RSS Feed for Latest Medical Headlines on RxPG News

Medical Research Health Special Topics World

 
  Home
 
   Health
 Aging
 Asian Health
 Events
 Fitness
 Food & Nutrition
 Happiness
 Men's Health
 Mental Health
 Occupational Health
 Parenting
 Public Health
 Sleep Hygiene
 Women's Health
 
   Healthcare
 Africa
 Australia
 Canada Healthcare
 China Healthcare
 India Healthcare
 New Zealand
 South Africa
 UK
 USA
 World Healthcare
 
   Latest Research
 Aging
 Alternative Medicine
 Anaethesia
 Biochemistry
 Biotechnology
 Cancer
 Cardiology
 Clinical Trials
 Cytology
 Dental
 Dermatology
 Embryology
 Endocrinology
 ENT
 Environment
 Epidemiology
 Gastroenterology
 Genetics
  Cloning
  Genetic Disorders
   Brachydactyly
   Fragile X Syndrome
   Huntington's
   MSUD
   Progeria
  X Chromosome
 Gynaecology
 Haematology
 Immunology
 Infectious Diseases
 Medicine
 Metabolism
 Microbiology
 Musculoskeletal
 Nephrology
 Neurosciences
 Obstetrics
 Ophthalmology
 Orthopedics
 Paediatrics
 Pathology
 Pharmacology
 Physiology
 Physiotherapy
 Psychiatry
 Radiology
 Rheumatology
 Sports Medicine
 Surgery
 Toxicology
 Urology
 
   Medical News
 Awards & Prizes
 Epidemics
 Launch
 Opinion
 Professionals
 
   Special Topics
 Ethics
 Euthanasia
 Evolution
 Feature
 Odd Medical News
 Climate
Search

Latest Research : Genetics : Genetic Disorders
  Last Updated: Nov 2, 2013 - 11:52:55 AM

Latest Research : Genetics : Genetic Disorders
XXYY syndrome- features and treatment options elucidated by researchers
Researchers at the UC Davis M.I.N.D. Institute and The Children's Hospital in Denver have conducted the largest study to date describing the medical and psychological characteristics of a rare genetic disorder in which males have two "X" and two "Y" chromosomes, rather than the normal one of each. The study, published in the June 15, 2008, issue of the American Journal of Medical Genetics Part A, also offers treatment recommendations for men and boys with the disorder.
Aug 24, 2008 - 1:16:40 AM

Latest Research : Genetics : Genetic Disorders
Switching genes to overdrive improves muscular dystrophy symptoms in mice
Scientists at Dana-Farber Cancer Institute have shown in a laboratory study that revving up a crucial set of muscle genes counteracts the damage caused by a form of muscular dystrophy.
Apr 1, 2007 - 11:56:50 AM

Latest Research : Genetics : Genetic Disorders
Gene mutation associated with X-linked mental retardation revealed
Researchers have identified a novel gene mutation that causes X-linked mental retardation for which there was no previously known molecular diagnosis, according to an article to be published electronically on Tuesday, March 20, 2007 in The American Journal of Human Genetics.
Mar 19, 2007 - 10:53:10 PM

Latest Research : Genetics : Genetic Disorders : Huntington's
Link between Huntington's and abnormal cholesterol levels in brain discovered
Mayo Clinic researchers have discovered a protein interaction that may explain how the deadly Huntington's disease affects the brain. The findings, published in and featured on the cover of the current issue of Human Molecular Genetics, show how the mutated Huntington's protein interacts with another protein to cause dramatic accumulation of cholesterol in the brain.
Dec 3, 2006 - 3:10:30 PM

Latest Research : Genetics : Genetic Disorders
Williams Syndrome, the brain and music
Children with Williams syndrome, a rare genetic disorder, just love music and will spend hours listening to or making music. Despite averaging an IQ score of 60, many possess a great memory for songs, an uncanny sense of rhythm, and the kind of auditory acuity, than can discern differences between different vacuum cleaner brands.
Oct 5, 2006 - 12:58:00 AM

Latest Research : Genetics : Genetic Disorders
Exploring genetics of congenital malformations
New research published in the August issue of the Journal of Cell Biology explains for the first time why congenital heart defects so often occur with limb deformities. In their research into the molecular mechanisms that control embryonic limb and heart development, Northwestern University researcher Hans-Georg Simon and his laboratory group recently identified a new protein, LMP4, which binds and regulates activity of the Tbx4 and Tbx5 transcription factors. Tbx5 and Tbx4 proteins play a key role in limb and heart formation in virtually all vertebrates, from fish to birds to mice to humans.
Aug 19, 2006 - 9:42:00 PM

Latest Research : Genetics : Genetic Disorders
FDA Approves Idursulfase As First Treatment for Hunter Syndrome
The Food and Drug Administration (FDA) approved Elaprase (idursulfase), the first product for the treatment of Hunter syndrome (Mucopolysaccharidosis II, or MPS II), a rare inherited disease which can lead to premature death. Elaprase is a new molecular entity, which is an active ingredient never before marketed in the United States.
Aug 2, 2006 - 12:30:00 PM

