107 related articles for article (PubMed ID: 10602993)
1. A deletion on chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidate.
Paige AJ; Kiernan BW; Varela A; Rogers MJ; Hughes D; Steel KP; Brown SD
Mamm Genome; 2000 Jan; 11(1):51-7. PubMed ID: 10602993
[TBL] [Abstract][Full Text] [Related]
2. Genetic mapping of the whirler mutation.
Rogers MJ; Fleming J; Kiernan BW; Mburu P; Varela A; Brown SD; Steel KP
Mamm Genome; 1999 May; 10(5):513-9. PubMed ID: 10337627
[TBL] [Abstract][Full Text] [Related]
3. Linkage analysis of the whirler deafness gene on mouse chromosome 4.
Fleming J; Rogers MJ; Brown SD; Steel KP
Genomics; 1994 May; 21(1):42-8. PubMed ID: 8088814
[TBL] [Abstract][Full Text] [Related]
4. Human orosomucoid polymorphism: molecular basis of the three common ORM1 alleles, ORM1*F1, ORM1*F2, and ORM1*S.
Yuasa I; Umetsu K; Vogt U; Nakamura H; Nanba E; Tamaki N; Irizawa Y
Hum Genet; 1997 Mar; 99(3):393-8. PubMed ID: 9050929
[TBL] [Abstract][Full Text] [Related]
5. Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.
Mburu P; Mustapha M; Varela A; Weil D; El-Amraoui A; Holme RH; Rump A; Hardisty RE; Blanchard S; Coimbra RS; Perfettini I; Parkinson N; Mallon AM; Glenister P; Rogers MJ; Paige AJ; Moir L; Clay J; Rosenthal A; Liu XZ; Blanco G; Steel KP; Petit C; Brown SD
Nat Genet; 2003 Aug; 34(4):421-8. PubMed ID: 12833159
[TBL] [Abstract][Full Text] [Related]
6. Elongation of hair cell stereocilia is defective in the mouse mutant whirler.
Holme RH; Kiernan BW; Brown SD; Steel KP
J Comp Neurol; 2002 Aug; 450(1):94-102. PubMed ID: 12124769
[TBL] [Abstract][Full Text] [Related]
7. Orosomucoid (ORM) typing by isoelectric focusing: evidence for gene duplication of ORM1 and genetic polymorphism of ORM2.
Yuasa I; Suenaga K; Umetsu K; Ito K; Robinet-Levy M
Hum Genet; 1987 Nov; 77(3):255-8. PubMed ID: 3679210
[TBL] [Abstract][Full Text] [Related]
8. Fine mapping of the circling (cir) gene on the distal portion of mouse chromosome 9.
Cho KI; Lee JW; Kim KS; Lee EJ; Suh JG; Lee HJ; Kim HT; Hong SH; Chung WH; Chang KT; Hyun BH; Oh YS; Ryoo ZY
Comp Med; 2003 Dec; 53(6):642-8. PubMed ID: 14727813
[TBL] [Abstract][Full Text] [Related]
9. Orosomucoid (ORM) typing by isoelectric focusing: evidence for an additional duplicated ORM1 locus haplotype and close linkage of two ORM loci.
Yuasa I; Umetsu K; Suenaga K
Am J Hum Genet; 1988 Aug; 43(2):165-9. PubMed ID: 3400642
[TBL] [Abstract][Full Text] [Related]
10. The circling mouse (C57BL/6J-cir) has a 40-kilobase genomic deletion that includes the transmembrane inner ear (tmie) gene.
Cho KI; Suh JG; Lee JW; Hong SH; Kang TC; Oh YS; Ryoo ZY
Comp Med; 2006 Dec; 56(6):476-81. PubMed ID: 17219777
[TBL] [Abstract][Full Text] [Related]
11. Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21.
Merry DE; Lesko JG; Sosnoski DM; Lewis RA; Lubinsky M; Trask B; van den Engh G; Collins FS; Nussbaum RL
Am J Hum Genet; 1989 Oct; 45(4):530-40. PubMed ID: 2491012
[TBL] [Abstract][Full Text] [Related]
12. Orosomucoid system: 17 additional orosomucoid variants and proposal for a new nomenclature.
Yuasa I; Weidinger S; Umetsu K; Suenaga K; Ishimoto G; Eap BC; Duche JC; Baumann P
Vox Sang; 1993; 64(1):47-55. PubMed ID: 8447119
[TBL] [Abstract][Full Text] [Related]
13. A comparative transcript map and candidates for mutant phenotypes in the Tyrp1 (brown) deletion complex homologous to human 9p21-23.
Simpson EH; Suffolk R; Bell JA; Jordan SA; Johnson DK; Hunsicker PR; Weber JS; Justice MJ; Jackson IJ
Mamm Genome; 2000 Jan; 11(1):58-63. PubMed ID: 10602994
[TBL] [Abstract][Full Text] [Related]
14. Orosomucoid (ORM) typing by isoelectric focusing: evidence for several new variants including ORM1 and ORM2 silent alleles.
Yuasa I; Umetsu K; Suenaga K; Ikebuchi J; Suzuki T
Vox Sang; 1990; 58(2):129-34. PubMed ID: 2339522
[TBL] [Abstract][Full Text] [Related]
15. Reverse genetics in the mouse and its application to the study of deafness.
Rinchik EM; Johnson DK; Margolis FL; Jackson IJ; Russell LB; Carpenter DA
Ann N Y Acad Sci; 1991; 630():80-92. PubMed ID: 1952626
[TBL] [Abstract][Full Text] [Related]
16. Genetic polymorphisms of orosomucoid on the Han population in Nanjing of China.
Li JH; Xu JQ; Li Y; Zhuang YY; Gong JB
Clin Chim Acta; 1999 Oct; 288(1-2):161-8. PubMed ID: 10529468
[TBL] [Abstract][Full Text] [Related]
17. Orosomucoid (ORM) typing by isoelectric focusing: evidence of two structural loci ORM1 and ORM2.
Yuasa I; Umetsu K; Suenaga K; Robinet-Levy M
Hum Genet; 1986 Oct; 74(2):160-1. PubMed ID: 3770743
[TBL] [Abstract][Full Text] [Related]
18. Subtyping of orosomucoid 1 (ORM1) by isoelectric focusing in agarose and polyacrylamide gels.
Thymann M; Weidinger S
Electrophoresis; 1988 Aug; 9(8):380-3. PubMed ID: 3234379
[TBL] [Abstract][Full Text] [Related]
19. Orosomucoid (ORM 1) subtyping and formal genetics.
Luckenbach C; Kömpf J; Ritter H
Hum Genet; 1991 Aug; 87(4):429-32. PubMed ID: 1879829
[TBL] [Abstract][Full Text] [Related]
20. Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Kurima K; Peters LM; Yang Y; Riazuddin S; Ahmed ZM; Naz S; Arnaud D; Drury S; Mo J; Makishima T; Ghosh M; Menon PS; Deshmukh D; Oddoux C; Ostrer H; Khan S; Riazuddin S; Deininger PL; Hampton LL; Sullivan SL; Battey JF; Keats BJ; Wilcox ER; Friedman TB; Griffith AJ
Nat Genet; 2002 Mar; 30(3):277-84. PubMed ID: 11850618
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
