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European Journal of Human Genetics : EJHG
|
August 19, 2010
Characterization of novel SLC6A8 variants with the use of splice-site analysis tools and implementation of a newly developed LOVD database
Ofir T Betsalel, Efraim H Rosenberg, Ligia S Almeida, et al.
Oncotarget
|
September 20, 2014
Splice variant transcripts of the anterior gradient 2 gene as a marker of prostate cancer
Antje Neeb, Simon Hefele, Stefanie Bormann, et al.
American Journal of Human Genetics
|
December 24, 2019
Pathogenic Bi-allelic Mutations in NDUFAF8 Cause Leigh Syndrome with an Isolated Complex I Deficiency
Charlotte L Alston, Mike T Veling, Juliana Heidler, et al.
Oncotarget
|
January 28, 2016
Prostate extracellular vesicles in patient plasma as a liquid biopsy platform for prostate cancer using nanoscale flow cytometry
Colleen N Biggs, Khurram M Siddiqui, Ali A Al-Zahrani, et al.
Nature Communications
|
May 27, 2024
Proteomic analysis of the urothelial cancer landscape
Franz F Dressler, Falk Diedrichs, Deema Sabtan, et al.
Mabs
|
February 28, 2018
When monoclonal antibodies are not monospecific: Hybridomas frequently express additional functional variable regions
Andrew R M Bradbury, Nathan D Trinklein, Holger Thie, et al.
Nature Medicine
|
May 20, 2014
Neutrophil granulocytes recruited upon translocation of intestinal bacteria enhance graft-versus-host disease via tissue damage
Lukas Schwab, Luise Goroncy, Senthilnathan Palaniyandi, et al.
Seizure
|
January 29, 2016
Effectiveness of antiepileptic therapy in patients with PCDH19 mutations
Jan Lotte, Thomas Bast, Peter Borusiak, et al.
The Journal of Experimental Medicine
|
May 21, 2024
Correction: Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect
Tamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
The Journal of Experimental Medicine
|
May 9, 2024
Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect
Tamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
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of 8
Search research articles
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Showing results (71-80 of 80) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 80 results.
European Journal of Human Genetics : EJHG
|
August 19, 2010
Characterization of novel SLC6A8 variants with the use of splice-site analysis tools and implementation of a newly developed LOVD database
Ofir T Betsalel, Efraim H Rosenberg, Ligia S Almeida, et al.
Oncotarget
|
September 20, 2014
Splice variant transcripts of the anterior gradient 2 gene as a marker of prostate cancer
Antje Neeb, Simon Hefele, Stefanie Bormann, et al.
American Journal of Human Genetics
|
December 24, 2019
Pathogenic Bi-allelic Mutations in NDUFAF8 Cause Leigh Syndrome with an Isolated Complex I Deficiency
Charlotte L Alston, Mike T Veling, Juliana Heidler, et al.
Oncotarget
|
January 28, 2016
Prostate extracellular vesicles in patient plasma as a liquid biopsy platform for prostate cancer using nanoscale flow cytometry
Colleen N Biggs, Khurram M Siddiqui, Ali A Al-Zahrani, et al.
Nature Communications
|
May 27, 2024
Proteomic analysis of the urothelial cancer landscape
Franz F Dressler, Falk Diedrichs, Deema Sabtan, et al.
Mabs
|
February 28, 2018
When monoclonal antibodies are not monospecific: Hybridomas frequently express additional functional variable regions
Andrew R M Bradbury, Nathan D Trinklein, Holger Thie, et al.
Nature Medicine
|
May 20, 2014
Neutrophil granulocytes recruited upon translocation of intestinal bacteria enhance graft-versus-host disease via tissue damage
Lukas Schwab, Luise Goroncy, Senthilnathan Palaniyandi, et al.
Seizure
|
January 29, 2016
Effectiveness of antiepileptic therapy in patients with PCDH19 mutations
Jan Lotte, Thomas Bast, Peter Borusiak, et al.
The Journal of Experimental Medicine
|
May 21, 2024
Correction: Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect
Tamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
The Journal of Experimental Medicine
|
May 9, 2024
Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect
Tamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
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of 8