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Replicative Stress Coincides with Impaired Nuclear DNA Damage Response in COX4-1 Deficiency.
Published in:
International Journal of Molecular Sciences, 2022, v. 23, n. 8, p. 4149, doi. 10.3390/ijms23084149
By:
- Douiev, Liza;
- Miller, Chaya;
- Keller, Guy;
- Benyamini, Hadar;
- Abu-Libdeh, Bassam;
- Saada, Ann
Publication type:
Article
Two transgenic mouse models for ß-subunit components of succinate-CoA ligase yielding pleiotropic metabolic alterations.
Published in:
Biochemical Journal, 2016, v. 473, n. 20, p. 3463, doi. 10.1042/BCJ20160594
By:
- Kacso, Gergely;
- Ravasz, Dora;
- Doczi, Judit;
- Németh, Beáta;
- Madgar, Ory;
- Saada, Ann;
- Ilin, Polina;
- Miller, Chaya;
- Ostergaard, Elsebet;
- Iordanov, Iordan;
- Adams, Daniel;
- Vargedo, Zsuzsanna;
- Masatake Araki;
- Kimi Araki;
- Mai Nakahara;
- Haruka Ito;
- Gál, Aniko;
- Molnár, Mária J.;
- Nagy, Zsolt;
- Patocs, Attila
Publication type:
Article
Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy.
Published in:
European Journal of Human Genetics, 2015, v. 23, n. 2, p. 159, doi. 10.1038/ejhg.2014.85
By:
- Abdulhag, Ulla Najwa;
- Soiferman, Devorah;
- Schueler-Furman, Ora;
- Miller, Chaya;
- Shaag, Avraham;
- Elpeleg, Orly;
- Edvardson, Simon;
- Saada, Ann
Publication type:
Article
Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy.
Published in:
European Journal of Human Genetics, 2011, v. 19, n. 4, p. 394, doi. 10.1038/ejhg.2010.214
By:
- Smits, Paulien;
- Saada, Ann;
- Wortmann, Saskia B.;
- Heister, Angelien J.;
- Brink, Maaike;
- Pfundt, Rolph;
- Miller, Chaya;
- Haas, Dorothea;
- Hantschmann, Ralph;
- Rodenburg, Richard J. T.;
- Smeitink, Jan A. M.;
- van den Heuvel, Lambert P.
Publication type:
Article
Frameshifting in the expression of the <em>Escherichia coli</em> trpR gene.
Published in:
Molecular Microbiology, 1992, v. 6, n. 19, p. 2777, doi. 10.1111/j.1365-2958.1992.tb01457.x
By:
- Benhar, Itah;
- Miller, Chaya;
- Engelberg-Kulka, Hanna
Publication type:
Article
Expanding the Mot1 subfamily: 89B helicase encodes a new Drosophila melanogaster SNF2-related protein which binds to multiple sites on polytene chromosomes.
Published in:
Nucleic Acids Research, 1996, v. 24, n. 16, p. 3121, doi. 10.1093/nar/24.16.3121
By:
- Goldman-Levi, Ronit;
- Miller, Chaya;
- Bogoch, Joel;
- Zak, Naomi B.
Publication type:
Article
Defective mitochondrial translation caused by a ribosomal protein (MRPS16) mutation.
Published in:
Annals of Neurology, 2004, v. 56, n. 5, p. 734
By:
- Chaya Miller;
- Ann Saada;
- Nava Shaul;
- Naama Shabtai;
- Efrat Ben‐Shalom;
- Avraham Shaag;
- Eli Hershkovitz;
- Orly Elpeleg
Publication type:
Article
Combined OXPHOS complex I and IV defect, due to mutated complex I assembly factor C20ORF7.
Published in:
Journal of Inherited Metabolic Disease, 2012, v. 35, n. 1, p. 125, doi. 10.1007/s10545-011-9348-y
By:
- Saada, Ann;
- Edvardson, Shimon;
- Shaag, Avraham;
- Chung, Wendy;
- Segel, Reeval;
- Miller, Chaya;
- Jalas, Chaim;
- Elpeleg, Orly
Publication type:
Article
Upregulation of COX4-2 via HIF-1α in Mitochondrial COX4-1 Deficiency.
Published in:
Cells (2073-4409), 2021, v. 10, n. 2, p. 452, doi. 10.3390/cells10020452
By:
- Douiev, Liza;
- Miller, Chaya;
- Ruppo, Shmuel;
- Benyamini, Hadar;
- Abu-Libdeh, Bassam;
- Saada, Ann;
- Bai, Yidong
Publication type:
Article

Found: 9