"Cloning and sequence analysis of a cDNA encoding human non-selective type of endothelin receptor."
Nakamuta M. , Takayanagi R. , Sakai Y. , Sakamoto S. , Hagiwara H. , Mizuno T. , Saito Y. , Hirose S. , Yamamoto M. , Nawata H.
Biochem. Biophys. Res. Commun.177:34-39(1991) [PubMed] [Europe PMC] [Abstract]

"Molecular cloning of a non-isopeptide-selective human endothelin receptor."
Ogawa Y. , Nakao K. , Arai H. , Nakagawa O. , Hosoda K. , Suga S. , Nakanishi S. , Imura H.
Biochem. Biophys. Res. Commun.178:248-255(1991) [PubMed] [Europe PMC] [Abstract]

"Cloning and functional expression of human cDNA for the ETB endothelin receptor."
Sakamoto A. , Yanagisawa M. , Sakurai T. , Takuwa Y. , Yanagisawa H. , Masaki T.
Biochem. Biophys. Res. Commun.178:656-663(1991) [PubMed] [Europe PMC] [Abstract]

"Molecular cloning of human endothelin (ET) receptors ETA and ETB."
Haendler B. , Hechler U. , Schleuning W.-D.
J. Cardiovasc. Pharmacol.20:S1-S4(1992) [PubMed] [Europe PMC] [Abstract]

"Molecular cloning of human endothelin receptors and their expression in vascular endothelial cells and smooth muscle cells."
Arai H. , Nakao K. , Hosoda K. , Ogawa Y. , Nakagawa O. , Komatsu Y. , Imura H.
Jpn. Circ. J.56:1303-1307(1992) [PubMed] [Europe PMC] [Abstract]

"The human endothelin-B receptor gene. Structural organization and chromosomal assignment."
Arai H. , Nakao K. , Takaya K. , Hosoda K. , Ogawa Y. , Nakanishi S. , Imura H.
J. Biol. Chem.268:3463-3470(1993) [PubMed] [Europe PMC] [Abstract]

"Molecular characterization and regulation of the human endothelin receptors."
Elshourbagy N.A. , Korman D.R. , Wu H.L. , Sylvester D.R. , Lee J.A. , Nuthalaganti P. , Bergsma D.J. , Kumar C.S. , Nambi P.
J. Biol. Chem.268:3873-3879(1993) [PubMed] [Europe PMC] [Abstract]

"Cloning and expression of an endothelin receptor subtype B from human prostate that mediates contraction."
Webb M.L. , Chao C.-C. , Rizzo M. , Shapiro R.A. , Neubauer M. , Liu E.C.K. , Aversa C.R. , Brittain R.J. , Treiger B.
Mol. Pharmacol.47:730-737(1995) [PubMed] [Europe PMC] [Abstract]

"Molecular characterization of a novel human endothelin receptor splice variant."
Elshourbagy N.A. , Adamou J.E. , Gagnon A.W. , Wu H.L. , Pullen M. , Nambi P.
J. Biol. Chem.271:25300-25307(1996) [PubMed] [Europe PMC] [Abstract]

"Novel endothelin B receptor transcripts with the potential of generating a new receptor."
Tsutsumi M. , Liang G. , Jones P.A.
Gene228:43-49(1999) [PubMed] [Europe PMC] [Abstract]

"cDNA clones of human proteins involved in signal transduction sequenced by the Guthrie cDNA resource center (www.cdna.org)."
Warren C.N. , Aronstam R.S. , Sharma S.V.
Submitted (2003-04) to the EMBL/GenBank/DDBJ databases

Totoki Y. , Toyoda A. , Takeda T. , Sakaki Y. , Tanaka A. , Yokoyama S. , Ohara O. , Nagase T. , Kikuno R.F.
Submitted (2005-03) to the EMBL/GenBank/DDBJ databases

"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]

