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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 mutation in the hairless gene causes hair loss and skin wrinkling in mice.

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

Inactivating both p53 and Rb genes in mice speeds up aggressive skin cancer development.

The fer-ts mutation in plants prevents root hair growth at high temperatures.

Deleting podoplanin in mice promotes hair growth by enhancing cell migration.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

GhDET2 is crucial for cotton fiber growth.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Nelfb is essential for dermal fat development and survival.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.

Targeting the TNFRSF1B gene may help treat hair loss.

Changing the amount of PLC5 in Arabidopsis affects root growth and drought resistance, with less PLC5 slowing root growth and more PLC5 improving drought tolerance but hindering root hair growth.

RNase L hinders hair follicle regeneration by altering immune signals.

RORA plays a key role in controlling seasonal hair molting by affecting hair follicle cell activity.

ROR-alpha may increase the growth of certain breast cancer cells by boosting aromatase, which could affect breast cancer prognosis.

Dermal EZH2 controls skin cell development and hair growth in mice.

PH-762 shows promise in treating skin cancer by effectively targeting and silencing PD-1 in tumors with minimal side effects.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

New genetic mutations causing hair loss were found in a Chinese family.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Paeoniflorin protects brain cells by involving a specific protein and neurosteroids.

Reducing SFRP1 can promote hair growth and may help treat hair loss.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

PBX1 reduces aging and cell death in stem cells by boosting SIRT1 and lowering PARP1.

Rat dermal papilla cells have unique properties and interact differently with their environment compared to other skin cells.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.