Latest Research : Genetics : Genetic Disorders : Huntington's
PARP1 inhibitors can protect Huntington's disease affected cells from damage
An enzyme known to be critical for the repair of damaged cells and the maintenance of cellular energy may be a useful target for new strategies to treat Huntington's disease (HD) and other disorders characterized by low cellular energy levels. In the August issue of Chemistry & Biology, a research team from the MassGeneral Institute for Neurodegenerative Disease (MIND) describes their discovery of a novel inhibitor of Poly (ADP-ribose) polymerase (PARP1) and their findings that PARP1 inhibitors can protect HD-affected cells from damage in laboratory assays.
Jul 30, 2006 - 2:41:00 AM

Latest Research : Genetics : Genetic Disorders : Huntington's
Gene therapy protects neurons in Huntington's disease
Researchers at Rush University Medical Center, Chicago, and Ceregene Inc., San Diego, have successfully used gene therapy to preserve motor function and stop the anatomic, cellular changes that occur in the brains of mice with Huntington's disease (HD). This is the first study to demonstrate that, using this delivery method, symptom onset might be prevented in HD mice with this treatment.
Jun 30, 2006 - 3:02:00 AM

Latest Research : Genetics : Genetic Disorders : Huntington's
Huntingtin cleavage is caused by caspase-6
Researchers at the University of British Columbia's Centre for Molecular Medicine and Therapeutics (CMMT) have provided ground-breaking evidence for a cure for Huntington disease in a mouse offering hope that this disease can be relieved in humans.
Jun 17, 2006 - 8:10:00 PM

Latest Research : Genetics : Genetic Disorders
The risk of transmission of genetic disorders through donor's sperm
As medical technology continues to advance, fertility procedures such as in-vitro fertilization and donor insemination are becoming more commonplace. However, a study in the May issue of The Journal of Pediatrics warns that, even after thorough screenings of sperm donors, genetic disorders can be transmitted to the conceived children.

May 19, 2006 - 7:25:00 PM

Latest Research : Genetics : Genetic Disorders : MSUD
Liver transplants provide metabolic cure for maple syrup urine disease
Liver transplants cured the metabolic symptoms of 11 patients with a rare but devastating genetic condition known as Maple Syrup Urine Disease (MSUD), according to a study by researchers from Children's Hospital of Pittsburgh and the Clinic for Special Children.
Apr 11, 2006 - 10:28:00 PM

Latest Research : Genetics : Genetic Disorders
Spinocerebellar ataxia type 5 (SCA5) gene pinpointed
Researchers at the University of Minnesota Medical School have discovered the gene responsible for a type of ataxia, an incurable degenerative brain disease affecting movement and coordination.
Jan 23, 2006 - 4:12:00 PM

Latest Research : Genetics : Genetic Disorders
Scientists probe connection between regulatory DNA and disease
Through the Human Genome Project, the HapMap Project and other efforts, we are beginning to identify genes that are modified in some diseases. More difficult to measure and identify are the regulatory regions in DNA – the 'managers' of genes – that control gene activity and might be important in causing disease.
Dec 17, 2005 - 3:34:00 PM

Latest Research : Genetics : Genetic Disorders : Progeria
Farnesyl Transferase Inhibitors in Hutchinson-Gilford progeria syndrome
Johns Hopkins scientists have discovered that a drug currently being tested against cancers might help children with a rare, fatal condition called Hutchinson-Gilford progeria syndrome, which causes rapid, premature aging.
Children with progeria appear normal until they're 6 months to a year old, but then begin developing symptoms normally associated with old age -- wrinkled skin, hair loss, brittle bones and atherosclerosis, which usually causes their deaths by about age 13. There's no known treatment.

Sep 28, 2005 - 1:20:00 PM

Latest Research : Genetics : Genetic Disorders : Huntington's
Clioquinol, an antibiotic shows new promise for Huntington's Disease
Clioquinol, an antibiotic that was banned for internal use in the United States in 1971 but is still used in topical applications, appears to block the genetic action of Huntington's disease in mice and in cell culture, according to a study reported by San Francisco VA Medical Center (SFVAMC) researchers.
Sep 12, 2005 - 6:14:00 PM

Latest Research : Genetics : Genetic Disorders : Progeria
Anti-cancer drugs might work in aging disease
Working together, scientists at the National Institutes of Health and the University of North Carolina at Chapel Hill have developed a promising new strategy for treating a form of progeria. That rare but deadly and heartbreaking genetic disease causes children to age remarkably fast and die almost always before they complete their teens.
Aug 30, 2005 - 7:45:00 PM

Latest Research : Genetics : Genetic Disorders : Progeria
Lamin research project provides clues about premature aging
A step towards understanding cell mutations that cause a variety of human diseases, particularly in children -- including that which brings about premature aging and early death -- has been taken by researchers at the Hebrew University of Jerusalem Silberman Institute of Life Sciences and the John Hopkins University School of Medicine.
Aug 30, 2005 - 7:42:00 PM

Latest Research : Genetics : Genetic Disorders : Progeria
Drug prevents cell abnormality leading to progeria
Genetic disease causes accelerated aging, death in children
Aug 30, 2005 - 7:39:00 PM