NIEHS SNPs program
Submitted (2004-02) to the EMBL/GenBank/DDBJ databases

"The DNA sequence and analysis of human chromosome 13."
Dunham A. , Matthews L.H. , Burton J. , Ashurst J.L. , Howe K.L. , Ashcroft K.J. , Beare D.M. , Burford D.C. , Hunt S.E. , Griffiths-Jones S. , Jones M.C. , Keenan S.J. , Oliver K. , Scott C.E. , Ainscough R. , Almeida J.P. , Ambrose K.D. , Andrews D.T. , Ashwell R.I.S. , Babbage A.K. , Bagguley C.L. , Bailey J. , Bannerjee R. , Barlow K.F. , Bates K. , Beasley H. , Bird C.P. , Bray-Allen S. , Brown A.J. , Brown J.Y. , Burrill W. , Carder C. , Carter N.P. , Chapman J.C. , Clamp M.E. , Clark S.Y. , Clarke G. , Clee C.M. , Clegg S.C. , Cobley V. , Collins J.E. , Corby N. , Coville G.J. , Deloukas P. , Dhami P. , Dunham I. , Dunn M. , Earthrowl M.E. , Ellington A.G. , Faulkner L. , Frankish A.G. , Frankland J. , French L. , Garner P. , Garnett J. , Gilbert J.G.R. , Gilson C.J. , Ghori J. , Grafham D.V. , Gribble S.M. , Griffiths C. , Hall R.E. , Hammond S. , Harley J.L. , Hart E.A. , Heath P.D. , Howden P.J. , Huckle E.J. , Hunt P.J. , Hunt A.R. , Johnson C. , Johnson D. , Kay M. , Kimberley A.M. , King A. , Laird G.K. , Langford C.J. , Lawlor S. , Leongamornlert D.A. , Lloyd D.M. , Lloyd C. , Loveland J.E. , Lovell J. , Martin S. , Mashreghi-Mohammadi M. , McLaren S.J. , McMurray A. , Milne S. , Moore M.J.F. , Nickerson T. , Palmer S.A. , Pearce A.V. , Peck A.I. , Pelan S. , Phillimore B. , Porter K.M. , Rice C.M. , Searle S. , Sehra H.K. , Shownkeen R. , Skuce C.D. , Smith M. , Steward C.A. , Sycamore N. , Tester J. , Thomas D.W. , Tracey A. , Tromans A. , Tubby B. , Wall M. , Wallis J.M. , West A.P. , Whitehead S.L. , Willey D.L. , Wilming L. , Wray P.W. , Wright M.W. , Young L. , Coulson A. , Durbin R.M. , Hubbard T. , Sulston J.E. , Beck S. , Bentley D.R. , Rogers J. , Ross M.T. more...
Nature428:522-528(2004) [PubMed] [Europe PMC] [Abstract]

Mural R.J. , Istrail S. , Sutton G.G. , Florea L. , Halpern A.L. , Mobarry C.M. , Lippert R. , Walenz B. , Shatkay H. , Dew I. , Miller J.R. , Flanigan M.J. , Edwards N.J. , Bolanos R. , Fasulo D. , Halldorsson B.V. , Hannenhalli S. , Turner R. , Yooseph S. , Lu F. , Nusskern D.R. , Shue B.C. , Zheng X.H. , Zhong F. , Delcher A.L. , Huson D.H. , Kravitz S.A. , Mouchard L. , Reinert K. , Remington K.A. , Clark A.G. , Waterman M.S. , Eichler E.E. , Adams M.D. , Hunkapiller M.W. , Myers E.W. , Venter J.C. more...
Submitted (2005-07) to the EMBL/GenBank/DDBJ databases

"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]

"Significance of novel endothelin-B receptor gene polymorphisms in Hirschsprung's disease: predominance of a novel variant (561C/T) in patients with co-existing Down's syndrome."
Zaahl M.G. , du Plessis L. , Warnich L. , Kotze M.J. , Moore S.W.
Mol. Cell. Probes17:49-54(2003) [PubMed] [Europe PMC] [Abstract]

