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Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

Using neurohormones to control keratin can lead to new skin disease treatments.

Blocking Wnt/β-catenin signaling with EGF receptor is necessary for proper hair growth.

Hedgehog signaling is crucial for mammary gland development over hair follicles.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

New treatments targeting the Hedgehog pathway can help treat advanced skin cancer but may have side effects and their effectiveness in early stages is unknown.

We need better ways to test and understand SARMs to make safer and more effective treatments.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

The circadian clock in skin cells controls their growth and rest cycles.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

A specific gene mutation causes long hair in Angora rabbits.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

TMPRSS2 is crucial for COVID-19 infection and is a potential target for treatment.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Activated ras can protect kidney cells from a certain substance that causes cell death.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Mechanical forces are crucial for shaping cells and forming tissues during development.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

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

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

SPT6 prevents excessive skin inflammation by blocking a feedback loop.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.

TBX3 gene affects pigmentation and marking formation in Dun Mongolian horses.

CCCA and LPP may be related hair loss conditions influenced by genetics and environment, needing early treatment.