Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Wilson Castillo-Tandazo"'
Autor:
Paul Schutzmeier, Augusto Focil Baquerizo, Wilson Castillo-Tandazo, Nicholas Focil, Stephan Bose-O’Reilly
Publikováno v:
Environmental Health, Vol 17, Iss 1, Pp 1-15 (2018)
Abstract Background Chronic mercury intoxication is a severe health issue and occurs especially in gold mining communities. Common chelators used for improving mercury elimination are not everywhere available and challenged by poor cell wall penetrat
Externí odkaz:
https://doaj.org/article/046104dd88664d84b582ae440ea34e7f
Autor:
Wilson Castillo-Tandazo, Monique F Smeets, Vincent Murphy, Rui Liu, Charlotte Hodson, Jörg Heierhorst, Andrew J Deans, Carl R Walkley
Publikováno v:
PLoS Genetics, Vol 15, Iss 7, p e1008266 (2019)
Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive disorder characterized by skin rash (poikiloderma), skeletal dysplasia, small stature, juvenile cataracts, sparse or absent hair, and predisposition to specific malignancies such as osteos
Externí odkaz:
https://doaj.org/article/01bd7b3d2de84365b18d2557fe19cc5a
Publikováno v:
Experimental Hematology. 82:1-7
Acute lymphoblastic leukemia (ALL) is the most common childhood cancer. Therapies for pediatric ALL have improved such that more than 80% of patients survive to 5 years post-therapy, and most survive to adulthood. These ALL patients experience long-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e04b4d7e3a94f3d9785056f81cc54866
https://doi.org/10.1016/j.exphem.2020.01.010
https://doi.org/10.1016/j.exphem.2020.01.010
Publikováno v:
Current Osteoporosis Reports. 17:343-352
Purpose of Review Osteosarcoma (OS) is the most common cancer of bone, yet is classified as a rare cancer. Treatment and outcomes for OS have not substantively changed in several decades. While the decoding of the OS genome greatly advanced the under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d0e118fc05a6139f3e92157df0c9685
https://doi.org/10.1007/s11914-019-00534-w
https://doi.org/10.1007/s11914-019-00534-w
Publikováno v:
Mol Cell Biol
Rothmund-Thomson syndrome (RTS) is an autosomal recessive disorder characterized by defects in the skeletal system, such as bone hypoplasia, short stature, low bone mass, and an increased incidence of osteosarcoma. RTS type 2 patients have germ line
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::460a7914d9d2415214e911fd4caa480f
https://pubmed.ncbi.nlm.nih.gov/33361189
https://pubmed.ncbi.nlm.nih.gov/33361189
Rothmund-Thomson Syndrome (RTS) is an autosomal recessive disorder characterized by poikiloderma, sparse or absent hair, and defects in the skeletal system such as bone hypoplasia, short stature, low bone mass, and an increased incidence of osteosarc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9dcfab24a0fd1a0d325910115205ec2
https://doi.org/10.1101/2020.11.11.379214
https://doi.org/10.1101/2020.11.11.379214
Autor:
Carl R. Walkley, Wilson Castillo-Tandazo, Anthony J. Mutsaers, Mannu K Walia, Thomas J. Martin
Publikováno v:
Journal of Cellular Biochemistry. 119:4241-4250
Osteosarcoma (OS) is the most common cancer of bone in children and young adults. Despite extensive research efforts, there has been no significant improvement in patient outcome for many years. An improved understanding of the biology of this cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a6f14270f9fb4d002d23c58fb984b75
https://doi.org/10.1002/jcb.26601
https://doi.org/10.1002/jcb.26601
Autor:
Joerg Heierhorst, Rui Liu, Monique Smeets, Charlotte Hodson, Carl R. Walkley, Wilson Castillo-Tandazo, Vincent J. Murphy, Andrew J. Deans
Publikováno v:
PLoS Genetics, Vol 15, Iss 7, p e1008266 (2019)
PLoS Genetics
PLoS Genetics
Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive disorder characterized by skin rash (poikiloderma), skeletal dysplasia, small stature, juvenile cataracts, sparse or absent hair, and predisposition to specific malignancies such as osteos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::634fde3ff33dc7dce1ce22cfa04ae38d
https://doaj.org/article/01bd7b3d2de84365b18d2557fe19cc5a
https://doaj.org/article/01bd7b3d2de84365b18d2557fe19cc5a
3059 – PROTEIN TRUNCATING, BUT NOT HELICASE INACTIVATING, RECQL4 MUTATIONS CAUSE BONE MARROW FAILURE
Publikováno v:
Experimental Hematology. 88:S56
Rothmund-Thomson Syndrome (RTS) is a rare autosomal recessive disorder characterized by skin rash, skeletal dysplasias, premature ageing, and caused by mutations in RECQL4. RTS is a familial cancer syndrome, with hematological cancers amongst the mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b91c25c185ec8878c6be26ae4772a9c2
https://doi.org/10.1016/j.exphem.2020.09.076
https://doi.org/10.1016/j.exphem.2020.09.076
Autor:
Wilson Castillo-Tandazo, Stephan Bose-O'Reilly, Augusto Focil Baquerizo, Nicholas Focil, Paul Schutzmeier
Publikováno v:
Environmental Health
Environmental Health, Vol 17, Iss 1, Pp 1-15 (2018)
Environmental Health, Vol 17, Iss 1, Pp 1-15 (2018)
BACKGROUND: Chronic mercury intoxication is a severe health issue and occurs especially in gold mining communities. Common chelators used for improving mercury elimination are not everywhere available and challenged by poor cell wall penetration. Thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87452eade510e0fa9682486463983121
https://zenodo.org/record/1412030
https://zenodo.org/record/1412030