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Frontiers in Neurology
|
August 15, 2020
<i>SETD5</i> Gene Haploinsufficiency in Three Patients With Suspected KBG Syndrome
Milena Crippa, Ilaria Bestetti, Silvia Maitz, et al.
The Journal of Biological Chemistry
|
August 5, 2010
Partial agonist and antagonist activities of a mutant scorpion beta-toxin on sodium channels
Izhar Karbat, Nitza Ilan, Joel Z Zhang, et al.
Physical Review Letters
|
September 25, 2020
Quantum-Limited Squeezed Light Detection with a Camera
Elisha S Matekole, Savannah L Cuozzo, Nikunjkumar Prajapati, et al.
Journal of Complementary & Integrative Medicine
|
October 13, 2018
Postoperative analgesia by adding acupuncture to conventional therapy, a non-randomized controlled trial
Ilana Levy, Samuel Attias, Lior Cohen, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2017
Novel homozygous missense mutation in NT5C2 underlying hereditary spastic paraplegia SPG45
Rachel Straussberg, Alexandros Onoufriadis, Osnat Konen, et al.
The Israel Medical Association Journal : IMAJ
|
June 29, 2023
Effect of Magnetic Resonance Imaging on Acute Surgical Treatment of Pregnant Patients: A Single Institution Study
Jonathan Abraham Demma, Lisandro Luques, Lior Cohen, et al.
European Journal of Biochemistry
|
June 6, 2003
An 'Old World' scorpion beta-toxin that recognizes both insect and mammalian sodium channels
Dalia Gordon, Nitza Ilan, Noam Zilberberg, et al.
The FEBS Journal
|
March 16, 2007
The unique pharmacology of the scorpion alpha-like toxin Lqh3 is associated with its flexible C-tail
Izhar Karbat, Roy Kahn, Lior Cohen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 15, 2016
A Biallelic Mutation in the Homologous Recombination Repair Gene SPIDR Is Associated With Human Gonadal Dysgenesis
Pola Smirin-Yosef, Nehama Zuckerman-Levin, Shay Tzur, et al.
American Journal of Human Genetics
|
January 27, 2015
Keppen-Lubinsky syndrome is caused by mutations in the inwardly rectifying K+ channel encoded by KCNJ6
Andrea Masotti, Paolo Uva, Laura Davis-Keppen, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 76) with videos related to
Sort By:
Page
of 8
Frontiers in Neurology
|
August 15, 2020
<i>SETD5</i> Gene Haploinsufficiency in Three Patients With Suspected KBG Syndrome
Milena Crippa, Ilaria Bestetti, Silvia Maitz, et al.
The Journal of Biological Chemistry
|
August 5, 2010
Partial agonist and antagonist activities of a mutant scorpion beta-toxin on sodium channels
Izhar Karbat, Nitza Ilan, Joel Z Zhang, et al.
Physical Review Letters
|
September 25, 2020
Quantum-Limited Squeezed Light Detection with a Camera
Elisha S Matekole, Savannah L Cuozzo, Nikunjkumar Prajapati, et al.
Journal of Complementary & Integrative Medicine
|
October 13, 2018
Postoperative analgesia by adding acupuncture to conventional therapy, a non-randomized controlled trial
Ilana Levy, Samuel Attias, Lior Cohen, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2017
Novel homozygous missense mutation in NT5C2 underlying hereditary spastic paraplegia SPG45
Rachel Straussberg, Alexandros Onoufriadis, Osnat Konen, et al.
The Israel Medical Association Journal : IMAJ
|
June 29, 2023
Effect of Magnetic Resonance Imaging on Acute Surgical Treatment of Pregnant Patients: A Single Institution Study
Jonathan Abraham Demma, Lisandro Luques, Lior Cohen, et al.
European Journal of Biochemistry
|
June 6, 2003
An 'Old World' scorpion beta-toxin that recognizes both insect and mammalian sodium channels
Dalia Gordon, Nitza Ilan, Noam Zilberberg, et al.
The FEBS Journal
|
March 16, 2007
The unique pharmacology of the scorpion alpha-like toxin Lqh3 is associated with its flexible C-tail
Izhar Karbat, Roy Kahn, Lior Cohen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 15, 2016
A Biallelic Mutation in the Homologous Recombination Repair Gene SPIDR Is Associated With Human Gonadal Dysgenesis
Pola Smirin-Yosef, Nehama Zuckerman-Levin, Shay Tzur, et al.
American Journal of Human Genetics
|
January 27, 2015
Keppen-Lubinsky syndrome is caused by mutations in the inwardly rectifying K+ channel encoded by KCNJ6
Andrea Masotti, Paolo Uva, Laura Davis-Keppen, et al.
Page
of 8