Dinucleotide repeat polymorphism in Gs-alpha subunit gene (GNAS1) on chromosome 20

Multi-dendrite fragmentation dynamics in acoustic flow with oscillating cavitation bubbles revealed in situ by synchrotron X-ray radiography.

Ultrasonics sonochemistry·2025

Patients with persistent symptoms after COVID-19 attending a multidisciplinary evaluation: Characteristics, medical conclusions, and satisfaction.

Journal of psychosomatic research·2023

Development and validation of an individualized nomogram for predicting the high-volume (> 5) central lymph node metastasis in papillary thyroid microcarcinoma.

Journal of endocrinological investigation·2021

Construction and validation of a nomogram for predicting cervical lymph node metastasis in classic papillary thyroid carcinoma.

Journal of endocrinological investigation·2021

Resting beta-cells - A functional reserve?

Diabetes & metabolism·2016

Cell-cell adhesion in the immune system.

Immunology today·2014

iHaptenAb: an integrated hapten-antibody database for rational hapten design and antibody discovery.

Nucleic acids research·2026

Sparsomycin inhibits translation through a conserved mechanism across all domains of life.

Nucleic acids research·2026

Crystal structures of type T archaeal ribonuclease P Rpp30, Rpp30/Pop5, and L7Ae provide insights into a reduced RNase P.

Nucleic acids research·2026

Partitioning of parental histones between leading and lagging strands is modulated by DNA polymerase dosage.

Nucleic acids research·2026

RNase E resolves toxic condensates by counteracting phase separation of Type II RhlB helicases.

Nucleic acids research·2026

A CRISPR/Cas9-induced blunt-end telomere system in S. pombe reveals RNase H2-dependent RNA primer removal at the terminal Okazaki fragment of lagging telomeres.

Nucleic acids research·2026

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

American journal of medical genetics. Part A·2026

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

International journal of molecular sciences·2026

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

International journal of molecular sciences·2026

4-Phenylbutyrate Rescue in GABRA1 Variants Associated with Developmental Epileptic Encephalopathies: From Cell and Mouse Models to Humans.

Cells·2026

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Journal of medical genetics·2026

Ultrasound-guided renal artery administration of angiopoietin-1 RNA therapy slows the progression of preclinical WT1 glomerular disease.

Science translational medicine·2026

Related Experiment Videos

Dinucleotide repeat polymorphism in Gs-alpha subunit gene (GNAS1) on chromosome 20

Related Concept Videos

Multi-dendrite fragmentation dynamics in acoustic flow with oscillating cavitation bubbles revealed in situ by synchrotron X-ray radiography.

Patients with persistent symptoms after COVID-19 attending a multidisciplinary evaluation: Characteristics, medical conclusions, and satisfaction.

Development and validation of an individualized nomogram for predicting the high-volume (> 5) central lymph node metastasis in papillary thyroid microcarcinoma.

Construction and validation of a nomogram for predicting cervical lymph node metastasis in classic papillary thyroid carcinoma.

Resting beta-cells - A functional reserve?

Cell-cell adhesion in the immune system.

iHaptenAb: an integrated hapten-antibody database for rational hapten design and antibody discovery.

Sparsomycin inhibits translation through a conserved mechanism across all domains of life.

Crystal structures of type T archaeal ribonuclease P Rpp30, Rpp30/Pop5, and L7Ae provide insights into a reduced RNase P.

Partitioning of parental histones between leading and lagging strands is modulated by DNA polymerase dosage.

RNase E resolves toxic condensates by counteracting phase separation of Type II RhlB helicases.

A CRISPR/Cas9-induced blunt-end telomere system in S. pombe reveals RNase H2-dependent RNA primer removal at the terminal Okazaki fragment of lagging telomeres.

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

4-Phenylbutyrate Rescue in GABRA1 Variants Associated with Developmental Epileptic Encephalopathies: From Cell and Mouse Models to Humans.

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Ultrasound-guided renal artery administration of angiopoietin-1 RNA therapy slows the progression of preclinical WT1 glomerular disease.

Related Experiment Videos

Dinucleotide repeat polymorphism in Gs-alpha subunit gene (GNAS1) on chromosome 20

Related Concept Videos

Related Articles