Levinson DF, Holmans P, Straub RE, Owen MJ, Wildenauer DB, Gejman PV, Pulver AE, Laurent C, Kendler KS, Walsh D, Norton N, Williams NM, Schwab SG, Lerer B, Mowry BJ, Sanders AR, Antonarakis SE, Blouin JL, DeLeuze JF, Mallet J: Multicenter linkage study of Schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: Schizophrenia linkage collaborative group III. Am J Hum Genet. 2000, 67: 652-663. 10.1086/303041.
Article
PubMed Central
CAS
PubMed
Google Scholar
Riley BP, McGuffin P: Linkage and associated studies of Schizophrenia. Am J Med Genet. 2000, 97: 23-44. 10.1002/(SICI)1096-8628(200021)97:1<23::AID-AJMG5>3.0.CO;2-K.
Article
CAS
PubMed
Google Scholar
Baron M: Genetics of Schizophrenia and the New Millenium: Progress and Pitfalls. Am J Med Genet. 2001, 68: 299-312. 10.1086/318212.
CAS
Google Scholar
Gurling H, Kalsi G, Brynjolfson J, Sigmundsson T, Sherrington R, Mankoo B, Read T, Murphy PBE, McQuillin A, Petursson H, Curtis D: Genomewide genetic linkage analysis confirms the presence of susceptibility loci for Schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8q21-22 and provides support for linkage to Schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23. Am J Hum Genet. 2001, 68: 661-673. 10.1086/318788.
Article
PubMed Central
CAS
PubMed
Google Scholar
Thaker G, Carpenter JW: Advances in Schizophrenia. Nature Medicine. 2001, 7: 667-671. 10.1038/89040.
Article
CAS
PubMed
Google Scholar
Waterworth DM, Bassett AS, Brzustowicz LM: Recent advances in the genetics of Schizophrenia. CMLS. 2002, 59: 331-348. 10.1007/s00018-002-8426-6.
Article
PubMed Central
CAS
Google Scholar
Williams J, Spurlock G, Holmans P, Mant R, Murphy K, Jones Lea, Cardno A, Asherson P, Blackwood D, Muir W, Meszaros K, Aschauer H, al MJe: A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and Schizophrenia. Mol Psychiatry. 1998, 3: 141-149. 10.1038/sj.mp.4000376.
Article
CAS
PubMed
Google Scholar
Dubertret C, Gorwood P, Ades J, Feingold J, Schwartz JC, Sokoloff P: Meta-analysis of DRD3 gene and Schizophrenia: ethnic heterogeneity and significant association in Caucasians. Am J Med Genet. 1998, 81: 318-322. 10.1002/(SICI)1096-8628(19980710)81:4<318::AID-AJMG8>3.0.CO;2-P.
Article
CAS
PubMed
Google Scholar
Zubenko G, Hughes H, Stiffler J, Zubenko W, BB K: Genome survey for susceptibility loci for recurrent, early-onset major depression: Results at 10 cM resolution. Am J Med Genet. 2002, 114: 413-422. 10.1002/ajmg.10381.
Article
PubMed
Google Scholar
Blouin JL, Dombroski BA, Nath SK, Lasseter VK, Wolyniec PS, Nestadt G, Thornquist M, Ullrich G, McGrath J, Kasch L, Lamacz M, Thomas MG, Gehrig C, Radhakrishna U, Snyder SE, Balk KG, Neufeld K, Swartz KL, DeMarchi N, Papadimitriou GN, Dikeos DG, Stefanis CN, Chakravarti A, Childs B, Pulver AE: Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21. Nat Genet. 1998, 20: 70-73. 10.1038/1734.
Article
CAS
PubMed
Google Scholar
Brzustowicz LM, Honer WG, Chow EW, Little D, Hogan J, Hodgkinson K, Bassett AS: Linkage of familial Schizophrenia to chromosome 13q32. Am J Hum Genet. 1999, 65: 1096-1103. 10.1086/302579.
Article
PubMed Central
CAS
PubMed
Google Scholar
Detera-Wadleigh SD, Badner JA, Berrettini WH, Yoshikawa T, Goldin LR, Turner G, Rollins DY, Moses T, Sanders AR, Karkera JD, Esterling LE, Zeng J, Ferraro TN, Guroff JJ, Kazuba D, Maxwell ME, Nurnberger JI, Gershon ES: A high-density genome scan detects evidence for a Bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2. Proc Natl Acad Sci U S A. 1999, 96: 5604-5609. 10.1073/pnas.96.10.5604.
Article
PubMed Central
CAS
PubMed
Google Scholar
Badner JA, Gershon ES: Meta analysis of whole-genome linkage scans of Bipolar disorder and Schizophrenia. Mol Psychiatry. 2002, 7: 405-411. 10.1038/sj.mp.4001012.
