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A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

The TG5 gene affects beef cattle weight, and the CC genotype leads to higher weights.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

RNA editing significantly affects hair growth and follicle cycling in the Tianzhu white yak.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

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

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

Transglutaminase does not modify human hair.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

Complex basal cell carcinomas need personalized treatment due to unique genetic mutations.

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

CYP154C7 enzyme can effectively modify steroids and is promising for commercial use.

BRG1 is essential for skin cells to move and heal wounds properly.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

Certain genetic variations can make people more likely to experience hair loss and low white blood cell count from azathioprine.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

KRT81 gene variations in sheep affect wool weight but not fiber length or thickness.

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.