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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

ILC1-like cells can independently cause alopecia areata by affecting hair follicles.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

CCC1 is crucial for pH balance in plant cells, affecting growth and stress tolerance.

Different types of sun exposure damage skin cells and immune cells, with chronic exposure leading to more severe and lasting damage.

Melatonin may help with nerve pain, a hepatitis C drug is effective but has side effects, a treatment for mouth sores works but can cause blood issues, ear reconstruction with an implant is safe, HIV transmission from mother to child in Taiwan is now 0% with treatment, certain blood problems are more common in people with a tongue condition, a gene and being overweight are linked to hair loss in some women, a new technique could reduce radiation for lung nodule patients, a hepatitis treatment may lower cancer recurrence after a procedure, and adding extra screening improves tuberculosis detection in patients with lung infections.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

Mice without the IL-6 gene had more hair growth after injury due to higher activity of a related protein, Stat3.

Certain MC4R gene variants are linked to higher BMI in obese women with PCOS but do not cause PCOS.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

The Itpr3 gene causes a specific hair pattern in mice.

The KRTAP21-2 gene affects wool length and quality in sheep.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

Lychee fruit polyphenol (Oligonol®) may regulate genes linked to cell growth and inflammation in human scalp cells.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

The KRTAP36-2 gene in sheep affects wool yield.

The study suggests that analyzing DNA can help treat hair loss, but more research is needed.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

The conclusion is that more research is needed to understand if the drug finasteride causes Post-Finasteride Syndrome or if it's due to individual genetic makeup.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Alopecia areata involves immune response and gene changes affecting hair loss.