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Anna Walczak

Showing results (31-40 of 65) with videos related to

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Polski Przeglad Chirurgiczny|July 6, 2012
The -2518 A/G MCP-1 polymorphism as a risk factor of inflammatory bowel diseaseAnna Walczak, Karolina Przybyłowska, Andrzej Sygut, et al.
American Journal of Medical Genetics. Part A|August 27, 2021
A recurrent de novo variant supports KCNC2 involvement in the pathogenesis of developmental and epileptic encephalopathyMałgorzata Rydzanicz, Piotr Zwoliński, Piotr Gasperowicz, et al.
Polski Przeglad Chirurgiczny|November 21, 2017
An association of the MCP-1 and CCR2 single nucleotide polymorphisms with colorectal cancer prevalenceAnna Walczak, Karolina Przybyłowska-Sygut, Andrzej Sygut, et al.
Neurologia I Neurochirurgia Polska|August 28, 2017
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) - A Polish family with novel SACS mutationsMagdalena Krygier, Agnieszka Konkel, Michał Schinwelski, et al.
Inorganic Chemistry|June 11, 2021
Charge Neutral [Cu<sub>2</sub>L<sub>2</sub>] and [Pd<sub>2</sub>L<sub>2</sub>] Metallocycles: Self-Assembly, Aggregation, and CatalysisMichał Kołodziejski, Aidan J Brock, Gracjan Kurpik, et al.
Ophthalmic Genetics|November 3, 2017
Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish populationMilena Molasy, Anna Walczak, Karolina Przybyłowska-Sygut, et al.
American Journal of Medical Genetics. Part A|February 3, 2022
Postzygotic mosaicism of a novel PTPN11 mutation in monozygotic twins discordant for metachondromatosisMałgorzata Rydzanicz, Wojciech Glinkowski, Anna Walczak, et al.
Seizure|August 15, 2024
The epilepsy phenotype of KCNK4-related neurodevelopmental diseaseMagdalena Krygier, Szymon Ziętkiewicz, Weronika Talaśka-Liczbik, et al.
European Journal of Medical Genetics|October 21, 2021
Efficacy and safety of sirolimus therapy in familial hypoinsulinemic hypoglycemia caused by AKT2 mutation inherited from the mosaic fatherMarya Dushar, Jędrzej Nowaczyk, Beata Pyrżak, et al.
Angewandte Chemie (International Ed. in English)|July 8, 2025
A Multistate Adaptive System of Topologically Distinct Chiral AssembliesWiktoria Adamska, Grzegorz Markiewicz, Anna Walczak, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Polski Przeglad Chirurgiczny|July 6, 2012
The -2518 A/G MCP-1 polymorphism as a risk factor of inflammatory bowel diseaseAnna Walczak, Karolina Przybyłowska, Andrzej Sygut, et al.
American Journal of Medical Genetics. Part A|August 27, 2021
A recurrent de novo variant supports KCNC2 involvement in the pathogenesis of developmental and epileptic encephalopathyMałgorzata Rydzanicz, Piotr Zwoliński, Piotr Gasperowicz, et al.
Polski Przeglad Chirurgiczny|November 21, 2017
An association of the MCP-1 and CCR2 single nucleotide polymorphisms with colorectal cancer prevalenceAnna Walczak, Karolina Przybyłowska-Sygut, Andrzej Sygut, et al.
Neurologia I Neurochirurgia Polska|August 28, 2017
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) - A Polish family with novel SACS mutationsMagdalena Krygier, Agnieszka Konkel, Michał Schinwelski, et al.
Inorganic Chemistry|June 11, 2021
Charge Neutral [Cu<sub>2</sub>L<sub>2</sub>] and [Pd<sub>2</sub>L<sub>2</sub>] Metallocycles: Self-Assembly, Aggregation, and CatalysisMichał Kołodziejski, Aidan J Brock, Gracjan Kurpik, et al.
Ophthalmic Genetics|November 3, 2017
Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish populationMilena Molasy, Anna Walczak, Karolina Przybyłowska-Sygut, et al.
American Journal of Medical Genetics. Part A|February 3, 2022
Postzygotic mosaicism of a novel PTPN11 mutation in monozygotic twins discordant for metachondromatosisMałgorzata Rydzanicz, Wojciech Glinkowski, Anna Walczak, et al.
Seizure|August 15, 2024
The epilepsy phenotype of KCNK4-related neurodevelopmental diseaseMagdalena Krygier, Szymon Ziętkiewicz, Weronika Talaśka-Liczbik, et al.
European Journal of Medical Genetics|October 21, 2021
Efficacy and safety of sirolimus therapy in familial hypoinsulinemic hypoglycemia caused by AKT2 mutation inherited from the mosaic fatherMarya Dushar, Jędrzej Nowaczyk, Beata Pyrżak, et al.
Angewandte Chemie (International Ed. in English)|July 8, 2025
A Multistate Adaptive System of Topologically Distinct Chiral AssembliesWiktoria Adamska, Grzegorz Markiewicz, Anna Walczak, et al.
Pageof 7