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Astrobiology
|
January 30, 2018
The UK Centre for Astrobiology: A Virtual Astrobiology Centre. Accomplishments and Lessons Learned, 2011-2016
Charles S Cockell, Beth Biller, Casey Bryce, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 4, 2016
mTOR Inhibitors for the Treatment of Severe Congenital Hyperinsulinism: Perspectives on Limited Therapeutic Success
Marie Szymanowski, Maria Salomon Estebanez, Raja Padidela, et al.
Diabetes
|
May 2, 2015
Altered Phenotype of β-Cells and Other Pancreatic Cell Lineages in Patients With Diffuse Congenital Hyperinsulinism in Infancy Caused by Mutations in the ATP-Sensitive K-Channel
Rachel J Salisbury, Bing Han, Rachel E Jennings, et al.
The Pharmacogenomics Journal
|
May 28, 2021
Gene expression signatures predict response to therapy with growth hormone
Adam Stevens, Philip Murray, Chiara De Leonibus, et al.
Cell Death & Disease
|
October 21, 2020
EVI1 phosphorylation at S436 regulates interactions with CtBP1 and DNMT3A and promotes self-renewal
Roberto Paredes, James R Kelly, Bethany Geary, et al.
Nucleic Acids Research
|
August 14, 2018
Erratum: EVI1 carboxy-terminal phosphorylation is ATM-mediated and sustains transcriptional modulation and self-renewal via enhanced CtBP1 association
Roberto Paredes, Marion Schneider, Adam Stevens, et al.
Nucleic Acids Research
|
June 26, 2018
EVI1 carboxy-terminal phosphorylation is ATM-mediated and sustains transcriptional modulation and self-renewal via enhanced CtBP1 association
Roberto Paredes, Marion Schneider, Adam Stevens, et al.
Cell Death & Disease
|
June 16, 2017
Acquired cross-linker resistance associated with a novel spliced BRCA2 protein variant for molecular phenotyping of BRCA2 disruption
Stefan Meyer, Adam Stevens, Roberto Paredes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 18, 2020
A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome
Sara Cuvertino, Verity Hartill, Alice Colyer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 24, 2020
Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome
Sara Cuvertino, Verity Hartill, Alice Colyer, et al.
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Search research articles
Search
Showing results (71-80 of 80) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 80 results.
Astrobiology
|
January 30, 2018
The UK Centre for Astrobiology: A Virtual Astrobiology Centre. Accomplishments and Lessons Learned, 2011-2016
Charles S Cockell, Beth Biller, Casey Bryce, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 4, 2016
mTOR Inhibitors for the Treatment of Severe Congenital Hyperinsulinism: Perspectives on Limited Therapeutic Success
Marie Szymanowski, Maria Salomon Estebanez, Raja Padidela, et al.
Diabetes
|
May 2, 2015
Altered Phenotype of β-Cells and Other Pancreatic Cell Lineages in Patients With Diffuse Congenital Hyperinsulinism in Infancy Caused by Mutations in the ATP-Sensitive K-Channel
Rachel J Salisbury, Bing Han, Rachel E Jennings, et al.
The Pharmacogenomics Journal
|
May 28, 2021
Gene expression signatures predict response to therapy with growth hormone
Adam Stevens, Philip Murray, Chiara De Leonibus, et al.
Cell Death & Disease
|
October 21, 2020
EVI1 phosphorylation at S436 regulates interactions with CtBP1 and DNMT3A and promotes self-renewal
Roberto Paredes, James R Kelly, Bethany Geary, et al.
Nucleic Acids Research
|
August 14, 2018
Erratum: EVI1 carboxy-terminal phosphorylation is ATM-mediated and sustains transcriptional modulation and self-renewal via enhanced CtBP1 association
Roberto Paredes, Marion Schneider, Adam Stevens, et al.
Nucleic Acids Research
|
June 26, 2018
EVI1 carboxy-terminal phosphorylation is ATM-mediated and sustains transcriptional modulation and self-renewal via enhanced CtBP1 association
Roberto Paredes, Marion Schneider, Adam Stevens, et al.
Cell Death & Disease
|
June 16, 2017
Acquired cross-linker resistance associated with a novel spliced BRCA2 protein variant for molecular phenotyping of BRCA2 disruption
Stefan Meyer, Adam Stevens, Roberto Paredes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 18, 2020
A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome
Sara Cuvertino, Verity Hartill, Alice Colyer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 24, 2020
Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome
Sara Cuvertino, Verity Hartill, Alice Colyer, et al.
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