Search

everythinglearnresearchcommunity

for

Search:↓

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

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

The conclusion is that women under 35 should start fertility checks after 12 months of trying to conceive, women over 35 after 6 months, and women over 40 should start immediately. The checks should include ovulation status, reproductive tract structure, and male partner's semen evaluation.

The document concludes that recent studies help tell apart desmoplastic trichoepitheliomas from other skin tumors, but more research is needed for clear differentiation.

Tradescantia plants can effectively test for the toxicity of harmful algae.

A woman with a rare scalp lymphoma had unusual hair loss after treatment.

The vitamin D receptor has many roles in the body beyond managing calcium, affecting the immune system, hair growth, muscles, fat, bone marrow, and cancer cells.

People with Down syndrome have higher rates of certain immune-related conditions and need special medical attention.

Mice lacking fibromodulin have disrupted healing patterns, leading to abnormal skin repair and scarring.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

Identified genes linked to male-pattern baldness may help develop new treatments.

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

Skin aging is caused by stem cell damage and can potentially be delayed with treatments like antioxidants and stem cell therapy.

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

EGFR helps control how hair grows and forms without needing p53 protein.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

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.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Hair in mammals likely evolved from glandular structures, not scales.

Keeping β-catenin levels high in mammary cells disrupts their development and branching.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Scientists turned rat thymus cells into stem cells that can help repair skin and hair.

Different types of cell death affect skin health and inflammation, and understanding them could improve treatments for skin diseases.

Cytokeratin 19 and cytokeratin 15 are key markers for monitoring the quality and self-renewing potential of engineered skin.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.