"The organization and the complete nucleotide sequence of the human NADH-cytochrome b5 reductase gene."
Tomatsu S. , Kobayashi Y. , Fukumaki Y. , Yubisui T. , Orii T. , Sakaki Y.
Gene80:353-361(1989) [PubMed] [Europe PMC] [Abstract]

Voice M.W.
Submitted (1996-11) to the EMBL/GenBank/DDBJ databases

Yoon B. , Chung H. , Ko E. , Lee D.
Submitted (2001-03) to the EMBL/GenBank/DDBJ databases

Lan F.
Submitted (1998-08) to the EMBL/GenBank/DDBJ databases

NIEHS SNPs program
Submitted (2003-07) to the EMBL/GenBank/DDBJ databases

"Cloning of human full-length CDSs in BD Creator(TM) system donor vector."
Kalnine N. , Chen X. , Rolfs A. , Halleck A. , Hines L. , Eisenstein S. , Koundinya M. , Raphael J. , Moreira D. , Kelley T. , LaBaer J. , Lin Y. , Phelan M. , Farmer A.
Submitted (2003-08) to the EMBL/GenBank/DDBJ databases

"A genome annotation-driven approach to cloning the human ORFeome."
Collins J.E. , Wright C.L. , Edwards C.A. , Davis M.P. , Grinham J.A. , Cole C.G. , Goward M.E. , Aguado B. , Mallya M. , Mokrab Y. , Huckle E.J. , Beare D.M. , Dunham I.
Genome Biol.5:R84.1-R84.11(2004) [PubMed] [Europe PMC] [Abstract]

"Complete sequencing and characterization of 21,243 full-length human cDNAs."
Ota T. , Suzuki Y. , Nishikawa T. , Otsuki T. , Sugiyama T. , Irie R. , Wakamatsu A. , Hayashi K. , Sato H. , Nagai K. , Kimura K. , Makita H. , Sekine M. , Obayashi M. , Nishi T. , Shibahara T. , Tanaka T. , Ishii S. , Yamamoto J. , Saito K. , Kawai Y. , Isono Y. , Nakamura Y. , Nagahari K. , Murakami K. , Yasuda T. , Iwayanagi T. , Wagatsuma M. , Shiratori A. , Sudo H. , Hosoiri T. , Kaku Y. , Kodaira H. , Kondo H. , Sugawara M. , Takahashi M. , Kanda K. , Yokoi T. , Furuya T. , Kikkawa E. , Omura Y. , Abe K. , Kamihara K. , Katsuta N. , Sato K. , Tanikawa M. , Yamazaki M. , Ninomiya K. , Ishibashi T. , Yamashita H. , Murakawa K. , Fujimori K. , Tanai H. , Kimata M. , Watanabe M. , Hiraoka S. , Chiba Y. , Ishida S. , Ono Y. , Takiguchi S. , Watanabe S. , Yosida M. , Hotuta T. , Kusano J. , Kanehori K. , Takahashi-Fujii A. , Hara H. , Tanase T.-O. , Nomura Y. , Togiya S. , Komai F. , Hara R. , Takeuchi K. , Arita M. , Imose N. , Musashino K. , Yuuki H. , Oshima A. , Sasaki N. , Aotsuka S. , Yoshikawa Y. , Matsunawa H. , Ichihara T. , Shiohata N. , Sano S. , Moriya S. , Momiyama H. , Satoh N. , Takami S. , Terashima Y. , Suzuki O. , Nakagawa S. , Senoh A. , Mizoguchi H. , Goto Y. , Shimizu F. , Wakebe H. , Hishigaki H. , Watanabe T. , Sugiyama A. , Takemoto M. , Kawakami B. , Yamazaki M. , Watanabe K. , Kumagai A. , Itakura S. , Fukuzumi Y. , Fujimori Y. , Komiyama M. , Tashiro H. , Tanigami A. , Fujiwara T. , Ono T. , Yamada K. , Fujii Y. , Ozaki K. , Hirao M. , Ohmori Y. , Kawabata A. , Hikiji T. , Kobatake N. , Inagaki H. , Ikema Y. , Okamoto S. , Okitani R. , Kawakami T. , Noguchi S. , Itoh T. , Shigeta K. , Senba T. , Matsumura K. , Nakajima Y. , Mizuno T. , Morinaga M. , Sasaki M. , Togashi T. , Oyama M. , Hata H. , Watanabe M. , Komatsu T. , Mizushima-Sugano J. , Satoh T. , Shirai Y. , Takahashi Y. , Nakagawa K. , Okumura K. , Nagase T. , Nomura N. , Kikuchi H. , Masuho Y. , Yamashita R. , Nakai K. , Yada T. , Nakamura Y. , Ohara O. , Isogai T. , Sugano S. more...
Nat. Genet.36:40-45(2004) [PubMed] [Europe PMC] [Abstract]

