Remitting diabetes: a new genetic subgroup?

Widening the phenotypic spectrum caused by pathogenic PDX1 variants in individuals with neonatal diabetes.

BMJ open diabetes research & care·2024

The impact of prolonged walking on fasting plasma glucose in type 2 diabetes: A randomised controlled crossover study.

Diabetic medicine : a journal of the British Diabetic Association·2024

A homozygous TARS2 variant is a novel cause of syndromic neonatal diabetes.

Diabetic medicine : a journal of the British Diabetic Association·2024

Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization.

Wellcome open research·2024

Ethnic differences in the manifestation of early-onset type 2 diabetes.

BMJ open diabetes research & care·2024

Precision treatment of beta-cell monogenic diabetes: a systematic review.

Communications medicine·2024

Islet Autoantibody Patterns Vary by Race and Ethnicity and Area Deprivation Index for Individuals at Risk for Type 1 Diabetes.

Diabetes care·2026

Continuous Glucose Monitoring Metrics and Risks of Severe Hypoglycemia and Diabetic Ketoacidosis in Type 1 Diabetes: A Pooled Analysis.

Diabetes care·2026

The Gain-of-Function GLP1R R131Q Variant Preserves β-Cell Function and Enhances Response to GLP-1 Receptor Agonists.

Diabetes care·2026

Type 2 Diabetes and Longitudinal Changes in Cortical and Trabecular Bone Density, Microarchitecture, and Strength: The Framingham Study.

Diabetes care·2026

In Utero Exposure to Preexisting or Gestational Diabetes Mellitus Increases Incidence of Diabetes in the Children of First Nations and Non-First Nations Mothers: A Retrospective Cohort Study.

Diabetes care·2026

Diagnostic Tools to Establish the Presence of Peripheral Arterial Disease in People With Diabetes (DMPAD): A Multicenter Comparative Diagnostic Accuracy Study.

Diabetes care·2026

Broken chromosomes don't stay home: Tunneling nanotubes carry damaged DNA between human cells.

Molecular cell·2026

Human acrocentric chromosome short-arm de novo mutation and recombination.

Cell·2026

Ophthalmic Manifestations of KIF11-Associated Microcephaly With or Without Chorioretinopathy, Lymphedema, or Intellectual Disability: A Case Report of a Novel Variant.

The American journal of case reports·2026

MAGIC populations: a next-generation framework for dissecting complex quantitative traits and accelerating molecular breeding in crops.

Frontiers in plant science·2026

Genome evolution and long-term demographic history in true crocodiles.

G3 (Bethesda, Md.)·2026

Cytoplasmic RBM20 granules modulate non-RBM20 target splicing through interactions with other splicing factors.

Nucleic acids research·2026

Related Experiment Videos

Remitting diabetes: a new genetic subgroup?

Related Concept Videos

Widening the phenotypic spectrum caused by pathogenic PDX1 variants in individuals with neonatal diabetes.

The impact of prolonged walking on fasting plasma glucose in type 2 diabetes: A randomised controlled crossover study.

A homozygous TARS2 variant is a novel cause of syndromic neonatal diabetes.

Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization.

Ethnic differences in the manifestation of early-onset type 2 diabetes.

Precision treatment of beta-cell monogenic diabetes: a systematic review.

Islet Autoantibody Patterns Vary by Race and Ethnicity and Area Deprivation Index for Individuals at Risk for Type 1 Diabetes.

Continuous Glucose Monitoring Metrics and Risks of Severe Hypoglycemia and Diabetic Ketoacidosis in Type 1 Diabetes: A Pooled Analysis.

The Gain-of-Function GLP1R R131Q Variant Preserves β-Cell Function and Enhances Response to GLP-1 Receptor Agonists.

Type 2 Diabetes and Longitudinal Changes in Cortical and Trabecular Bone Density, Microarchitecture, and Strength: The Framingham Study.

In Utero Exposure to Preexisting or Gestational Diabetes Mellitus Increases Incidence of Diabetes in the Children of First Nations and Non-First Nations Mothers: A Retrospective Cohort Study.

Diagnostic Tools to Establish the Presence of Peripheral Arterial Disease in People With Diabetes (DMPAD): A Multicenter Comparative Diagnostic Accuracy Study.

Broken chromosomes don't stay home: Tunneling nanotubes carry damaged DNA between human cells.

Human acrocentric chromosome short-arm de novo mutation and recombination.

Ophthalmic Manifestations of KIF11-Associated Microcephaly With or Without Chorioretinopathy, Lymphedema, or Intellectual Disability: A Case Report of a Novel Variant.

MAGIC populations: a next-generation framework for dissecting complex quantitative traits and accelerating molecular breeding in crops.

Genome evolution and long-term demographic history in true crocodiles.

Cytoplasmic RBM20 granules modulate non-RBM20 target splicing through interactions with other splicing factors.

Related Experiment Videos

Remitting diabetes: a new genetic subgroup?

Related Concept Videos

Related Articles