Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Eugenio Taboada"'
Publikováno v:
Molecular & Cellular Oncology, Vol 4, Iss 3 (2017)
The Hippo pathway is an important signaling pathway that controls cell proliferation and apoptosis. It is evolutionarily conserved in mammals and is stimulated by cell–cell contact, inhibiting cell proliferation in response to increased cell densit
Externí odkaz:
https://doaj.org/article/b99bc46ee7f34999b64ce68835421929
Autor:
Uttam Garg, Darcy K. Weidemann, Eugenio Taboada, Clarence C. Frazee, Katherine L. Kurzinski, Tarak Srivastava
Publikováno v:
Pediatric Nephrology. 36:4137-4140
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2e624bc43b2a6b3c9c7608d00ce9cde
https://doi.org/10.1007/s00467-021-05263-w
https://doi.org/10.1007/s00467-021-05263-w
Autor:
Katherine L. Kurzinski, Tarak Srivastava, Darcy K. Weidemann, Clarence C. Frazee, Uttam Garg, Eugenio Taboada
Publikováno v:
Pediatric nephrology (Berlin, Germany). 36(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e15e8db7f8fdbfdf411b772f78c56ab6
https://pubmed.ncbi.nlm.nih.gov/34606003
https://pubmed.ncbi.nlm.nih.gov/34606003
Publikováno v:
Pediatr Allergy Immunol Pulmonol
Glomus tumors (GTs) are rare, usually benign, mesenchymal neoplasms typically located in the cutaneous tissues of the extremities. Visceral locations have been reported in ∼5% of cases. The average age at diagnosis is 42 years. GTs originating in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9072404941ce65593558c51d939bab83
https://europepmc.org/articles/PMC7057049/
https://europepmc.org/articles/PMC7057049/
Publikováno v:
Journal of pediatric and adolescent gynecology. 32(5)
Background Turner syndrome is a genetic disorder resulting from the absence of or structural abnormality of one X chromosome. The presence of Y chromosome material in girls with Turner syndrome confers an increased risk of benign and malignant germ c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91da64e931686af0a2cfb788ed8a0d5b
https://pubmed.ncbi.nlm.nih.gov/31279777
https://pubmed.ncbi.nlm.nih.gov/31279777
Autor:
Katherine M Chastain, Terrie G Flatt, Atif A. Ahmed, John Herriges, Linda D. Cooley, Eugenio Taboada, Robert E. Garola, Laura C. McCarthy
Publikováno v:
Journal of pediatric hematology/oncology. 41(8)
Neuroblastoma (NB) in children older than 10 years is rare. We reviewed our archives for patients with NB aged 10 to 18 years and summarized their clinicopathologic/genetic records. Of 96 patients, 4 patients were identified in this age group. Four t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a608932df52093bdde7bf653095fb152
https://pubmed.ncbi.nlm.nih.gov/30973487
https://pubmed.ncbi.nlm.nih.gov/30973487
Autor:
Jean Baptiste Lepichon, Xinping Liu, Laurie D. Smith, Richard W. Gross, Stephen F. Kingsmore, Eugenio Taboada, Keith A. Coffman, Carol J Saunders, Margaret Gibson, Emily G. Farrow, Isabelle Thiffault, Neil A. Miller, Melanie Patterson, Sung Ho Moon
Publikováno v:
Human Mutation. 36:301-306
Mitochondriopathies are a group of clinically heterogeneous genetic diseases caused by defects in mitochondrial metabolism, bioenergetic efficiency, and/or signaling functions. The large majority of proteins involved in mitochondrial function are enc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6a479735dc47174583b9236f0d31db9
https://doi.org/10.1002/humu.22743
https://doi.org/10.1002/humu.22743
Autor:
Carol J Saunders, Nicole P. Safina, Sultan Habeebu, Isabelle Thiffault, Priya Skaria, Eugenio Taboada, Alex Kats, Atif A. Ahmed
Publikováno v:
American journal of medical genetics. Part A. 176(2)
Arthrogryposis multiplex congenita affects approximately 1 in 3,000 individuals of different ethnic backgrounds and displays an equal incidence in males and females. The underlying mechanism for congenital contracture of the joints is decreased fetal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f14ef99d4e776eafcddc0c6e574eeb6
https://pubmed.ncbi.nlm.nih.gov/29274205
https://pubmed.ncbi.nlm.nih.gov/29274205
Autor:
Sarah Mc Dermott, Elena Repnikova, Midhat S. Farooqi, Weijie Li, Nazia Tabassum Iqbal, Jdl Nolen, Eugenio Taboada, Jennifer Roberts, Michael Silvey
Publikováno v:
Pathology - Research and Practice. 215:152578
Epsilon gamma delta beta (eγδβ)0 - thalassemia is a very rare disorder that results from large deletions in the β-globin gene cluster which abolish all regional globin chain gene expression from that allele. Since it is an exceedingly rare cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::983be5a65d29c0f0b347100725eca496
https://doi.org/10.1016/j.prp.2019.152578
https://doi.org/10.1016/j.prp.2019.152578
Publikováno v:
Human Pathology. 37:914-918
Papillary glioneuronal tumor is a recently described central nervous system neoplasm that almost always occurs adjacent to the lateral ventricle. We present a case of this rare entity, representing the 21st case of this lesion, which exhibits a mixed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d25c51700aa427b90b2431294d28286
https://doi.org/10.1016/j.humpath.2006.01.031
https://doi.org/10.1016/j.humpath.2006.01.031