Search

everythinglearnresearchcommunity

for

Search:↓

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

The RapidHIT ID system can effectively get DNA profiles from hair roots with enough cells.

Researchers found two new genetic variants linked to Alzheimer's disease.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

K25, K27, and K28 are found in all inner root sheath layers of hair, while K26 is only in the cuticle.

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

Scientists found 53 keratin genes in yaks that are important for hair growth and share similarities with those in other animals.

miR-214-3p helps nerve repair and recovery.

A new non-invasive method can analyze skin mRNA to understand skin diseases better.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

AD198 is more effective than doxorubicin in stopping certain dog cancer cells.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

UC.145 may be a new biomarker for predicting gastric cancer.

A rabbit gene important for hair development was identified and detailed.

The 4C32 gene may help in mouse skin development and differentiation.

Three molecular subtypes of advanced skin T-cell lymphoma were identified, with potential biomarkers for predicting treatment response and disease progression.

Blocking CXCR4 may help treat hidradenitis suppurativa.

BroadAMP-GPT effectively creates antimicrobial peptides to fight drug-resistant bacteria.

Long non-coding RNAs play a key role in yak hair growth cycles.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

Intermediate filaments are crucial for cell structure and function, regulated by specific genes and proteins.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

LHX2 is crucial for development, tissue repair, and preventing diseases.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.