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The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Specialized ribosomes affect aging in human skin cells.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

The document tests knowledge and decision-making in hematology through multiple-choice questions.

The document provides 70 multiple choice questions to improve haematology skills.

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

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

Removing centrosomes from skin cells leads to thinner skin and stops hair growth, but does not greatly affect skin cell differentiation.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Non-coding RNAs play key roles in the hair growth cycle of Angora rabbits.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

A new gene, JMJD1C, may affect testosterone levels in men.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

The modified wash test is better than TrichoScan® for diagnosing hair loss.

DHT affects bone growth by altering gene activity in osteoblasts, potentially complicating steroid use.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.