Association of genotype and total cholesterol in MZ twins

[Tumor cells transfer between the patient and laboratory animal as a basic methodological approach to the study of cancerogenesis and identification of biomarkers].

Rozhledy v chirurgii : mesicnik Ceskoslovenske chirurgicke spolecnosti·2017

[Postpancreatectomy haemorrhage (PPH), prevalence, diagnosis and management].

Rozhledy v chirurgii : mesicnik Ceskoslovenske chirurgicke spolecnosti·2016

[The survival of patients with radically non-resectable pancreatic cancer].

Rozhledy v chirurgii : mesicnik Ceskoslovenske chirurgicke spolecnosti·2016

[Current status regarding surgical treatment of pancreatic cancer in the Czech Republic].

Rozhledy v chirurgii : mesicnik Ceskoslovenske chirurgicke spolecnosti·2016

Frailty and Constellations of Factors in Aging HIV-infected and Uninfected Women--The Women's Interagency HIV Study.

The Journal of frailty & aging·2016

[Surgical therapy of pancreatic cancer - 5 years survival].

Rozhledy v chirurgii : mesicnik Ceskoslovenske chirurgicke spolecnosti·2016

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

Clinical genetics·2026

A Novel De Novo STAG1 Variant at the RAD21 Binding Interface Is Associated With Hypoglycemia, Recurrent Fever, Immunodeficiency and Features of Classical Cohesinopathies.

Clinical genetics·2026

Pathogenicity of NUSAP1 Variants Is Defined by NMD-Escape: Evidence From Two Novel Cases and Systematic Population-Based Variant Analysis.

Clinical genetics·2026

Biallelic ABCA13 Loss-of-Function Variants in a Child With Neurodevelopmental Delay: A Case Report.

Clinical genetics·2026

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Clinical genetics·2026

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Clinical genetics·2026

Genetic landscape of pediatric seizures in Southeast China: identification of a novel GLI3 frameshift variant through whole-exome sequencing.

Annals of medicine and surgery (2012)·2026

RECQL correlates with immune infiltration and serves as a prognostic biomarker and therapeutic predictor in gastric cancer.

Translational cancer research·2026

Decreased H3K79 acetylation and dysregulation of neurodevelopmental genes in fetal down syndrome.

Translational pediatrics·2026

Insulin resistance evaluated by estimated glucose disposal rate and its association with cardiometabolic risk factors among adolescents in Northeast China.

Frontiers in nutrition·2026

Polygenic score for sleep duration in relation to the risk of Alzheimer's disease: results from the UK biobank.

Frontiers in dementia·2026

Related Experiment Videos

Association of genotype and total cholesterol in MZ twins

Related Concept Videos

[Tumor cells transfer between the patient and laboratory animal as a basic methodological approach to the study of cancerogenesis and identification of biomarkers].

[Postpancreatectomy haemorrhage (PPH), prevalence, diagnosis and management].

[The survival of patients with radically non-resectable pancreatic cancer].

[Current status regarding surgical treatment of pancreatic cancer in the Czech Republic].

Frailty and Constellations of Factors in Aging HIV-infected and Uninfected Women--The Women's Interagency HIV Study.

[Surgical therapy of pancreatic cancer - 5 years survival].

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

A Novel De Novo STAG1 Variant at the RAD21 Binding Interface Is Associated With Hypoglycemia, Recurrent Fever, Immunodeficiency and Features of Classical Cohesinopathies.

Pathogenicity of NUSAP1 Variants Is Defined by NMD-Escape: Evidence From Two Novel Cases and Systematic Population-Based Variant Analysis.

Biallelic ABCA13 Loss-of-Function Variants in a Child With Neurodevelopmental Delay: A Case Report.

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Genetic landscape of pediatric seizures in Southeast China: identification of a novel GLI3 frameshift variant through whole-exome sequencing.

RECQL correlates with immune infiltration and serves as a prognostic biomarker and therapeutic predictor in gastric cancer.

Decreased H3K79 acetylation and dysregulation of neurodevelopmental genes in fetal down syndrome.

Insulin resistance evaluated by estimated glucose disposal rate and its association with cardiometabolic risk factors among adolescents in Northeast China.

Polygenic score for sleep duration in relation to the risk of Alzheimer's disease: results from the UK biobank.

Related Experiment Videos

Association of genotype and total cholesterol in MZ twins

Related Concept Videos

Related Articles