-
1
-
-
30344454700
-
Renal ultrasonography not required in babies with isolated minor ear anomalies
-
Deshpande SA, Watson H. 2006. Renal ultrasonography not required in babies with isolated minor ear anomalies. Arch. Dis. Child. Fetal Neonatal. Ed. 91(1):F29-30
-
(2006)
Arch. Dis. Child. Fetal Neonatal. Ed
, vol.91
, Issue.1
-
-
Deshpande, S.A.1
Watson, H.2
-
2
-
-
40949156813
-
Mild external ear malformations and renal tract abnormalities: A meta-analysis
-
Cuestas E, Bur C, Bongiovanni V. 2006. Mild external ear malformations and renal tract abnormalities: a meta-analysis. Rev. Fac. Cien. Med. Univ. Nac. Cordoba 63(1):46-52
-
(2006)
Rev. Fac. Cien. Med. Univ. Nac. Cordoba
, vol.63
, Issue.1
, pp. 46-52
-
-
Cuestas, E.1
Bur, C.2
Bongiovanni, V.3
-
3
-
-
34247872867
-
Association of isolated preauricular tags and nephrourological anomalies: Case-control study
-
Lizama M, Cavagnaro F, Arau R, et al. 2007. Association of isolated preauricular tags and nephrourological anomalies: case-control study. Pediatr. Nephrol. 22(5):658-60
-
(2007)
Pediatr. Nephrol
, vol.22
, Issue.5
, pp. 658-660
-
-
Lizama, M.1
Cavagnaro, F.2
Arau, R.3
-
4
-
-
0035433966
-
Syndromic ear anomalies and renal ultrasounds
-
Wang RY, Earl DL, Ruder RO, et al. 2001. Syndromic ear anomalies and renal ultrasounds. Pediatrics 108(2):E32
-
(2001)
Pediatrics
, vol.108
, Issue.2
-
-
Wang, R.Y.1
Earl, D.L.2
Ruder, R.O.3
-
5
-
-
33745613785
-
Hair cell development: Commitment through differentiation
-
Kelley MW. 2006. Hair cell development: commitment through differentiation. Brain Res. 1091(1):172-85
-
(2006)
Brain Res
, vol.1091
, Issue.1
, pp. 172-185
-
-
Kelley, M.W.1
-
6
-
-
0032842838
-
Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia
-
Xu PX, Adams J, Peters H, et al. 1999. Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia. Nat. Genet. 23(1):113-17
-
(1999)
Nat. Genet
, vol.23
, Issue.1
, pp. 113-117
-
-
Xu, P.X.1
Adams, J.2
Peters, H.3
-
7
-
-
33748964769
-
Eya1 regulates the growth of otic epithelium and interacts with Pax2 during the development of all sensory areas in the inner ear
-
Zou D, Silvius D, Rodrigo-Blomqvist S, et al. 2006. Eya1 regulates the growth of otic epithelium and interacts with Pax2 during the development of all sensory areas in the inner ear. Dev. Biol. 298(2):430-41
-
(2006)
Dev. Biol
, vol.298
, Issue.2
, pp. 430-441
-
-
Zou, D.1
Silvius, D.2
Rodrigo-Blomqvist, S.3
-
8
-
-
0041326752
-
The role of Six1 in mammalian auditory system development
-
Zheng W, Huang L,Wei ZB, et al. 2003. The role of Six1 in mammalian auditory system development. Development 130(17):3989-4000
-
(2003)
Development
, vol.130
, Issue.17
, pp. 3989-4000
-
-
Zheng, W.1
Huang, L.2
Wei, Z.B.3
-
9
-
-
0037147757
-
Expression of the transcription factors GATA3 and Pax2 during development of the mammalian inner ear
-
Lawoko-Kerali G, Rivolta MN, Holley M. 2002. Expression of the transcription factors GATA3 and Pax2 during development of the mammalian inner ear. J. Comp. Neurol. 442(4):378-91
-
(2002)
J. Comp. Neurol
, vol.442
, Issue.4
, pp. 378-391
-
-
Lawoko-Kerali, G.1
Rivolta, M.N.2
Holley, M.3
-
10
-
-
3042826801
-
The role of Pax2 in mouse inner ear development
-
Burton Q, Cole LK, Mulheisen M, et al. 2004. The role of Pax2 in mouse inner ear development. Dev. Biol. 272(1):161-75
-
(2004)
Dev. Biol
, vol.272
, Issue.1
, pp. 161-175
-
-
Burton, Q.1
Cole, L.K.2
Mulheisen, M.3
-
11
-
-
31644438184
-
Pax 2/8-regulated Gata 3 expression is necessary for morphogenesis and guidance of the nephric duct in the developing kidney
-
Grote D, Souabni A, Busslinger M, et al. 2006. Pax 2/8-regulated Gata 3 expression is necessary for morphogenesis and guidance of the nephric duct in the developing kidney. Development 133(1):53-61
-
(2006)
Development
, vol.133
, Issue.1
, pp. 53-61
-
-
Grote, D.1
Souabni, A.2
Busslinger, M.3
-
12
-
-
0035215311
-
Regulation of ureteric bud outgrowth by Pax2-dependent activation of the glial derived neurotrophic factor gene
-
Brophy PD, Ostrom L, Lang KM, et al. 2001. Regulation of ureteric bud outgrowth by Pax2-dependent activation of the glial derived neurotrophic factor gene. Development 128(23):4747-56
-
(2001)
Development
, vol.128
, Issue.23
, pp. 4747-4756
-
-
Brophy, P.D.1
Ostrom, L.2
Lang, K.M.3
-
13
-
-
0029953417
-
Pax2 contributes to inner ear patterning and optic nerve trajectory
-
Torres M, Gomez-Pardo E, Gruss P. 1996. Pax2 contributes to inner ear patterning and optic nerve trajectory. Development 122(11):3381-91
