Search research articles
Contact Us
Filters
Showing results (81-90 of 89) with videos related to
Page
of 9
Sort By:
You have reached the last page of results.
This site can display upto 89 results.
The Journal of Biological Chemistry
|
September 6, 2019
The SH3 domains of the protein kinases ITK and LCK compete for adjacent sites on T cell-specific adapter protein
Thorny Cesilie Bie Andersen, Per Eugen Kristiansen, Zsuzsa Huszenicza, et al.
Human Molecular Genetics
|
June 14, 2021
A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge-Weber syndrome
Roar Fjær, Katarzyna Marciniak, Olav Sundnes, et al.
Brain : a Journal of Neurology
|
February 1, 2022
ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequences
Dulika Sumathipala, Petter Strømme, Zohreh Fattahi, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine
|
July 19, 2021
Improving outcomes of hypoglossal nerve stimulation therapy: current practice, future directions, and research gaps. Proceedings of the 2019 International Sleep Surgery Society Research Forum
Maria V Suurna, Ofer Jacobowitz, Jolie Chang, et al.
Sleep & Breathing = Schlaf & Atmung
|
November 20, 2020
Sleep medicine in otolaryngology units: an international survey
Giovanni Cammaroto, Giulia Bianchi, Henry Zhang, et al.
Brain : a Journal of Neurology
|
February 2, 2023
BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening
Trine Tangeraas, Juliana R Constante, Paul Hoff Backe, et al.
European Journal of Human Genetics : EJHG
|
January 19, 2018
Biallelic variants in KIF14 cause intellectual disability with microcephaly
Periklis Makrythanasis, Reza Maroofian, Asbjørg Stray-Pedersen, et al.
Sleep & Breathing = Schlaf & Atmung
|
September 14, 2021
Correction to: Sleep medicine in otolaryngology units: an international survey
Giovanni Cammaroto, Giulia Bianchi, Henry Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 17, 2026
Biallelic SUPT4H1 Variants Cause a Multisystem Neurodevelopmental Disorder Associated with Disrupted Transcription
Christina Canavati, Mari Oppebøen, Radha Verma, et al.
Page
of 9
Search research articles
Search
Showing results (81-90 of 89) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 89 results.
The Journal of Biological Chemistry
|
September 6, 2019
The SH3 domains of the protein kinases ITK and LCK compete for adjacent sites on T cell-specific adapter protein
Thorny Cesilie Bie Andersen, Per Eugen Kristiansen, Zsuzsa Huszenicza, et al.
Human Molecular Genetics
|
June 14, 2021
A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge-Weber syndrome
Roar Fjær, Katarzyna Marciniak, Olav Sundnes, et al.
Brain : a Journal of Neurology
|
February 1, 2022
ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequences
Dulika Sumathipala, Petter Strømme, Zohreh Fattahi, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine
|
July 19, 2021
Improving outcomes of hypoglossal nerve stimulation therapy: current practice, future directions, and research gaps. Proceedings of the 2019 International Sleep Surgery Society Research Forum
Maria V Suurna, Ofer Jacobowitz, Jolie Chang, et al.
Sleep & Breathing = Schlaf & Atmung
|
November 20, 2020
Sleep medicine in otolaryngology units: an international survey
Giovanni Cammaroto, Giulia Bianchi, Henry Zhang, et al.
Brain : a Journal of Neurology
|
February 2, 2023
BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening
Trine Tangeraas, Juliana R Constante, Paul Hoff Backe, et al.
European Journal of Human Genetics : EJHG
|
January 19, 2018
Biallelic variants in KIF14 cause intellectual disability with microcephaly
Periklis Makrythanasis, Reza Maroofian, Asbjørg Stray-Pedersen, et al.
Sleep & Breathing = Schlaf & Atmung
|
September 14, 2021
Correction to: Sleep medicine in otolaryngology units: an international survey
Giovanni Cammaroto, Giulia Bianchi, Henry Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 17, 2026
Biallelic SUPT4H1 Variants Cause a Multisystem Neurodevelopmental Disorder Associated with Disrupted Transcription
Christina Canavati, Mari Oppebøen, Radha Verma, et al.
Page
of 9