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RXRα is crucial for proper immune response and links diet to immune function.

CD34+ and CD34- melanocyte stem cells have different regenerative abilities.

Goats with BSE or scrapie show varying symptoms, and using only clinical signs may not detect all scrapie cases.

Hair becomes gray and thin as we age, and while most hair loss in older people is due to genetics, there's a chance for gray hair to regain color under certain conditions.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Scientists successfully made a human growth factor in a plant, which could help with hair growth and bone development.

Scientists restored fertility in male mice lacking a key fertility gene by using a modified gene.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

GDNF helps grow hair and heal skin wounds by acting on hair stem cells.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

A man with X-ALD improved after treatment, highlighting the need to consider X-ALD in similar patients and test their relatives.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

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.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

The document concluded that more research is needed to understand how estrogen affects the enzyme involved in hirsutism development.

Using animal names for skin conditions helps with learning and memory.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

The RapidHIT ID system can effectively get DNA profiles from hair roots with enough cells.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

The research showed that Vitamin D and its receptor are important for healthy bones and normal hair and skin in rats.

Gene therapy helped rats with a specific type of rickets grow hair without severe inflammation.