Gene Mutations Linked to IBD in Children
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Gene Mutations Linked to IBD in Children
View full resource at webmd.com
Tags: IBD, Genetic, Disease and Condition, Genes, Children's Health
Most Recently Shared on November 18, 2009 at 11:42 pm By:
Gene Mutations Linked to IBD in Children: Rare genetic mutations may trigger inflammatory bowel disease (IBD) in yo... http://bit.ly/1n1P40
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Spontaneous gene glitches linked to autism risk with older dads, April 4, 2012 News Release - National Institutes of Health (NIH)
nih.gov — “Researchers have turned up a new clue to the workings of a possible environmental factor in: fathers were four times more likely than mothers to transmit tiny, spontaneous mutations to their children with the disorders. Moreover, the number of such transmitted genetic glitches increased with paternal age. The discovery may help to explain earlier evidence linking autism risk to older fathers.” View full resource at nih.gov
Most Recently Shared on April 4, 2012 at 8:05 pm By:
News: Spontaneous gene glitches linked to autism risk with older dads http://t.co/NvLdbzMC
Multiple Genes Linked To Differences In Cystic Fibrosis Identified
medicalnewstoday.com — “Cystic fibrosis (CF) is a devastating disease caused by mutations in the CFTR gene. In Canada, one in every 3,600 children born has the disease.Researchers have long been puzzled as to h” View full resource at medicalnewstoday.com
Most Recently Shared on April 4, 2012 at 7:05 am By:
Multiple Genes Linked To Differences In Cystic Fibrosis Identified http://t.co/N93B1N5w #gastrointestinal
Advanced-Stage Neuroblastoma Diagnosis Age Linked To Genetic Mutation - QualityPoint Technologies
qualitypointtech.net — “In children and young adults with advanced-stage neuroblastoma (a cancerous tumor that develops from nerve tissue), researchers have identified that certain variations of the gene ATRX are associated with age at diagnosis. The study is published in the March 14 issue of JAMA. In children, neuroblastoma is the most prevalent extracranial (outside the cranium) solid tumor. The disease is responsible for 15% of all cancer-related deaths in children...” View full resource at qualitypointtech.net
Most Recently Shared on March 13, 2012 at 11:00 pm By:
Advanced-Stage Neuroblastoma Diagnosis Age Linked To Genetic Mutation: In children and young adults with advanced-... http://t.co/ZtgdBhPO
Advanced-Stage Neuroblastoma Diagnosis Age Linked To Genetic Mutation
medicalnewstoday.com — “In children and young adults with advanced-stage neuroblastoma (a cancerous tumor that develops from nerve tissue), researchers have identified that certain variations of the gene ATRX are associa” View full resource at medicalnewstoday.com
Most Recently Shared on March 13, 2012 at 9:05 pm By:
Advanced-Stage Neuroblastoma Diagnosis Age Linked To Genetic Mutation http://t.co/Znbmrlgr #healthnews
New Genetic Studies Suggest Why Autism Is More Common In Boys Than Girls | Care2 Causes
care2.com — “Three new studies in Neuron reports that hundreds of spontaneous genetic mutations have been linked to autism. Such CBS News describes the findings as a shocker, previous research has indicated that de novo or spontaneous gene mutations can be linked to the neurodevelopmental disorder. As Time magazine says, the new studies differ from previous genetic studies, which looked at families with at least two autistic children; such families may represent cases in which inherited genetic mutations may” View full resource at care2.com
Most Recently Shared on June 10, 2011 at 5:22 am By:
Researchers link spontaneous gene mutations to autism
medicalxpress.com — “(Medical Xpress) -- Using high-throughput gene sequencing technology, researchers have identified several harmful spontaneous gene mutations in children with autism spectrum disorders (ASDs) that may cause the disorder.” View full resource at medicalxpress.com
Most Recently Shared on May 16, 2011 at 12:33 pm By:
Researchers link spontaneous gene mutations to autism http://tw.medicalxpress.com/224753585
Research Suggests Link Between 'Handedness' and Dyslexia - Drugs.com MedNews
drugs.com — “New genetic mapping of children with reading difficulties suggests that those who carry a particular gene mutation are particularly well-skilled in the use of t” View full resource at drugs.com
Most Recently Shared on November 5, 2010 at 5:11 pm By:
Research Suggests Link Between 'Handedness' and Dyslexia: FRIDAY, Nov. 5 -- New genetic mapping of childre... http://bit.ly/abq66y #drug
