We now have an excellent model for this childhood disorder to learn about
the molecular causes of disease and to test for potential therapeutic strategies.
Identifying
the molecular causes of disease represented a major breakthrough in the history of medicine, moving the discipline from pattern recognition and therapeutic strategies based on syndromic pathophysiology to molecular mechanism and evidence ‐ based therapies derived from clinical trials designed on the basis of molecular mechanism.
Not exact matches
The notion that antisense oligonucleotides might inhibit the progression
of genetic
diseases or tumor -
causing viruses dates back to the late 1970s, when legendary
molecular biologist Paul Zamecnik and colleague Mary Stephenson demonstrated the method's viability against the Rous sarcoma virus.
These studies helped illuminate some
of the
molecular mechanisms by which these fungal pathogens
cause disease in the banana.
«I do think the science is becoming mature enough that we are starting to understand really at a
molecular level how a lot
of these
diseases are
caused,» Fontoura said.
Researchers from Instituto de Medicina
Molecular (iMM) Lisboa have created a chimera virus that allows the study
of molecules to treat cancers
caused by human herpes virus infection in mice models
of disease.
The team identified 345 regions
of the genome where they could pinpoint the likely
molecular causes underlying a person's predisposition to immune - related
diseases such as inflammatory bowel
disease, type 1 diabetes and multiple sclerosis.
«We found that a particular vaginal bacterium, Gardnerella vaginalis, did not
cause infection during exposure to the urinary tract, but it damaged the cells on the surface
of the bladder and
caused E. coli from a previous UTI to start multiplying, leading to another bout
of disease,» said the study's senior author, Amanda Lewis, PhD, an assistant professor
of molecular microbiology and
of obstetrics and gynecology at Washington University.
Mooney added, «Understanding and characterizing potentially functional HD protein interactions gives scientists new tools to connect genomic, genetic, proteomic and other
molecular changes to identify the
causes of this deadly
disease.
Detection and
molecular characterization
of Ebola viruses
causing disease in human and nonhuman primates
This can result in a serious genetic
disease that can
cause anemia, neuro - cognitive impairment, and even early death,» says the study's lead - author, Dr. Jean - Louis Guéant, director
of the Inserm unit
of Nutrition - Genetics - Environmental Risks at University
of Lorraine and head
of the Department
of Molecular Medicine and Personalized Therapeutics — National Center
of Inborn Errors
of Metabolism at the University Regional Hospital
of Nancy.
«Clearly, there are basic
molecular mechanisms
of aging that
cause the various
diseases that disable and ultimately kill us.»
By studying how these genes
cause defects in fly and mouse models, we can improve our insights into the mechanisms related to human
disease,» said corresponding author and Dr. Hugo J. Bellen, professor
of neuroscience and
molecular and human genetics at Baylor College
of Medicine and an investigator at the Howard Hughes Medical Institute.
The first clue to the importance
of this
molecular mimicry in herpes stromal keratitis (HSK), an autoimmune
disease of the eye
caused by infection with herpes virus 1 (HSV - 1), came about 3 years ago.
«Gastrointestinal
diseases are a major
cause of mortality in wild and captive pandas but scientists understand very little about their digestive process,» says co-author Ashli Brown Johnson, state chemist and Mississippi State University associate professor
of biochemistry,
molecular biology, entomology and plant pathology.
While researching the
molecular causes of heart failure and new ways to treat it, a Charité - based working group, led by Prof. Dr. Ulrich Kintscher, found that changes in adipose (fat) tissue lipid metabolism affect
disease development.
The researchers are investigating other mutations identified through the genetic screen and plan to undertake more genetic analysis
of HLHS patients to better understand the
molecular and genetic factors that
cause the
disease.
Bloomfield said updating the ELN recommendations was prompted by new insights into the
molecular and genomic
causes of the
disease, by the development
of new genetic tests and tests for detecting minimal residual
disease and by the development
of novel anti-leukemic agents.
Understanding its
molecular causes and risk factors has been challenging because most cases develop sporadically without inherited genetic mutations, and because
of the gradual progression
of symptoms over the course
of disease.
Scientists at the Max Planck Institute for
Molecular Genetics in Berlin have found seven new genes that can
cause this genetic
disease: Mutations
of these genes on the X chromosome lead to various forms
of intellectual disability.
While the
disease is
caused by a single gene mutation, the manifestation
of the
disease at a
molecular level is nevertheless highly complex and involves multiple cellular processes.
Published online ahead
of print in the leading microbiology journal
Molecular Microbiology, the researchers have identified a building block common to many types
of bacterial «virulence factors» (the bacterial proteins which act as weapons to
cause disease, such as toxins or degrading enzymes).
In the scientific article «Histone mutations separate R loops from genome instability induction» published in
Molecular Cell, the researchers state that RNA joins with DNA by chance or because
of a
disease, the structure
of the chromatin, the protein envelope
of the chromosomes is altered,
causing breaks in the DNA.
With the successful demonstration
of the MRI probe, Northwestern researchers now have established the
molecular basis for the
cause, detection by non-invasive MR imaging and treatment
of Alzheimer's
disease.
Using this approach, these investigators found that nodes (genes) with high connectivity tend to have lower levels
of change in expression than peripheral nodes, consistent with the notion that
disease ‐
causing genes are typically not central hubs in a
molecular module.
