-
1
-
-
0016563163
-
Editorial: The primary glomerular filtration barrier - Basement membrane or epithelial slits?
-
Farquhar MG. Editorial: The primary glomerular filtration barrier - basement membrane or epithelial slits? Kidney Int 1975; 8:197-211.
-
(1975)
Kidney Int
, vol.8
, pp. 197-211
-
-
Farquhar, M.G.1
-
2
-
-
0035722242
-
Glomerular endothelial cells and podocytes jointly synthesize laminin-1 and -11 chains
-
DOI 10.1046/j.1523-1755.2001.0600031037.x
-
St. John PL, Abrahamson DR. Glomerular endothelial cells and podocytes jointly synthesize laminin-1 and -11 chains. Kidney Int 2001; 60:1037-46. (Pubitemid 34205803)
-
(2001)
Kidney International
, vol.60
, Issue.3
, pp. 1037-1046
-
-
ST., J.P.L.1
Abrahamson, D.R.2
-
3
-
-
0021855102
-
Origin of the glomerular basement membrane visualized after in vivo labeling of laminin in newborn rat kidneys
-
DOI 10.1083/jcb.100.6.1988
-
Abrahamson DR. Origin of the glomerular basement membrane visualized after in vivo labeling of laminin in newborn rat kidneys. J Cell Biol 1985; 100:1988-2000. (Pubitemid 15042096)
-
(1985)
Journal of Cell Biology
, vol.100
, Issue.6
, pp. 1988-2000
-
-
Abrahamson, D.R.1
-
4
-
-
67649687035
-
Cellular origins of type IV collagen networks in developing glomeruli
-
Abrahamson DR, Hudson BG, Stroganova L, Borza DB, St. John PL. Cellular origins of type IV collagen networks in developing glomeruli. J Am Soc Nephrol 2009; 20:1471-9.
-
(2009)
J Am Soc Nephrol
, vol.20
, pp. 1471-1479
-
-
Abrahamson, D.R.1
Hudson, B.G.2
Stroganova, L.3
Borza, D.B.4
St. John, P.L.5
-
5
-
-
0025008077
-
The tight junction protein ZO-1 is concentrated along slit diaphragms of the glomerular epithelium
-
Schnabel E, Anderson JM, Farquhar MG. The tight junction protein ZO-1 is concentrated along slit diaphragms of the glomerular epithelium. J Cell Biol 1990; 111:1255-63.
-
(1990)
J Cell Biol
, vol.111
, pp. 1255-1263
-
-
Schnabel, E.1
Anderson, J.M.2
Farquhar, M.G.3
-
6
-
-
33751161268
-
The cellular basis of kidney development
-
Dressler GR. The cellular basis of kidney development. Annu Rev Cell Dev Biol 2006; 22:509-29.
-
(2006)
Annu Rev Cell Dev Biol
, vol.22
, pp. 509-529
-
-
Dressler, G.R.1
-
7
-
-
66049109286
-
Glomerular endothelial cell fenestrations: An integral component of the glomerular filtration barrier
-
Satchell SC, Braet F. Glomerular endothelial cell fenestrations: An integral component of the glomerular filtration barrier. Am J Physiol Renal Physiol 2009; 296:947-56.
