Gene Loss Causes Leukemia
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Gene Loss Causes Leukemia
View full resource at disabled-world.com
Most Recently Shared on May 17, 2010 at 6:08 pm By:
Study links genes to common forms of glaucoma
medicalxpress.com — “Results from the largest genetic study of glaucoma, a leading cause of blindness and vision loss worldwide, showed that two genetic variations are associated with primary open angle glaucoma (POAG), a common form of the disease. The identification of genes responsible for this disease is the first step ...” View full resource at medicalxpress.com
Most Recently Shared on April 26, 2012 at 8:56 pm By:
PhysOrg Health News Health News
Study links genes to common forms of glaucoma http://t.co/Tywm9scK
ApoE4 gene could cause early loss of synapses in Alzheimer's disease
news-medical.net — “Today, researchers at the Blanchette Rockefeller Neurosciences Institute (BRNI) at West Virginia University in Morgantown, West Virginia reported a significant advance in understanding how different forms of the ApoE gene raise the risk for Alzheimer's disease.” View full resource at news-medical.net
Most Recently Shared on March 17, 2012 at 10:21 am By:
Alzheimers News: ApoE4 gene could cause early loss of synapses in Alzheimer's disease: Today, researchers at the... http://t.co/Pjbj6Qjw
ApoE4 gene could cause early loss of synapses in Alzheimer's disease
news-medical.net — “Today, researchers at the Blanchette Rockefeller Neurosciences Institute (BRNI) at West Virginia University in Morgantown, West Virginia reported a significant advance in understanding how different forms of the ApoE gene raise the risk for Alzheimer's disease.” View full resource at news-medical.net
Most Recently Shared on March 17, 2012 at 10:12 am By:
ApoE4 gene could cause early loss of synapses in Alzheimer's disease: Today, researchers at the Blanchette Rocke... http://t.co/mck4sCTG
BMC Genetics | Abstract | Association of single nucleotide polymorphic sites in candidate genes with aggressiveness and deoxynivalenol production in Fusarium graminearum causing wheat head blight
biomedcentral.com — “Fusarium graminearum sensu stricto (s.s.) is an ubiquitous pathogen of cereals. The economic impact of Fusarium head blight (FHB) is characterized by crop losses and mycotoxin contamination. Our objective was to associate SNP diversity within candidate genes with phenotypic traits. A total of 77 F. graminearum s.s. isolates was tested for severity of fungal infection (=aggressiveness) and deoxynivalenol (DON) production in an inoculated field experiment at two locations in each of two years. For” View full resource at biomedcentral.com
Most Recently Shared on March 13, 2012 at 3:30 pm By:
BioMed Central Medical Journal
RT @bmc_series: Aggressive genes identified in wheat fungus http://t.co/qunIvaFr #BMCGenetics #genetics #plant #biology #pathogens
Genome Medicine | Abstract | Systems-level analysis of age-related macular degeneration reveals global biomarkers and phenotype-specific functional networks
genomemedicine.com — “Age-related macular degeneration (AMD) is a leading cause of blindness that affects the central region of the retinal pigmented epithelium (RPE), choroid, and neural retina. Initially characterized by an accumulation of sub-RPE deposits, AMD leads to progressive retinal degeneration, and in advanced cases, irreversible vision loss. Although genetic analysis, animal models, and cell culture systems have yielded important insights into AMD, the molecular pathways underlying AMD's onset and progres” View full resource at genomemedicine.com
Most Recently Shared on February 24, 2012 at 1:49 pm By:
BioMed Central Medical Journal
RT @genomemedicine: Systems approach reveals novel #gene signatures associated with age-related macular degeneration http://t.co/BlVKhaxX
Shedding Light On Gene Destruction Linked To Aggressive Prostate Cancer
medicalnewstoday.com — “Researchers at Queen's University have identified a possible cause for the loss of a tumour suppressor gene (known as PTEN) that can lead to the development of more aggressive forms of prostate ca” View full resource at medicalnewstoday.com
Most Recently Shared on January 29, 2012 at 8:05 am By:
Shedding Light On Gene Destruction Linked To Aggressive Prostate Cancer http://t.co/XwQ2fja3 #prostate
Protein gives clue to hearing loss | NHS Choices | Nursing Times
nursingtimes.net — “Gene research may provide a clue to the causes of deafness, according to the Daily Mirror.” View full resource at nursingtimes.net
Most Recently Shared on January 11, 2012 at 1:01 am By:
Behind the Headlines Protein gives clue to hearing loss: Gene research may provide a clue to the causes of deafn... http://t.co/xI7RSEaW
