Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Jeffrey D Goldsmith"'
Autor:
Panagiotis A Konstantinopoulos, Elena Fountzilas, Jeffrey D Goldsmith, Manoj Bhasin, Kamana Pillay, Nancy Francoeur, Towia A Libermann, Mark C Gebhardt, Dimitrios Spentzos
Publikováno v:
PLoS ONE, Vol 5, Iss 4, p e9747 (2010)
BACKGROUND: Diagnosis of soft tissue sarcomas (STS) is challenging. Many remain unclassified (not-otherwise-specified, NOS) or grouped in controversial categories such as malignant fibrous histiocytoma (MFH), with unclear therapeutic value. We analyz
Externí odkaz:
https://doaj.org/article/1287b21eeb1b4f89a0bf4c17e502a4e7
Autor:
Amy E. O’Connell, Sathuwarman Raveenthiraraj, Luiz Fernando Silva Oliveira, Comfort Adegboye, Venkata Siva Dasuri, Wanshu Qi, Radhika S. Khetani, Akaljot Singh, Nambirajam Sundaram, Jasmine Lin, Prathima Nandivada, Lorena Rincón-Cruz, Jeffrey D. Goldsmith, Jay R. Thiagarajah, Diana L. Carlone, Jerrold R. Turner, Pankaj B. Agrawal, Michael Helmrath, David T. Breault
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 18, Iss 2, Pp 101349- (2024)
Background & aims: Humans with WNT2B deficiency have severe intestinal disease, including significant inflammatory injury, highlighting a critical role for WNT2B. We sought to understand how WNT2B contributes to intestinal homeostasis. Methods: We in
Externí odkaz:
https://doaj.org/article/73ecaa07cd064534a6b295fa2a02c92d
Autor:
Meri Kalashyan, Krishnan Raghunathan, Haley Oller, Marie-Theres Bayer, Lissette Jimenez, Joseph T. Roland, Elena Kolobova, Susan J. Hagen, Jeffrey D. Goldsmith, Mitchell D. Shub, James R. Goldenring, Izumi Kaji, Jay R. Thiagarajah
Publikováno v:
The Journal of Clinical Investigation, Vol 133, Iss 20 (2023)
Microvillus inclusion disease (MVID), caused by loss-of-function mutations in the motor protein myosin Vb (MYO5B), is a severe infantile disease characterized by diarrhea, malabsorption, and acid/base instability, requiring intensive parenteral suppo
Externí odkaz:
https://doaj.org/article/c92ae08826724d77b38d9aae71d0c007
Autor:
Katherine Culbreath, Gregory Keefe, Emily Nes, Steven J. Staffa, Alexandra N. Carey, Tom Jaksic, Jeffrey D. Goldsmith, Biren P. Modi, Jodie D. Ouahed, Lissette Jimenez
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 76:468-474
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6507c6f022afb98bd6536465f748e808
https://doi.org/10.1097/mpg.0000000000003718
https://doi.org/10.1097/mpg.0000000000003718
Autor:
Beate C. Beinvogl, Jeffrey D. Goldsmith, Ramalingam Arumugam, Michelle Kennedy, Mani Mokalla, Paul A. Rufo, Menno Verhave
Publikováno v:
Case Reports in Pediatrics, Vol 2020 (2020)
A two-and-one-half-year-old previously healthy female presented with a ten-week history of watery diarrhea, nonbilious and nonbloody emesis, and low-grade fevers. She was found to have severe hypoalbuminemia and hypogammaglobulinemia. Her symptoms pe
Externí odkaz:
https://doaj.org/article/e124f5ad690940b39757aa4ff787650e
Autor:
Amy E. O’Connell, Sathuwarman Raveenthiraraj, Comfort Adegboye, Wanshu Qi, Radhika S. Khetani, Akaljot Singh, Nambirajam Sundaram, Chidera Emeonye, Jasmine Lin, Jeffrey D. Goldsmith, Jay R. Thiagarajah, Diana L. Carlone, Jerrold R. Turner, Pankaj B. Agrawal, Michael Helmrath, David T. Breault
Publikováno v:
bioRxiv
Background and aimsWNT2B is a canonical Wnt ligand previously thought to be fully redundant with other Wnts in the intestinal epithelium. However, humans with WNT2B deficiency have severe intestinal disease, highlighting a critical role for WNT2B. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f32e2c49e942178dbaff1d00bcd608e
https://doi.org/10.1101/2023.04.21.537894
https://doi.org/10.1101/2023.04.21.537894
Autor:
Victor L, Fox, Inbar S, Spofford, Brian D, Crompton, Mathew B, Yurgelun, Craig W, Lillehei, Jeffrey D, Goldsmith
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 75:e49-e52
Serrated polyps are pathological neoplastic lesions in the colon with subtle gross morphology leading to underreporting during colonoscopy. While detection rates are increasing in average-risk adult screening colonoscopy, the rate of detection during
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a23b876ae847d0640261fafb9e908f01
https://doi.org/10.1097/mpg.0000000000003546
https://doi.org/10.1097/mpg.0000000000003546
Autor:
Katelyn, Dannheim, Jodie, Ouahed, Michael, Field, Scott, Snapper, Bram P, Raphael, Sarah C, Glover, Phyllis R, Bishop, Natalie, Bhesania, Daniel, Kamin, Jay, Thiagarajah, Jeffrey D, Goldsmith
Publikováno v:
Am J Surg Pathol
Mutations in the tetratricopeptide repeat domain 7A (TTC7A) gene are a rare cause of congenital enteropathy that can result in significant morbidity. TTC7A deficiency leads to disruption of the intestinal epithelium. The histopathology of this condit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d035a8b52c80bb95375dc483d4ee16e7
https://doi.org/10.1097/pas.0000000000001856
https://doi.org/10.1097/pas.0000000000001856
Autor:
Meri Kalashyan, Krishnan Raghunathan, Haley Oller, Marie-Bayer Theres, Lissette Jimenez, Joseph T. Roland, Elena Kolobova, Susan J Hagen, Jeffrey D. Goldsmith, Mitchell D. Shub, James R. Goldenring, Izumi Kaji, Jay R. Thiagarajah
Publikováno v:
bioRxiv
Microvillus Inclusion Disease (MVID), caused by loss-of-function mutations in the motor protein Myosin Vb (MYO5B), is a severe infantile disease characterized by diarrhea, malabsorption, and acid-base instability, requiring intensive parenteral suppo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90d81b0c39f873291cb28607e6bfb76d
https://europepmc.org/articles/PMC9900906/
https://europepmc.org/articles/PMC9900906/
Autor:
Sonja, Chen, Jeffrey D, Goldsmith, Rima, Fawaz, Alyaa, Al-Ibraheemi, Antonio R, Perez-Atayde, Sara O, Vargas
Publikováno v:
The American journal of surgical pathology. 45(8)
Congenital tufting enteropathy (CTE) is a rare heritable cause of intractable diarrhea due to EPCAM mutation. Pathologic findings include intestinal villous atrophy, tufted discohesive tear-drop-shaped epithelium, and a normal brush border. In affect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::94e393432cb331184ed76a019785f9ff
https://pubmed.ncbi.nlm.nih.gov/33756496
https://pubmed.ncbi.nlm.nih.gov/33756496