Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Anna Abramowicz

Showing results (1-10 of 10) with videos related to

Pageof 1
Sort By:
Developmental Period Medicine|September 4, 2014
Neurofibromin in neurofibromatosis type 1 - mutations in NF1gene as a cause of diseaseAnna Abramowicz, Monika Gos
Postepy Higieny I Medycyny Doswiadczalnej (Online)|December 17, 2015
[Neurofibromin - protein structure and cellular functions in the context of neurofibromatosis type I pathogenesis]Anna Abramowicz, Monika Gos
Journal of Applied Genetics|March 20, 2019
Correction to: Splicing mutations in human genetic disorders: examples, detection, and confirmationAnna Abramowicz, Monika Gos
Postepy Biochemii|February 5, 2013
[RAS/MAPK signal transduction pathway and its role in the pathogenesis of Noonan syndrome]Monika Gos, Monika Leszkiewicz, Anna Abramowicz
Journal of Hazardous Materials|May 6, 2021
Heavy metal- and organic-matter pollution due to self-heating coal-waste dumps in the Upper Silesian Coal Basin (Poland)Ádám Nádudvari, Barbara Kozielska, Anna Abramowicz, et al.
American Journal of Medical Genetics. Part A|May 26, 2018
MAP2K2 mutation as a cause of cardio-facio-cutaneous syndrome in an infant with a severe and fatal course of the diseaseMonika Gos, Robert Smigiel, Teresa Kaczan, et al.
The Science of the Total Environment|April 26, 2024
Botryoidal and spherulitic hematite as experimental evidence of highly acidic conditions in burning coal-waste dumps and potentially on MarsJustyna Ciesielczuk, Monika J Fabiańska, Krzysztof Gaidzik, et al.
Genes|December 23, 2023
Research on the Pathogenesis of Cognitive and Neurofunctional Impairments in Patients with Noonan Syndrome: The Role of Rat Sarcoma-Mitogen Activated Protein Kinase Signaling Pathway Gene DisturbancesNatalia Braun-Walicka, Agnieszka Pluta, Tomasz Wolak, et al.
Genes|September 7, 2016
Towards a Better Molecular Diagnosis of FMR1-Related Disorders-A Multiyear Experience from a Reference LabSylwia Olimpia Rzońca, Monika Gos, Daniel Szopa, et al.
Journal of Medical Genetics|March 22, 2015
Rare variants in SOS2 and LZTR1 are associated with Noonan syndromeGuilherme Lopes Yamamoto, Meire Aguena, Monika Gos, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Developmental Period Medicine|September 4, 2014
Neurofibromin in neurofibromatosis type 1 - mutations in NF1gene as a cause of diseaseAnna Abramowicz, Monika Gos
Postepy Higieny I Medycyny Doswiadczalnej (Online)|December 17, 2015
[Neurofibromin - protein structure and cellular functions in the context of neurofibromatosis type I pathogenesis]Anna Abramowicz, Monika Gos
Journal of Applied Genetics|March 20, 2019
Correction to: Splicing mutations in human genetic disorders: examples, detection, and confirmationAnna Abramowicz, Monika Gos
Postepy Biochemii|February 5, 2013
[RAS/MAPK signal transduction pathway and its role in the pathogenesis of Noonan syndrome]Monika Gos, Monika Leszkiewicz, Anna Abramowicz
Journal of Hazardous Materials|May 6, 2021
Heavy metal- and organic-matter pollution due to self-heating coal-waste dumps in the Upper Silesian Coal Basin (Poland)Ádám Nádudvari, Barbara Kozielska, Anna Abramowicz, et al.
American Journal of Medical Genetics. Part A|May 26, 2018
MAP2K2 mutation as a cause of cardio-facio-cutaneous syndrome in an infant with a severe and fatal course of the diseaseMonika Gos, Robert Smigiel, Teresa Kaczan, et al.
The Science of the Total Environment|April 26, 2024
Botryoidal and spherulitic hematite as experimental evidence of highly acidic conditions in burning coal-waste dumps and potentially on MarsJustyna Ciesielczuk, Monika J Fabiańska, Krzysztof Gaidzik, et al.
Genes|December 23, 2023
Research on the Pathogenesis of Cognitive and Neurofunctional Impairments in Patients with Noonan Syndrome: The Role of Rat Sarcoma-Mitogen Activated Protein Kinase Signaling Pathway Gene DisturbancesNatalia Braun-Walicka, Agnieszka Pluta, Tomasz Wolak, et al.
Genes|September 7, 2016
Towards a Better Molecular Diagnosis of FMR1-Related Disorders-A Multiyear Experience from a Reference LabSylwia Olimpia Rzońca, Monika Gos, Daniel Szopa, et al.
Journal of Medical Genetics|March 22, 2015
Rare variants in SOS2 and LZTR1 are associated with Noonan syndromeGuilherme Lopes Yamamoto, Meire Aguena, Monika Gos, et al.
Pageof 1