Study In Fruit Flies Has Implications For Autism, Other Cognitive Impairment Syndromes
medicalnewstoday.com — “The most common form of heritable cognitive impairment is Fragile X Syndrome, caused by mutation or malfunction of the FMR1 gene. Loss of FMR1 function is also the most common genetic cause of aut” View full resource at medicalnewstoday.com
Most Recently Shared on November 1, 2011 at 8:06 am By:
Study In Fruit Flies Has Implications For Autism, Other Cognitive Impairment Syndromes: The most common form of ... http://t.co/MLazq4s5
NIH scientists discover link among spectrum of childhood diseases, October 31, 2011 News Release - National Institutes of Health (NIH)
nih.gov — “An international collaboration of scientists, including researchers at the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), a part of the National Institutes of Health, has identified a genetic mutation that causes a rare childhood disease characterized predominantly by inflammation and fat loss.” View full resource at nih.gov
Most Recently Shared on October 31, 2011 at 6:49 pm By:
NIH scientists discover link among spectrum of childhood diseases. #gene #rheu #inflammation #CANDLE http://t.co/4QyrzNru
Gene Responsible For Relapses In Young Leukemia Patients
medicalnewstoday.com — “One of the causes of resistance to cancer treatment in children is now beginning to be elucidated. Acute lymphoblastic leukemia patients with a particular form of the ATF5 gene are at higher risk” View full resource at medicalnewstoday.com
Most Recently Shared on October 28, 2011 at 8:05 am By:
Gene Responsible For Relapses In Young Leukemia Patients http://t.co/eVEZ1whc #genetics
Tantalizing glimmers about roles of CCR2 gene, Th17 cell and a missing monocyte
news-medical.net — “An estimated 1.3 million people in the United States suffer from rheumatoid arthritis. The causes behind this chronic disease — which can exhibit itself as pain, swelling, stiffness, deformation, and loss of function in the joints — have eluded scientists for centuries. A new study by UNC researchers offers tantalizing glimmers about the roles of a gene called CCR2, an immune system cell called Th17 cell, and a missing monocyte.” View full resource at news-medical.net
Most Recently Shared on October 11, 2011 at 2:48 pm By:
Scott Strumello Patient Expert
Tantalizing glimmers about roles of CCR2 gene, Th17 cell and a missing monocyte http://t.co/9MuZ9mxb
New Insight Into The Cellular Defects In Huntington's Disease
medicalnewstoday.com — “Huntington's disease is a devastating neurogenerative disorder that causes a progressive loss of functional capacity and reduced life span. It is an inherited condition caused by a mutant HTT gene” View full resource at medicalnewstoday.com
Most Recently Shared on October 11, 2011 at 10:06 am By:
New Insight Into The Cellular Defects In Huntington's Disease http://t.co/me0WZ8al #huntingtons
Newly Identified DNA Repair Defect Linked To Increased Risk Of Leukemia Relapse
medicalnewstoday.com — “St. Jude Children's Research Hospital scientists tie low levels of a key DNA repair protein to loss of regulatory genes in a study that offers new clues about why acute lymphoblastic leukemia some” View full resource at medicalnewstoday.com
Most Recently Shared on September 27, 2011 at 7:05 am By:
Newly Identified DNA Repair Defect Linked To Increased Risk Of Leukemia Relapse http://mnt.to/3ZTg #genetics
Gene mutation shown to cause leukemia and lymphedema
sciencedaily.com — “Researchers have discovered a gene that when mutated can cause lymphedema (swollen limbs due to a failure of the lymph system), immune abnormalities, deafness and leukemia. The identification of the gene responsible for causing this rare combination of medical conditions, known as Emberger syndrome, could allow earlier identification and treatment of those at risk.” View full resource at sciencedaily.com
Most Recently Shared on September 7, 2011 at 1:35 pm By:
#Gene mutation shown to cause #leukemia & #lymphedema: #raredisorder http://t.co/mT8bSzc via @AddThis
Gene mutation shown to cause leukemia and lymphedema
sciencedaily.com — “Researchers have discovered a gene that when mutated can cause lymphedema (swollen limbs due to a failure of the lymph system), immune abnormalities, deafness and leukemia. The identification of the gene responsible for causing this rare combination of medical conditions, known as Emberger syndrome, could allow earlier identification and treatment of those at risk.” View full resource at sciencedaily.com
Most Recently Shared on September 6, 2011 at 12:13 pm By:
Jamie Inman M.A., LMFT Therapist and ePatient
Gene mutation shown to cause leukemia and lymphedema http://t.co/WJnXGFN via @addthis
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