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A protein called CBP is found in prostate cancer and can increase the effectiveness of certain prostate cancer treatments.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

New genes and pathways are important for testosterone production and male sexual development.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

The KRTAP27-1 gene variations in sheep may affect wool length and weight.

CIPK13 and CIPK18 genes are crucial for root hair growth in plants.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

ATP-sensitive potassium channels are important for hair growth.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

Genetic differences affect COVID-19 severity and treatment effectiveness.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.