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Personalized treatment based on detailed tumor analysis successfully managed and reduced the patient's aggressive hair follicle cancer.

Newborn mouse skin cells can grow hair and this process can be recreated in adult cells to potentially help with hair loss.

Genomic prediction can improve breeding strategies for Korean Sapsaree dogs.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

Suppressing eIF4E can prevent hair loss from chemotherapy.

KLB and EIF3C genes are key for early diagnosis of vitiligo and alopecia areata.

Rare genetic variants contribute to male pattern hair loss, but there's no link to severe COVID-19.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Type 1/17 inflammation in psoriasis increases skin cell growth due to a molecule that could be a new treatment target.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

ESR2 gene linked to female-pattern hair loss.

Overexpression of R-spondin 3 leads to sparse hair and impaired hair regeneration.

The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Overexpression of E2F1 can lead to skin tumors and disrupt hair growth.