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European Journal of Human Genetics : EJHG
|
June 26, 2003
Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of cases
Barbara Burwinkel, Bin Hu, Anja Schroers, et al.
Blood Advances
|
June 21, 2024
Neurobeachin regulates hematopoietic progenitor differentiation and survival by modulating Notch activity
Miguel Ganuza, Antonio Morales-Hernández, Alanna Van Huizen, et al.
Experimental Hematology
|
January 13, 2009
Neurobeachin (NBEA) is a target of recurrent interstitial deletions at 13q13 in patients with MGUS and multiple myeloma
Julie O'Neal, Feng Gao, Anjum Hassan, et al.
Frontiers in Synaptic Neuroscience
|
August 31, 2018
Molecular Dissection of Neurobeachin Function at Excitatory Synapses
Daniele Repetto, Johannes Brockhaus, Hong J Rhee, et al.
Nature Communications
|
March 29, 2024
Remodeling of the postsynaptic proteome in male mice and marmosets during synapse development
Takeshi Kaizuka, Takehiro Suzuki, Noriyuki Kishi, et al.
Human Genetics
|
May 26, 1998
Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinase PHKA2 gene
B Burwinkel, L Amat, R G Gray, et al.
DNA and Cell Biology
|
February 9, 2005
Rat synapsin 1 promoter mediated transgene expression in testicular cell types
K A Street, G Xu, K L Hall, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
February 8, 2025
Cost-Effectiveness of a Digitally Supported Care Management Program for Caregivers of People With Dementia
Michelle Pfaff, Wolfgang Hoffmann, Melanie Boekholt, et al.
Aging & Mental Health
|
November 22, 2017
Supporting family dementia caregivers: testing the efficacy of dementia care management on multifaceted caregivers' burden
I Zwingmann, W Hoffmann, B Michalowsky, et al.
Annals of Neurology
|
March 20, 1998
Mutation analysis in myophosphorylase deficiency (McArdle's disease)
M Vorgerd, C Kubisch, B Burwinkel, et al.
Page
of 28
Search research articles
Search
Showing results (121-130 of 272) with videos related to
Sort By:
Page
of 28
European Journal of Human Genetics : EJHG
|
June 26, 2003
Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of cases
Barbara Burwinkel, Bin Hu, Anja Schroers, et al.
Blood Advances
|
June 21, 2024
Neurobeachin regulates hematopoietic progenitor differentiation and survival by modulating Notch activity
Miguel Ganuza, Antonio Morales-Hernández, Alanna Van Huizen, et al.
Experimental Hematology
|
January 13, 2009
Neurobeachin (NBEA) is a target of recurrent interstitial deletions at 13q13 in patients with MGUS and multiple myeloma
Julie O'Neal, Feng Gao, Anjum Hassan, et al.
Frontiers in Synaptic Neuroscience
|
August 31, 2018
Molecular Dissection of Neurobeachin Function at Excitatory Synapses
Daniele Repetto, Johannes Brockhaus, Hong J Rhee, et al.
Nature Communications
|
March 29, 2024
Remodeling of the postsynaptic proteome in male mice and marmosets during synapse development
Takeshi Kaizuka, Takehiro Suzuki, Noriyuki Kishi, et al.
Human Genetics
|
May 26, 1998
Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinase PHKA2 gene
B Burwinkel, L Amat, R G Gray, et al.
DNA and Cell Biology
|
February 9, 2005
Rat synapsin 1 promoter mediated transgene expression in testicular cell types
K A Street, G Xu, K L Hall, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
February 8, 2025
Cost-Effectiveness of a Digitally Supported Care Management Program for Caregivers of People With Dementia
Michelle Pfaff, Wolfgang Hoffmann, Melanie Boekholt, et al.
Aging & Mental Health
|
November 22, 2017
Supporting family dementia caregivers: testing the efficacy of dementia care management on multifaceted caregivers' burden
I Zwingmann, W Hoffmann, B Michalowsky, et al.
Annals of Neurology
|
March 20, 1998
Mutation analysis in myophosphorylase deficiency (McArdle's disease)
M Vorgerd, C Kubisch, B Burwinkel, et al.
Page
of 28