"Endothelin-1 and ETA receptor expression in vascular smooth muscle cells from human placenta: a new ETA receptor messenger ribonucleic acid is generated by alternative splicing of exon 3."
Bourgeois C. , Robert B. , Rebourcet R. , Mondon F. , Mignot T.-M. , Duc-Goiran P. , Ferre F.
J. Clin. Endocrinol. Metab.82:3116-3123(1997) [PubMed] [Europe PMC] [Abstract]

"Palmitoylation of human endothelinB. Its critical role in G protein coupling and a differential requirement for the cytoplasmic tail by G protein subtypes."
Okamoto Y. , Ninomiya H. , Tanioka M. , Sakamoto A. , Miwa S. , Masaki T.
J. Biol. Chem.272:21589-21596(1997) [PubMed] [Europe PMC] [Abstract]

"Mutations in Hirschsprung disease: when does a mutation contribute to the phenotype."
Hofstra R.M.W. , Osinga J. , Buys C.H.C.M.
Eur. J. Hum. Genet.5:180-185(1997) [PubMed] [Europe PMC] [Abstract]

"A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease."
Puffenberger E.G. , Hosoda K. , Washington S.S. , Nakao K. , Dewit D. , Yanagisawa M. , Chakravarti A.
Cell79:1257-1266(1994) [PubMed] [Europe PMC] [Abstract]

"Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease."
Attie T. , Till M. , Pelet A. , Amiel J. , Edery P. , Boutrand L. , Munnich A. , Lyonnet S.
Hum. Mol. Genet.4:2407-2409(1995) [PubMed] [Europe PMC] [Abstract]

"Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population."
Auricchio A. , Casari G. , Staiano A. , Ballabio A.
Hum. Mol. Genet.5:351-354(1996) [PubMed] [Europe PMC] [Abstract]

"Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease."
Amiel J. , Attie T. , Jan D. , Pelet A. , Edery P. , Bidaud C. , Lacombe D. , Tam P. , Simeoni J. , Flori E. , Nihoul-Fekete C. , Munnich A. , Lyonnet S.
Hum. Mol. Genet.5:355-357(1996) [PubMed] [Europe PMC] [Abstract]

"A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)."
Hofstra R.M.W. , Tan-Sindhunata G. , Wu Y. , Kamsteeg E.-J. , Stulp R.P. , van Ravenswaaij-Arts C. , Majoor-Krakauer D. , Angrist M. , Chakravarti A. , Meijers C. , Buys C.H.C.M.
Nat. Genet.12:445-447(1996) [PubMed] [Europe PMC] [Abstract]

"Phenotypic variation in a family with mutations in two Hirschsprung-related genes (RET and endothelin receptor B)."
Svensson P.J. , Anvret M. , Molander M.L. , Nordenskjold A.
Hum. Genet.103:145-148(1998) [PubMed] [Europe PMC] [Abstract]

"Functional characterization of three mutations of the endothelin B receptor gene in patients with Hirschsprung's disease: evidence for selective loss of Gi coupling."
Fuchs S. , Amiel J. , Claudel S. , Lyonnet S. , Corvol P. , Pinet F.
Mol. Med.7:115-124(2001) [PubMed] [Europe PMC] [Abstract]

"ABCD syndrome is caused by a homozygous mutation in the EDNRB gene."
Verheij J.B. , Kunze J. , Osinga J. , van Essen A.J. , Hofstra R.M.
Am. J. Med. Genet.108:223-225(2002) [PubMed] [Europe PMC] [Abstract]

"SOX10 mutations in chronic intestinal pseudo-obstruction suggest a complex physiopathological mechanism."
Pingault V. , Girard M. , Bondurand N. , Dorkins H. , Van Maldergem L. , Mowat D. , Shimotake T. , Verma I. , Baumann C. , Goossens M.
Hum. Genet.111:198-206(2002) [PubMed] [Europe PMC] [Abstract]