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The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

Genetic factors could lead to personalized treatments for hair loss.

Allopregnanolone changes gene expression in glioblastoma cells.

Advancements in nanoformulations for CRISPR-Cas9 genome editing can respond to specific triggers for controlled gene editing, showing promise in treating incurable diseases, but challenges like precision and system design complexity still need to be addressed.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

Stem cell therapies could be a promising alternative for hair loss treatment, but more research is needed to understand their full potential and safety.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

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

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

A specific gene mutation causes long hair in Angora rabbits.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Forensic DNA Phenotyping accurately predicts physical traits and is used in investigations, but needs more diverse population data for confirmation.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Using existing drugs for new purposes could be a cost-effective way to treat chest pain and non-clogged heart arteries, with some drugs for lung blood pressure showing promise but needing more testing.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

Researchers identified specific genes that are important for mouse skin cell development and healing.