Novel intronic polymorphism (+1675G/A) in the human angiotensin II subtype 2 receptor gene

Measurement of the centrality dependence of the charged-particle pseudorapidity distribution in proton-lead collisions at [Formula: see text] TeV with the ATLAS detector.

The European physical journal. C, Particles and fields·2017

C-Peptide, Baseline and Postprandial Insulin Resistance after a Carbohydrate-Rich Test Meal - Evidence for an Increased Insulin Clearance in PCOS Patients?

Geburtshilfe und Frauenheilkunde·2017

Measurement of the Inelastic Proton-Proton Cross Section at sqrt[s]=13 TeV with the ATLAS Detector at the LHC.

Physical review letters·2016

Search for Higgs and Z Boson Decays to ϕγ with the ATLAS Detector.

Physical review letters·2016

Identification of boosted, hadronically decaying W bosons and comparisons with ATLAS data taken at [Formula: see text] TeV.

The European physical journal. C, Particles and fields·2016

Observation of Long-Range Elliptic Azimuthal Anisotropies in sqrt[s]=13 and 2.76 TeV pp Collisions with the ATLAS Detector.

Physical review letters·2016

Bayesian Integration of Tumor Mutational Signatures and Somatic Features Refines Pathogenicity Assessment of Germline Mismatch Repair Variants.

Human mutation·2026

First Cornelia de Lange Syndrome Type 4 Caused by the Gonadal Mosaicism of RAD21 Deletion.

Human mutation·2026

TRACE: A Framework for Integrating Transcript Relevance Into ACMG/AMP Variant Interpretation.

Human mutation·2026

Association Between Mutation Context-Associated RUNX1 Transcriptional States and Immune-Stromal Heterogeneity in Nonsmall Cell Lung Cancer.

Human mutation·2026

The Role of Genetic Variation in Phenotypic Variability in Loeys-Dietz Syndrome.

Human mutation·2026

Functional Validation of a Novel Homozygous TTN Splice-Site Variant Reveals Aberrant Splicing in Hypertrophic Cardiomyopathy.

Human mutation·2026

Previously unreported pathogenic variant in FOXC1 causing Axenfeld-Rieger syndrome with significant ocular anterior segment dysgenesis.

BMJ case reports·2026

Selective Sinus Replacement for a Patient With an Unruptured Sinus of Valsalva Aneurysm.

Annals of thoracic surgery short reports·2026

Y-incision aortic annular enlargement using the arc patch modification: a step-by-step tutorial.

Multimedia manual of cardiothoracic surgery : MMCTS·2026

Evaluation of surgical outcomes and intervention threshold for small-angle acute acquired comitant esotropia.

Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie·2026

Enhanced abrupt autofocusing and depth-of-focus of circular Airy derivative beams via controlled asymmetry.

Optics letters·2026

Pseudonaja textilis venom factor Va circumvents natural regulatory mechanisms via a unique A2 domain region.

Journal of thrombosis and haemostasis : JTH·2026

Related Experiment Videos

Novel intronic polymorphism (+1675G/A) in the human angiotensin II subtype 2 receptor gene

Related Concept Videos

Measurement of the centrality dependence of the charged-particle pseudorapidity distribution in proton-lead collisions at [Formula: see text] TeV with the ATLAS detector.

C-Peptide, Baseline and Postprandial Insulin Resistance after a Carbohydrate-Rich Test Meal - Evidence for an Increased Insulin Clearance in PCOS Patients?

Measurement of the Inelastic Proton-Proton Cross Section at sqrt[s]=13 TeV with the ATLAS Detector at the LHC.

Search for Higgs and Z Boson Decays to ϕγ with the ATLAS Detector.

Identification of boosted, hadronically decaying W bosons and comparisons with ATLAS data taken at [Formula: see text] TeV.

Observation of Long-Range Elliptic Azimuthal Anisotropies in sqrt[s]=13 and 2.76 TeV pp Collisions with the ATLAS Detector.

Bayesian Integration of Tumor Mutational Signatures and Somatic Features Refines Pathogenicity Assessment of Germline Mismatch Repair Variants.

First Cornelia de Lange Syndrome Type 4 Caused by the Gonadal Mosaicism of RAD21 Deletion.

TRACE: A Framework for Integrating Transcript Relevance Into ACMG/AMP Variant Interpretation.

Association Between Mutation Context-Associated RUNX1 Transcriptional States and Immune-Stromal Heterogeneity in Nonsmall Cell Lung Cancer.

The Role of Genetic Variation in Phenotypic Variability in Loeys-Dietz Syndrome.

Functional Validation of a Novel Homozygous TTN Splice-Site Variant Reveals Aberrant Splicing in Hypertrophic Cardiomyopathy.

Previously unreported pathogenic variant in FOXC1 causing Axenfeld-Rieger syndrome with significant ocular anterior segment dysgenesis.

Selective Sinus Replacement for a Patient With an Unruptured Sinus of Valsalva Aneurysm.

Y-incision aortic annular enlargement using the arc patch modification: a step-by-step tutorial.

Evaluation of surgical outcomes and intervention threshold for small-angle acute acquired comitant esotropia.

Enhanced abrupt autofocusing and depth-of-focus of circular Airy derivative beams via controlled asymmetry.

Pseudonaja textilis venom factor Va circumvents natural regulatory mechanisms via a unique A2 domain region.

Related Experiment Videos

Novel intronic polymorphism (+1675G/A) in the human angiotensin II subtype 2 receptor gene

Related Concept Videos

Related Articles