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International Journal of Molecular Sciences
|
August 10, 2024
Rare Germline Variants in the Adenomatous Polyposis Coli Gene Associated with Dental and Osseous Anomalies
Gergely Büki, Gréta Antal, Judit Bene
Current Molecular Medicine
|
April 11, 2023
Microhomology-Mediated Break-Induced Replication: A Possible Molecular Mechanism of the Formation of a Large CNV in <i>FBN1</i> Gene in a Patient with Marfan Syndrome
Gergely Buki, Kinga Hadzsiev, Judit Bene
Nutrition & Diabetes
|
March 18, 2018
Role of carnitine and its derivatives in the development and management of type 2 diabetes
Judit Bene, Kinga Hadzsiev, Bela Melegh
International Journal of Molecular Sciences
|
September 28, 2023
Copy Number Variations in Neuropsychiatric Disorders
Gergely Büki, Kinga Hadzsiev, Judit Bene
Frontiers in Genetics
|
April 22, 2022
Editorial: Copy Number Variation in Rare Disorders
Katalin Komlósi, Attila Gyenesei, Judit Bene
Current Molecular Medicine
|
November 16, 2019
Mass Spectrometric Analysis of L-carnitine and its Esters: Potential Biomarkers of Disturbances in Carnitine Homeostasis
Judit Bene, Andras Szabo, Katalin Komlósi, et al.
Advances in Experimental Medicine and Biology
|
May 22, 2003
Mapping of possible laminin binding sites of Y. pestis plasminogen activator (Pla) via phage display
Orsolya Benedek, Judit Bene, Béla Melegh, et al.
Scandinavian Journal of Clinical and Laboratory Investigation
|
March 4, 2011
Dynamic adaptive changes of the serum carnitine esters during and after L-carnitine supplementation in patients with maintenance haemodialysis
Judit Bene, Botond Csiky, Katalin Komlosi, et al.
Molecular Genetics and Metabolism Reports
|
March 12, 2024
Importance and application of WES in fetal genetic diagnostics: Identification of novel <i>ASPM</i> mutation in a fetus with microcephaly
Renata Szalai, Agnes Till, Attila Gyenesei, et al.
European Journal of Human Genetics : EJHG
|
May 8, 2003
Congenital cataract as the first symptom of a neuromuscular disease caused by a novel single large-scale mitochondrial DNA deletion
Judit Bene, Edit Nádasi, György Kosztolányi, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 77) with videos related to
Sort By:
Page
of 8
International Journal of Molecular Sciences
|
August 10, 2024
Rare Germline Variants in the Adenomatous Polyposis Coli Gene Associated with Dental and Osseous Anomalies
Gergely Büki, Gréta Antal, Judit Bene
Current Molecular Medicine
|
April 11, 2023
Microhomology-Mediated Break-Induced Replication: A Possible Molecular Mechanism of the Formation of a Large CNV in <i>FBN1</i> Gene in a Patient with Marfan Syndrome
Gergely Buki, Kinga Hadzsiev, Judit Bene
Nutrition & Diabetes
|
March 18, 2018
Role of carnitine and its derivatives in the development and management of type 2 diabetes
Judit Bene, Kinga Hadzsiev, Bela Melegh
International Journal of Molecular Sciences
|
September 28, 2023
Copy Number Variations in Neuropsychiatric Disorders
Gergely Büki, Kinga Hadzsiev, Judit Bene
Frontiers in Genetics
|
April 22, 2022
Editorial: Copy Number Variation in Rare Disorders
Katalin Komlósi, Attila Gyenesei, Judit Bene
Current Molecular Medicine
|
November 16, 2019
Mass Spectrometric Analysis of L-carnitine and its Esters: Potential Biomarkers of Disturbances in Carnitine Homeostasis
Judit Bene, Andras Szabo, Katalin Komlósi, et al.
Advances in Experimental Medicine and Biology
|
May 22, 2003
Mapping of possible laminin binding sites of Y. pestis plasminogen activator (Pla) via phage display
Orsolya Benedek, Judit Bene, Béla Melegh, et al.
Scandinavian Journal of Clinical and Laboratory Investigation
|
March 4, 2011
Dynamic adaptive changes of the serum carnitine esters during and after L-carnitine supplementation in patients with maintenance haemodialysis
Judit Bene, Botond Csiky, Katalin Komlosi, et al.
Molecular Genetics and Metabolism Reports
|
March 12, 2024
Importance and application of WES in fetal genetic diagnostics: Identification of novel <i>ASPM</i> mutation in a fetus with microcephaly
Renata Szalai, Agnes Till, Attila Gyenesei, et al.
European Journal of Human Genetics : EJHG
|
May 8, 2003
Congenital cataract as the first symptom of a neuromuscular disease caused by a novel single large-scale mitochondrial DNA deletion
Judit Bene, Edit Nádasi, György Kosztolányi, et al.
Page
of 8