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Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Skin cells called dermal fibroblasts are important for skin growth, hair growth, and wound healing.

Wnt signaling is crucial for skin development and hair growth.

Human mitochondrial DNA polymerase makes very few errors, crucial for preventing degenerative diseases.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

A new 3D culture system helps grow and study mouse skin stem cells for a long time.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Adding a second method to PROTACs could improve cancer treatment.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

The research found specific genes and pathways that control fur development and color in young American minks.

Certain cancer drugs interact with skin bacteria to cause acne-like rashes.

Long scalp hair evolved for cooling and social signaling.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

Key genes and pathways improve wool quality in Zhexi Angora rabbits.

Basement membrane changes are crucial for hair follicle development.

Melanocytes are important for normal body functions and have potential uses in regenerative medicine and disease treatment.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

The KRTAP36-2 gene in sheep affects wool yield.

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.