Maternal Serotonin Deficiencies Linked with ADHD in Offspring - Kansas City infoZine News
infozine.com — “Mothers Whose Gene Sequencing Showed Mutations Likely to Cause Low Levels of Serotonin Had Children Who Were at Higher Risk of Adhd (attention-deficit Hyperactivity Disorder) Than Control Individuals or Offspring of Fathers with the Mutations.” View full resource at infozine.com
Most Recently Shared on October 6, 2010 at 6:40 pm By:
Maternal Serotonin Deficiencies Linked with ADHD in Offspring http://bit.ly/apRktr #ADHD
Researchers target vascular disease linked to cancer-causing gene mutation
physorg.com — “Researchers have discovered how a genetic disease known mainly for its life-threatening tumors also can cause sudden death from cardiovascular disease in children, and are mounting a clinical trial to develop treatments for the problem.” View full resource at physorg.com
Most Recently Shared on March 23, 2010 at 7:50 pm By:
Researchers target vascular disease linked to cancer-causing gene mutation http://tw.physorg.com/188577269
Targeting vascular disease linked to cancer-causing gene mutation
feeds.sciencedaily.com — “Researchers have discovered how a genetic disease known mainly for its life-threatening tumors also can cause sudden death from cardiovascular disease in children, and are mounting a clinical trial to develop treatments for the problem.” View full resource at feeds.sciencedaily.com
Most Recently Shared on March 23, 2010 at 7:12 pm By:
Targeting vascular disease linked to cancer-causing gene mutation: Researchers have discovered how a genetic disea... http://bit.ly/dzOfmJ
Nephrology: New gene linked to kidney disease
sciencedaily.com — “Nephronophthisis (NPHP) is the most common genetic cause of kidney failure in children. Ten causative genes (NPHP1-NPHP9 and NPHP11), all of which generate proteins that localize to a cellular complex known as the primary cilia-centrosome complex, have been identified previously. A team of researchers has now identified an association between mutations in the XPNPEP3 gene and an NPHP-like nephropathy in two consanguineous families, one in northern Finland and one in Turkey.” View full resource at sciencedaily.com
Most Recently Shared on March 7, 2010 at 3:45 pm By:
Gene Mutation Linked to Poor Survival in Children with Medulloblastoma | Children's Brain Tumor Foundation
cbtf.org — “Gene Mutation Linked to Poor Survival in Children with Medulloblastoma | Children's Brain Tumor Foundation” View full resource at cbtf.org
Most Recently Shared on February 24, 2010 at 2:17 pm By:
"Gene Mutation Linked To Poor Survival in Children With Medulloblastoma". This is what I was Dx with in 1995. #YPGCBTF http://bit.ly/aBRxTw
NCI Cancer Bulletin for February 9, 2010 - National Cancer Institute
cancer.gov — “NCI's biweekly online newsletter provides useful, timely information about cancer research to the cancer community.” View full resource at cancer.gov
Most Recently Shared on February 9, 2010 at 11:50 pm By:
Gene mutation linked to poor survival in children with medulloblastoma http://bit.ly/d9xUTN
Investigators Identify Gene Mutations That Predispose Patients With Becker Muscular Dystrophy To Early Onset Cardiomyopathy
medicalnewstoday.com — “Investigators in the research institute at nationwide children's hospital have identified a link between specific modifications of the dystrophin gene and the age of cardiac disease onset in patie” View full resource at medicalnewstoday.com
Most Recently Shared on January 14, 2010 at 4:19 pm By:
Investigators Identify Gene Mutations That Predispose Patients With Becker Muscular Dystrophy To Early Onset Cardiomyo... http://mnt.to/3whQ
Investigators Identify Gene Mutations that Predispose Patients with Becker Muscular Dystrophy to Early Onset Cardiomyopathy
newswise.com — “Investigators in The Research Institute at Nationwide Children's Hospital have identified a link between specific modifications of the dystrophin gene and the age of cardiac disease onset in patients with Becker muscular dystrophy (BMD). This information could help clinicians provide early cardiac intervention for BMD patients based on genetic testing results performed on a blood sample.” View full resource at newswise.com
Most Recently Shared on January 13, 2010 at 8:39 pm By:
Investigators Identify Gene Mutations that Predispose Patients with Becker Muscular Dystrophy to Early Onset Cardi... http://bit.ly/7VSDjp
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Gene Mutations Linked to IBD in Children: Rare genetic mutations may trigger inflammatory bowel disease (IBD) i.. http://bit.ly/1n1P40
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