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Large Language Models in Drug Development: A Review by Harvard's George Church Lab

Large Language Models in Drug Development: A Review by Harvard's George Church Lab

This article discusses the significant potential of LLMs in understanding disease mechanisms, drug discovery, and clinical trials—three fundamental stages of drug development. This article is authorized by the DrugAI team to medicine.net.

Large Language Models in Drug Development: A Review by Harvard's George Church Lab

This article discusses the significant potential of LLMs in understanding disease mechanisms, drug discovery, and clinical trials—three fundamental stages of drug development. This article is authorized by the DrugAI team to medicine.net.
Parkinson's disease study develops analytical pipeline to identify unexploited genes

Parkinson's disease study develops analytical pipeline to identify unexploited genes

byHiroshima UniversityA pipeline to explore candidate target genes using transcriptomics and unknomics. Credit: Takayuki Suzuki/Hiroshima UniversityA research team from Hiroshima University has

Parkinson's disease study develops analytical pipeline to identify unexploited genes

byHiroshima UniversityA pipeline to explore candidate target genes using transcriptomics and unknomics. Credit: Takayuki Suzuki/Hiroshima UniversityA research team from Hiroshima University has
Dyslexia and ADHD share genetic links, study shows

Dyslexia and ADHD share genetic links, study shows

byUniversity of EdinburghGenetic relationships between ten neurodevelopmental and psychiatric disorders. Credit:Molecular Psychiatry(2024). DOI: 10.1038/s41380-024-02649-8Scientists

Dyslexia and ADHD share genetic links, study shows

byUniversity of EdinburghGenetic relationships between ten neurodevelopmental and psychiatric disorders. Credit:Molecular Psychiatry(2024). DOI: 10.1038/s41380-024-02649-8Scientists
Genetic analysis sheds light on the role of IFT140 in polycystic kidney disease

Genetic analysis sheds light on the role of IFT140 in polycystic kidney disease

byTokyo Medical and Dental UniversityThrough a comprehensive genetic analysis of patients with PKD but no family history of the disease, researchers found that a mutation in theIFT140&nbsp

Genetic analysis sheds light on the role of IFT140 in polycystic kidney disease

byTokyo Medical and Dental UniversityThrough a comprehensive genetic analysis of patients with PKD but no family history of the disease, researchers found that a mutation in theIFT140&nbsp
TAAR1 gene mutations may be a missing link in understanding neuropsychiatric disorders, researchers suggest

TAAR1 gene mutations may be a missing link in understanding neuropsychiatric disorders, researchers suggest

by Genomic PressThe association between TAAR1 variants, neuropsychiatric disorders, and therapeutic response. TAAR1 mutations (only selected mutations are shown for clarity) in patients with neuropsyc

TAAR1 gene mutations may be a missing link in understanding neuropsychiatric disorders, researchers suggest

by Genomic PressThe association between TAAR1 variants, neuropsychiatric disorders, and therapeutic response. TAAR1 mutations (only selected mutations are shown for clarity) in patients with neuropsyc
Unraveling schizophrenia: New insights into genetic and environmental interplay

Unraveling schizophrenia: New insights into genetic and environmental interplay

by Genomic PressCredit: Pixabay/CC0 Public DomainIn the complex landscape of mental health research, a new viewpoint offers a critical examination of how genes and environment conspire to influence sc

Unraveling schizophrenia: New insights into genetic and environmental interplay

by Genomic PressCredit: Pixabay/CC0 Public DomainIn the complex landscape of mental health research, a new viewpoint offers a critical examination of how genes and environment conspire to influence sc
Study deciphers pathological mechanisms of spermatogenic impairment in cryptorchidism

Study deciphers pathological mechanisms of spermatogenic impairment in cryptorchidism

byChinese Academy of SciencesSpermatogenic failure in cryptorchidism is due to abnormal spermatogonia, activated mast cells, and impaired testicular niche. Credit: Wang Xiaoyan and Zhuang ZiyanC

Study deciphers pathological mechanisms of spermatogenic impairment in cryptorchidism

byChinese Academy of SciencesSpermatogenic failure in cryptorchidism is due to abnormal spermatogonia, activated mast cells, and impaired testicular niche. Credit: Wang Xiaoyan and Zhuang ZiyanC
Gene therapy offers promise for treating glaucoma and age-related macular degeneration

Gene therapy offers promise for treating glaucoma and age-related macular degeneration

byTrinity College DublinCredit:International Journal of Molecular Sciences(2024). DOI: 10.3390/ijms25168876Scientists from Trinity College Dublin have developed a highly promising ge

Gene therapy offers promise for treating glaucoma and age-related macular degeneration

byTrinity College DublinCredit:International Journal of Molecular Sciences(2024). DOI: 10.3390/ijms25168876Scientists from Trinity College Dublin have developed a highly promising ge
Researchers report encouraging first evidence of effective new gene therapy to treat multiple sulfatase deficiency

Researchers report encouraging first evidence of effective new gene therapy to treat multiple sulfatase deficiency

byChildren's Hospital of PhiladelphiaCredit:Molecular Therapy(2024). DOI: 10.1016/j.ymthe.2024.08.015Researchers from Children's Hospital of Philadelphia (CHOP) have tested a

Researchers report encouraging first evidence of effective new gene therapy to treat multiple sulfatase deficiency

byChildren's Hospital of PhiladelphiaCredit:Molecular Therapy(2024). DOI: 10.1016/j.ymthe.2024.08.015Researchers from Children's Hospital of Philadelphia (CHOP) have tested a
How newly identified biomarkers could reveal risk factors for sudden infant death syndrome

How newly identified biomarkers could reveal risk factors for sudden infant death syndrome

byUniversity of California, San FranciscoCredit: CC0 Public DomainResearchers at UC San Francisco are getting closer to being able to predict sudden infant death syndrome, or SIDS.In a study&nbs

How newly identified biomarkers could reveal risk factors for sudden infant death syndrome

byUniversity of California, San FranciscoCredit: CC0 Public DomainResearchers at UC San Francisco are getting closer to being able to predict sudden infant death syndrome, or SIDS.In a study&nbs
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