Search

everythinglearnresearchcommunity

for

Search:↓

Certain gene variations may increase the risk of hair loss in Egyptians.

The document concludes that while there are promising methods to control CRISPR/Cas9 gene editing, more research is needed to overcome challenges related to safety and effectiveness for clinical use.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

New treatments for advanced skin cancer are improving patient outcomes, but drug resistance and finding the right treatment combinations are still big challenges.

The Rotterdam Study aims to understand various diseases in older adults.

Some common medications can harm male fertility, but many effects can be reversed.

Certain immune molecules and stress affect hair loss, and while genes play a role, more research is needed to fully understand and treat it.

PTEN helps control the number and health of skin stem cells by working with the protein BMAL1.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Notch/CSL signaling controls hair follicle differentiation through Wnt5a and FoxN1.

Whale genes show changes that help them live in water, like less hair and better flippers.

ELL is crucial for gene transcription related to skin cell growth.

Cashmere and milk goats have different hair growth cycles and gene expressions, which could help improve wool production.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Hdac1 and Hdac2 help maintain and protect the cells that control hair growth.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

Meis1 is crucial for skin health and tumor development.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

The research provides insights into hair follicle growth in forest musk deer by identifying key genes and pathways involved.

Hairlessness in mammals is caused by combined changes in genes and regulatory regions.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

Researchers identified genes that may affect hair growth in Cashmere goats.

The Ovol2-Zeb1 circuit is crucial for skin healing and hair growth by guiding cell movement and growth.

Ovol2 is crucial for hair growth and skin healing by controlling cell movement and growth.

The vitamin D receptor is essential for skin stem cells to grow, move, and become different cell types needed for skin healing.