"The DNA sequence of human chromosome 22."
Dunham I. , Hunt A.R. , Collins J.E. , Bruskiewich R. , Beare D.M. , Clamp M. , Smink L.J. , Ainscough R. , Almeida J.P. , Babbage A.K. , Bagguley C. , Bailey J. , Barlow K.F. , Bates K.N. , Beasley O.P. , Bird C.P. , Blakey S.E. , Bridgeman A.M. , Buck D. , Burgess J. , Burrill W.D. , Burton J. , Carder C. , Carter N.P. , Chen Y. , Clark G. , Clegg S.M. , Cobley V.E. , Cole C.G. , Collier R.E. , Connor R. , Conroy D. , Corby N.R. , Coville G.J. , Cox A.V. , Davis J. , Dawson E. , Dhami P.D. , Dockree C. , Dodsworth S.J. , Durbin R.M. , Ellington A.G. , Evans K.L. , Fey J.M. , Fleming K. , French L. , Garner A.A. , Gilbert J.G.R. , Goward M.E. , Grafham D.V. , Griffiths M.N.D. , Hall C. , Hall R.E. , Hall-Tamlyn G. , Heathcott R.W. , Ho S. , Holmes S. , Hunt S.E. , Jones M.C. , Kershaw J. , Kimberley A.M. , King A. , Laird G.K. , Langford C.F. , Leversha M.A. , Lloyd C. , Lloyd D.M. , Martyn I.D. , Mashreghi-Mohammadi M. , Matthews L.H. , Mccann O.T. , Mcclay J. , Mclaren S. , McMurray A.A. , Milne S.A. , Mortimore B.J. , Odell C.N. , Pavitt R. , Pearce A.V. , Pearson D. , Phillimore B.J.C.T. , Phillips S.H. , Plumb R.W. , Ramsay H. , Ramsey Y. , Rogers L. , Ross M.T. , Scott C.E. , Sehra H.K. , Skuce C.D. , Smalley S. , Smith M.L. , Soderlund C. , Spragon L. , Steward C.A. , Sulston J.E. , Swann R.M. , Vaudin M. , Wall M. , Wallis J.M. , Whiteley M.N. , Willey D.L. , Williams L. , Williams S.A. , Williamson H. , Wilmer T.E. , Wilming L. , Wright C.L. , Hubbard T. , Bentley D.R. , Beck S. , Rogers J. , Shimizu N. , Minoshima S. , Kawasaki K. , Sasaki T. , Asakawa S. , Kudoh J. , Shintani A. , Shibuya K. , Yoshizaki Y. , Aoki N. , Mitsuyama S. , Roe B.A. , Chen F. , Chu L. , Crabtree J. , Deschamps S. , Do A. , Do T. , Dorman A. , Fang F. , Fu Y. , Hu P. , Hua A. , Kenton S. , Lai H. , Lao H.I. , Lewis J. , Lewis S. , Lin S.-P. , Loh P. , Malaj E. , Nguyen T. , Pan H. , Phan S. , Qi S. , Qian Y. , Ray L. , Ren Q. , Shaull S. , Sloan D. , Song L. , Wang Q. , Wang Y. , Wang Z. , White J. , Willingham D. , Wu H. , Yao Z. , Zhan M. , Zhang G. , Chissoe S. , Murray J. , Miller N. , Minx P. , Fulton R. , Johnson D. , Bemis G. , Bentley D. , Bradshaw H. , Bourne S. , Cordes M. , Du Z. , Fulton L. , Goela D. , Graves T. , Hawkins J. , Hinds K. , Kemp K. , Latreille P. , Layman D. , Ozersky P. , Rohlfing T. , Scheet P. , Walker C. , Wamsley A. , Wohldmann P. , Pepin K. , Nelson J. , Korf I. , Bedell J.A. , Hillier L.W. , Mardis E. , Waterston R. , Wilson R. , Emanuel B.S. , Shaikh T. , Kurahashi H. , Saitta S. , Budarf M.L. , McDermid H.E. , Johnson A. , Wong A.C.C. , Morrow B.E. , Edelmann L. , Kim U.J. , Shizuya H. , Simon M.I. , Dumanski J.P. , Peyrard M. , Kedra D. , Seroussi E. , Fransson I. , Tapia I. , Bruder C.E. , O'Brien K.P. , Wilkinson P. , Bodenteich A. , Hartman K. , Hu X. , Khan A.S. , Lane L. , Tilahun Y. , Wright H. more...
Nature402:489-495(1999) [PubMed] [Europe PMC] [Abstract]

