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The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

GhPLDα1 helps thicken cotton fiber walls by boosting cellulose production.

AP-1 controls tumor cell type by affecting key signaling pathways.

The main enzyme found in pubic skin that could be targeted to treat excessive hair growth is 5 alpha-R2.

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

The research identified specific genes that are active in the cells crucial for hair growth.

Recognizing scalp symptoms in PRP is crucial for proper diagnosis and treatment.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Proretinal nanoparticles are a safe and effective way to deliver retinal to the skin.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

Your genes, especially IL-1a, can predict how well a hair growth treatment with platelet rich plasma will work for you.

Blocking CYP17A1 enzyme may help improve certain brain function issues related to dopamine.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Lichen planopilaris is a rare, chronic condition causing hair loss, mainly in middle-aged women, and early treatment is important to prevent permanent baldness.

Sfrp2 increases during hair follicle catagen phase and slows keratinocyte growth.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

ADF8 and ADF11 help root hairs grow by responding to hormones and environmental signals.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

TRPA1 and TRPV1 channels don't affect mechanotransduction in rat sinus hair follicles.

CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.