians and pathologists in Western and South Australia, have identified two new variants of a gene, known to regulate glycogen availability for muscle development.
International Journal of Surgical Oncology is a peer-reviewed, open access journal that publishes original research articles, review articles, and clinical studies in all areas of surgical oncology.
Emory receives NINDS grant for biomarker research on Parkinson's News-Medical.net Led by F.
ORLANDO—CT texture analysis of primary tumors may be a potential imaging biomarker in localized esophageal cancer following neoadjuvant chemotherapy, according to research being presented at the 2013 Cancer ...
RT @EricTopol: Genomics at Your Fingertips http://t.co/iehVcVfP by @drkevincampbell HT @cyphergenomics #CDoM
DAI provides potential imaging biomarker to indicate brain tumor response to RT Medical Xpress Diffusion abnormality index (DAI) shows promise as an imaging biomarker to measure brain tumor response to radiation therapy, according to research being...
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Bioscience Technology New Schizophrenia Diagnostic Method Found - Bioscience Technology Bioscience Technology Researchers have discovered a method for physical diagnosis of schizophrenia by collecting tissue from the nose Schizophrenia, a...
NanoVelcro Chip device captures and isolates potentially high-risk cancer cells
The discovery of activating mutations in EGFR radically changed the treatment options for these patients, and, indeed, treatment of advanced stage patients with EGFR-mutated tumors with erlotinib (in the US) is now front-line ...
Elevated levels of Cyclin D1b could function as a novel biomarker of lethal metastatic disease in prostate cancer patients, according to a pre-clinical study published ahead of print on December 21...Read the whole entry... »...
Although the presence of an EGFR mutation is a predictive marker for response to EGFR tyrosine kinase inhibitor therapy in patients with non-small cell lung cancer, the mutation is not a prognostic factor.
Multiple sclerosis (MS) is a central nervous system (CNS) disorder characterised by demyelination and neurodegeneration. Although hallmarks of recovery (remyelination and repair) have been documented in early MS, the regenerative capacity of the adult CNS per se remains uncertain with the wide held belief that it is either limited or non-existent. The neural cell adhesion molecule (NCAM) is a cell adhesion molecule that has been widely implicated in axonal outgrowth, guidance and fasciculation. Here, we used in vitro and in vivo studies in MS to investigate the role of NCAM in disease progression.
A new diagnostic test that uses metabolomic analysis may be a safe and easy screening method to detect pancreatic cancer, researchers in Japan said.
Lung cancer is a tricky disease and there is a graveyard littered with lung cancer drugs that failed in clinical trial.Targeted approaches like Xalkori from Pfizer (PFE) and Tarceva from Roche (RHHBY.OB) work for small segmen...
Despite all we have learned about the importance of sensitizing EGFR mutations in defining the management of advanced NSCLC, our education regarding the relevance of this molecular target in optimizing clinical outcomes continues.
Heidi Rehm has been using disease-targeted gene panels to diagnose patients in her clinical molecular genetics practice for a decade. Having adopted next-generation sequencing approaches two years ago, and whole-genome and whole-exome sequencing for some patients in the past year, she is a pioneer in applying genomics in the clinic.
IBM is turning Watson loose on lung cancer, offering up a cloud-based service designed to let doctors from around the country find the best-possible treatments for their patients.
Via Alex Butler
OncLive BATTLE-2: Next-Generation of Biomarker-Driven Trials OncLive While the number of known mutations and matching targeted agents is relatively limited at present, clinical trials are being designed to identify effective therapies for specific...
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Sarah Cannon and the UCL Cancer Institute of the UK establish a genetic sequencing platform for cancer patients focused on identifying driver mutations with "actionable" available treatments. This platform also requires less tissue for the testing and may be performed at a lower cost than traditional gene sequencing.