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

Marzena Kucharczyk

Showing results (1-10 of 15) with videos related to

Pageof 2
Sort By:
Journal of Inorganic Biochemistry|February 8, 2008
Structural features of the Cu(2+)-vancomycin complexMarzena Kucharczyk, Magdalena Brzezowska, Anna Maciag, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
1.15 Mb microdeletion in chromosome band 20p13 associated with moderate developmental delay-additional case and data's reviewAleksandra Jezela-Stanek, Marzena Kucharczyk, Magdalena Pelc, et al.
American Journal of Medical Genetics. Part A|February 21, 2012
Minimal clinical findings in a patient with 15qter microdeletion syndrome: delineation of the associated phenotypeAleksandra Jezela-Stanek, Marzena Kucharczyk, Magdalena Pelc, et al.
Clinical Dysmorphology|March 7, 2012
History and molecular characteristics of a patient with terminal deletion of 14q. Is this another syndrome with a striking phenotype?Aleksandra Jezela-Stanek, Marzena Kucharczyk, Anna Gutkowska, et al.
Ginekologia Polska|October 24, 2015
Trends in prenatal diagnosis of non-specific multiple malformations disorders with reference to the own experience and research study on Smith-Lemli-Opitz syndromeAleksandra Jezela-Stanek, Ewa Małunowicz, Siejka Anna, et al.
American Journal of Medical Genetics. Part A|August 12, 2014
The first case of a patient with de novo partial distal 16q tetrasomy and a data's reviewMarzena Kucharczyk, Andrzej Kochański, Aleksandra Jezela-Stanek, et al.
Biomedical Papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia|February 19, 2015
Oculocutaneous albinism in a patient with 17p13.2-pter duplication - a review on the molecular syndromology of 17p13 duplicationMarzena Kucharczyk, Aleksandra Jezela-Stanek, Dorota Gieruszczak-Bialek, et al.
Journal of Inorganic Biochemistry|December 8, 2009
Cu(II) ion interaction with teicoplanin-vancomycin's analogMagdalena Brzezowska, Marzena Kucharczyk-Klamińska, Francesca Bernardi, et al.
American Journal of Medical Genetics. Part A|April 1, 2016
Additional data on the clinical phenotype of Helsmoortel-Van der Aa syndrome associated with a novel truncating mutation in ADNP geneMałgorzata Krajewska-Walasek, Dorota Jurkiewicz, Dorota Piekutowska-Abramczuk, et al.
Bioinorganic Chemistry and Applications|March 13, 2010
DNA oxidative cleavage induced by the novel peptide derivatives of 3-(quinoxalin-6-yl)alanine in combination with Cu(II) or Fe(II) ionsWojciech Szczepanik, Marzena Kucharczyk-Klamińska, Piotr Stefanowicz, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of Inorganic Biochemistry|February 8, 2008
Structural features of the Cu(2+)-vancomycin complexMarzena Kucharczyk, Magdalena Brzezowska, Anna Maciag, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
1.15 Mb microdeletion in chromosome band 20p13 associated with moderate developmental delay-additional case and data's reviewAleksandra Jezela-Stanek, Marzena Kucharczyk, Magdalena Pelc, et al.
American Journal of Medical Genetics. Part A|February 21, 2012
Minimal clinical findings in a patient with 15qter microdeletion syndrome: delineation of the associated phenotypeAleksandra Jezela-Stanek, Marzena Kucharczyk, Magdalena Pelc, et al.
Clinical Dysmorphology|March 7, 2012
History and molecular characteristics of a patient with terminal deletion of 14q. Is this another syndrome with a striking phenotype?Aleksandra Jezela-Stanek, Marzena Kucharczyk, Anna Gutkowska, et al.
Ginekologia Polska|October 24, 2015
Trends in prenatal diagnosis of non-specific multiple malformations disorders with reference to the own experience and research study on Smith-Lemli-Opitz syndromeAleksandra Jezela-Stanek, Ewa Małunowicz, Siejka Anna, et al.
American Journal of Medical Genetics. Part A|August 12, 2014
The first case of a patient with de novo partial distal 16q tetrasomy and a data's reviewMarzena Kucharczyk, Andrzej Kochański, Aleksandra Jezela-Stanek, et al.
Biomedical Papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia|February 19, 2015
Oculocutaneous albinism in a patient with 17p13.2-pter duplication - a review on the molecular syndromology of 17p13 duplicationMarzena Kucharczyk, Aleksandra Jezela-Stanek, Dorota Gieruszczak-Bialek, et al.
Journal of Inorganic Biochemistry|December 8, 2009
Cu(II) ion interaction with teicoplanin-vancomycin's analogMagdalena Brzezowska, Marzena Kucharczyk-Klamińska, Francesca Bernardi, et al.
American Journal of Medical Genetics. Part A|April 1, 2016
Additional data on the clinical phenotype of Helsmoortel-Van der Aa syndrome associated with a novel truncating mutation in ADNP geneMałgorzata Krajewska-Walasek, Dorota Jurkiewicz, Dorota Piekutowska-Abramczuk, et al.
Bioinorganic Chemistry and Applications|March 13, 2010
DNA oxidative cleavage induced by the novel peptide derivatives of 3-(quinoxalin-6-yl)alanine in combination with Cu(II) or Fe(II) ionsWojciech Szczepanik, Marzena Kucharczyk-Klamińska, Piotr Stefanowicz, et al.
Pageof 2