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ABCC8
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Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?
2017 |
Second Faculty of Medicine
publication
Aetiology and treatment of neonatal diabetes
2019 |
Second Faculty of Medicine
publication
Whole Exome Sequencing Analysis of ABCC8 and ABCD2 Genes Associating With Clinical Course of Breast Carcinoma
2015 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
High incidence of heterozygous ABCC8 and HNF1A mutations in Czech patients with congenital hyperinsulinism
2015 |
First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
publication
Protein expression and localization of ABC transporters in pancreatic adenocarcinoma: prognostic role of ABCC8
2023 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Congenital hyperinsulinism caused by novel homozygous katp channel gene variants may be linked to unexplained neonatal deaths among kurdish consanguineous families
2020 |
Second Faculty of Medicine
publication
Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generations
2011 |
Second Faculty of Medicine, Third Faculty of Medicine
publication
Severe Hyperinsulinemic Hypoglycemia in a Neonate: Response to Sirolimus Therapy
2015 |
Second Faculty of Medicine
publication
Congenital hyperinsulinism: Loss of B-cell self-control
2016 |
Second Faculty of Medicine
publication
Treatment of diabetes in small children
2019 |
Second Faculty of Medicine
publication
The expression profile of ATP-binding cassette transporter genes in breast carcinoma
2013 |
First Faculty of Medicine, Central Library of Charles University
publication
The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia
2015 |
Second Faculty of Medicine
publication
Reprogramming of Human Pancreatic Organoid Cells into Insulin-Producing beta-Like Cells by Small Molecules and in Vitro Transcribed Modified mRNA Encoding Neurogenin 3 Transcription Factor
2019 |
First Faculty of Medicine, Faculty of Physical Education and Sport
publication
The invaluable role of consanguinity in providing insight into paediatric endocrine conditions: Lessons learned from congenital hyperinsulinism, monogenic diabetes, and short stature
2022 |
Second Faculty of Medicine
publication
Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia
2012 |
Faculty of Medicine in Pilsen
publication
Differences in Transcript Levels of ABC Transporters Between Pancreatic Adenocarcinoma and Nonneoplastic Tissues
2013 |
First Faculty of Medicine, Central Library of Charles University
publication
Role of Genetic Variation in ABC Transporters in Breast Cancer Prognosis and Therapy Response
2020 |
Faculty of Medicine in Pilsen
publication
The role of ABC transporters in progression and clinical outcome of colorectal cancer
2012 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq
2024 |
Second Faculty of Medicine