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October 9, 2024
Rapid identification of primary atopic disorders (PAD) by a clinical landmark-guided, upfront use of genomic sequencing
Tim Niehues, Sandra von Hardenberg, Eunike Velleuer
The Journal of Nutritional Biochemistry
|
November 28, 2017
ApoE is a major determinant of hepatic bile acid homeostasis in mice
Sandra von Hardenberg, Carsten Gnewuch, Gerd Schmitz, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
Diagnostic genomic sequencing in critically ill children
Bernd Auber, Gunnar Schmidt, Chen Du, et al.
Frontiers in Pediatrics
|
June 5, 2023
A holistic approach to maximise diagnostic output in trio exome sequencing
Sandra von Hardenberg, Hannah Wallaschek, Chen Du, et al.
Oncotarget
|
June 17, 2015
Leupaxin stimulates adhesion and migration of prostate cancer cells through modulation of the phosphorylation status of the actin-binding protein caldesmon
Sascha Dierks, Sandra von Hardenberg, Thomas Schmidt, et al.
Clinical Immunology (Orlando, Fla.)
|
April 24, 2025
A novel hemizygous nonsense variant in DOCK11 causes systemic inflammation and immunodeficiency
Abdulwahab Elsayed, Sandra von Hardenberg, Faranaz Atschekzei, et al.
Frontiers in Pediatrics
|
April 25, 2024
Current genetic diagnostics in inborn errors of immunity
Sandra von Hardenberg, Isabel Klefenz, Doris Steinemann, et al.
The Journal of Allergy and Clinical Immunology
|
June 12, 2024
Phenotypic and pathomechanistic overlap between tapasin and TAP deficiencies
Abdulwahab Elsayed, Sandra von Hardenberg, Faranaz Atschekzei, et al.
Journal of the Peripheral Nervous System : JPNS
|
January 19, 2026
Broadening the Clinical Spectrum of Axonal Hereditary Neuropathies: A Comparative Case Study on DNAJB2- and HINT1-Related Disease
Bogdan Bjelica, Corinna Hendrich, Sandra von Hardenberg, et al.
RMD Open
|
July 3, 2026
Rare variants in genes related to inborn errors of immunity in patients with rheumatoid arthritis and secondary immunodeficiency
Faranaz Atschekzei, Natalia Dubrowinskaja, Manfred Anim, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 38) with videos related to
Sort By:
Page
of 4
Allergologie Select
|
October 9, 2024
Rapid identification of primary atopic disorders (PAD) by a clinical landmark-guided, upfront use of genomic sequencing
Tim Niehues, Sandra von Hardenberg, Eunike Velleuer
The Journal of Nutritional Biochemistry
|
November 28, 2017
ApoE is a major determinant of hepatic bile acid homeostasis in mice
Sandra von Hardenberg, Carsten Gnewuch, Gerd Schmitz, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
Diagnostic genomic sequencing in critically ill children
Bernd Auber, Gunnar Schmidt, Chen Du, et al.
Frontiers in Pediatrics
|
June 5, 2023
A holistic approach to maximise diagnostic output in trio exome sequencing
Sandra von Hardenberg, Hannah Wallaschek, Chen Du, et al.
Oncotarget
|
June 17, 2015
Leupaxin stimulates adhesion and migration of prostate cancer cells through modulation of the phosphorylation status of the actin-binding protein caldesmon
Sascha Dierks, Sandra von Hardenberg, Thomas Schmidt, et al.
Clinical Immunology (Orlando, Fla.)
|
April 24, 2025
A novel hemizygous nonsense variant in DOCK11 causes systemic inflammation and immunodeficiency
Abdulwahab Elsayed, Sandra von Hardenberg, Faranaz Atschekzei, et al.
Frontiers in Pediatrics
|
April 25, 2024
Current genetic diagnostics in inborn errors of immunity
Sandra von Hardenberg, Isabel Klefenz, Doris Steinemann, et al.
The Journal of Allergy and Clinical Immunology
|
June 12, 2024
Phenotypic and pathomechanistic overlap between tapasin and TAP deficiencies
Abdulwahab Elsayed, Sandra von Hardenberg, Faranaz Atschekzei, et al.
Journal of the Peripheral Nervous System : JPNS
|
January 19, 2026
Broadening the Clinical Spectrum of Axonal Hereditary Neuropathies: A Comparative Case Study on DNAJB2- and HINT1-Related Disease
Bogdan Bjelica, Corinna Hendrich, Sandra von Hardenberg, et al.
RMD Open
|
July 3, 2026
Rare variants in genes related to inborn errors of immunity in patients with rheumatoid arthritis and secondary immunodeficiency
Faranaz Atschekzei, Natalia Dubrowinskaja, Manfred Anim, et al.
Page
of 4