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Further testing of paclitaxel poliglumex for this cancer treatment is not justified.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

pCLCA2 protein may help maintain skin structure and function.

Mitochondrial activity varies in cells before they stop growing, affecting their growth potential.

Prenatal diagnosis of trichothiodystrophy is possible in the second trimester using fetal eyebrow biopsy, with sulfur content analysis being more reliable.

Disrupting β-catenin signaling in certain cells causes anorectal malformations.

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

Cronkhite-Canada syndrome is a rare condition causing gut polyps, hair loss, skin changes, and nail issues, often with a poor outlook.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

TSC2-/meth cells can cause skin lesions, hair growth, and lung issues, and may be treated with chromatin remodeling agents.

The FGF5 gene determines hair length in dogs.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

Over a third of women thought to have non-classical congenital adrenal hyperplasia didn't have it confirmed by genetic tests.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Cetuximab can cause eyelash growth, which is rare but manageable.

scMC effectively separates biological signals from technical noise in single-cell genomics data.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

Electron Beam Tomography (EBT) is a useful additional test to stress testing for detecting heart disease.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

KRT72 gene helps form hair.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

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