-
(2009)
Am J Physiol Renal Physiol
, vol.296
, pp. 947-956
-
-
Satchell, S.C.1
Braet, F.2
-
9
-
-
42149122041
-
Properties of the glomerular barrier and mechanisms of proteinuria
-
DOI 10.1152/physrev.00055.2006
-
Haraldsson B, Nystrom J, Deen WM. Properties of the glomerular barrier and mechanisms of proteinuria. Physiol Rev 2008; 88:451-87. (Pubitemid 351522745)
-
(2008)
Physiological Reviews
, vol.88
, Issue.2
, pp. 451-487
-
-
Haraldsson, B.1
Nystrom, J.2
Deen, W.M.3
-
11
-
-
22544480570
-
A simplified laminin nomenclature
-
DOI 10.1016/j.matbio.2005.05.006, PII S0945053X0500065X
-
Aumailley M, Bruckner-Tuderman L, Carter WG, Deutzmann R, Edgar D, Ekblom P, et al. A simplified laminin nomenclature. Matrix Biol 2005; 24:326-32. (Pubitemid 41021635)
-
(2005)
Matrix Biology
, vol.24
, Issue.5
, pp. 326-332
-
-
Aumailley, M.1
Bruckner-Tuderman, L.2
Carter, W.G.3
Deutzmann, R.4
Edgar, D.5
Ekblom, P.6
Engel, J.7
Engvall, E.8
Hohenester, E.9
Jones, J.C.R.10
Kleinman, H.K.11
Marinkovich, M.P.12
Martin, G.R.13
Mayer, U.14
Meneguzzi, G.15
Miner, J.H.16
Miyazaki, K.17
Patarroyo, M.18
Paulsson, M.19
Quaranta, V.20
Sanes, J.R.21
Sasaki, T.22
Sekiguchi, K.23
Sorokin, L.M.24
Talts, J.F.25
Tryggvason, K.26
Uitto, J.27
Virtanen, I.28
Von Der, M.K.29
Wewer, U.M.30
Yamada, Y.31
Yurchenco, P.D.32
more..
-
12
-
-
0033519279
-
Laminin polymerization induces a receptor-cytoskeleton network
-
DOI 10.1083/jcb.145.3.619
-
Colognato H, Winkelmann DA, Yurchenco PD. Laminin polymerization induces a receptor-cytoskeleton network. J Cell Biol 1999; 145:619-31. (Pubitemid 29215724)
-
(1999)
Journal of Cell Biology
, vol.145
, Issue.3
, pp. 619-631
-
-
Colognato, H.1
Winkelmann, D.A.2
Yurchenco, P.D.3
-
13
-
-
0030919488
-
The laminin alpha chains: Expression, developmental transitions, and chromosomal locations of alpha1-5, identification of heterotrimeric laminins 8- 11, and cloning of a novel alpha3 isoform
-
DOI 10.1083/jcb.137.3.685
-
Miner JH, Patton BL, Lentz SI, Gilbert DJ, Snider WD, Jenkins NA, et al. The laminin alpha chains: expression, developmental transitions and chromosomal locations of alpha1-5, identification of heterotrimeric laminins 8-11 and cloning of a novel alpha3 isoform. J Cell Biol 1997; 137:685-701. (Pubitemid 27200670)
-
(1997)
Journal of Cell Biology
, vol.137
, Issue.3
, pp. 685-701
-
-
Miner, J.H.1
Patton, B.L.2
Lentz, S.I.3
Gilbert, D.J.4
Snider, W.D.5
Jenkins, N.A.6
Copeland, N.G.7
Sanes, J.R.8
-
14
-
-
0028171098
-
Collagen IV α3, α4 and α5 chains in rodent basal laminae: Sequence, distribution, association with laminins and developmental switches
-
Miner JH, Sanes JR. Collagen IV α3, α4 and α5 chains in rodent basal laminae: Sequence, distribution, association with laminins and developmental switches. J Cell Biol 1994; 127:879-91.