-
(1996)
Development
, vol.122
, Issue.11
, pp. 3381-3391
-
-
Torres, M.1
Gomez-Pardo, E.2
Gruss, P.3
-
14
-
-
0034096902
-
Gata3 loss leads to embryonic lethality due to noradrenaline deficiency of the sympathetic nervous system
-
Lim KC, Lakshmanan G, Crawford SE, et al. 2000. Gata3 loss leads to embryonic lethality due to noradrenaline deficiency of the sympathetic nervous system. Nat. Genet. 25(2):209-12
-
(2000)
Nat. Genet
, vol.25
, Issue.2
, pp. 209-212
-
-
Lim, K.C.1
Lakshmanan, G.2
Crawford, S.E.3
-
15
-
-
0028174023
-
Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret
-
Schuchardt A, D'Agati V, Larsson-Blomberg L, et al. 1994. Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret. Nature 367(6461):380-83
-
(1994)
Nature
, vol.367
, Issue.6461
, pp. 380-383
-
-
Schuchardt, A.1
D'Agati, V.2
Larsson-Blomberg, L.3
-
16
-
-
33748151500
-
Odd-skipped related 1 is required for development of the metanephric kidney and regulates formation and differentiation of kidney precursor cells
-
James RG, Kamei CN,Wang Q, et al. 2006. Odd-skipped related 1 is required for development of the metanephric kidney and regulates formation and differentiation of kidney precursor cells. Development 133(15):2995-3004
-
(2006)
Development
, vol.133
, Issue.15
, pp. 2995-3004
-
-
James, R.G.1
Kamei, C.N.2
Wang, Q.3
-
18
-
-
42049083603
-
SIX1 mutation screening in 247 branchio-oto-renal syndrome families: A recurrent missense mutation associated with BOR
-
Kochhar A, Orten DJ, Sorensen JL, et al. 2008. SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR. Hum. Mutat. 29(4):565
-
(2008)
Hum. Mutat
, vol.29
, Issue.4
, pp. 565
-
-
Kochhar, A.1
Orten, D.J.2
Sorensen, J.L.3
-
19
-
-
0016880752
-
Familial branchio-oto-renal dysplasia: A new addition to the branchial arch syndromes
-
Melnick M, Bixler D, Nance WE, et al. 1976. Familial branchio-oto-renal dysplasia: a new addition to the branchial arch syndromes. Clin. Genet. 9(1):25-34
-
(1976)
Clin. Genet
, vol.9
, Issue.1
, pp. 25-34
-
-
Melnick, M.1
Bixler, D.2
Nance, W.E.3
-
20
-
-
0019165942
-
Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss
-
Fraser FC, Sproule JR, Halal F. 1980. Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss. Am. J. Med. Genet. 7(3):341-49
-
(1980)
Am. J. Med. Genet
, vol.7
, Issue.3
, pp. 341-349
-
-
Fraser, F.C.1
Sproule, J.R.2
Halal, F.3
-
21
-
-
2642566992
-
Branchio-oto-renal syndrome: The mutation spectrum in EYA1 and its phenotypic consequences
-
Chang EH, Menezes M, Meyer NC, et al. 2004. Branchio-oto-renal syndrome: the mutation spectrum in EYA1 and its phenotypic consequences. Hum. Mutat. 23(6):582-89
-
(2004)
Hum. Mutat
, vol.23
, Issue.6
, pp. 582-589
-
-
Chang, E.H.1
Menezes, M.2
Meyer, N.C.3
-
22
-
-
1642561731
-
Ear and kidney syndromes: Molecular versus clinical approach
-
Izzedine H, Tankere F, Launay-Vacher V, et al. 2004. Ear and kidney syndromes: molecular versus clinical approach. Kidney Int. 65(2):369-85
-
(2004)
Kidney Int
, vol.65
, Issue.2
, pp. 369-385
-
-
Izzedine, H.1
Tankere, F.2
Launay-Vacher, V.3
-
23
-
-
0031046284
-
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family
-
Abdelhak S, Kalatzis V, Heilig R, et al. 1997. A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family. Nat. Genet. 15(2):157-64
-
(1997)
Nat. Genet
, vol.15
, Issue.2
, pp. 157-164
-
-
Abdelhak, S.1
Kalatzis, V.2
Heilig, R.3
-
24
-
-
42049094684
-
Branchio-oto-renal syndrome (BOR): Novel mutations in the EYA1 gene, and a review of the mutational genetics of BOR
-
Orten DJ, Fischer SM, Sorensen JL, et al. 2008. Branchio-oto-renal syndrome (BOR): novel mutations in the EYA1 gene, and a review of the mutational genetics of BOR. Hum. Mutat. 29(4):537-44
-
(2008)
Hum. Mutat
, vol.29
, Issue.4
, pp. 537-544
-
-
Orten, D.J.1
Fischer, S.M.2
Sorensen, J.L.3
-
25
-
-
0031760440
-
Eya1 expression in the developing ear and kidney: Towards the understanding of the pathogenesis of branchio-oto-renal (BOR) syndrome
-
Kalatzis V, Sahly I, El-Amraoui A, et al. 1998. Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of branchio-oto-renal (BOR) syndrome. Dev. Dyn. 213(4):486-99
-
(1998)
Dev. Dyn
, vol.213
, Issue.4
, pp. 486-499
-
-
Kalatzis, V.1
Sahly, I.2
El-Amraoui, A.3
-
26
-
-
2542620650
-
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes
-
Ruf RG, Xu PX, Silvius D, et al. 2004. SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes. Proc. Natl. Acad. Sci. USA 101(21):8090-95
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, Issue.21