Article
CAS
PubMed
Google Scholar
Chrisitan S, McDonough J, Liu C-y, Shaikh S, Vlamakis V, Badner J, Chakravarti A, Gershon E: An evaluation of the assembly of an approximately 15-Mb region on human chromosome 13q32-q33 linked to Bipolar disorder and Schizophrenia. Genomics. 2002, 79: 635-656. 10.1006/geno.2002.6765.
Article
Google Scholar
Liu C, Badner JA, SL C, Guroff JJ, Detera-Wadleigh SD, Gershon ES: Fine Mapping Supports Previous Linkage Evidence for a Bipolar Disorder Susceptibility Locus on 13q32. Am J Med Genet. 2001, 105: 375-380. 10.1002/ajmg.1358.
Article
CAS
PubMed
Google Scholar
Fei YJ, Kanai Y, Nussberger S, Ganapathy V, Leibach FH, Romero MF, Singh SK, Boron WF, Hediger MA: Expression cloning of a mammalian proton-coupled oligopeptide transporter. Nature. 1994, 368: 563-566. 10.1038/368563a0.
Article
CAS
PubMed
Google Scholar
Liang R, Fei Y, Prasad P, Ramamoorthy S, Han H, Yang-Feng T, Hediger M, Ganapathy V, Leibach F: Human intestinal H(+)/ peptide cotransporter: cloning, functional expression, and chromosomal localization. J Biol Chem. 1995, 20: 6456-6463.
Google Scholar
Adibi SA: The oligopeptide transporter (Pept-1) in human intestine: biology and function. Gastroenterology. 1997, 113: 332-340.
Article
CAS
PubMed
Google Scholar
Tamai I, Nakanihsi T, Nakahara H, Sai Y, Ganapathy V, Leibach F: Improvement of L-do-pa absorption by dipeptidyl derivation, utilizing peptide transporter PepT1. J Pharm Sci. 1998, 87: 1542-1546. 10.1021/js980186o.
Article
CAS
PubMed
Google Scholar
Oh D, Han H, Amidon G: Drug transport and targeting. Intestinal transport. Pharm Biotechnol. 1999, 12: 59-88.
Article
CAS
PubMed
Google Scholar
Veugelers M, Vermeesch J, Reekmans G, Steinfeld R, Marynen P, David G: Characterization of glypican-5 and chromosomal localization of human GPC5, a new member of the Glypican gene family. Genomics. 1997, 40: 24-30. 10.1006/geno.1996.4518.
Article
CAS
PubMed
Google Scholar
Saunders S, Paine-Saunders S, Lander A: Expression of the cell surface proteoglycan glypican-5 is developmentally regulated in kidney, limb, and brain. Dev Biol. 1997, 190: 78-93. 10.1006/dbio.1997.8690.
Article
CAS
PubMed
Google Scholar
Paine-Saunders S, Viviano B, Saunders S: GPC6, a novel member of the glypican gene family, encodes a product structurally related to GPC4 and is colocalized with GPC5 on human chromosome 13. Genomics. 1999, 57: 455-458. 10.1006/geno.1999.5793.
Article
CAS
PubMed
Google Scholar
Brown S, Russo J, Chitayat D, Warburton D: The 13q- syndrome: the molecular definition of a critical deletion region in band 13q32. Am J Hum Genet. 1995, 57: 859-866.
PubMed Central
CAS
PubMed
Google Scholar
Yamaguchi Y: Heparan sulfate proteoglycans in the nervous system: their div roles in neurogenesis, axon guidance, and synaptogenesis. Semin Cell Dev Biol. 2001, 12: 99-106. 10.1006/scdb.2000.0238.
Article
CAS
PubMed
Google Scholar
Nakato H, Futch T, Selleck S: The division abnormally delayed (dally) gene: A putative integral membrane proteoglycan required for cell division patterning during postembryonic development of the nervous system in Drosophila. Development. 1995, 121: 3687-3702.
CAS
PubMed
Google Scholar
Gonzalez A, Kaya M, Shi W, Song H, Testa J, Penn L, Filmus J: OCI-5/GPC3, a glypican encoded by a gene that is mutated in the Simpson-Golabi-Behmel overgrowth syndrome, induces apoptosis in a cell line-specific manner. J Cell Biol. 1998, 141: 1407-1414. 10.1083/jcb.141.6.1407.
Article
PubMed Central
CAS
PubMed
Google Scholar
Veugelers M, Cat B, Muyldermans S, Reekmans G, Delande N, Frints S, Legius E, Fryns J, Schrander-Stumpel C, Weidle B, Magdalena N, David G: Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene. Hum Mol Genet. 2000, 9: 1321-1328. 10.1093/hmg/9.9.1321.
