User profiles for "author:M Zatyka"
Malgorzata ZatykaInstitute of Cancer and Genomic Sciences University of Birmingham UK Verified email at bham.ac.uk Cited by 2306 |
Control of genes for conjugative transfer of plasmids and other mobile elements
Conjugative transfer is a primary means of spread of mobile genetic elements (plasmids and
transposons) between bacteria. It leads to the dissemination and evolution of the genes …
transposons) between bacteria. It leads to the dissemination and evolution of the genes …
Dysregulation of autophagy as a common mechanism in lysosomal storage diseases
E Seranova, KJ Connolly, M Zatyka… - Essays in …, 2017 - portlandpress.com
The lysosome plays a pivotal role between catabolic and anabolic processes as the nexus
for signalling pathways responsive to a variety of factors, such as growth, nutrient …
for signalling pathways responsive to a variety of factors, such as growth, nutrient …
Epigenetic Inactivation of the RASSF1A 3p21.3 Tumor Suppressor Gene in Both Clear Cell and Papillary Renal Cell Carcinoma
Renal cell carcinoma (RCC), the most common adult kidney neoplasm, is
histopathologically heterogeneous, with most sporadic RCCs (∼ 80%) classified as clear …
histopathologically heterogeneous, with most sporadic RCCs (∼ 80%) classified as clear …
The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation
…, U Leimer, D Bartsch, M Zatyka… - Proceedings of the …, 2002 - National Acad Sciences
In the last few years, several genes involved in X-specific mental retardation (MR) have
been identified by using genetic analysis. Although it is likely that additional genes …
been identified by using genetic analysis. Although it is likely that additional genes …
Conjugative-DNA transfer processes
EL Zechner*, F. de la Cruz, R. Eisenbrandt, AM Grahn, G. Koraimann, E. Lanka*, G. Muth, W.
Pansegrau, CM Thomas, BM Wilkins and M. Zatyka3. 1. IntroductionConjugation is the …
Pansegrau, CM Thomas, BM Wilkins and M. Zatyka3. 1. IntroductionConjugation is the …
Identification of cyclin D1 and other novel targets for the von Hippel-Lindau tumor suppressor gene by expression array analysis and investigation of cyclin D1 …
Germ-line mutations in the von Hippel-Lindau (VHL) tumor suppressor disease are
associatedwith a high risk of retinal and cerebellar hemangioblastomas, renalcell carcinoma …
associatedwith a high risk of retinal and cerebellar hemangioblastomas, renalcell carcinoma …
[HTML][HTML] Autophagy in rare (nonlysosomal) neurodegenerative diseases
Neurodegenerative diseases (NDDs) comprise conditions with impaired neuronal function
and loss and may be associated with a build-up of aggregated proteins with altered …
and loss and may be associated with a build-up of aggregated proteins with altered …
Sulfate and thiosulfate transport in Escherichia coli K-12: evidence for a functional overlapping of sulfate-and thiosulfate-binding proteins
In Escherichia coli, sulfate and thiosulfate ions are transported by an ABC-type transporter
consisting of both the membrane components (the products of cysT, cysW, and cysA genes) …
consisting of both the membrane components (the products of cysT, cysW, and cysA genes) …
Sodium-potassium ATPase β1 subunit is a molecular partner of Wolframin, an endoplasmic reticulum protein involved in ER stress
Wolfram syndrome, an autosomal recessive disorder characterized by diabetes mellitus and
optic atrophy, is caused by mutations in the WFS1 gene encoding an endoplasmic reticulum …
optic atrophy, is caused by mutations in the WFS1 gene encoding an endoplasmic reticulum …
Microarray based analysis of 3p25‐p26 deletions (3p‐syndrome)
…, RM Barber, F Rahman, M Zatyka… - American Journal of …, 2009 - Wiley Online Library
Distal deletion of chromosome 3p25‐pter (3p‐syndrome) produces a distinct clinical
syndrome characterized by low birth weight, mental retardation, telecanthus, ptosis, and …
syndrome characterized by low birth weight, mental retardation, telecanthus, ptosis, and …