, pp. 8090-8095
-
-
Ruf, R.G.1
Xu, P.X.2
Silvius, D.3
-
27
-
-
34147143953
-
Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome
-
Hoskins BE, Cramer CH, Silvius D, et al. 2007. Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome. Am. J. Hum. Genet. 80(4):800-4
-
(2007)
Am. J. Hum. Genet
, vol.80
, Issue.4
, pp. 800-804
-
-
Hoskins, B.E.1
Cramer, C.H.2
Silvius, D.3
-
28
-
-
0026728345
-
Brief report: Autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia
-
Bilous RW,Murty G, Parkinson DB, et al. 1992. Brief report: autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia. N. Engl. J. Med. 327(15):1069-74
-
(1992)
N. Engl. J. Med
, vol.327
, Issue.15
, pp. 1069-1074
-
-
Bilous, R.W.1
Murty, G.2
Parkinson, D.B.3
-
29
-
-
0034721115
-
GATA3 haplo-insufficiency causes human HDR syndrome
-
Van Esch H, Groenen P, Nesbit MA, et al. 2000. GATA3 haplo-insufficiency causes human HDR syndrome. Nature 406(6794):419-22
-
(2000)
Nature
, vol.406
, Issue.6794
, pp. 419-422
-
-
Van Esch, H.1
Groenen, P.2
Nesbit, M.A.3
-
30
-
-
0029047090
-
The GATA-3 gene is expressed during human kidney embryogenesis
-
Labastie MC, Catala M, Gregoire JM, et al. 1995. The GATA-3 gene is expressed during human kidney embryogenesis. Kidney Int. 47(6):1597-603
-
(1995)
Kidney Int
, vol.47
, Issue.6
, pp. 1597-1603
-
-
Labastie, M.C.1
Catala, M.2
Gregoire, J.M.3
-
31
-
-
33750248983
-
Characteristics of hearing loss in HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome
-
van Looij MA, Meijers-Heijboer H, Beetz R, et al. 2006. Characteristics of hearing loss in HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome. Audiol. Neurootol. 11(6):373-79
-
(2006)
Audiol. Neurootol
, vol.11
, Issue.6
, pp. 373-379
-
-
van Looij, M.A.1
Meijers-Heijboer, H.2
Beetz, R.3
-
32
-
-
0033833143
-
Competence, specification and commitment in otic placode induction
-
Groves AK, Bronner-Fraser M. 2000. Competence, specification and commitment in otic placode induction. Development 127(16):3489-99
-
(2000)
Development
, vol.127
, Issue.16
, pp. 3489-3499
-
-
Groves, A.K.1
Bronner-Fraser, M.2
-
33
-
-
0032818483
-
Renal-coloboma syndrome: A multi-system developmental disorder caused by PAX2 mutations
-
Eccles MR, Schimmenti LA. 1999. Renal-coloboma syndrome: a multi-system developmental disorder caused by PAX2 mutations. Clin. Genet. 56(1):1-9
-
(1999)
Clin. Genet
, vol.56
, Issue.1
, pp. 1-9
-
-
Eccles, M.R.1
Schimmenti, L.A.2
-
34
-
-
0031963876
-
Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome
-
Kohlhase J, Wischermann A, Reichenbach H, et al. 1998. Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome. Nat. Genet. 18(1):81-83
-
(1998)
Nat. Genet
, vol.18
, Issue.1
, pp. 81-83
-
-
Kohlhase, J.1
Wischermann, A.2
Reichenbach, H.3
-
35
-
-
33748593397
-
SALL1 mutations in sporadic Townes-Brocks syndrome are of predominantly paternal origin without obvious paternal age effect
-
Bohm J, Munk-Schulenburg S, Felscher S, et al. 2006. SALL1 mutations in sporadic Townes-Brocks syndrome are of predominantly paternal origin without obvious paternal age effect. Am. J. Med. Genet. A 140(18):1904-8
-
(2006)
Am. J. Med. Genet. A
, vol.140
, Issue.18
, pp. 1904-1908
-
-
Bohm, J.1
Munk-Schulenburg, S.2
Felscher, S.3
-
36
-
-
33646175897
-
Detection of heterozygous SALL1 deletions by quantitative real time PCR proves the contribution of a SALL1 dosage effect in the pathogenesis of Townes-Brocks syndrome
-
Borozdin W, Steinmann K, Albrecht B, et al. 2006. Detection of heterozygous SALL1 deletions by quantitative real time PCR proves the contribution of a SALL1 dosage effect in the pathogenesis of Townes-Brocks syndrome. Hum. Mutat. 27(2):211-12
-
(2006)
Hum. Mutat
, vol.27
, Issue.2
, pp. 211-212
-
-
Borozdin, W.1
Steinmann, K.2
Albrecht, B.3
-
37
-
-
33750117655
-
Essential roles of Sall family genes in kidney development
-
Nishinakamura R, Osafune K. 2006. Essential roles of Sall family genes in kidney development. J. Physiol. Sci. 56(2):131-36
-
(2006)
J. Physiol. Sci
, vol.56
, Issue.2
, pp. 131-136
-
-
Nishinakamura, R.1
Osafune, K.2
-
38
-
-
0034840126
-
Murine homolog of SALL1 is essential for ureteric bud invasion in kidney development
-
Nishinakamura R, Matsumoto Y, Nakao K, et al. 2001. Murine homolog of SALL1 is essential for ureteric bud invasion in kidney development. Development 128(16):3105-15
-
(2001)
Development
, vol.128
, Issue.16
, pp. 3105-3115
-
-
Nishinakamura, R.1
Matsumoto, Y.2
Nakao, K.3
-
39
