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Journal of Medical Genetics
|
May 23, 2020
Bi-allelic <i>TTC5</i> variants cause delayed developmental milestones and intellectual disability
Arisha Rasheed, Evren Gumus, Maha Zaki, et al.
Journal of Phycology
|
October 22, 2024
A cry for kelp: Evidence for polyphenolic inhibition of Oxford Nanopore sequencing of brown algae
William S Pearman, Vanessa Arranz, Jose I Carvajal, et al.
Psychological Medicine
|
May 27, 2022
Does the impact of bereavement vary between same and different gender partnerships? A representative national, cross-sectional study
Liadh Timmins, Alexandra Pitman, Michael King, et al.
Human Mutation
|
June 10, 2020
First clinical and myopathological description of a myofibrillar myopathy with congenital onset and homozygous mutation in FLNC
Heike Kölbel, Andreas Roos, Peter F M van der Ven, et al.
Oncogenesis
|
December 12, 2019
PPP2R2A prostate cancer haploinsufficiency is associated with worse prognosis and a high vulnerability to B55α/PP2A reconstitution that triggers centrosome destabilization
Ziran Zhao, Alison Kurimchak, Anna S Nikonova, et al.
Annals of the American Thoracic Society
|
July 1, 2020
Comparison of Multiple Breath Washout and Spirometry in Children with Primary Ciliary Dyskinesia and Cystic Fibrosis and Healthy Controls
BreAnna Kinghorn, Sharon McNamara, Alan Genatossio, et al.
Biorxiv : the Preprint Server for Biology
|
February 13, 2023
Organism-Wide Analysis of Sepsis Reveals Mechanisms of Systemic Inflammation
Michihiro Takahama, Ashwini Patil, Katherine Johnson, et al.
Gates Open Research
|
February 12, 2024
Protocol and statistical analysis plan for a randomized controlled trial of the effect of intravenous iron on anemia in Malawian pregnant women in their third trimester (REVAMP - TT)
Rebecca Harding, Ernest Moya, Ricardo Ataíde, et al.
Neuron
|
February 9, 2022
Suppression of premature transcription termination leads to reduced mRNA isoform diversity and neurodegeneration
Geneva R LaForce, Jordan S Farr, Jingyi Liu, et al.
Annals of Neurology
|
October 15, 2019
POPDC3 Gene Variants Associate with a New Form of Limb Girdle Muscular Dystrophy
John Vissing, Katherine Johnson, Ana Töpf, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 117) with videos related to
Sort By:
Page
of 12
Journal of Medical Genetics
|
May 23, 2020
Bi-allelic <i>TTC5</i> variants cause delayed developmental milestones and intellectual disability
Arisha Rasheed, Evren Gumus, Maha Zaki, et al.
Journal of Phycology
|
October 22, 2024
A cry for kelp: Evidence for polyphenolic inhibition of Oxford Nanopore sequencing of brown algae
William S Pearman, Vanessa Arranz, Jose I Carvajal, et al.
Psychological Medicine
|
May 27, 2022
Does the impact of bereavement vary between same and different gender partnerships? A representative national, cross-sectional study
Liadh Timmins, Alexandra Pitman, Michael King, et al.
Human Mutation
|
June 10, 2020
First clinical and myopathological description of a myofibrillar myopathy with congenital onset and homozygous mutation in FLNC
Heike Kölbel, Andreas Roos, Peter F M van der Ven, et al.
Oncogenesis
|
December 12, 2019
PPP2R2A prostate cancer haploinsufficiency is associated with worse prognosis and a high vulnerability to B55α/PP2A reconstitution that triggers centrosome destabilization
Ziran Zhao, Alison Kurimchak, Anna S Nikonova, et al.
Annals of the American Thoracic Society
|
July 1, 2020
Comparison of Multiple Breath Washout and Spirometry in Children with Primary Ciliary Dyskinesia and Cystic Fibrosis and Healthy Controls
BreAnna Kinghorn, Sharon McNamara, Alan Genatossio, et al.
Biorxiv : the Preprint Server for Biology
|
February 13, 2023
Organism-Wide Analysis of Sepsis Reveals Mechanisms of Systemic Inflammation
Michihiro Takahama, Ashwini Patil, Katherine Johnson, et al.
Gates Open Research
|
February 12, 2024
Protocol and statistical analysis plan for a randomized controlled trial of the effect of intravenous iron on anemia in Malawian pregnant women in their third trimester (REVAMP - TT)
Rebecca Harding, Ernest Moya, Ricardo Ataíde, et al.
Neuron
|
February 9, 2022
Suppression of premature transcription termination leads to reduced mRNA isoform diversity and neurodegeneration
Geneva R LaForce, Jordan S Farr, Jingyi Liu, et al.
Annals of Neurology
|
October 15, 2019
POPDC3 Gene Variants Associate with a New Form of Limb Girdle Muscular Dystrophy
John Vissing, Katherine Johnson, Ana Töpf, et al.
Page
of 12