Latest Research : Genetics : Genetic Disorders : Progeria
Farnesyltransferase inhibitors (FTIs) might be useful in Hutchinson-Gilford Progeria Syndrome
In a surprising development, a research team led by the National Human Genome Research Institute (NHGRI), part of the National Institutes of Health (NIH), has found that a class of experimental anti-cancer drugs also shows promise in laboratory studies for treating a fatal genetic disorder that causes premature aging.
Aug 30, 2005 - 7:33:00 PM

Latest Research : Genetics : Genetic Disorders
Lorenzo's oil (LO) reduced the risk of developing severe X-linked adrenoleukodystrophy (ALD)
Treatment of boys with X-linked adrenoleukodystrophy (ALD) with Lorenzo's oil (LO) reduced their risk of developing the severe debilitating form of the disease, according to a study in the July issue of the Archives of Neurology, one of the JAMA/Archives journals.
Jul 12, 2005 - 12:26:00 PM

Latest Research : Genetics : Genetic Disorders : Fragile X Syndrome
Understanding the interaction of Fragile X mental retardation protein and kissing complex RNAs
Fragile X syndrome is the most common inherited form of mental retardation, affecting approximately 1 in 3600 males and 1 in 4000-6000 females.
Apr 18, 2005 - 4:57:00 AM

Latest Research : Genetics : Genetic Disorders
Roberts Gene ESCO2 Discovered to be behind "PSEUDOTHALIDOMIDE" Syndrome
A team of scientists from Colombia, the United States and elsewhere has successfully completed a 15-year-plus search for the genetic problems behind the very rare Roberts syndrome, whose physical manifestations often include cleft lip and palate and shortened limbs that resemble those of babies whose mothers took thalidomide during pregnancy.
Apr 12, 2005 - 1:02:00 PM

Latest Research : Genetics : Genetic Disorders : Huntington's
Potential therapeutic target for Huntington's disease
Researchers studying yeast cells have identified a metabolic enzyme as a potential therapeutic target for treating Huntington's disease, a fatal inherited neurodegenerative disorder for which there is currently no effective treatment.
Apr 7, 2005 - 6:14:00 PM

Latest Research : Genetics : Genetic Disorders : Brachydactyly
Putting a finger on shortened digits
Brachydactyly is a group of inherited disorders of the hands that are characterized by shortened fingers and abnormal joint formation.
Apr 3, 2005 - 1:44:00 PM

<< prev next >>

 
Headlines
Health  
Intake of low energy dense food better than skipping meals
Molecular hub links obesity, heart disease to high blood pressure
Bird flu mutation study offers vaccine clue
Youth with type 1 diabetes may suffer health risks when transitioning from pediatric to adult care
Promoting poultry health through diet
Creeping epidemic of obesity hits Asia Pacific region
NOAA adds red tide alerts to Beach Hazards Statements
University-developed omega-3-rich ground beef available soon
Institute of Medicine report details for monitoring safety of childhood immunization schedule
Moms go online for seeking parenting advice
Healthcare  
Flu pandemic infected one in five
Stigma preventing leprosy-cured from getting jobs
Measles, Mumps make a comeback in US
Melinda Gates calls on Akhilesh Yadav
'Movies, TV impact tobacco users more than newspapers'
Rockland to open three new hospitals in NCR
Spice Global enters healthcare business with hospital in Delhi
Delhi to expedite recruitment of doctors
India adds spice to US life, keeps it healthy
BRICS to strengthen cooperation in health sector
Latest Research  
Moderate to severe psoriasis linked to chronic kidney disease, say experts
Licensing deal marks coming of age for University of Washington, University of Alabama-Birmingham
Simple blood or urine test to identify blinding disease
Physician job satisfaction driven by quality of patient care
Book explores undiscovered economics of everyday life
Gene and stem cell therapy combination could aid wound healing
Solving the internet capacity crunch
Breathing new life into preterm baby research
Perceptions of the role of the state shape water services provision
UltraHaptics -- it's magic in the air
Medical News  
NHRC issues notice to Kerala over infant deaths
Advanced breast cancer detecting machine comes to India
'Dispel myths about vitiligo'
NHRC summons Odisha chief secretary
Woman dies of swine flu in UP
Maharashtra, GE to modernise rural health care
Hypertension: India's silent killer
Need cautious effort to eradicate polio: Experts
Ayurveda experts develop online personalised health regimen
Soon a detailed study on 'diabesity': Doctors
Special Topics  
MPs express anguish at Delhi gang-rape, Shinde assures fast trial
Worrying rise in number of medical students in prostitution over last 10 years
Behold India's unfolding democratic revolution
Chinese woman cuts open her belly to save surgery cost
Improved Sense of Smell Produced Smarter Mammals
Two-year-old world's first to have extra DNA strand
172,155 kidney stones removed from one patient!
'Primodial Soup' theory for origin of life rejected in paper
Human species could have killed Neanderthal man
History, geography also seem to shape our genome

All rights reserved by RxPG
Contact Us