-
-
35648970547
-
Renal dysgenesis and KAL1 gene defects in patients with sporadic Kallmann syndrome
-
Georgopoulos NA, Koika V, Galli-Tsinopoulou A, et al. 2007. Renal dysgenesis and KAL1 gene defects in patients with sporadic Kallmann syndrome. Fertil. Steril. 88(5):1311-17
-
(2007)
Fertil. Steril
, vol.88
, Issue.5
, pp. 1311-1317
-
-
Georgopoulos, N.A.1
Koika, V.2
Galli-Tsinopoulou, A.3
-
40
-
-
0036159074
-
Conductive hearing loss associated with Kallmann's syndrome
-
Coatesworth AP, Woodhead CJ. 2002. Conductive hearing loss associated with Kallmann's syndrome. J. Laryngol. Otol. 116(2):125-26
-
(2002)
J. Laryngol. Otol
, vol.116
, Issue.2
, pp. 125-126
-
-
Coatesworth, A.P.1
Woodhead, C.J.2
-
41
-
-
0032953341
-
Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: Implications for the developmental anomalies of X chromosome-linked Kallmann syndrome
-
Hardelin JP, Julliard AK, Moniot B, et al. 1999. Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: implications for the developmental anomalies of X chromosome-linked Kallmann syndrome. Dev. Dyn. 215(1):26-44
-
(1999)
Dev. Dyn
, vol.215
, Issue.1
, pp. 26-44
-
-
Hardelin, J.P.1
Julliard, A.K.2
Moniot, B.3
-
42
-
-
33845213880
-
Localization of anosmin-1a and anosmin-1b in the inner ear and neuromasts of zebrafish
-
Ernest S, Guadagnini S, Prevost MC, et al. 2007. Localization of anosmin-1a and anosmin-1b in the inner ear and neuromasts of zebrafish. Gene. Exp. Patterns 7(3):274-81
-
(2007)
Gene. Exp. Patterns
, vol.7
, Issue.3
, pp. 274-281
-
-
Ernest, S.1
Guadagnini, S.2
Prevost, M.C.3
-
43
-
-
33846850357
-
FGFR1 and anosmin-1 underlying genetically distinct forms of Kallmann syndrome are coexpressed and interact in olfactory bulbs
-
Ayari B, Soussi-Yanicostas N. 2007. FGFR1 and anosmin-1 underlying genetically distinct forms of Kallmann syndrome are coexpressed and interact in olfactory bulbs. Dev. Genes Evol. 217(2):169-75
-
(2007)
Dev. Genes Evol
, vol.217
, Issue.2
, pp. 169-175
-
-
Ayari, B.1
Soussi-Yanicostas, N.2
-
44
-
-
3042738924
-
Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport
-
Blacque OE, Reardon MJ, Li C, et al. 2004. Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport. Genes Dev. 18(13):1630-42
-
(2004)
Genes Dev
, vol.18
, Issue.13
, pp. 1630-1642
-
-
Blacque, O.E.1
Reardon, M.J.2
Li, C.3
-
45
-
-
38349000827
-
Intraflagellar transport motors in cilia: Moving along the cell's antenna
-
Scholey JM. 2008. Intraflagellar transport motors in cilia: moving along the cell's antenna. J. Cell Biol. 180(1):23-29
-
(2008)
J. Cell Biol
, vol.180
, Issue.1
, pp. 23-29
-
-
Scholey, J.M.1
-
46
-
-
28844460656
-
Cilia and centrosomes: A unifying pathogenic concept for cystic kidney disease?
-
Hildebrandt F, Otto E. 2005. Cilia and centrosomes: a unifying pathogenic concept for cystic kidney disease? Nat. Rev. Genet. 6(12):928-40
-
(2005)
Nat. Rev. Genet
, vol.6
, Issue.12
, pp. 928-940
-
-
Hildebrandt, F.1
Otto, E.2
-
47
-
-
18144431330
-
Linking cilia to Wnts
-
Germino GG. 2005. Linking cilia to Wnts. Nat. Genet. 37(5):455-57
-
(2005)
Nat. Genet
, vol.37
, Issue.5
, pp. 455-457
-
-
Germino, G.G.1
-
48
-
-
0024472754
-
The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome
-
Green JS, Parfrey PS, Harnett JD, et al. 1989. The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome. N. Engl. J. Med. 321(15):1002-9
-
(1989)
N. Engl. J. Med
, vol.321
, Issue.15
, pp. 1002-1009
-
-
Green, J.S.1
Parfrey, P.S.2
Harnett, J.D.3
-
49
-
-
34249978500
-
Bardet-Biedl syndrome: Beyond the cilium
-
Tobin JL, Beales PL. 2007. Bardet-Biedl syndrome: beyond the cilium. Pediatr. Nephrol. 22(7):926-36
-
(2007)
Pediatr. Nephrol
, vol.22
, Issue.7
, pp. 926-936
-
-
Tobin, J.L.1
Beales, P.L.2
-
50
-
-
0142104970
-
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome
-
Ansley SJ, Badano JL, Blacque OE, et al. 2003. Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome. Nature 425(6958):628-33
-
(2003)
Nature
, vol.425
, Issue.6958
, pp. 628-633
-
-
Ansley, S.J.1
Badano, J.L.2
Blacque, O.E.3
-
51
-
-
20144386878
-
MKKS/BBS6, a divergent chaperonin-like protein linked to the obesity disorder Bardet-Biedl syndrome, is a novel centrosomal component required for cytokinesis
-
Kim JC, Ou YY, Badano JL, et al. 2005. MKKS/BBS6, a divergent chaperonin-like protein linked to the obesity disorder Bardet-Biedl syndrome, is a novel centrosomal component required for cytokinesis. J. Cell Sci. 118(Pt. 5):1007-20
-
(2005)
J. Cell Sci
, vol.118
, Issue.PART. 5
