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BioWorld - Tuesday, February 17, 2026
Home » Topics » Disease categories and therapies » Genetic/congenital

Genetic/congenital
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Credit: Darryl Leja, NHGRI
Genetic/Congenital

Study hits shared risk between schizophrenia, bipolar disease on the nose

Nov. 15, 2022
By Anette Breindl
Researchers have identified miR-124 signaling and its effects on AMPA receptor neurotransmission as a biological mechanism linking the shared risk scores of schizophrenia and bipolar disorders to their shared symptoms. The work, which appeared online in Neuron on Nov. 14, 2022, focused on schizophrenia and bipolar disorder, which are both highly heritable disorders that share substantial risk. Beyond their implications for those two specific disorders, the findings illustrate a path to connecting risk scores and behaviors via their biological link.
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Biomarkers

Missense mutation in ARSK linked to a subtype of MPS

Nov. 9, 2022
Researchers from Children's Hospital Los Angeles presented data from a study that linked a homozygous missense mutation in ARSK to a new subtype of the lysosomal storage disease mucopolysaccharidoses (MPS).
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Triglyceride fat accumulated inside liver cells
Endocrine/Metabolic

At AASLD 2022, polygenic risk score subtypes in NAFLD

Nov. 8, 2022
By Anette Breindl
Modern molecular techniques have progressed to the point where sequencing can seem almost quaint. At the Basic Science Symposium of the American Association for the Study of Liver Diseases 2022 meeting (AASLD 2022), new techniques were on full display, with sessions devoted to epigenetics, microbiome analysis and spatial transcriptomics. But the first session was still on genetic variants in all their forms – rare variants, common variants and nongermline mutations.
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Lungs
Respiratory

Tavanta Therapeutics reports in vitro data on TAVT-135 for cystic fibrosis

Nov. 7, 2022
Modulators of cystic fibrosis transmembrane...
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Endocrine/Metabolic

JCR to develop BBB-penetrating α-L-fucosidase JR-471 for fucosidosis

Nov. 4, 2022
JCR Pharmaceuticals Co. Ltd. has decided to develop a new drug candidate, JR-471, a blood-brain barrier (BBB)-penetrating α-L-fucosidase for the treatment of patients with the inherited lysosomal storage disorder fucosidosis.
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DNA illustration
Biomarkers

New case report of Charcot-Marie-Tooth type 2S disease treated with ASO

Nov. 3, 2022
Charcot-Marie-Tooth disease (CMT) is a heterogeneous group of congenital disorders characterized by peripheral neuropathy.
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Skeletal system
Biomarkers

GPC6 marker tied to skeletal dysplasia

Oct. 31, 2022
Protein glypican 6 (GPC6) belongs to the proteoglycan family, which is linked to glycosylphosphatidylinositol (GPI)-anchored heparan sulfate.
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Zebrafish
Neurology/Psychiatric

Novel POMT1 knockout zebrafish model of congenital muscular dystrophy

Oct. 31, 2022
Dystroglycanopathies are a subset of rare congenital muscular dystrophies (CMDs) caused by dysregulation in the assemblage of glycans on the α-dystroglycan (α-DG) transmembrane glycoprotein.
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DNA illustration
Biomarkers

Pathogenic ELOC gene variants as a novel cause for VHL disease

Oct. 28, 2022
To date, only inactivating germline variations in the VHL gene have been linked to von Hippel-Lindau...
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A young C. elegans adult
Genetic/Congenital

Proteostasis disruption links menopause to aging in C. elegans

Oct. 25, 2022
By Anette Breindl

Disrupted meiosis, the cell division process that leads to the production of reproductive cells in sexually reproducing organisms, led to a decline in overall health by triggering an accelerating aging signature in the roundworm Caenorhabditis elegans.

The work is “the first direct evidence that manipulating the health of reproductive cells leads to premature aging and a decline in healthspan,” senior author Arjumand Ghazi, an associate professor of pediatrics, developmental biology, and cell biology and physiology at the University of Pittsburgh and the University of Pittsburgh Medical Center (UPMC) Children’s Hospital, said in a press release.
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