Résultat de recherche

Candidate Predisposition Variants in Kaposi Sarcoma as Detected by Whole-Genome...

Human embryonic stem cells reveal recurrent genomic instability at 20q...

Human embryonic stem cells and genomic instability.

Recurrent genomic instability of chromosome 1q in neural derivatives of...

Early transcriptional changes linked to naturally occurring Huntington's...

Urine-derived cells provide a readily accessible cell type for feeder-free...

High N-glycan multiplicity is critical for neuronal adhesion and sensitizes...

Human SNORA31 variations impair cortical neuron-intrinsic immunity to HSV-1...

Identification of an Endoglin Variant Associated With HCV-Related Liver...

Homozygous NLRP1 gain-of-function mutation in siblings with a syndromic...

Prevalence and risk factors for latent tuberculosis infection among healthcare...

A deep intronic splice mutation of STAT3 underlies hyper IgE syndrome by...

Pleiotropic effects for Parkin and LRRK2 in leprosy type-1 reactions and...

Inherited IFNAR1 deficiency in otherwise healthy patients with adverse...

Severe influenza pneumonitis in children with inherited TLR3 deficienc...

Effectiveness and safety of the tri-iodothyronine analogue Triac in children...

Glibenclamide oral suspension: Suitable and effective in patients with...

Effectiveness and safety of long-term treatment with sulfonylureas in patients...

Thyroid Hypoplasia in Congenital Hypothyroidism Associated with Thyroid...

Mutations in BOREALIN cause thyroid dysgenesis.