Search

for
Search:

Learn

0 / 0 results

— no results

Research

5 / 53 results

research Identification of Compound Heterozygous Mutations in AP1B1 Leading to the Newly Described Recessive Keratitis–Ichthyosis–Deafness (KIDAR) Syndrome

11 citations , January 2021 in “British Journal of Dermatology”

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

research Characterization of Novel TMEM173 Mutation with Additive IFIH1 Risk Allele

1 citations , August 2018 in “bioRxiv (Cold Spring Harbor Laboratory)”

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

research Novel TMEM173 Mutation and the Role of Disease-Modifying Alleles

47 citations , December 2019 in “Frontiers in immunology”

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

research Lipid-Based Liquid Crystals as Drug Delivery Vehicles for Antimicrobial Peptides

5 citations , January 2017 in “Chalmers Publication Library (Chalmers University of Technology)”

Cubosomes enhance antimicrobial peptide stability and effectiveness.

research Hair Transplantation Surgery Versus Other Modalities of Treatment in Androgenetic Alopecia: A Narrative Review

2 citations , March 2021 in “Cosmetics”

Hair transplant surgery is the most effective, safe, and satisfying treatment for hair loss.

View more "ap1b1" in research →

Community Join

0 / 0 results

— no results