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The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

Food deprivation increases MST enzyme in the brain, possibly affecting energy balance.

Mettl3 is essential for normal tissue development and self-renewal by regulating gene expression.

Researchers created an efficient method to extract DNA from marmoset hair, reducing blood chimerism.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

A specific group of early-stage melanocytes is reduced in vitiligo-affected skin, which may explain treatment resistance.

Humans lost body hair relatively recently in evolution.

Two siblings were diagnosed with Trichothiodystrophy, identified by brittle hair and low sulfur content.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Removing part of the vitamin D receptor stops vitamin D from working properly.

Researchers created an efficient method to extract DNA from marmoset hair, avoiding blood chimerism.

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.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

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

Targeting ATM could help manage heart cell enlargement due to pressure overload.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

TCDD changes skin cell growth and keratin production in mice.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

In situ DNA labeling in hair can help predict forensic DNA analysis success.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Early detection and treatment of Menkes disease with copper injections are crucial for better outcomes.

Vitamin B12 deficiency can cause darkening of all nails.

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