-
(1994)
J Cell Biol
, vol.127
, pp. 879-891
-
-
Miner, J.H.1
Sanes, J.R.2
-
15
-
-
16644399795
-
The molecular basis of goodpasture and alport syndromes: Beacons for the discovery of the collagen IV family
-
DOI 10.1097/01.ASN.0000141462.00630.76
-
Hudson BG. The molecular basis of Goodpasture and Alport syndromes: beacons for the discovery of the collagen IV family. J Am Soc Nephrol 2004; 15:2514-27. (Pubitemid 41103358)
-
(2004)
Journal of the American Society of Nephrology
, vol.15
, Issue.10
, pp. 2514-2527
-
-
Hudson, B.G.1
-
16
-
-
33846029867
-
Molecular recognition in the assembly of collagens: Terminal noncollagenous domains are key recognition modules in the formation of triple helical protomers
-
DOI 10.1074/jbc.R600025200
-
Khoshnoodi J, Cartailler JP, Alvares K, Veis A, Hudson BG. Molecular recognition in the assembly of collagens: Terminal noncollagenous domains are key recognition modules in the formation of triple helical protomers. J Biol Chem 2006; 281:38117-21. (Pubitemid 46041935)
-
(2006)
Journal of Biological Chemistry
, vol.281
, Issue.50
, pp. 38117-38121
-
-
Khoshnoodi, J.1
Cartailler, J.-P.2
Alvares, K.3
Veis, A.4
Hudson, B.G.5
-
17
-
-
0031754846
-
Role of distinct type IV collagen networks in glomerular development and function
-
DOI 10.1046/j.1523-1755.1998.00188.x
-
Harvey SJ, Zheng K, Sado Y, Naito I, Ninomiya Y, Jacobs RM, et al. Role of distinct type IV collagen networks in glomerular development and function. Kidney Int 1998; 54:1857-66. (Pubitemid 28533613)
-
(1998)
Kidney International
, vol.54
, Issue.6
, pp. 1857-1866
-
-
Harvey, S.J.1
Zheng, K.2
Sado, Y.3
Naito, I.4
Ninomiya, Y.5
Jacobs, R.M.6
Hudson, B.G.7
Thorner, P.S.8
-
18
-
-
0031000529
-
Isoform switching of type IV collagen is developmentally arrested in X- linked Aport syndrome leading to increased susceptibility of renal basement membranes to endoproteolysis
-
Kalluri R, Shield CF, III, Todd P, Hudson BG, Neilson EG. Isoform switching of type IV collagen is developmentally arrested in X-linked Alport syndrome leading to increased susceptibility of renal basement membranes to endoproteolysis. J Clin Invest 1997; 99:2470-8. (Pubitemid 27227726)
-
(1997)
Journal of Clinical Investigation
, vol.99
, Issue.10
, pp. 2470-2478
-
-
Kalluri, R.1
Shield III, C.F.2
Todd, P.3
Hudson, B.G.4
Neilson, E.G.5
-
19
-
-
0036405396
-
Binding of mouse nidogen-2 to basement membrane components and cells and its expression in embryonic and adult tissues suggest complementary functions of the two nidogens
-
DOI 10.1006/excr.2002.5611
-
Salmivirta K, Talts JF, Olsson M, Sasaki T, Timpl R, Ekblom P. Binding of mouse nidogen-2 to basement membrane components and cells and its expression in embryonic and adult tissues suggest complementary functions of the two nidogens. Exp Cell Res 2002; 279:188-201. (Pubitemid 35217548)
-
(2002)
Experimental Cell Research
, vol.279
, Issue.2
, pp. 188-201
-
-
Salmivirta, K.1
Talts, J.F.2
Olsson, M.3
Sasaki, T.4
Timpl, R.5
Ekblom, P.6
-
20
-
-
22544456862
-
Compound genetic ablation of nidogen 1 and 2 causes basement membrane defects and perinatal lethality in mice
-
DOI 10.1128/MCB.25.15.6846-6856.2005
-
Bader BL, Smyth N, Nedbal S, Miosge N, Baranowsky A, Mokkapati S, et al. Compound genetic ablation of nidogen 1 and 2 causes basement membrane defects and perinatal lethality in mice. Mol Cell Biol 2005; 25:6846-56. (Pubitemid 41023254)
-
(2005)
Molecular and Cellular Biology
, vol.25
, Issue.15
, pp. 6846-6856
-
-
Bader, B.L.1
Smyth, N.2
Nedbal, S.3
Miosge, N.4
Baranowsky, A.5
Mokkapati, S.6
Murshed, M.7
Nischt, R.8
-
21
-
-
15644366697
-
Agrin is a major heparan sulfate proteoglycan in the human glomerular basement membrane
-
Groffen AJ, Ruegg MA, Dijkman H, van de Velden TJ, Buskens CA, van den Born J, et al. Agrin is a major heparan sulfate proteoglycan in the human glomerular basement membrane. J Histochem Cytochem 1998; 46:19-27. (Pubitemid 28030506)
-
(1998)
