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Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The research explains how a human enzyme binds and processes its substrate, which could relate to its role in biological functions and hair loss.

The study created a test that found hormonal and toxic effects in plant and fungal extracts using prostate cancer cells.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

Vitamin D boosts a specific gene activity in kidney cells that could improve heart and kidney function.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

The document concludes that pregnancy and cancer share immune evasion tactics, but more research is needed before using checkpoint blockade immunotherapy in pregnant cancer patients to avoid harm to the placenta.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

Researchers found new potential treatments for conditions related to the androgen receptor, like male hormonal contraception, by testing thousands of compounds.

Dutasteride may help reduce brain plaque linked to Alzheimer's by affecting cell energy structures and waste removal.

New methods have helped find cells that create other cells in the body.

Mesenchymal Stem Cells (MSCs) are promising for multiple therapies, but more research is needed to fully understand and optimize their use.

CRISPR/Cas systems show promise for cancer treatment by targeting miRNAs, but delivery and specificity challenges remain.

New treatments for prostate cancer and BPH show promise, including novel compounds that target hormone synthesis and response.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

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.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

NIPT can help detect potential maternal cancer, and GIPXplore can identify immune diseases in pregnancies.

Temozolomide improves survival in grade III glioma patients without harming quality of life.

Finasteride doesn't affect omeprazole metabolism in Japanese people.

Different substances that activate or block the androgen receptor can affect male development and treat conditions like prostate cancer.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

Lengthening telomeres may reverse aging and extend lifespan.

Activating TLR5 in the gut can extend lifespan and improve health in aged mice.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.