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Human Molecular Genetics
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May 23, 2013
A Y328C missense mutation in spermine synthase causes a mild form of Snyder-Robinson syndrome
Zhe Zhang, Joy Norris, Vera Kalscheuer, et al.
Journal of Chemical Information and Modeling
|
May 20, 2025
<i>In Silico</i> Screening for Small Molecules to Alter Calpain Proteolysis through Modulating Conformation Changes Induced by Heterodimerization
Pitambar Poudel, Ivan Shapovalov, Shailesh Kumar Panday, et al.
Plos One
|
June 27, 2013
Cancer missense mutations alter binding properties of proteins and their interaction networks
Hafumi Nishi, Manoj Tyagi, Shaolei Teng, et al.
International Journal of Molecular Sciences
|
August 7, 2021
Computational Investigation of the pH Dependence of Stability of Melanosome Proteins: Implication for Melanosome formation and Disease
Mahesh Koirala, H B Mihiri Shashikala, Jacob Jeffries, et al.
Journal of Alzheimer'S Disease : JAD
|
October 15, 2013
A novel p.Leu(381)Phe mutation in presenilin 1 is associated with very early onset and unusually fast progressing dementia as well as lysosomal inclusions typically seen in Kufs disease
Natalia Dolzhanskaya, Michael A Gonzalez, Fiorella Sperziani, et al.
BMC Biophysics
|
May 16, 2012
DelPhi: a comprehensive suite for DelPhi software and associated resources
Lin Li, Chuan Li, Subhra Sarkar, et al.
The Journal of Physical Chemistry. B
|
February 14, 2006
Coating single-walled carbon nanotubes with phospholipids
Yonnie Wu, JoAn S Hudson, Qi Lu, et al.
Journal of Computational Chemistry
|
June 26, 2019
DelPhi Suite: New Developments and Review of Functionalities
Chuan Li, Zhe Jia, Arghya Chakravorty, et al.
Journal of Human Genetics
|
March 13, 2019
Three additional patients with EED-associated overgrowth: potential mutation hotspots identified?
Catherine J Spellicy, Yunhui Peng, Leah Olewiler, et al.
European Journal of Human Genetics : EJHG
|
January 24, 2018
Key apoptotic genes APAF1 and CASP9 implicated in recurrent folate-resistant neural tube defects
Catherine J Spellicy, Joy Norris, Renee Bend, et al.
Page
of 16
Search research articles
Search
Showing results (131-140 of 151) with videos related to
Sort By:
Page
of 16
Human Molecular Genetics
|
May 23, 2013
A Y328C missense mutation in spermine synthase causes a mild form of Snyder-Robinson syndrome
Zhe Zhang, Joy Norris, Vera Kalscheuer, et al.
Journal of Chemical Information and Modeling
|
May 20, 2025
<i>In Silico</i> Screening for Small Molecules to Alter Calpain Proteolysis through Modulating Conformation Changes Induced by Heterodimerization
Pitambar Poudel, Ivan Shapovalov, Shailesh Kumar Panday, et al.
Plos One
|
June 27, 2013
Cancer missense mutations alter binding properties of proteins and their interaction networks
Hafumi Nishi, Manoj Tyagi, Shaolei Teng, et al.
International Journal of Molecular Sciences
|
August 7, 2021
Computational Investigation of the pH Dependence of Stability of Melanosome Proteins: Implication for Melanosome formation and Disease
Mahesh Koirala, H B Mihiri Shashikala, Jacob Jeffries, et al.
Journal of Alzheimer'S Disease : JAD
|
October 15, 2013
A novel p.Leu(381)Phe mutation in presenilin 1 is associated with very early onset and unusually fast progressing dementia as well as lysosomal inclusions typically seen in Kufs disease
Natalia Dolzhanskaya, Michael A Gonzalez, Fiorella Sperziani, et al.
BMC Biophysics
|
May 16, 2012
DelPhi: a comprehensive suite for DelPhi software and associated resources
Lin Li, Chuan Li, Subhra Sarkar, et al.
The Journal of Physical Chemistry. B
|
February 14, 2006
Coating single-walled carbon nanotubes with phospholipids
Yonnie Wu, JoAn S Hudson, Qi Lu, et al.
Journal of Computational Chemistry
|
June 26, 2019
DelPhi Suite: New Developments and Review of Functionalities
Chuan Li, Zhe Jia, Arghya Chakravorty, et al.
Journal of Human Genetics
|
March 13, 2019
Three additional patients with EED-associated overgrowth: potential mutation hotspots identified?
Catherine J Spellicy, Yunhui Peng, Leah Olewiler, et al.
European Journal of Human Genetics : EJHG
|
January 24, 2018
Key apoptotic genes APAF1 and CASP9 implicated in recurrent folate-resistant neural tube defects
Catherine J Spellicy, Joy Norris, Renee Bend, et al.
Page
of 16