, pp. 1007-1020
-
-
Kim, J.C.1
Ou, Y.Y.2
Badano, J.L.3
-
52
-
-
0033062278
-
New criteria for improved diagnosis of Bardet-Biedl syndrome: Results of a population survey
-
Beales PL, Elcioglu N, Woolf AS, et al. 1999. New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey. J. Med. Genet. 36(6):437-46
-
(1999)
J. Med. Genet
, vol.36
, Issue.6
, pp. 437-446
-
-
Beales, P.L.1
Elcioglu, N.2
Woolf, A.S.3
-
53
-
-
27144460671
-
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates
-
Ross AJ, May-Simera H, Eichers ER, et al. 2005. Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates. Nat. Genet. 37(10):1135-40
-
(2005)
Nat. Genet
, vol.37
, Issue.10
, pp. 1135-1140
-
-
Ross, A.J.1
May-Simera, H.2
Eichers, E.R.3
-
54
-
-
0033609103
-
Situs inversus and embryonic ciliary morphogenesis defects in mouse mutants lacking the KIF3A subunit of kinesin-II
-
Marszalek JR, Ruiz-Lozano P, Roberts E, et al. 1999. Situs inversus and embryonic ciliary morphogenesis defects in mouse mutants lacking the KIF3A subunit of kinesin-II. Proc. Natl. Acad. Sci. USA 96(9):5043-48
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, Issue.9
, pp. 5043-5048
-
-
Marszalek, J.R.1
Ruiz-Lozano, P.2
Roberts, E.3
-
55
-
-
0037884961
-
Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease
-
Lin F, Hiesberger T, Cordes K, et al. 2003. Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease. Proc. Natl. Acad. Sci. USA 100(9):5286-91
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, Issue.9
, pp. 5286-5291
-
-
Lin, F.1
Hiesberger, T.2
Cordes, K.3
-
56
-
-
44349116202
-
Acute kidney injury and aberrant planar cell polarity induce cyst formation in mice lacking renal cilia
-
Patel V, Li L, Cobo-Stark P, et al. 2008. Acute kidney injury and aberrant planar cell polarity induce cyst formation in mice lacking renal cilia. Hum. Mol. Genet. 17(11):1578-90
-
(2008)
Hum. Mol. Genet
, vol.17
, Issue.11
, pp. 1578-1590
-
-
Patel, V.1
Li, L.2
Cobo-Stark, P.3
-
57
-
-
0034042763
-
The Oak Ridge polycystic kidney (orpk) disease gene is required for left-right axis determination
-
Murcia NS, Richards WG, Yoder BK, et al. 2000. The Oak Ridge polycystic kidney (orpk) disease gene is required for left-right axis determination. Development 127(11):2347-55
-
(2000)
Development
, vol.127
, Issue.11
, pp. 2347-2355
-
-
Murcia, N.S.1
Richards, W.G.2
Yoder, B.K.3
-
58
-
-
49449091433
-
The Oak Ridge polycystic kidney mouse: Modeling ciliopathies of mice and men
-
Lehman JM, Michaud EJ, Schoeb TR, et al. 2008. The Oak Ridge polycystic kidney mouse: modeling ciliopathies of mice and men. Dev. Dyn. 237(8):1960-71
-
(2008)
Dev. Dyn
, vol.237
, Issue.8
, pp. 1960-1971
-
-
Lehman, J.M.1
Michaud, E.J.2
Schoeb, T.R.3
-
59
-
-
37549052499
-
Ciliary proteins link basal body polarization to planar cell polarity regulation
-
Jones C, Roper VC, Foucher I, et al. 2008. Ciliary proteins link basal body polarization to planar cell polarity regulation. Nat. Genet. 40(1):69-77
-
(2008)
Nat. Genet
, vol.40
, Issue.1
, pp. 69-77
-
-
Jones, C.1
Roper, V.C.2
Foucher, I.3
-
60
-
-
37749054886
-
Kif3a constrains beta-catenin-dependent Wnt signalling through dual ciliary and nonciliary mechanisms
-
Corbit KC, Shyer AE, Dowdle WE, et al. 2008. Kif3a constrains beta-catenin-dependent Wnt signalling through dual ciliary and nonciliary mechanisms. Nat. Cell Biol. 10(1):70-76
-
(2008)
Nat. Cell Biol
, vol.10
, Issue.1
, pp. 70-76
-
-
Corbit, K.C.1
Shyer, A.E.2
Dowdle, W.E.3
-
61
-
-
33644624937
-
Ciliogenesis defects in embryos lacking inturned or fuzzy function are associated with failure of planar cell polarity and Hedgehog signaling
-
Park TJ, Haigo SL, Wallingford JB. 2006. Ciliogenesis defects in embryos lacking inturned or fuzzy function are associated with failure of planar cell polarity and Hedgehog signaling. Nat. Genet. 38(3):303-11
-
(2006)
Nat. Genet
, vol.38
, Issue.3
, pp. 303-311
-
-
Park, T.J.1
Haigo, S.L.2
Wallingford, J.B.3
-
62
-
-
35648985644
-
Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response
-
Gerdes JM, Liu Y, Zaghloul NA, et al. 2007. Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response. Nat. Genet. 39(11):1350-60
-
(2007)
Nat. Genet
, vol.39
, Issue.11
, pp. 1350-1360
-
-
Gerdes, J.M.1
Liu, Y.2
Zaghloul, N.A.3
-
63
-
-
70449232246
-
Retinal degeneration combined with obesity, diabetes mellitus and neurogenous deafness: A specific syndrome (not hitherto described) distinct from the Laurence-Moon-Bardet-Biedl syndrome: a clinical, endocrinological and genetic examination based on a large pedigree