"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res.14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]

"Molecular cloning of cDNAs of human liver and placenta NADH-cytochrome b5 reductase."
Yubisui T. , Naitoh Y. , Zenno S. , Tamura M. , Takeshita M. , Sakaki Y.
Proc. Natl. Acad. Sci. U.S.A.84:3609-3613(1987) [PubMed] [Europe PMC] [Abstract]

"Upregulation of voltage-gated Na+ channel expression and metastatic potential in human breast cancer: correlative studies on cell lines and biopsy tissues."
Diss J.K.J. , Fraser S.P. , Coombes R.C. , Djamgoz M.B.A.
Submitted (2001-04) to the EMBL/GenBank/DDBJ databases

"The NH2-terminal structures of human and rat liver microsomal NADH-cytochrome b5 reductases."
Murakami K. , Yubisui T. , Takeshita M. , Miyata T.
J. Biochem.105:312-317(1989) [PubMed] [Europe PMC] [Abstract]

"Complete amino acid sequence of NADH-cytochrome b5 reductase purified from human erythrocytes."
Yubisui T. , Miyata T. , Iwanaga S. , Tamura M. , Takeshita M.
J. Biochem.99:407-422(1986) [PubMed] [Europe PMC] [Abstract]

"Amino acid sequence of NADH-cytochrome b5 reductase of human erythrocytes."
Yubisui T. , Miyata T. , Iwanaga S. , Tamura M. , Yoshida S. , Takeshita M. , Nakajima H.
J. Biochem.96:579-582(1984) [PubMed] [Europe PMC] [Abstract]

"An erythroid-specific transcript generates the soluble form of NADH-cytochrome b5 reductase in humans."
Bulbarelli A. , Valentini A. , De Silvestris M. , Cappellini M.D. , Borgese N.
Blood92:310-319(1998) [PubMed] [Europe PMC] [Abstract]

"Role of cysteine residues in human NADH-cytochrome b5 reductase studied by site-directed mutagenesis. Cys-273 and Cys-283 are located close to the NADH-binding site but are not catalytically essential."
Shirabe K. , Yubisui T. , Nishino T. , Takeshita M.
J. Biol. Chem.266:7531-7536(1991) [PubMed] [Europe PMC] [Abstract]

"A quantitative atlas of mitotic phosphorylation."
Dephoure N. , Zhou C. , Villen J. , Beausoleil S.A. , Bakalarski C.E. , Elledge S.J. , Gygi S.P.
Proc. Natl. Acad. Sci. U.S.A.105:10762-10767(2008) [PubMed] [Europe PMC] [Abstract]

"Lysine acetylation targets protein complexes and co-regulates major cellular functions."
Choudhary C. , Kumar C. , Gnad F. , Nielsen M.L. , Rehman M. , Walther T.C. , Olsen J.V. , Mann M.
Science325:834-840(2009) [PubMed] [Europe PMC] [Abstract]

"Initial characterization of the human central proteome."
Burkard T.R. , Planyavsky M. , Kaupe I. , Breitwieser F.P. , Buerckstuemmer T. , Bennett K.L. , Superti-Furga G. , Colinge J.
BMC Syst. Biol.5:17-17(2011) [PubMed] [Europe PMC] [Abstract]

"Structure of human erythrocyte NADH-cytochrome b5 reductase."
Bando S. , Takano T. , Yubisui T. , Shirabe K. , Takeshita M. , Nakagawa A.
Acta Crystallogr. D60:1929-1934(2004) [PubMed] [Europe PMC] [Abstract]