Journal of Histochemistry and Cytochemistry
, vol.46
, Issue.1
, pp. 19-27
-
-
Groffen, A.J.1
Ruegg, M.A.2
Dijkman, H.3
Van De, V.T.J.4
Buskens, C.A.5
Van Den, B.J.6
Assmann, K.J.7
Monnens, L.A.8
Veerkamp, J.H.9
Van Den, H.L.P.10
-
22
-
-
32344447256
-
Assembly of the postsynaptic membrane at the neuromuscular junction: Paradigm lost
-
DOI 10.1016/j.conb.2005.12.003, PII S0959438805001856, Development
-
Kummer TT, Misgeld T, Sanes JR. Assembly of the postsynaptic membrane at the neuromuscular junction: Paradigm lost. Curr Opin Neurobiol 2006; 16:74-82. (Pubitemid 43221856)
-
(2006)
Current Opinion in Neurobiology
, vol.16
, Issue.1
, pp. 74-82
-
-
Kummer, T.T.1
Misgeld, T.2
Sanes, J.R.3
-
23
-
-
34547680445
-
Disruption of glomerular basement membrane charge through podocyte-specific mutation of agrin does not alter glomerular permselectivity
-
DOI 10.2353/ajpath.2007.061116
-
Harvey SJ, Jarad G, Cunningham J, Rops AL, van der Vlag J, Berden JH, et al. Disruption of glomerular basement membrane charge through podocyte-specific mutation of agrin does not alter glomerular permselectivity. Am J Pathol 2007; 171:139-52. (Pubitemid 47339234)
-
(2007)
American Journal of Pathology
, vol.171
, Issue.1
, pp. 139-152
-
-
Harvey, S.J.1
Jarad, G.2
Cunningham, J.3
Rops, A.L.4
Van Der, V.J.5
Berden, J.H.6
Moeller, M.J.7
Holzman, L.B.8
Burgess, R.W.9
Miner, J.H.10
-
24
-
-
0034650304
-
Defective glomerulogenesis in the absence of laminin α5 demonstrates a developmental role for the kidney glomerular basement membrane
-
DOI 10.1006/dbio.1999.9546
-
Miner JH, Li C. Defective glomerulogenesis in the absence of lamininα5 demonstrates a developmental role for the kidney glomerular basement membrane. Dev Biol 2000; 217:278-89. (Pubitemid 30060876)
-
(2000)
Developmental Biology
, vol.217
, Issue.2
, pp. 278-289
-
-
Miner, J.H.1
Li, C.2
-
25
-
-
0344921338
-
Mesangial cells organize the glomerular capillaries by adhering to the G domain of laminin alpha5 in the glomerular basement membrane
-
DOI 10.1083/jcb.200211121
-
Kikkawa Y, Virtanen I, Miner JH. Mesangial cells organize the glomerular capillaries by adhering to the G domain of laminin alpha5 in the glomerular basement membrane. J Cell Biol 2003; 161:187-96. (Pubitemid 36459090)
-
(2003)
Journal of Cell Biology
, vol.161
, Issue.1
, pp. 187-196
-
-
Kikkawa, Y.1
Virtanen, I.2
Miner, J.H.3
-
26
-
-
0032015551
-
Positionally cloned gene for a novel glomerular protein - Nephrin - Is mutated in congenital nephrotic syndrome
-
Kestila M, Lenkkeri U, Mannikko M, Lamerdin J, McCready P, Putaala H, et al. Positionally cloned gene for a novel glomerular protein - nephrin - is mutated in congenital nephrotic syndrome. Mol Cell 1998; 1:575-82. (Pubitemid 128374693)
-
(1998)
Molecular Cell
, vol.1
, Issue.4
, pp. 575-582
-
-
Kestila, M.1
Lenkkeri, U.2
Mannikko, M.3
Lamerdin, J.4
McCready, P.5
Putaala, H.6
Ruotsalainen, V.7
Morita, T.8
Nissinen, M.9
Herva, R.10
Kashtan, C.E.11
Peltonen, L.12
Holmberg, C.13
Olsen, A.14
Tryggvason, K.15
-
27
-
-
77950515351
-
Genetics of nephrotic syndrome: Connecting molecular genetics to podocyte physiology
-
Machuca E, Benoit G, Antignac C. Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology. Hum Mol Genet 2009; 18:185-94.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 185-194
-
-
Machuca, E.1
Benoit, G.2
Antignac, C.3
-
28
-
-
33746770477
-
The glomerular basement membrane: Not gone, just forgotten
-
DOI 10.1172/JCI29488
-
Farquhar MG. The glomerular basement membrane: not gone, just forgotten. J Clin Invest 2006; 116:2090-3. (Pubitemid 44162317)
-
(2006)
Journal of Clinical Investigation
, vol.116
, Issue.8
, pp. 2090-2093
-
-
Farquhar, M.G.1
-
29
-
-
77950625211
-
Maintenance of glomerular filtration barrier integrity requires laminin alpha5
-
Goldberg S, Adair-Kirk TL, Senior RM, Miner JH. Maintenance of glomerular filtration barrier integrity requires laminin alpha5. J Am Soc Nephrol 2010; 21:579-86.