-
Alstrom CH, Hallgren B, Nilsson LB, et al. 1959. Retinal degeneration combined with obesity, diabetes mellitus and neurogenous deafness: a specific syndrome (not hitherto described) distinct from the Laurence-Moon-Bardet-Biedl syndrome: a clinical, endocrinological and genetic examination based on a large pedigree. Acta Psychiatr. Neurol. Scand. Suppl. 129:1-35
-
(1959)
Acta Psychiatr. Neurol. Scand. Suppl
, vol.129
, pp. 1-35
-
-
Alstrom, C.H.1
Hallgren, B.2
Nilsson, L.B.3
-
65
-
-
18544391142
-
Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alstrom syndrome
-
Hearn T, Renforth GL, Spalluto C, et al. 2002. Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alstrom syndrome. Nat. Genet. 31(1):79-83
-
(2002)
Nat. Genet
, vol.31
, Issue.1
, pp. 79-83
-
-
Hearn, T.1
Renforth, G.L.2
Spalluto, C.3
-
66
-
-
26444443136
-
Alms1-disrupted mice recapitulate human Alstrom syndrome
-
Collin GB, Cyr E, Bronson R, et al. 2005. Alms1-disrupted mice recapitulate human Alstrom syndrome. Hum. Mol. Genet. 14(16):2323-33
-
(2005)
Hum. Mol. Genet
, vol.14
, Issue.16
, pp. 2323-2333
-
-
Collin, G.B.1
Cyr, E.2
Bronson, R.3
-
67
-
-
34249871086
-
Nephronophthisis-associated ciliopathies
-
Hildebrandt F, Zhou W. 2007. Nephronophthisis-associated ciliopathies. J. Am. Soc. Nephrol. 18(6):1855-71
-
(2007)
J. Am. Soc. Nephrol
, vol.18
, Issue.6
, pp. 1855-1871
-
-
Hildebrandt, F.1
Zhou, W.2
-
68
-
-
0041592700
-
Mutations inINVSencoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
-
Otto EA, Schermer B, Obara T, et al. 2003. Mutations inINVSencoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination. Nat. Genet. 34(4):413-20
-
(2003)
Nat. Genet
, vol.34
, Issue.4
, pp. 413-420
-
-
Otto, E.A.1
Schermer, B.2
Obara, T.3
-
69
-
-
0026573062
-
Senior-Loken syndrome. Case reports of two siblings and association with sensorineural deafness
-
Clarke MP, Sullivan TJ, Francis C, et al. 1992. Senior-Loken syndrome. Case reports of two siblings and association with sensorineural deafness. Br. J. Ophthalmol. 76(3):171-72
-
(1992)
Br. J. Ophthalmol
, vol.76
, Issue.3
, pp. 171-172
-
-
Clarke, M.P.1
Sullivan, T.J.2
Francis, C.3
-
70
-
-
33748937382
-
Nephronophthisis type 1 deletion syndrome with neurological symptoms: Prevalence and significance of the association
-
Caridi G, Dagnino M, Rossi A, et al. 2006. Nephronophthisis type 1 deletion syndrome with neurological symptoms: prevalence and significance of the association. Kidney Int. 70(7):1342-47
-
(2006)
Kidney Int
, vol.70
, Issue.7
, pp. 1342-1347
-
-
Caridi, G.1
Dagnino, M.2
Rossi, A.3
-
71
-
-
13144262840
-
Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis
-
Karet FE, Gainza FJ, Gyory AZ, et al. 1998. Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis. Proc. Natl. Acad. Sci. USA 95(11):6337-42
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, Issue.11
, pp. 6337-6342
-
-
Karet, F.E.1
Gainza, F.J.2
Gyory, A.Z.3
-
72
-
-
0033812944
-
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing
-
Smith AN, Skaug J, Choate KA, et al. 2000. Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing. Nat. Genet. 26(1):71-75
-
(2000)
Nat. Genet
, vol.26
, Issue.1
, pp. 71-75
-
-
Smith, A.N.1
Skaug, J.2
Choate, K.A.3
-
73
-
-
0033358521
-
Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34
-
Karet FE, Finberg KE, Nayir A, et al. 1999. Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34. Am. J. Hum. Genet. 65(6):1656-65
-
(1999)
Am. J. Hum. Genet
, vol.65
, Issue.6
, pp. 1656-1665
-
-
Karet, F.E.1
Finberg, K.E.2
Nayir, A.3
-
74
-
-
18744379726
-
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss
-
Stover EH, Borthwick KJ, Bavalia C, et al. 2002. Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss. J. Med. Genet. 39(11):796-803
-
(2002)
J. Med. Genet
, vol.39
, Issue.11
, pp. 796-803
-
-
Stover, E.H.1
Borthwick, K.J.2
Bavalia, C.3
-
75
-
-
41449091581
-
Audiometric and imaging characteristics of distal renal tubular acidosis and deafness
-
Joshua B, Kaplan DM, Raveh E, et al. 2008. Audiometric and imaging characteristics of distal renal tubular acidosis and deafness. J. Laryngol. Otol. 122(2):193-98
-
(2008)
J. Laryngol. Otol
, vol.122
, Issue.2
, pp. 193-198
-
-
Joshua, B.1
Kaplan, D.M.2
Raveh, E.3
-
76
-
-
33644860224
-
Molecular investigation and long-term clinical progress in Greek Cypriot families with recessive distal renal tubular acidosis and sensorineural deafness due to mutations in the ATP6V1B1 gene