Article
CAS
PubMed
Google Scholar
Li M, Shuman C, Fei Y, Cutiongco E, Bender H, Stevens C, Wilkins-Haug L, Day-Salvatore D, Yong S, Geraghty M, Squire J, Weksberg R: GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome. Am J Med Genet. 2001, 102: 161-168. 10.1002/1096-8628(20010801)102:2<161::AID-AJMG1453>3.0.CO;2-O.
Article
CAS
PubMed
Google Scholar
Veugelers M, De Cat B, Delande N, Esselens C, Bonk I, Vermeesch J, Marynen P, Fryns J, David G: A 4-Mb BAC/PAC contig and complete genomic structure of the GPC5/GPC6 gene cluster on chromosome 13q32. Matrix Biol. 2001, 20: 375-385. 10.1016/S0945-053X(01)00143-3.
Article
CAS
PubMed
Google Scholar
Syrrou M, Keymolen K, Devriendt K, Holvoet M, Reinhilde T, Verhofstadt K, Fryns J-P: Glypican 1 gene: Good candidate for brachydactyly type E. Am J med Genet. 2002, 108: 310-314. 10.1002/ajmg.10266.
Article
PubMed
Google Scholar
Uttri A, Johns S, Sadee W: Genomic Structure of Proton-Coupled Oligopeptide Transporter SLC15A1 and pH-Sensing regulatory Splice Variant. AAPS PharmSci. 2001, 3: E6-10.1208/ps030106.
Google Scholar
Bolger M, Haworth I, Yeung A, Ann D, Grafenstein H, Alvarez S, Okamoto C, Kim K, Basu S, Wu S, Lee V: Structure, Function, and Molecular Modeling Approaches to teh Study ofthe Intenstinal Dipeptide Tranporter PepT1. J Pharm Sci. 1998, 87: 1286-1291. 10.1021/js980090u.
Article
CAS
PubMed
Google Scholar
Yeung A, Basu S, Wu S, Chu C, Okamoto C, Alvarez S, Grafenstein H, Shen W, Kim K, Bolger M, Haworth I, Ann D, Lee V: Molecular Identification of a Role for Tyrosine 167 in the Function of the Human Intestinal Proton-Coupled Dipeptide transporter (SLC15A1). Biochem Biophys Res Commum. 1998, 250: 103-107. 10.1006/bbrc.1998.9283.
Article
CAS
Google Scholar
Lee V, Chu C, Mahlin E, Basu S, Ann D, Bolger M, Haworth I, Yeung A, Wu S, Alvarez S, Okamoto C: Biopharmaceutics of Transmucosal Peptide and Protein Drug Administration: Role of Transport Mechanisms with a Focul on the Involvement of PepT1. J Controlled Rel. 1999, 62: 129-140. 10.1016/S0168-3659(99)00030-9.
Article
CAS
Google Scholar
Chen X, Steel A, Hediger MA: Functional Roles of Histidine and Tyrosine Residues in the H(+)-Peptide Transporter PepT1. Biochem Biophys REs Commum. 2000, 272: 726-730. 10.1006/bbrc.2000.2851.
Article
CAS
Google Scholar
Li M, Squire J, Weksberg R: Molecular genetics of Wiedemann-Beckwith syndrome. Am J Med Genet. 1998, 79: 253-259. 10.1002/(SICI)1096-8628(19981002)79:4<253::AID-AJMG5>3.0.CO;2-N.
Article
CAS
PubMed
Google Scholar
Shanske A, Ferreira J, Leonard J, Fuller P, Marion R: Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13. Am J Med Genet. 2001, 102: 231-236. 10.1002/ajmg.1451.
Article
CAS
PubMed
Google Scholar
Ujike H, Takehisa Y, Takaki M, Tanaka Y, Nakata K, Takeda T, Kodama M, Fujiwara Y, Yamamoto A, Kuroda S: NOTCH4 gene polymorphism and susceptibility to Schizophrenia and schizoaffective disorder. Neurosci Lett. 2001, 301: 41-44. 10.1016/S0304-3940(01)01602-0.
Article
CAS
PubMed
Google Scholar
Van Camp G, Willems P, Smith R: Nonsyndromic hearing impairment: unparalleled heterogeneity. Am J Hum Genet. 1997, 60: 758-764.
PubMed Central
CAS
PubMed
Google Scholar
Rabionet R, Zelante L, Lopez-Bigas N, D'Agruma L, Melchionda S, Restagno G, Arbones M, Gasparini P, Estivill X: Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene. Hum Genet. 2000, 106: 40-44. 10.1007/s004390051007.
Article
CAS
PubMed
Google Scholar
Muzny DM, Metzker M, Bouck J, Gorrell J, Ding Y, Maxim E, Gibbs R: Using BODIPY dye-primer chemistry in large-scale sequencing. IEEE Engineering in Med Biol. 1998, 17 (6): 88-93. 10.1109/51.731327.
Article
CAS
Google Scholar