-
(2010)
J Am Soc Nephrol
, vol.21
, pp. 579-586
-
-
Goldberg, S.1
Adair-Kirk, T.L.2
Senior, R.M.3
Miner, J.H.4
-
30
-
-
0025292712
-
Identification of mutations in the COL4A5 collagen gene in Alport syndrome
-
Barker DF, Hostikka SL, Zhou J, Chow LT, Oliphant AR, Gerken SC, et al. Identification of mutations in the COL4A5 collagen gene in Alport syndrome. Science 1990; 248:1224-7.
-
(1990)
Science
, vol.248
, pp. 1224-1227
-
-
Barker, D.F.1
Hostikka, S.L.2
Zhou, J.3
Chow, L.T.4
Oliphant, A.R.5
Gerken, S.C.6
-
31
-
-
0034110693
-
Alport syndromes: Phenotypic heterogeneity of progressive hereditary nephritis
-
Kashtan CE. Alport syndromes: Phenotypic heterogeneity of progressive hereditary nephritis. Pediatr Nephrol 2000; 14:502-12. (Pubitemid 30319244)
-
(2000)
Pediatric Nephrology
, vol.14
, Issue.6
, pp. 502-512
-
-
Kashtan, C.E.1
-
32
-
-
0026740928
-
Distribution of the α1 and α2 chains of collagen IV and of collagens V and VI in Alport syndrome
-
Kashtan CE, Kim Y. Distribution of the α1 and α2 chains of collagen IV and of collagens V and VI in Alport syndrome. Kidney Int 1992; 42:115-26.
-
(1992)
Kidney Int
, vol.42
, pp. 115-126
-
-
Kashtan, C.E.1
Kim, Y.2
-
33
-
-
33745841589
-
-/- Alport mice
-
DOI 10.1681/ASN.2006020165
-
Kang JS, Wang XP, Miner JH, Morello R, Sado Y, Abrahamson DR, et al. Loss of alpha3/alpha4(IV) collagen from the glomerular basement membrane induces a strain-dependent isoform switch to alpha5alpha6(IV) collagen associated with longer renal survival in Col4a3-/- Alport mice. J Am Soc Nephrol 2006; 17:1962-9. (Pubitemid 44036180)
-
(2006)
Journal of the American Society of Nephrology
, vol.17
, Issue.7
, pp. 1962-1969
-
-
Kang, J.S.1
Wang, X.-P.2
Miner, J.H.3
Morello, R.4
Sado, Y.5
Abrahamson, D.R.6
Borza, D.-B.7
-
34
-
-
33645498692
-
Role of COL4A1 in small-vessel disease and hemorrhagic stroke
-
Gould DB, Phalan FC, van Mil SE, Sundberg JP, Vahedi K, Massin P, et al. Role of COL4A1 in small-vessel disease and hemorrhagic stroke. N Engl J Med 2006; 354:1489-96.
-
(2006)
N Engl J Med
, vol.354
, pp. 1489-1496
-
-
Gould, D.B.1
Phalan, F.C.2
Van Mil, S.E.3
Sundberg, J.P.4
Vahedi, K.5
Massin, P.6
-
35
-
-
37549015654
-
COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms and muscle cramps
-
Plaisier E, Gribouval O, Alamowitch S, Mougenot B, Prost C, Verpont MC, et al. COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms and muscle cramps. N Engl J Med 2007; 357:2687-95.
