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Stem Cell Research
|
February 26, 2018
Generation of a human induced pluripotent stem cell (iPSC) line from a 51-year-old female with attention-deficit/hyperactivity disorder (ADHD) carrying a duplication of SLC2A3
Charline Jansch, Katharina Günther, Jonas Waider, et al.
Scientific Reports
|
June 28, 2016
Hypoxia-inducible factor 3A gene expression and methylation in adipose tissue is related to adipose tissue dysfunction
Susanne Pfeiffer, Jacqueline Krüger, Anna Maierhofer, et al.
Human Molecular Genetics
|
November 26, 2008
Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment
Eberhard Schneider, Tina Märker, Angelika Daser, et al.
European Journal of Dermatology : EJD
|
December 3, 2019
Memory CD4+ T cells lacking expression of CCR7 promote pro-inflammatory cytokine production in patients with diffuse cutaneous systemic sclerosis
Giovanni Almanzar, Marc Schmalzing, Matthias Klein, et al.
Developmental Cell
|
July 11, 2006
In vitro-differentiated embryonic stem cells give rise to male gametes that can generate offspring mice
Karim Nayernia, Jessica Nolte, Hans W Michelmann, et al.
Molecular Neurobiology
|
January 9, 2026
Expansion of Molecular and Clinical Aspects of EPS8L2 (DFNB106)-Associated Hearing Loss Emphasizes a Potential Therapeutic Window
Daniel Owrang, Aboulfazl Rad, Masoome Alerasool, et al.
Human Genomics
|
March 6, 2024
Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome
Asuman Koparir, Caroline Lekszas, Kemal Keseroglu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 2, 2021
Lipid droplets in mammalian eggs are utilized during embryonic diapause
Roberta Arena, Simona Bisogno, Łukasz Gąsior, et al.
International Journal of Molecular Sciences
|
January 8, 2020
Novel Loss-of-Function Variants in <i>CDC14A</i> are Associated with Recessive Sensorineural Hearing Loss in Iranian and Pakistani Patients
Julia Doll, Susanne Kolb, Linda Schnapp, et al.
EXCLI Journal
|
February 28, 2022
Hypermethylation of <i>RAD9A</i> intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformation
Danuta Galetzka, Julia Böck, Lukas Wagner, et al.
Page
of 19
Search research articles
Search
Showing results (141-150 of 190) with videos related to
Sort By:
Page
of 19
Stem Cell Research
|
February 26, 2018
Generation of a human induced pluripotent stem cell (iPSC) line from a 51-year-old female with attention-deficit/hyperactivity disorder (ADHD) carrying a duplication of SLC2A3
Charline Jansch, Katharina Günther, Jonas Waider, et al.
Scientific Reports
|
June 28, 2016
Hypoxia-inducible factor 3A gene expression and methylation in adipose tissue is related to adipose tissue dysfunction
Susanne Pfeiffer, Jacqueline Krüger, Anna Maierhofer, et al.
Human Molecular Genetics
|
November 26, 2008
Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment
Eberhard Schneider, Tina Märker, Angelika Daser, et al.
European Journal of Dermatology : EJD
|
December 3, 2019
Memory CD4+ T cells lacking expression of CCR7 promote pro-inflammatory cytokine production in patients with diffuse cutaneous systemic sclerosis
Giovanni Almanzar, Marc Schmalzing, Matthias Klein, et al.
Developmental Cell
|
July 11, 2006
In vitro-differentiated embryonic stem cells give rise to male gametes that can generate offspring mice
Karim Nayernia, Jessica Nolte, Hans W Michelmann, et al.
Molecular Neurobiology
|
January 9, 2026
Expansion of Molecular and Clinical Aspects of EPS8L2 (DFNB106)-Associated Hearing Loss Emphasizes a Potential Therapeutic Window
Daniel Owrang, Aboulfazl Rad, Masoome Alerasool, et al.
Human Genomics
|
March 6, 2024
Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome
Asuman Koparir, Caroline Lekszas, Kemal Keseroglu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 2, 2021
Lipid droplets in mammalian eggs are utilized during embryonic diapause
Roberta Arena, Simona Bisogno, Łukasz Gąsior, et al.
International Journal of Molecular Sciences
|
January 8, 2020
Novel Loss-of-Function Variants in <i>CDC14A</i> are Associated with Recessive Sensorineural Hearing Loss in Iranian and Pakistani Patients
Julia Doll, Susanne Kolb, Linda Schnapp, et al.
EXCLI Journal
|
February 28, 2022
Hypermethylation of <i>RAD9A</i> intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformation
Danuta Galetzka, Julia Böck, Lukas Wagner, et al.
Page
of 19