Search results: Sage Journals

Restricted accessResearch articleFirst published November, 2015

Study on the particle swarm optimization based on double mutation

Xian Wen Luo, Zuo Ying Liu

Journal of Computational Methods in Sciences and Engineering

Restricted accessOtherFirst published August, 2010

Mutational Analysis of the MECP2 Gene in Tunisian Patients With Rett Syndrome: A Novel Double Mutation

Nourhene Fendri-Kriaa, Emna Mkaouar-Rebai, Dorsaf Moalla [...]

Journal of Child Neurology

Free accessResearch articleFirst published April, 2018

Acquisition of double mutation in gyrA caused high resistance to sitafloxacin in Helicobacter pylori after unsuccessful eradication with sitafloxacin-containing regimens

Hideki Mori, Hidekazu Suzuki, Juntaro Matsuzaki [...]

United European Gastroenterology Journal

Restricted accessResearch articleFirst published March, 1994

Dissection of the Molecular Consequences of a Double Mutation Causing a Human Lysosomal Disease

Aija Riikonen, Elina Ikonen, Raija Sormunen [...]

DNA and Cell Biology

Open accessCase reportFirst published 2024

Double Hit in Clear-Cell Renal Cell Carcinoma With Germline Pathogenic ATM Mutation and Somatic VHL Mutation

Kok Hoe Chan, Nicolas Duque Clavijo, Gustavo Ayala [...]

Journal of Investigative Medicine High Impact Case Reports

Restricted accessBrief reportFirst published February, 2021

A Novel Double RET E768D/L790F Mutation Associated with a MEN2B-Like Phenotype

Annie Mathew, Soeren Latteyer, Karin Frank-Raue [...]

Thyroid®

Restricted accessResearch articleFirst published August 8, 2016

Expression of the Alzheimer’s Disease Mutations AβPP695sw and PSEN1M146I in Double-Transgenic Göttingen Minipigs

Jannik E. Jakobsen, Marianne G. Johansen, Mette Schmidt [...]

Journal of Alzheimer’s Disease

Restricted accessResearch articleFirst published July, 2017

Clinical,Molecular,and Computational Analysis in Patients With a Novel Double Mutation and a New Synonymous Variant in MeCP2: Report of the First Missense Mutation Within the AT-hook1 Cluster in Rett Syndrome

Marwa Kharrat, Yosra Kamoun, Fatma Kamoun [...]

Journal of Child Neurology

Restricted accessResearch articleFirst published June, 1987

Use of λ Exonuclease for Efficient Oligonucleotide-Mediated Site-Directed Deletion and Point Mutation of Double-Stranded DNA

D.P. Palermo, G.F. Hess

DNA and Cell Biology

Restricted accessResearch articleFirst published February, 1995

Suppression of Single and Double Nonsense Mutations Introduced into the Diphtheria Toxin A-Chain Gene: A Potential Binary System for Toxin Gene Therapy

Donald F. Robinson, Ian H. Maxwell

Human Gene Therapy

Restricted accessResearch articleFirst published November, 2015

Study on the particle swarm optimization based on double mutation

Xian Wen Luo, Zuo Ying Liu

Journal of Computational Methods in Sciences and Engineering

Restricted accessOtherFirst published August, 2010

Mutational Analysis of the MECP2 Gene in Tunisian Patients With Rett Syndrome: A Novel Double Mutation

Nourhene Fendri-Kriaa, Emna Mkaouar-Rebai, Dorsaf Moalla [...]

Journal of Child Neurology

Free accessResearch articleFirst published April, 2018

Acquisition of double mutation in gyrA caused high resistance to sitafloxacin in Helicobacter pylori after unsuccessful eradication with sitafloxacin-containing regimens

Hideki Mori, Hidekazu Suzuki, Juntaro Matsuzaki [...]

United European Gastroenterology Journal

Restricted accessResearch articleFirst published March, 1994

Dissection of the Molecular Consequences of a Double Mutation Causing a Human Lysosomal Disease

Aija Riikonen, Elina Ikonen, Raija Sormunen [...]

DNA and Cell Biology

Open accessCase reportFirst published 2024

Double Hit in Clear-Cell Renal Cell Carcinoma With Germline Pathogenic ATM Mutation and Somatic VHL Mutation

Kok Hoe Chan, Nicolas Duque Clavijo, Gustavo Ayala [...]

Journal of Investigative Medicine High Impact Case Reports

Restricted accessBrief reportFirst published February, 2021

A Novel Double RET E768D/L790F Mutation Associated with a MEN2B-Like Phenotype

Annie Mathew, Soeren Latteyer, Karin Frank-Raue [...]

Thyroid®

Restricted accessResearch articleFirst published August 8, 2016

Expression of the Alzheimer’s Disease Mutations AβPP695sw and PSEN1M146I in Double-Transgenic Göttingen Minipigs

Jannik E. Jakobsen, Marianne G. Johansen, Mette Schmidt [...]

Journal of Alzheimer’s Disease

Restricted accessResearch articleFirst published July, 2017

Clinical,Molecular,and Computational Analysis in Patients With a Novel Double Mutation and a New Synonymous Variant in MeCP2: Report of the First Missense Mutation Within the AT-hook1 Cluster in Rett Syndrome

Marwa Kharrat, Yosra Kamoun, Fatma Kamoun [...]

Journal of Child Neurology

Restricted accessResearch articleFirst published June, 1987

Use of λ Exonuclease for Efficient Oligonucleotide-Mediated Site-Directed Deletion and Point Mutation of Double-Stranded DNA

D.P. Palermo, G.F. Hess

DNA and Cell Biology

Restricted accessResearch articleFirst published February, 1995

Suppression of Single and Double Nonsense Mutations Introduced into the Diphtheria Toxin A-Chain Gene: A Potential Binary System for Toxin Gene Therapy

Donald F. Robinson, Ian H. Maxwell

Human Gene Therapy