-
(2007)
N Engl J Med
, vol.357
, pp. 2687-2695
-
-
Plaisier, E.1
Gribouval, O.2
Alamowitch, S.3
Mougenot, B.4
Prost, C.5
Verpont, M.C.6
-
36
-
-
8444221929
-
Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities
-
DOI 10.1093/hmg/ddh284
-
Zenker M, Aigner T, Wendler O, Tralau T, Muntefering H, Fenski R, et al. Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities. Hum Mol Genet 2004; 13:2625-32. (Pubitemid 39485411)
-
(2004)
Human Molecular Genetics
, vol.13
, Issue.21
, pp. 2625-2632
-
-
Zenker, M.1
Aigner, T.2
Wendler, O.3
Tralau, T.4
Muntefering, H.5
Fenski, R.6
Pitz, S.7
Schumacher, V.8
Royer-Pokora, B.9
Wuhl, E.10
Cochat, P.11
Bouvier, R.12
Kraus, C.13
Mark, K.14
Madlon, H.15
Dotsch, J.16
Rascher, W.17
Maruniak-Chudek, I.18
Lennert, T.19
Neumann, L.M.20
Reis, A.21
more..
-
37
-
-
4744356720
-
Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: An autosomal recessive syndrome
-
DOI 10.1002/ajmg.a.30310
-
Zenker M, Tralau T, Lennert T, Pitz S, Mark K, Madlon H, et al. Congenital nephrosis, mesangial sclerosis and distinct eye abnormalities with microcoria: an autosomal recessive syndrome. Am J Med Genet A 2004; 130:138-45. (Pubitemid 39310500)
-
(2004)
American Journal of Medical Genetics
, vol.130 A
, Issue.2
, pp. 138-145
-
-
Zenker, M.1
Tralau, T.2
Lennert, T.3
Pitz, S.4
Mark, K.5
Madlon, H.6
Dotsch, J.7
Reis, A.8
Muntefering, H.9
Neumann, L.M.10
-
38
-
-
0029127384
-
The renal glomerulus of mice lacking s-laminin/laminin β2: Nephrosis despite molecular compensation by laminin β1
-
Noakes PG, Miner JH, Gautam M, Cunningham JM, Sanes JR, Merlie JP. The renal glomerulus of mice lacking s-laminin/laminin β2: Nephrosis despite molecular compensation by laminin β1. Nat Genet 1995; 10:400-6.
-
(1995)
Nat Genet
, vol.10
, pp. 400-406
-
-
Noakes, P.G.1
Miner, J.H.2
Gautam, M.3
Cunningham, J.M.4
Sanes, J.R.5
Merlie, J.P.6
-
39
-
-
0028908326
-
Aberrant differentiation of neuromuscular junctions in mice lacking s-laminin/laminin β2
-
Noakes PG, Gautam M, Mudd J, Sanes JR, Merlie JP. Aberrant differentiation of neuromuscular junctions in mice lacking s-laminin/laminin β2. Nature 1995; 374:258-62.
-
(1995)
Nature
, vol.374
, pp. 258-262
-
-
Noakes, P.G.1
Gautam, M.2
Mudd, J.3
Sanes, J.R.4
Merlie, J.P.5
-
40
-
-
0033216631
-
Disruption of laminin beta2 chain production causes alterations in morphology and function in the CNS
-
Libby RT, Lavallee CR, Balkema GW, Brunken WJ, Hunter DD. Disruption of laminin beta2 chain production causes alterations in morphology and function in the CNS. J Neurosci 1999; 19:9399-411. (Pubitemid 30228093)
-
(1999)
Journal of Neuroscience
, vol.19
, Issue.21
, pp. 9399-9411
-
-
Libby, R.T.1
Lavallee, C.R.2
Balkema, G.W.3
Brunken, W.J.4
Hunter, D.D.5
-
42
-
-
33748438381
-
Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders
-
DOI 10.1038/sj.ki.5001679, PII 5001679
-
Hasselbacher K, Wiggins RC, Matejas V, Hinkes BG, Mucha B, Hoskins BE, et al. Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders. Kidney Int 2006; 70:1008-12. (Pubitemid 44344069)
-
(2006)
Kidney International
, vol.70
, Issue.6
, pp. 1008-1012
-
-
Hasselbacher, K.1
Wiggins, R.C.2
Matejas, V.3
Hinkes, B.G.4
Mucha, B.5
Hoskins, B.E.6
Ozaltin, F.7
Nurnberg, G.8
Becker, C.9
Hangan, D.10
Pohl, M.11
Kuwertz-Broking, E.12
Griebel, M.13
Schumacher, V.14
Royer-Pokora, B.15
Bakkaloglu, A.16
Nurnberg, P.17
Zenker, M.18
Hildebrandt, F.19
-
43
-
-
77956293608
-
Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum
-
Matejas V, Hinkes B, Alkandari F, Al-Gazali L, Annexstad E, Aytac MB, et al. Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum. Hum Mutat 2010; 31:992-1002.