An international collaboration jointly led by scientists from Trinity College Dublin has shed new light on the origins and
molecular causes of age related degenerative conditions including Motor Neuron
Disease (MND).
Their
disease module revealed that two proteins previously linked to some forms
of the
disease were part
of the same
molecular pathway and that they work together to
cause errors in cell proliferation, which may be linked to the symptoms
of the
disease.
This can result in a serious genetic
disease that can
cause anemia, neuro - cognitive impairment, and even early death,» says the study's lead - author, Dr. Jean - Louis Guéant, director
of the Inserm unit
of Nutrition - Genetics - Environmental Risks at University
of Lorraine and head
of the Department
of Molecular Medicine and Personalized Therapeutics - National Center
of Inborn Errors
of Metabolism at the University Regional Hospital
of Nancy.
For instance, literally countless trials must be undertaken to ensure that a newly synthesized drug acts correctly on inhibiting a particular
molecular pathway, and countless experiments must be performed to ensure the responsibility
of that pathway as the
cause of a particular
disease.
CSHL is a private, non-profit research and education institution dedicated to exploring
molecular biology and genetics in order to advance the understanding and ability to diagnose and treat cancers, neurological
diseases, and other
causes of human suffering.
Among Desmond - Hellmann's most distinguishing contributions was establishing precision medicine — which aims to collect and analyze massive amounts
of data (genomic,
molecular, environmental and clinical) to identify the root
causes of diseases and to develop targeted therapies to treat them — as a goal for UCSF and the nation.
In addition to his other roles at the institute, he is director
of the Clinical
Molecular Genetics Training Program, an executive faculty member
of the Joint National Institutes
of Health - Johns Hopkins University Genetic Counseling Training Program, and the project officer for the Center for Inherited
Disease Research in Baltimore, a research center that analyzes common disorders
caused by the actions
of multiple genes and interactions with the environment.
Dr. Mucke has spent most
of his career uncovering the
molecular and cellular mechanisms that
cause memory loss and behavioral abnormalities in Alzheimer's
disease and related conditions.
«Although we first became aware
of prions because they
cause several bizarre neurological
diseases, the discovery that something so awesomely similar happens in organisms as different as humans and yeast makes us suspect that there is a fundamental, common biochemical process at work here,» said study director Susan Lindquist, PhD, professor
of molecular genetics and cell biology and an investigator in the Howard Hughes Medical Institute at the University
of Chicago.
To shed light on the putative
diseases and
causes of death in Tutankhamun's immediate lineage, we first used
molecular genetic methods to determine kinship within that lineage.
Dr Søren Tvorup Christensen (Department
of Biology) and Professor Lars Allan Larsen (Department
of Cellular and
Molecular Medicine) at the University
of Copenhagen, in collaboration with colleagues in Denmark and France, have spearheaded the recent discovery which sheds new light on the
causes of a range
of debilitating
diseases and birth defects.
Dr. Komáromy studies the
molecular causes of inherited eye
diseases in dogs and is working to develop gene therapies to stop vision loss.
«Having done a lot
of clinical interpretation for patients, my frustration over many years is that we can not diagnose the
causes of disease in most
of the rare
disease patients we test,» said Heidi Rehm, who is also the Chief Laboratory Director
of the Laboratory for
Molecular Medicine at Partners Personalized Medicine and an associate professor at Harvard Medical School.
Fruit flies serve as a good model organism for understanding the
molecular mechanisms behind many human
diseases — around 75 percent
of disease -
causing genes are found in the species in a similar form.
Kim Orth
of the University
of Texas Southwestern Medical Center and the Howard Hughes Medical Institute has worked to elucidate the activity
of bacterial virulence factors on the
molecular level, providing insights into how bacteria
cause disease and how eukaryotic host cells signalin response to infection.
The FLI investigates the
molecular causes for these aging - associated changes with the goal to uncover new approaches for therapies aiming to preserve the functioning
of the body's own stem cells and organs thereby reducing the risk
of diseases and cancer during aging.
Scientists at Washington University in St. Louis reached a new milestone in cancer research this month with the completion
of a comprehensive analysis
of the
molecular underpinnings
of the
causes of the
disease.
In spite
of worldwide research efforts, Parkinson's
disease's
molecular causes are still not clear.
Besides oxidation, glycation and the subsequent formation
of AGEs is one
of the major
molecular mechanisms
causing ongoing damage in your body, which leads to
disease, (premature) aging and, eventually, death.
The
molecular structure
of thyroid tissue is almost identical to that
of gluten and therefore the immune system may start sending antibodies not only against gluten proteins but against proteins found in different organs
causing autoimmune
diseases.
BIO * 235, Microbiology (4 credits / 6 contact hours) $ $ Laboratory Course Fee Gen Ed Competencies: Scientific Knowledge & Understanding, Scientific Reasoning This is an introduction to general microbiology.The course is designed to meet the needs
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cause disease and yet are essential to human well - being.
``... Initially the virus was identified in Greyhounds, and there was some speculation that the virus was exclusively
causing disease in Greyhounds,» said Dr. Ruben O. Donis, chief
of molecular genetics for the influenza branch at the CDC, who was part
of the group
of researchers.