-
Feldman M, Prikis M, Athanasiou Y, et al. 2006. Molecular investigation and long-term clinical progress in Greek Cypriot families with recessive distal renal tubular acidosis and sensorineural deafness due to mutations in the ATP6V1B1 gene. Clin. Genet. 69(2):135-44
-
(2006)
Clin. Genet
, vol.69
, Issue.2
, pp. 135-144
-
-
Feldman, M.1
Prikis, M.2
Athanasiou, Y.3
-
77
-
-
33646372973
-
Genetic investigation of autosomal recessive distal renal tubular acidosis: Evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 gene
-
Vargas-Poussou R, Houillier P, Le Pottier N, et al. 2006. Genetic investigation of autosomal recessive distal renal tubular acidosis: evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 gene. J. Am. Soc. Nephrol. 17(5):1437-43
-
(2006)
J. Am. Soc. Nephrol
, vol.17
, Issue.5
, pp. 1437-1443
-
-
Vargas-Poussou, R.1
Houillier, P.2
Le Pottier, N.3
-
78
-
-
0042166134
-
Molecular mechanisms of Bartter syndrome caused by mutations in the BSND gene
-
Hayama A, Rai T, Sasaki S, et al. 2003. Molecular mechanisms of Bartter syndrome caused by mutations in the BSND gene. Histochem. Cell Biol. 119(6):485-93
-
(2003)
Histochem. Cell Biol
, vol.119
, Issue.6
, pp. 485-493
-
-
Hayama, A.1
Rai, T.2
Sasaki, S.3
-
79
-
-
0028832124
-
Localization and functional characterization of rat kidney-specific chloride channel, ClC-K1
-
Uchida S, Sasaki S, Nitta K, et al. 1995. Localization and functional characterization of rat kidney-specific chloride channel, ClC-K1. J. Clin. Invest. 95(1):104-13
-
(1995)
J. Clin. Invest
, vol.95
, Issue.1
, pp. 104-113
-
-
Uchida, S.1
Sasaki, S.2
Nitta, K.3
-
80
-
-
0034920817
-
Intrarenal and cellular localization of CLC-K2 protein in the mouse kidney
-
Kobayashi K, Uchida S, Mizutani S, et al. 2001. Intrarenal and cellular localization of CLC-K2 protein in the mouse kidney. J. Am. Soc. Nephrol. 12(7):1327-34
-
(2001)
J. Am. Soc. Nephrol
, vol.12
, Issue.7
, pp. 1327-1334
-
-
Kobayashi, K.1
Uchida, S.2
Mizutani, S.3
-
81
-
-
0037171857
-
Deafness and renal tubular acidosis in mice lacking the K-Cl cotransporter Kcc4
-
Boettger T, Hubner CA, Maier H, et al. 2002. Deafness and renal tubular acidosis in mice lacking the K-Cl cotransporter Kcc4. Nature 416(6883):874-78
-
(2002)
Nature
, vol.416
, Issue.6883
, pp. 874-878
-
-
Boettger, T.1
Hubner, C.A.2
Maier, H.3
-
82
-
-
0035189356
-
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
-
Birkenhager R, Otto E, Schurmann MJ, et al. 2001. Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure. Nat. Genet. 29(3):310-14
-
(2001)
Nat. Genet
, vol.29
, Issue.3
, pp. 310-314
-
-
Birkenhager, R.1
Otto, E.2
Schurmann, M.J.3
-
84
-
-
1642366722
-
Salt wasting and deafness resulting from mutations in two chloride channels
-
Schlingmann KP, Konrad M, Jeck N, et al. 2004. Salt wasting and deafness resulting from mutations in two chloride channels. N. Engl. J. Med. 350(13):1314-19
-
(2004)
N. Engl. J. Med
, vol.350
, Issue.13
, pp. 1314-1319
-
-
Schlingmann, K.P.1
Konrad, M.2
Jeck, N.3
-
85
-
-
34249287054
-
Alport syndrome or progressive hereditary nephritis with hearing loss
-
Gubler MC, Heidet L, Antignac C. 2007. Alport syndrome or progressive hereditary nephritis with hearing loss. Nephrol. Ther. 3(3):113-20
-
(2007)
Nephrol. Ther
, vol.3
, Issue.3
, pp. 113-120
-
-
Gubler, M.C.1
Heidet, L.2
Antignac, C.3
-
86
-
-
2342647451
-
Autosomal-dominant Alport syndrome: Natural history of a disease due to COL4A3 or COL4A4 gene
-
Pescucci C, Mari F, Longo I, et al. 2004. Autosomal-dominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 gene. Kidney Int. 65(5):1598-603
-
(2004)
Kidney Int
, vol.65
, Issue.5
, pp. 1598-1603
-
-
Pescucci, C.1
Mari, F.2
Longo, I.3
-
87
-
-
34447573030
-
Alport syndrome and the X chromosome: Implications of a diagnosis of Alport syndrome in females
-
Kashtan CE. 2007. Alport syndrome and the X chromosome: implications of a diagnosis of Alport syndrome in females. Nephrol. Dial. Transpl. 22(6):1499-505
-
(2007)
Nephrol. Dial. Transpl
, vol.22
, Issue.6
, pp. 1499-1505
-
-
Kashtan, C.E.1
-
88
-
-
0141566829
-
X-linked Alport syndrome: Natural history and genotypephenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study
-
Jais JP, Knebelmann B, Giatras I, et al. 2003. X-linked Alport syndrome: natural history and genotypephenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study. J. Am. Soc. Nephrol. 14(10):2603-10
-
(2003)
J. Am. Soc. Nephrol
, vol.14
, Issue.10
, pp. 2603-2610
-
-
Jais, J.P.1
