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New compounds were made that effectively block a specific enzyme related to androgen conditions.

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LGR5 helps maintain corneal cell characteristics and prevents unwanted changes by controlling specific cell signaling pathways.

Differences in androgen receptor expression and tissue properties may lead to higher cryptorchidism risk in certain rats.

EFFC might be common but underreported.

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A patient with a rare disease had a unique genetic mutation linked to their symptoms.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

BI 2536 had limited effectiveness against several advanced cancers and caused significant side effects.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

LEKTI is crucial for skin barrier and immune function, affecting conditions like Netherton syndrome and atopic dermatitis.

Researchers found a non-functional sheep keratin gene due to mutations.

Tissue-engineered skin substitutes can model junctional epidermolysis bullosa and may help develop gene therapy.

Hit15 shows promise as a COVID-19 treatment by reducing virus infection and inflammation.

A rigid compound with a common structural motif was successfully synthesized.

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A girl had rickets due to a gene mutation affecting vitamin D response.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

ROR2 is crucial for hair follicle stem cell maintenance and self-renewal.

The three estrogen receptor genes are highly expressed in zebrafish neuromasts during development.

Eclipta alba IIHR Sel EA 43 is best for large-scale cultivation due to high growth, yield, and wedelolactone content.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A specific gene mutation causes woolly hair and hair loss.