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Blood
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July 15, 2004
A requirement for Notch1 distinguishes 2 phases of definitive hematopoiesis during development
Brandon K Hadland, Stacey S Huppert, Jyotshnabala Kanungo, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
February 2, 2018
Transcription factor GATA6: a novel marker and putative inducer of ductal metaplasia in biliary atresia
Tea Soini, Marjut Pihlajoki, Noora Andersson, et al.
Hepatology (Baltimore, Md.)
|
August 31, 2019
Sox9 Is a Modifier of the Liver Disease Severity in a Mouse Model of Alagille Syndrome
Joshua M Adams, Kari A Huppert, Eumenia C Castro, et al.
Nano Letters
|
September 17, 2014
Terahertz generation by dynamical photon drag effect in graphene excited by femtosecond optical pulses
J Maysonnave, S Huppert, F Wang, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
April 23, 2024
BiliQML: a supervised machine-learning model to quantify biliary forms from digitized whole slide liver histopathological images
Dominick J Hellen, Meredith E Fay, David H Lee, et al.
Hepatology (Baltimore, Md.)
|
April 6, 2023
ASO silencing of a glycosyltransferase, Poglut1 , improves the liver phenotypes in mouse models of Alagille syndrome
Nima Niknejad, Duncan Fox, Jennifer L Burwinkel, et al.
Cell Reports
|
May 24, 2016
Identification of a Paralog-Specific Notch1 Intracellular Domain Degron
Matthew R Broadus, Tony W Chen, Leif R Neitzel, et al.
Neoplasia (New York, N.Y.)
|
January 12, 2013
CITED1 expression in liver development and hepatoblastoma
Andrew J Murphy, Christian de Caestecker, Janene Pierce, et al.
Gastroenterology
|
May 30, 2025
Adeno-associated Virus-mediated Silencing of Sox4 Leads to Long-Term Amelioration of Liver Phenotypes in Mouse Models of Alagille Syndrome
Duncan Fox, Jun Xie, Jennifer L Burwinkel, et al.
Stem Cell Reports
|
January 15, 2021
Modeling Human Bile Acid Transport and Synthesis in Stem Cell-Derived Hepatocytes with a Patient-Specific Mutation
Hisamitsu Hayashi, Shuhei Osaka, Kokoro Sakabe, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 85) with videos related to
Sort By:
Page
of 9
Blood
|
July 15, 2004
A requirement for Notch1 distinguishes 2 phases of definitive hematopoiesis during development
Brandon K Hadland, Stacey S Huppert, Jyotshnabala Kanungo, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
February 2, 2018
Transcription factor GATA6: a novel marker and putative inducer of ductal metaplasia in biliary atresia
Tea Soini, Marjut Pihlajoki, Noora Andersson, et al.
Hepatology (Baltimore, Md.)
|
August 31, 2019
Sox9 Is a Modifier of the Liver Disease Severity in a Mouse Model of Alagille Syndrome
Joshua M Adams, Kari A Huppert, Eumenia C Castro, et al.
Nano Letters
|
September 17, 2014
Terahertz generation by dynamical photon drag effect in graphene excited by femtosecond optical pulses
J Maysonnave, S Huppert, F Wang, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
April 23, 2024
BiliQML: a supervised machine-learning model to quantify biliary forms from digitized whole slide liver histopathological images
Dominick J Hellen, Meredith E Fay, David H Lee, et al.
Hepatology (Baltimore, Md.)
|
April 6, 2023
ASO silencing of a glycosyltransferase, Poglut1 , improves the liver phenotypes in mouse models of Alagille syndrome
Nima Niknejad, Duncan Fox, Jennifer L Burwinkel, et al.
Cell Reports
|
May 24, 2016
Identification of a Paralog-Specific Notch1 Intracellular Domain Degron
Matthew R Broadus, Tony W Chen, Leif R Neitzel, et al.
Neoplasia (New York, N.Y.)
|
January 12, 2013
CITED1 expression in liver development and hepatoblastoma
Andrew J Murphy, Christian de Caestecker, Janene Pierce, et al.
Gastroenterology
|
May 30, 2025
Adeno-associated Virus-mediated Silencing of Sox4 Leads to Long-Term Amelioration of Liver Phenotypes in Mouse Models of Alagille Syndrome
Duncan Fox, Jun Xie, Jennifer L Burwinkel, et al.
Stem Cell Reports
|
January 15, 2021
Modeling Human Bile Acid Transport and Synthesis in Stem Cell-Derived Hepatocytes with a Patient-Specific Mutation
Hisamitsu Hayashi, Shuhei Osaka, Kokoro Sakabe, et al.
Page
of 9