-
(2010)
Hum Mutat
, vol.31
, pp. 992-1002
-
-
Matejas, V.1
Hinkes, B.2
Alkandari, F.3
Al-Gazali, L.4
Annexstad, E.5
Aytac, M.B.6
-
44
-
-
79955640326
-
A missense LAMB2 mutation causes congenital nephrotic syndrome by impairing laminin secretion
-
DOI: 10.1681/ASN.2010060632
-
Chen Y, Kikkawa Y, Miner JH. A missense LAMB2 mutation causes congenital nephrotic syndrome by impairing laminin secretion. J Amer Soc Nephrol 2011; 22; DOI: 10.1681/ASN.2010060632.
-
(2011)
J Amer Soc Nephrol
, vol.22
-
-
Chen, Y.1
Kikkawa, Y.2
Miner, J.H.3
-
45
-
-
33645548140
-
Transgenic isolation of skeletal muscle and kidney defects in laminin beta2 mutant mice: Implications for Pierson syndrome
-
Miner JH, Go G, Cunningham J, Patton BL, Jarad G. Transgenic isolation of skeletal muscle and kidney defects in laminin beta2 mutant mice: Implications for Pierson syndrome. Development 2006; 133:967-75.
-
(2006)
Development
, vol.133
, pp. 967-975
-
-
Miner, J.H.1
Go, G.2
Cunningham, J.3
Patton, B.L.4
Jarad, G.5
-
46
-
-
0037373006
-
Excess placental soluble fms-like tyrosine kinase 1 (sFlt1) may contribute to endothelial dysfunction hypertension, and proteinuria in preeclampsia
-
DOI 10.1172/JCI200317189
-
Maynard SE, Min JY, Merchan J, Lim KH, Li J, Mondal S, et al. Excess placental soluble fms-like tyrosine kinase 1 (sFlt1) may contribute to endothelial dysfunction, hypertension and proteinuria in preeclampsia. J Clin Invest 2003; 111:649-58. (Pubitemid 36278583)
-
(2003)
Journal of Clinical Investigation
, vol.111
, Issue.5
, pp. 649-658
-
-
Maynard, S.E.1
Min, J.-Y.2
Merchan, J.3
Lim, K.-H.4
Li, J.5
Mondal, S.6
Libermann, T.A.7
Morgan, J.P.8
Sellke, F.W.9
Stillman, I.E.10
Epstein, F.H.11
Sukhatme, V.P.12
Karumanchi, S.A.13
-
47
-
-
0037370325
-
Glomerular-specific alterations of VEGF-A expression lead to distinct congenital and acquired renal diseases
-
DOI 10.1172/JCI200317423
-
Eremina V, Sood M, Haigh J, Nagy A, Lajoie G, Ferrara N, et al. Glomerular-specific alterations of VEGF-A expression lead to distinct congenital and acquired renal diseases. J Clin Invest 2003; 111:707-16. (Pubitemid 36278589)
-
(2003)
Journal of Clinical Investigation
, vol.111
, Issue.5
, pp. 707-716
-
-
Eremina, V.1
Sood, M.2
Haigh, J.3
Nagy, A.4
Lajoie, G.5
Ferrara, N.6
Gerber, H.-P.7
Kikkawa, Y.8
Miner, J.H.9
Quaggin, S.E.10
|