"Structural role of serine 127 in the NADH-binding site of human NADH-cytochrome b5 reductase."
Yubisui T. , Shirabe K. , Takeshita M. , Kobayashi Y. , Fukumaki Y. , Sakaki Y. , Takano T.
J. Biol. Chem.266:66-70(1991) [PubMed] [Europe PMC] [Abstract]

"Exonic point mutations in NADH-cytochrome B5 reductase genes of homozygotes for hereditary methemoglobinemia, types I and III: putative mechanisms of tissue-dependent enzyme deficiency."
Katsube T. , Sakamoto N. , Kobayashi Y. , Seki R. , Hirano M. , Tanishima K. , Tomoda A. , Takazakura E. , Yubisui T. , Takeshita M. , Sakaki Y. , Fukumaki Y.
Am. J. Hum. Genet.48:799-808(1991) [PubMed] [Europe PMC] [Abstract]

"Enzymatic instability of NADH-cytochrome b5 reductase as a cause of hereditary methemoglobinemia type I (red cell type)."
Shirabe K. , Yubisui T. , Borgese N. , Tang C.-Y. , Hultquist D.E. , Takeshita M.
J. Biol. Chem.267:20416-20421(1992) [PubMed] [Europe PMC] [Abstract]

"An in-frame deletion of codon 298 of the NADH-cytochrome b5 reductase gene results in hereditary methemoglobinemia type II (generalized type). A functional implication for the role of the COOH-terminal region of the enzyme."
Shirabe K. , Fujimoto Y. , Yubisui T. , Takeshita M.
J. Biol. Chem.269:5952-5957(1994) [PubMed] [Europe PMC] [Abstract]

"Four new mutations in the NADH-cytochrome b5 reductase gene from patients with recessive congenital methemoglobinemia type II."
Vieira L.M. , Kaplan J.-C. , Kahn A. , Leroux A.
Blood85:2254-2262(1995) [PubMed] [Europe PMC] [Abstract]

"A high-frequency polymorphism of NADH-cytochrome b5 reductase in African-Americans."
Jenkins M.M. , Prchal J.T.
Hum. Genet.99:248-250(1997) [PubMed] [Europe PMC] [Abstract]

"Identification of a novel point mutation (Leu72-to-Pro) in the NADH-cytochrome b5 reductase gene of a patient with hereditary methaemoglobinaemia type I."
Wu Y.-S. , Huang C.-H. , Wan Y. , Huang Q.-J. , Zhu Z.-Y.
Br. J. Haematol.102:575-577(1998) [PubMed] [Europe PMC] [Abstract]

"Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH-cytochrome b5 reductase gene."
Higasa K. , Manabe J.I. , Yubisui T. , Sumimoto H. , Pung-Amritt P. , Tanphaichitr V.S. , Fukumaki Y.
Br. J. Haematol.103:922-930(1998) [PubMed] [Europe PMC] [Abstract]

"A novel mutation in the NADH-cytochrome b5 reductase gene of a Chinese patient with recessive congenital methemoglobinemia."
Wang Y. , Wu Y.-S. , Zheng P.-Z. , Yang W.-X. , Fang G.-A. , Tang Y.-C. , Xie F. , Lan F.-H. , Zhu Z.-Y.
Blood95:3250-3255(2000) [PubMed] [Europe PMC] [Abstract]

"Arginine-glutamine replacement at residue 57 of NADH-cytochrome b5 reductase in Chinese hereditary methemoglobinemia."
Huang C.-H. , Xie Y. , Wang Y. , Wu Y.-S.
Zhonghua Xue Ye Xue Za Zhi18:200-203(1997) [PubMed] [Europe PMC] [Abstract]

"Familial idiopathic methemoglobinemia revisited: original cases reveal 2 novel mutations in NADH-cytochrome b5 reductase."
Percy M.J. , Gillespie M.J.S. , Savage G. , Hughes A.E. , McMullin M.F. , Lappin T.R.J.
Blood100:3447-3449(2002) [PubMed] [Europe PMC] [Abstract]

"Recessive congenital methaemoglobinaemia: functional characterization of the novel D239G mutation in the NADH-binding lobe of cytochrome b5 reductase."
Percy M.J. , Crowley L.J. , Davis C.A. , McMullin M.F. , Savage G. , Hughes J. , McMahon C. , Quinn R.J.M. , Smith O. , Barber M.J. , Lappin T.R.J.
Br. J. Haematol.129:847-853(2005) [PubMed] [Europe PMC] [Abstract]