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Daniela Gasperikova

Showing results (41-50 of 46) with videos related to

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Plos One|May 5, 2017
Genetic analysis of single-minded 1 gene in early-onset severely obese children and adolescentsDaniela Stanikova, Marek Buzga, Patrik Krumpolec, et al.
Human Genetics|February 11, 2015
Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing lossGowri Nayak, Lukas Varga, Claire Trincot, et al.
Molecular Medicine (Cambridge, Mass.)|September 14, 2022
Variants influencing age at diagnosis of HNF1A-MODYAgnieszka H Ludwig-Słomczyńska, Michał T Seweryn, Piotr Radkowski, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|April 11, 2025
Improving mitochondria-associated endoplasmic reticulum membranes integrity as converging therapeutic strategy for rare neurodegenerative diseases and cancerMichal Cagalinec, Adnan Mohd, Silvia Borecka, et al.
Human Mutation|January 6, 2017
EIF2S3 Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMOMartina Skopkova, Friederike Hennig, Byung-Sik Shin, et al.
Diabetes|January 1, 2013
Mutations in HNF1A result in marked alterations of plasma glycan profileGaya Thanabalasingham, Jennifer E Huffman, Jayesh J Kattla, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Plos One|May 5, 2017
Genetic analysis of single-minded 1 gene in early-onset severely obese children and adolescentsDaniela Stanikova, Marek Buzga, Patrik Krumpolec, et al.
Human Genetics|February 11, 2015
Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing lossGowri Nayak, Lukas Varga, Claire Trincot, et al.
Molecular Medicine (Cambridge, Mass.)|September 14, 2022
Variants influencing age at diagnosis of HNF1A-MODYAgnieszka H Ludwig-Słomczyńska, Michał T Seweryn, Piotr Radkowski, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|April 11, 2025
Improving mitochondria-associated endoplasmic reticulum membranes integrity as converging therapeutic strategy for rare neurodegenerative diseases and cancerMichal Cagalinec, Adnan Mohd, Silvia Borecka, et al.
Human Mutation|January 6, 2017
EIF2S3 Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMOMartina Skopkova, Friederike Hennig, Byung-Sik Shin, et al.
Diabetes|January 1, 2013
Mutations in HNF1A result in marked alterations of plasma glycan profileGaya Thanabalasingham, Jennifer E Huffman, Jayesh J Kattla, et al.
Pageof 5