Chromosome News and Research

Latest Chromosome News and Research

Researchers identify genetic factor linked to development of diabetic peripheral neuropathy

Researchers from Joslin Diabetes Center, using a genome-wide association study, have identified a genetic factor linked to the development of diabetic peripheral neuropathy.

12 Jun 2019

Rettsyndrome.org funds research that will benefit boys and girls with MECP2-related disorders

Rettsyndrome.org announced their funding of two new research projects today. Jeannie T. Lee, MD, Ph.D. of Massachusetts General Hospital is awarded a two-year ANGEL Grant for $600,000 to focus on reactivating the silent X chromosome for Rett syndrome and Davut Pehlivan, MDof Baylor College of Medicine is awarded a two-year Mentored Clinical Fellowship for $250,000 to study MECP2 Duplication syndrome.

6 Jun 2019

Study clarifies how 3D organization of genome is regulated at onset of skeletal muscle formation

A new study from the University of Minnesota Medical School clarifies how the three-dimensional organization of the genome is regulated at the onset of skeletal muscle formation.

25 May 2019

Research sheds new light on the function of frequently mutated cancer protein

New research from The Wistar Institute sheds light on the function of the ARID1A protein, encoded by a gene that is among the most frequently mutated across human cancers.

24 May 2019

Novel program that provides comprehensive care for Turner syndrome earns national recognition

A novel program designed to provide comprehensive care for Turner syndrome at The University of Texas Health Science Center at Houston and UT Physicians is one of the first in the U.S. to be designated an adult clinic by the Turner Syndrome Global Alliance.

24 May 2019

Rutgers-led study pinpoints key gene linked to impaired memory in Down syndrome

Targeting a key gene before birth could someday help lead to a treatment for Down syndrome by reversing abnormal embryonic brain development and improving cognitive function after birth, according to a Rutgers-led study.

24 May 2019

Children's Tumor Foundation establishes significant research initiative to combat NF2

On the occasion of World NF2 Awareness Day, the Children's Tumor Foundation has announced the establishment of a significant research initiative dedicated to finding effective treatments for NF2, along with a substantial investment of $2.3 million in this bold new effort.

23 May 2019

Spatial configuration of the genome is not inherited, but set up during embryogenesis

The architecture of the DNA-protein complexes that make up the genome in each cell nucleus regulates the course of early embryonic development.

23 May 2019

Scientists create bacteria with man-made DNA

In a landmark research study, a living organism (E. coli) has been made using entirely human-made DNA.

21 May 2019

New approach to waking up sleeping genes could help people with Prader-Willi syndrome

New funding is enabling Walter and Eliza Hall Institute researchers to develop new approaches to potentially help people with Prader-Willi syndrome, a devastating and incurable genetic condition.

21 May 2019

Researchers identify first gene that predisposes to fainting

Fainting is not solely caused by external factors. Your genes also play a part. This has recently been documented by research team from the University of Copenhagen, Statens Serum Institut and Rigshospitalet.

16 May 2019

Researchers identify why lymphoma patients may become resistant to specific drug

With more targeted therapies being approved each year for cancer, the development of drug resistance to these agents is a growing concern.

16 May 2019

Study: Under-connectivity is the underlying cause of brain disorders

Under-connectivity, or too few connections in the brain, is the underlying cause of brain disorders like autism and schizophrenia, according to a recent study from investigators at the George Washington University Institute for Neuroscience.

10 May 2019

Sussex scientists discover new genetic defect that causes intellectual disability

Researchers at the University of Sussex have discovered a new genetic defect which causes a form of intellectual disability; a finding that will improve screening programmes and help to end a 'diagnostic odyssey' for families across the globe.

1 May 2019

Researchers use genomics to solve a 20-year case study

After 20 years, a patient's family received an answer to a decades-long genetic mystery. Their daughter had two rare disorders, Angelman syndrome and P450scc deficiency, which was detected after researchers found out she had uniparental disomy, two copies of chromosome 15 from one parent and none from another.

28 Apr 2019

MIT scientists reverse some behavioral symptoms of rare neurodevelopmental disorder

Williams Syndrome, a rare neurodevelopmental disorder that affects about one in 10,000 babies born in the United States, produces a range of symptoms including cognitive impairments, cardiovascular problems, and extreme friendliness, or hypersociability.

22 Apr 2019

New gene therapy cures babies with fatal 'Bubble Boy' disease

A new gene therapy created by US researchers appears to have cured eight infant boys born with a rare genetic disorder referred to as “Bubble Boy” disease.

18 Apr 2019

Maternal age has no effect on IVF success, conclude researchers

Researchers have shown that maternal age may not influence the implantation potential of embryos in IVF or the likelihood of miscarriage.

18 Apr 2019

Bacteria use viruses for self-recognition, study reveals

Bacterial cells that normally colonize our guts can distinguish themselves from other bacterial species using what's traditionally considered their enemy--a virus.

17 Apr 2019

Rare gut condition is more predictable from individual's genetic makeup, study finds

Hirschsprung disease - a rare condition where the failure of gut nerves to develop before birth leads to impaired bowel contractions that prevent infants from passing stool - is more predictable from an individual's genetic makeup than previously envisioned.

11 Apr 2019

Chromosome News and Research

Latest Chromosome News and Research

Researchers identify genetic factor linked to development of diabetic peripheral neuropathy

Rettsyndrome.org funds research that will benefit boys and girls with MECP2-related disorders

Study clarifies how 3D organization of genome is regulated at onset of skeletal muscle formation

Research sheds new light on the function of frequently mutated cancer protein

Novel program that provides comprehensive care for Turner syndrome earns national recognition

Rutgers-led study pinpoints key gene linked to impaired memory in Down syndrome

Children's Tumor Foundation establishes significant research initiative to combat NF2

Spatial configuration of the genome is not inherited, but set up during embryogenesis

Scientists create bacteria with man-made DNA

New approach to waking up sleeping genes could help people with Prader-Willi syndrome

Researchers identify first gene that predisposes to fainting

Researchers identify why lymphoma patients may become resistant to specific drug

Study: Under-connectivity is the underlying cause of brain disorders

Sussex scientists discover new genetic defect that causes intellectual disability

Researchers use genomics to solve a 20-year case study

MIT scientists reverse some behavioral symptoms of rare neurodevelopmental disorder

New gene therapy cures babies with fatal 'Bubble Boy' disease

Maternal age has no effect on IVF success, conclude researchers

Bacteria use viruses for self-recognition, study reveals

Rare gut condition is more predictable from individual's genetic makeup, study finds

From street to lab: Advancing controlled substance testing with handheld Raman and FTIR

Reimagining light scattering for biotherapeutics

Empowering genomics research with cloud-based innovation

Chromosome News and Research

Latest Chromosome News and Research

From street to lab: Advancing controlled substance testing with handheld Raman and FTIR

Reimagining light scattering for biotherapeutics

Empowering genomics research with cloud-based innovation

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