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Annals of the American Thoracic Society
|
February 8, 2024
Genetic Analysis of Obstructive Sleep Apnea and Its Relationship with Severe COVID-19
Satu Strausz, Elizabete Agafonova, Varvara Tiullinen, et al.
Journal of Chemical Theory and Computation
|
August 26, 2024
Effective Inclusion of Electronic Polarization Improves the Description of Electrostatic Interactions: The prosECCo75 Biomolecular Force Field
Ricky Nencini, Carmelo Tempra, Denys Biriukov, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 23, 2022
The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections
Samuel E Jones, Fahrisa I Maisha, Satu J Strausz, et al.
International Journal of Oncology
|
December 6, 2005
The importance of functional testing in the genetic assessment of Muir-Torre syndrome, a clinical subphenotype of HNPCC
Saara Ollila, Roslyn Fitzpatrick, Laura Sarantaus, et al.
Breast Cancer Research and Treatment
|
October 6, 2016
Impact of neoadjuvant therapy on eligibility for and frequency of breast conservation in stage II-III HER2-positive breast cancer: surgical results of CALGB 40601 (Alliance)
Mehra Golshan, Constance T Cirrincione, William M Sikov, et al.
Nucleic Acids Research
|
February 21, 1998
BTKbase, mutation database for X-linked agammaglobulinemia (XLA)
M Vihinen, O Brandau, L J Brandén, et al.
The Journal of Investigative Dermatology
|
November 29, 2021
Characterization of the CpG Island Hypermethylated Phenotype Subclass in Primary Melanomas
Kathleen Conway, Yihsuan S Tsai, Sharon N Edmiston, et al.
Acta Ophthalmologica
|
July 8, 2017
The Finnish national guideline for diagnosis, treatment and follow-up of patients with wet age-related macular degeneration
Raimo Tuuminen, Hannele Uusitalo-Järvinen, Vesa Aaltonen, et al.
Human Mutation
|
March 21, 2007
Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR)
Philip A Chan, Sekhar Duraisamy, Peter J Miller, et al.
Gastroenterology
|
November 15, 2006
Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein
Saara Ollila, Laura Sarantaus, Reetta Kariola, et al.
Page
of 63
Search research articles
Search
Showing results (451-460 of 628) with videos related to
Sort By:
Page
of 63
Annals of the American Thoracic Society
|
February 8, 2024
Genetic Analysis of Obstructive Sleep Apnea and Its Relationship with Severe COVID-19
Satu Strausz, Elizabete Agafonova, Varvara Tiullinen, et al.
Journal of Chemical Theory and Computation
|
August 26, 2024
Effective Inclusion of Electronic Polarization Improves the Description of Electrostatic Interactions: The prosECCo75 Biomolecular Force Field
Ricky Nencini, Carmelo Tempra, Denys Biriukov, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 23, 2022
The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections
Samuel E Jones, Fahrisa I Maisha, Satu J Strausz, et al.
International Journal of Oncology
|
December 6, 2005
The importance of functional testing in the genetic assessment of Muir-Torre syndrome, a clinical subphenotype of HNPCC
Saara Ollila, Roslyn Fitzpatrick, Laura Sarantaus, et al.
Breast Cancer Research and Treatment
|
October 6, 2016
Impact of neoadjuvant therapy on eligibility for and frequency of breast conservation in stage II-III HER2-positive breast cancer: surgical results of CALGB 40601 (Alliance)
Mehra Golshan, Constance T Cirrincione, William M Sikov, et al.
Nucleic Acids Research
|
February 21, 1998
BTKbase, mutation database for X-linked agammaglobulinemia (XLA)
M Vihinen, O Brandau, L J Brandén, et al.
The Journal of Investigative Dermatology
|
November 29, 2021
Characterization of the CpG Island Hypermethylated Phenotype Subclass in Primary Melanomas
Kathleen Conway, Yihsuan S Tsai, Sharon N Edmiston, et al.
Acta Ophthalmologica
|
July 8, 2017
The Finnish national guideline for diagnosis, treatment and follow-up of patients with wet age-related macular degeneration
Raimo Tuuminen, Hannele Uusitalo-Järvinen, Vesa Aaltonen, et al.
Human Mutation
|
March 21, 2007
Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR)
Philip A Chan, Sekhar Duraisamy, Peter J Miller, et al.
Gastroenterology
|
November 15, 2006
Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein
Saara Ollila, Laura Sarantaus, Reetta Kariola, et al.
Page
of 63