Knebelmann, B.2
Giatras, I.3
-
89
-
-
28144465642
-
Distribution of type IV collagen in the cochlea in Alport syndrome
-
Zehnder AF, Adams JC, Santi PA, et al. 2005. Distribution of type IV collagen in the cochlea in Alport syndrome. Arch. Otolaryngol. Head Neck Surg. 131(11):1007-13
-
(2005)
Arch. Otolaryngol. Head Neck Surg
, vol.131
, Issue.11
, pp. 1007-1013
-
-
Zehnder, A.F.1
Adams, J.C.2
Santi, P.A.3
-
90
-
-
45149089697
-
Case-control study of acute renal failure in patients with cystic fibrosis in the UK
-
Smyth A, Lewis S, Bertenshaw C, et al. 2008. Case-control study of acute renal failure in patients with cystic fibrosis in the UK. Thorax 63(6):532-35
-
(2008)
Thorax
, vol.63
, Issue.6
, pp. 532-535
-
-
Smyth, A.1
Lewis, S.2
Bertenshaw, C.3
-
91
-
-
0018185123
-
Ototoxicity of gentamicin: Clinical experience in a children's hospital
-
Echeverria P, Fina D, Norton S, et al. 1978. Ototoxicity of gentamicin: clinical experience in a children's hospital. Chemotherapy 24(4):267-71
-
(1978)
Chemotherapy
, vol.24
, Issue.4
, pp. 267-271
-
-
Echeverria, P.1
Fina, D.2
Norton, S.3
-
92
-
-
37549053577
-
A systemic gentamicin pathway across the stria vascularis
-
Dai CF, Steyger PS. 2008. A systemic gentamicin pathway across the stria vascularis. Hear. Res. 235(1-2):114-24
-
(2008)
Hear. Res
, vol.235
, Issue.1-2
, pp. 114-124
-
-
Dai, C.F.1
Steyger, P.S.2
-
93
-
-
19544392023
-
TRPV1 regulators mediate gentamicin penetration of cultured kidney cells
-
Myrdal SE, Steyger PS. 2005. TRPV1 regulators mediate gentamicin penetration of cultured kidney cells. Hear. Res. 204(1-2):170-82
-
(2005)
Hear. Res
, vol.204
, Issue.1-2
, pp. 170-182
-
-
Myrdal, S.E.1
Steyger, P.S.2
-
94
-
-
34547479230
-
Gentamicin-induced ototoxicity in hemodialysis patients is ameliorated by N-acetylcysteine
-
Feldman L, Efrati S, Eviatar E, et al. 2007. Gentamicin-induced ototoxicity in hemodialysis patients is ameliorated by N-acetylcysteine. Kidney Int. 72(3):359-63
-
(2007)
Kidney Int
, vol.72
, Issue.3
, pp. 359-363
-
-
Feldman, L.1
Efrati, S.2
Eviatar, E.3
-
95
-
-
35549002726
-
Ototoxicity caused by aminoglycosides
-
Bitner-Glindzicz M, Rahman S. 2007. Ototoxicity caused by aminoglycosides. BMJ 335(7624):784-85
-
(2007)
BMJ
, vol.335
, Issue.7624
, pp. 784-785
-
-
Bitner-Glindzicz, M.1
Rahman, S.2
-
96
-
-
67650767476
-
A maternal hereditary deafness pedigree of the A1555G mitochondrial mutation, causing aminoglycoside ototoxicity predisposition
-
Bai YH, Ren CC, Gong XR, et al. 2008. A maternal hereditary deafness pedigree of the A1555G mitochondrial mutation, causing aminoglycoside ototoxicity predisposition. J. Laryngol. Otol. 19:1-5
-
(2008)
J. Laryngol. Otol
, vol.19
, pp. 1-5
-
-
Bai, Y.H.1
Ren, C.C.2
Gong, X.R.3
-
97
-
-
41049098414
-
Prevention of cisplatin nephrotoxicity: State of the art and recommendations from the European Society of Clinical Pharmacy Special Interest Group on Cancer Care
-
Launay-Vacher V, Rey JB, Isnard-Bagnis C, et al. 2008. Prevention of cisplatin nephrotoxicity: state of the art and recommendations from the European Society of Clinical Pharmacy Special Interest Group on Cancer Care. Cancer Chemother. Pharmacol. 61(6):903-9
-
(2008)
Cancer Chemother. Pharmacol
, vol.61
, Issue.6
, pp. 903-909
-
-
Launay-Vacher, V.1
Rey, J.B.2
Isnard-Bagnis, C.3
-
98
-
-
41949141897
-
Hearing loss in pediatric oncology patients receiving carboplatin-containing regimens
-
Dean JB, Hayashi SS, Albert CM, et al. 2008. Hearing loss in pediatric oncology patients receiving carboplatin-containing regimens. J. Pediatr. Hematol. Oncol. 30(2):130-34
-
(2008)
J. Pediatr. Hematol. Oncol
, vol.30
, Issue.2
, pp. 130-134
-
-
Dean, J.B.1
Hayashi, S.S.2
Albert, C.M.3
-
99
-
-
33745278586
-
High accumulation of platinum-DNA adducts in strial marginal cells of the cochlea is an early event in cisplatin but not carboplatin ototoxicity
-
Thomas JP, Lautermann J, Liedert B, et al. 2006. High accumulation of platinum-DNA adducts in strial marginal cells of the cochlea is an early event in cisplatin but not carboplatin ototoxicity. Mol. Pharmacol. 70(1):23-29
-
(2006)
Mol. Pharmacol
, vol.70
, Issue.1
, pp. 23-29
-
-
Thomas, J.P.1
Lautermann, J.2
Liedert, B.3
-
100
-
-
49949088446
-
Cisplatin-induced cytoxicity: Is the nucleus relevant?
-
Sheikh-Hamad D. 2008. Cisplatin-induced cytoxicity: Is the nucleus relevant? Am. J. Physiol. Renal Physiol. 295(1):F42-43
-
(2008)
Am. J. Physiol. Renal Physiol
, vol.295
, Issue.1
-
-
Sheikh-Hamad, D.1
|