
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
IMMT
Introduction
Mitochondrial inner membrane protein is a protein that in humans is encoded by the IMMT gene.[1][2][3]
References
References
- ↑ Gieffers C, Korioth F, Heimann P, Ungermann C, Frey J (Jun 1997). “Mitofilin is a transmembrane protein of the inner mitochondrial membrane expressed as two isoforms”. Exp Cell Res. 232 (2): 395–9. doi:10.1006/excr.1997.3539. PMID 9168817.
- ↑ Icho T, Ikeda T, Matsumoto Y, Hanaoka F, Kaji K, Tsuchida N (Aug 1994). “A novel human gene that is preferentially transcribed in heart muscle”. Gene. 144 (2): 301–6. doi:10.1016/0378-1119(94)90394-8. PMID 8039717.
- ↑ “Entrez Gene: IMMT inner membrane protein, mitochondrial (mitofilin)”.
- ↑ Lehner, Ben; Semple Jennifer I; Brown Stephanie E; Counsell Damian; Campbell R Duncan; Sanderson Christopher M (Jan 2004). “Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region”. Genomics. United States. 83 (1): 153–67. doi:10.1016/S0888-7543(03)00235-0. ISSN 0888-7543. PMID 14667819.
Further reading
Further reading
- Dawson SJ, White LA (1992). “Treatment of Haemophilus aphrophilus endocarditis with ciprofloxacin”. J. Infect. 24 (3): 317–20. doi:10.1016/S0163-4453(05)80037-4. PMID 1602151.
- Maruyama K, Sugano S (1994). “Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides”. Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
- Bonaldo MF, Lennon G, Soares MB (1997). “Normalization and subtraction: two approaches to facilitate gene discovery”. Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
- Hillier LD, Lennon G, Becker M, et al. (1997). “Generation and analysis of 280,000 human expressed sequence tags”. Genome Res. 6 (9): 807–28. doi:10.1101/gr.6.9.807. PMID 8889549.
- Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). “Construction and characterization of a full length-enriched and a 5′-end-enriched cDNA library”. Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
- Hattori M, Fujiyama A, Taylor TD, et al. (2000). “The DNA sequence of human chromosome 21”. Nature. 405 (6784): 311–9. doi:10.1038/35012518. PMID 10830953.
- Liu J, Akoulitchev S, Weber A, et al. (2001). “Defective interplay of activators and repressors with TFIH in xeroderma pigmentosum”. Cell. 104 (3): 353–63. doi:10.1016/S0092-8674(01)00223-9. PMID 11239393.
- Bernert G, Fountoulakis M, Lubec G (2003). “Manifold decreased protein levels of matrin 3, reduced motor protein HMP and hlark in fetal Down’s syndrome brain”. Proteomics. 2 (12): 1752–7. doi:10.1002/1615-9861(200212)2:12<1752::AID-PROT1752>3.0.CO;2-Y. PMID 12469345.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). “Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences”. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS…9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Millar JK, Christie S, Porteous DJ (2004). “Yeast two-hybrid screens implicate DISC1 in brain development and function”. Biochem. Biophys. Res. Commun. 311 (4): 1019–25. doi:10.1016/j.bbrc.2003.10.101. PMID 14623284.
- Lehner B, Semple JI, Brown SE, et al. (2004). “Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region”. Genomics. 83 (1): 153–67. doi:10.1016/S0888-7543(03)00235-0. PMID 14667819.
- Goehler H, Lalowski M, Stelzl U, et al. (2004). “A protein interaction network links GIT1, an enhancer of huntingtin aggregation, to Huntington’s disease”. Mol. Cell. 15 (6): 853–65. doi:10.1016/j.molcel.2004.09.016. PMID 15383276.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). “The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)”. Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- John GB, Shang Y, Li L, et al. (2005). “The Mitochondrial Inner Membrane Protein Mitofilin Controls Cristae Morphology”. Mol. Biol. Cell. 16 (3): 1543–54. doi:10.1091/mbc.E04-08-0697. PMC 551514. PMID 15647377.
- Stelzl U, Worm U, Lalowski M, et al. (2005). “A human protein-protein interaction network: a resource for annotating the proteome”. Cell. 122 (6): 957–68. doi:10.1016/j.cell.2005.08.029. PMID 16169070.
- Lim J, Hao T, Shaw C, et al. (2006). “A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration”. Cell. 125 (4): 801–14. doi:10.1016/j.cell.2006.03.032. PMID 16713569.
- Camargo LM, Collura V, Rain JC, et al. (2007). “Disrupted in Schizophrenia 1 Interactome: evidence for the close connectivity of risk genes and a potential synaptic basis for schizophrenia”. Mol. Psychiatry. 12 (1): 74–86. doi:10.1038/sj.mp.4001880. PMID 17043677.
- Xie J, Marusich MF, Souda P, et al. (2007). “The mitochondrial inner membrane protein mitofilin exists as a complex with SAM50, metaxins 1 and 2, coiled-coil-helix coiled-coil-helix domain-containing protein 3 and 6 and DnaJC11”. FEBS Lett. 581 (18): 3545–9. doi:10.1016/j.febslet.2007.06.052. PMID 17624330.
