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Reviewers criticized the study for assuming drugs with similar side-effects work the same way and questioned the validity of its findings due to potential biases and data quality issues.

Genetic variations contribute to over 10% of recurrent early pregnancy loss cases.

A woman with Rhupus and Rowell syndrome was treated successfully with medication adjustments.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

LLPS is crucial for RALF signaling, aiding plant growth and stress resilience.

A fungal enzyme was used to make compounds more soluble, aiding drug discovery and crop protection.

Cell proteomic footprinting enhances cancer vaccine quality by ensuring correct antigen composition.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

The system aims to extend human lifespan to 130-150 years by improving cellular health and reducing stress.

The system aims to extend human lifespan to 130-150 years by improving cellular health and reducing stress.

The new method provides more accurate vibrational frequencies for drug molecules than traditional models.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

The new method found new shared genetic areas linked to both Type 2 Diabetes and Prostate Cancer.

Reductive stress messes up collagen balance and alters cell signaling in human skin cells, which could help treat certain skin diseases.

Scientists successfully created and analyzed the structure of a part of the human androgen receptor with specific modulators and a peptide to understand how it binds differently in various tissues.

A new method creates valuable compounds for drug discovery by breaking traditional chemical rules.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

The platform effectively grows lung cancer cell spheroids for drug testing.

Drug repurposing can create safer, cheaper treatments by finding new uses for existing drugs.

A patient with Rhupus was diagnosed with Rowell syndrome and treated with various medications.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.