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Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

PCOS is a genetic disorder affecting women's reproductive health, with treatments focused on symptoms like insulin resistance and fertility.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

The study provides insights into hair growth mechanisms in yaks.

Genes controlling hair growth and immune response are disrupted in male pattern baldness.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

Using hemocoagulase with platelet-rich plasma in hip replacement can lessen blood loss and improve healing and blood clotting.

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

Live imaging has advanced our understanding of stem cell behavior and raised new research questions.

Hair regrowth from severe alopecia areata treatment with baricitinib can vary, with faster results in those with shorter hair loss duration.

Merkel cells stabilize nerve endings in the skin, and they change independently of each other.

American men are older, more obese, and have longer infertility than Canadian men.

COVID-19 can cause various skin issues, but long-term skin problems are rare.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Fish teeth and taste bud densities are linked and can change between types due to shared genetic and molecular factors.

Low-dose radiation affects hair stem cell function and survival by changing their genetic material's structure.

Finger length ratios might help predict common hair loss.

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

Changes in skin microbes play a role in some skin diseases and could lead to new treatments.

Zebrafish are useful for studying and developing treatments for human skin diseases.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Most cases of Temporal Triangular Alopecia are found in early childhood and may be related to genetic conditions.