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Showing results (171-180 of 274) with videos related to

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Pediatric Diabetes|November 19, 2014
Chromosome 18q deletion syndrome with autoimmune diabetes mellitus: putative genomic loci for autoimmunity and immunodeficiencyAnna Hogendorf, Beata S Lipska-Zietkiewicz, Agnieszka Szadkowska, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|April 11, 2012
HbA1c-based diabetes diagnosis among patients with glucokinase mutation (GCK-MODY) is affected by a genetic variant of glucose-6-phosphatase (G6PC2)M Borowiec, W Fendler, P Dusatkova, et al.
Journal of Proteome Research|September 13, 2017
Serum Metabolic Fingerprinting Identified Putatively Annotated Sphinganine Isomer as a Biomarker of Wolfram SyndromeAgnieszka Zmyslowska, Michal Ciborowski, Maciej Borowiec, et al.
Molecular Biology Reports|June 24, 2010
MUTYH Tyr165Cys, OGG1 Ser326Cys and XPD Lys751Gln polymorphisms and head neck cancer susceptibility: a case control studyTomasz Sliwinski, Karolina Przybylowska, Lukasz Markiewicz, et al.
International Journal of Molecular Sciences|March 29, 2023
Evaluation of the Oral Bacterial Genome and Metabolites in Patients with Wolfram SyndromeE Zmysłowska-Polakowska, T Płoszaj, S Skoczylas, et al.
Pediatric Blood & Cancer|August 5, 2022
Challenges in the interpretation of a germline TERT variant in a patient with juvenile myelomonocytic leukemiaSzymon Janczar, Martin Kirschner, Fabian Beier, et al.
Leukemia Research|November 2, 2015
Preserved global histone H4 acetylation linked to ETV6-RUNX1 fusion and PAX5 deletions is associated with favorable outcome in pediatric B-cell progenitor acute lymphoblastic leukemiaK Janczar, S Janczar, A Pastorczak, et al.
Acta Diabetologica|October 18, 2018
Measurement of corneal thickness, optic nerve sheath diameter and retinal nerve fiber layer as potential new non-invasive methods in assessing a risk of cerebral edema in type 1 diabetes in childrenKrzysztof Jeziorny, Anna Niwald, Agnieszka Moll, et al.
International Journal of Molecular Sciences|July 29, 2023
Four Decades of Carrier Detection and Prenatal Diagnosis in Hemophilia A: Historical Overview, State of the Art and Future DirectionsRima Dardik, Szymon Janczar, Shadan Lalezari, et al.
Human Molecular Genetics|December 1, 2020
Double strand breaks (DSBs) as indicators of genomic instability in PATRR-mediated translocationsSarah Correll-Tash, Brenna Lilley, Harold Salmons Iv, et al.
Pageof 28

Showing results (171-180 of 274) with videos related to

Sort By:
Pageof 28
Pediatric Diabetes|November 19, 2014
Chromosome 18q deletion syndrome with autoimmune diabetes mellitus: putative genomic loci for autoimmunity and immunodeficiencyAnna Hogendorf, Beata S Lipska-Zietkiewicz, Agnieszka Szadkowska, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|April 11, 2012
HbA1c-based diabetes diagnosis among patients with glucokinase mutation (GCK-MODY) is affected by a genetic variant of glucose-6-phosphatase (G6PC2)M Borowiec, W Fendler, P Dusatkova, et al.
Journal of Proteome Research|September 13, 2017
Serum Metabolic Fingerprinting Identified Putatively Annotated Sphinganine Isomer as a Biomarker of Wolfram SyndromeAgnieszka Zmyslowska, Michal Ciborowski, Maciej Borowiec, et al.
Molecular Biology Reports|June 24, 2010
MUTYH Tyr165Cys, OGG1 Ser326Cys and XPD Lys751Gln polymorphisms and head neck cancer susceptibility: a case control studyTomasz Sliwinski, Karolina Przybylowska, Lukasz Markiewicz, et al.
International Journal of Molecular Sciences|March 29, 2023
Evaluation of the Oral Bacterial Genome and Metabolites in Patients with Wolfram SyndromeE Zmysłowska-Polakowska, T Płoszaj, S Skoczylas, et al.
Pediatric Blood & Cancer|August 5, 2022
Challenges in the interpretation of a germline TERT variant in a patient with juvenile myelomonocytic leukemiaSzymon Janczar, Martin Kirschner, Fabian Beier, et al.
Leukemia Research|November 2, 2015
Preserved global histone H4 acetylation linked to ETV6-RUNX1 fusion and PAX5 deletions is associated with favorable outcome in pediatric B-cell progenitor acute lymphoblastic leukemiaK Janczar, S Janczar, A Pastorczak, et al.
Acta Diabetologica|October 18, 2018
Measurement of corneal thickness, optic nerve sheath diameter and retinal nerve fiber layer as potential new non-invasive methods in assessing a risk of cerebral edema in type 1 diabetes in childrenKrzysztof Jeziorny, Anna Niwald, Agnieszka Moll, et al.
International Journal of Molecular Sciences|July 29, 2023
Four Decades of Carrier Detection and Prenatal Diagnosis in Hemophilia A: Historical Overview, State of the Art and Future DirectionsRima Dardik, Szymon Janczar, Shadan Lalezari, et al.
Human Molecular Genetics|December 1, 2020
Double strand breaks (DSBs) as indicators of genomic instability in PATRR-mediated translocationsSarah Correll-Tash, Brenna Lilley, Harold Salmons Iv, et al.
Pageof 28