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Research Breakthroughs

Maletic-Savatic lab discovers a novel marker of adult human neural stem cells

Maletic-Savatic lab discovers a novel marker of adult human neural stem cells

3/24/21
Study finds BASP-1 as a novel biomarker of adult human neural stem cells.
Researchers identify DNA elements that affect MECP2 expression

Researchers identify DNA elements that affect MECP2 expression

3/19/21
Researchers in the Zoghbi lab find DNA regions critical for MECP2 function, identifying potential therapeutic targets for Rett and MECP2 Duplication syndrome.
A preclinical study validates antisense oligonucleotides as a feasible approach to treat MECP2 duplication disorder

A preclinical study validates antisense oligonucleotides as a feasible approach to treat MECP2 duplication disorder

3/3/21
A novel "humanized" mouse model generated validates the use of antisense oligonucleotides to reverse the symptoms of MECP2 Duplication Syndrome.
Deep brain stimulation and exercise restore movement in ataxia

Deep brain stimulation and exercise restore movement in ataxia

3/1/21
Sillitoe lab finds deep brain stimulation of the cerebellum and exercise can reverse ataxia
Acthar® Gel (RCI) suppresses spasms in the TTX animal model of infantile spasms

Acthar® Gel (RCI) suppresses spasms in the TTX animal model of infantile spasms

2/5/21
Study finds high dosages of RCI were required to eliminate spasms and hypsarrhythmia-like activity in rodents.
EIF2AK2 variants cause symptoms akin to Pelizaeus-Merzbacher disease

EIF2AK2 variants cause symptoms akin to Pelizaeus-Merzbacher disease

12/21/20
Drs. Daniel Calame, Hsiao-Tuan Chao and team find a molecular cause for PMD patients without any mutations in PLP1 gene.
Novel gene variants that modify the risk of late-onset Alzheimer’s disease discovered

Novel gene variants that modify the risk of late-onset Alzheimer’s disease discovered

12/8/20
Lichtarge and Botas labs use a novel methodology to find 216 novel genetic modifiers of late-onset Alzheimer's disease.
A role for the slow oscillations of the neocortex in epileptic spasm generation

A role for the slow oscillations of the neocortex in epileptic spasm generation

12/7/20
The Swann lab discovers the source and mechanism of epileptic spasms.
BICRA gene provides answers to patients, doctors and scientists

BICRA gene provides answers to patients, doctors and scientists

11/23/20
Research from Bellen lab finds chromatin remodeling protein BICRA and the ncBAF complex function in neural development in humans and flies.
Low doses of insecticide trigger neurodegeneration in insects

Low doses of insecticide trigger neurodegeneration in insects

9/29/20
The Bellen lab in collaboration with Dr. Felipe Martelli's team in Melbourne explore the effects of low doses of insecticide, imidacloprid, on the physiology of fruit flies.
Regulating gene regulatory regions offers a novel mechanism to control ATXN1 levels

Regulating gene regulatory regions offers a novel mechanism to control ATXN1 levels

8/31/20
Researchers in the Zoghbi lab investigate the mechanisms involved in Ataxin-1 expression.
Novel regulators of myelin repair and regeneration discovered

Novel regulators of myelin repair and regeneration discovered

8/13/20
Researchers in Dr. HYun-Kyoung Lee identify a new regulator (Nedd4) and genetic pathway (Daam2-VHL-Nedd4) that controls myelin formation during development and after injury.
Dissecting the genetics of neurodevelopmental disorders – one cell at a time

Dissecting the genetics of neurodevelopmental disorders – one cell at a time

7/20/20
The Liu lab reveals genetic convergences between autism spectrum disorder and epilepsy during key neurodevelopmental stages.
Solving the CLN6 mystery in Batten's disease

Solving the CLN6 mystery in Batten's disease

6/30/20
Sardiello lab discovers how defective CLN6 can lead to Batten's disease.
Unraveling a novel role for TFEB in liver development, regeneration and biliary cancer

Unraveling a novel role for TFEB in liver development, regeneration and biliary cancer

6/17/20
Researchers in Drs. Ballabio and Pastore labs' identify a novel developmental role for transcription factor, TFEB in liver development and regeneration.
Research reveals a new way to predict genetic diseases

Research reveals a new way to predict genetic diseases

5/18/20
Wangler lab finds genes with more CpG in the first and second codons have a higher propensity to get mutated and so, can be used as good predictors of disease risk.
An international collaboration discovers novel neurodevelopmental syndrome

An international collaboration discovers novel neurodevelopmental syndrome

4/23/20
UDN researchers led by Dr. Bellen identify a new Cdk19-mediated neurodevelopmental disorder.
Solving the puzzle of Mitchell disease

Solving the puzzle of Mitchell disease

4/8/20
Bellen lab in collaboration with the UDN find a new neurological disorder.
Inappropriate cellular response to stress linked to a new neurological disorder

Inappropriate cellular response to stress linked to a new neurological disorder

3/24/20
Chao and Bellen labs finds pathogenic variants in the EIF2Ak family of kinases associated with a novel neurodevelopmental disorder with degenerative features.
Researchers learn to control brain cell that triggers tremor

Researchers learn to control brain cell that triggers tremor

3/18/20
Latest research from Dr. Roy Sillitoe's laboratory has made strides understanding of how tremor — the most common movement disorder — happens, opening the possibility of novel therapies for this condition.