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About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

Testing for the NUDT 15 variant is crucial before starting azathioprine, especially in Asians.

A gene mutation causes curly hair and hair loss in rats.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

Colorectal cancer's ability to spread is due to changes in many genes, not just one.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Prolactin levels and gene polymorphism are not linked to vitiligo severity but are related to BMI.

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

A new genetic variant in the EEF2K gene may contribute to polycystic ovary syndrome.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Using special RNA to target a mutant gene fixed hair problems in mice.

Most children with skin inflammation taking methotrexate had lab abnormalities, but liver issues often improved without changing the medication dose.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

TIP39 and PTH2R help control calcium levels and skin cell development.

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

Mutations in certain receptors can cause diseases and offer new treatment options.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

Dual-targeted therapy is effective and safe for difficult-to-treat inflammatory bowel disease.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

New mutations in the hairless gene may cause hair loss and affect bone development.

H19 may help cause PCOS by affecting CTGF levels, suggesting a new treatment target.

lncRNA MTC helps goat skin cells grow and may aid hair growth by controlling proteins linked to cell growth.

An antibiotic called co-trimoxazole can effectively treat autoimmune diseases.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

FGF13 gene changes cause excessive hair growth in a rare condition.