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Heliyon
|
January 27, 2025
Molecular docking and molecular dynamics simulation studies of inhibitor candidates against <i>Anopheles gambiae</i> 3-hydroxykynurenine transaminase and implications on vector control
Eunice O Adedeji, Olubanke O Ogunlana, Gbolahan O Oduselu, et al.
Frontiers in Microbiology
|
June 21, 2023
Machine learning on large scale perturbation screens for SARS-CoV-2 host factors identifies β-catenin/CBP inhibitor PRI-724 as a potent antiviral
Maximilian A Kelch, Antonella Vera-Guapi, Thomas Beder, et al.
Plos One
|
July 5, 2024
Combination of computational techniques and RNAi reveal targets in Anopheles gambiae for malaria vector control
Eunice O Adedeji, Thomas Beder, Claudia Damiani, et al.
Plos One
|
March 27, 2025
Correction: Combination of computational techniques and RNAi reveal targets in Anopheles gambiae for malaria vector control
Eunice O Adedeji, Thomas Beder, Claudia Damiani, et al.
The Journal of Pediatrics
|
March 6, 2004
Genotype-phenotype correlations in Noonan syndrome
Martin Zenker, Gernot Buheitel, Ralf Rauch, et al.
Journal of Human Genetics
|
April 25, 2019
SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy
Björn Fischer-Zirnsak, Rainer Koenig, Franz Alisch, et al.
Journal of Medical Genetics
|
October 24, 2006
Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations
Martin Zenker, Katarina Lehmann, Anna Leana Schulz, et al.
Human Mutation
|
June 14, 2014
Deletions in the 3' part of the NFIX gene including a recurrent Alu-mediated deletion of exon 6 and 7 account for previously unexplained cases of Marshall-Smith syndrome
Denny Schanze, Dorothée Neubauer, Valerie Cormier-Daire, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
March 9, 2010
Osteopathia striata with cranial sclerosis owing to WTX gene defect
Bram Perdu, Fenna de Freitas, Suzanne G M Frints, et al.
Bone
|
January 11, 2020
Biallelic variants in KYNU cause a multisystemic syndrome with hand hyperphalangism
Nadja Ehmke, Kristina Cusmano-Ozog, Rainer Koenig, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 35) with videos related to
Sort By:
Page
of 4
Heliyon
|
January 27, 2025
Molecular docking and molecular dynamics simulation studies of inhibitor candidates against <i>Anopheles gambiae</i> 3-hydroxykynurenine transaminase and implications on vector control
Eunice O Adedeji, Olubanke O Ogunlana, Gbolahan O Oduselu, et al.
Frontiers in Microbiology
|
June 21, 2023
Machine learning on large scale perturbation screens for SARS-CoV-2 host factors identifies β-catenin/CBP inhibitor PRI-724 as a potent antiviral
Maximilian A Kelch, Antonella Vera-Guapi, Thomas Beder, et al.
Plos One
|
July 5, 2024
Combination of computational techniques and RNAi reveal targets in Anopheles gambiae for malaria vector control
Eunice O Adedeji, Thomas Beder, Claudia Damiani, et al.
Plos One
|
March 27, 2025
Correction: Combination of computational techniques and RNAi reveal targets in Anopheles gambiae for malaria vector control
Eunice O Adedeji, Thomas Beder, Claudia Damiani, et al.
The Journal of Pediatrics
|
March 6, 2004
Genotype-phenotype correlations in Noonan syndrome
Martin Zenker, Gernot Buheitel, Ralf Rauch, et al.
Journal of Human Genetics
|
April 25, 2019
SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy
Björn Fischer-Zirnsak, Rainer Koenig, Franz Alisch, et al.
Journal of Medical Genetics
|
October 24, 2006
Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations
Martin Zenker, Katarina Lehmann, Anna Leana Schulz, et al.
Human Mutation
|
June 14, 2014
Deletions in the 3' part of the NFIX gene including a recurrent Alu-mediated deletion of exon 6 and 7 account for previously unexplained cases of Marshall-Smith syndrome
Denny Schanze, Dorothée Neubauer, Valerie Cormier-Daire, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
March 9, 2010
Osteopathia striata with cranial sclerosis owing to WTX gene defect
Bram Perdu, Fenna de Freitas, Suzanne G M Frints, et al.
Bone
|
January 11, 2020
Biallelic variants in KYNU cause a multisystemic syndrome with hand hyperphalangism
Nadja Ehmke, Kristina Cusmano-Ozog, Rainer Koenig, et al.
Page
of 4