-
1
-
-
0029984364
-
Structure of the human laminin gamma 2 chain gene (LAMC2): Alternative splicing with different tissue distribution of two transcripts
-
Airenne T, Haakana H, Sainio K et al. (1996) Structure of the human laminin gamma 2 chain gene (LAMC2): alternative splicing with different tissue distribution of two transcripts. Genomics 32:54-64
-
(1996)
Genomics
, vol.32
, pp. 54-64
-
-
Airenne, T.1
Haakana, H.2
Sainio, K.3
-
2
-
-
0034039814
-
Differential expression of mouse laminin gamma2 and gamma2* chain transcripts
-
Airenne T, Lin Y, Olsson M et al. (2000) Differential expression of mouse laminin gamma2 and gamma2* chain transcripts. Cell Tissue Res 300:129-137
-
(2000)
Cell Tissue Res
, vol.300
, pp. 129-137
-
-
Airenne, T.1
Lin, Y.2
Olsson, M.3
-
3
-
-
0038824761
-
Customized molecular phenotyp-ing by quantitative gene expression and pattern recognition analysis
-
Akilesh S, Shaffer DJ, Roopenian D (2003) Customized molecular phenotyp-ing by quantitative gene expression and pattern recognition analysis. Genome Res 13:1719-1727
-
(2003)
Genome Res
, vol.13
, pp. 1719-1727
-
-
Akilesh, S.1
Shaffer, D.J.2
Roopenian, D.3
-
4
-
-
24944468060
-
Epidermolysis bullosa hereditaria. 3. A histologic study of changes in teeth in the polydysplastic dystrophic and lethal forms
-
Arwill T, Olsson O, Bergenholtz A (1965) Epidermolysis bullosa hereditaria. 3. A histologic study of changes in teeth in the polydysplastic dystrophic and lethal forms. Oral Surg Oral Med Oral Pathol 19:723-744
-
(1965)
Oral Surg Oral Med Oral Pathol
, vol.19
, pp. 723-744
-
-
Arwill, T.1
Olsson, O.2
Bergenholtz, A.3
-
5
-
-
58249107829
-
Type XVII collagen is a key player in tooth enamel formation
-
Asaka T, Akiyama M, Domon T et al. (2009) Type XVII collagen is a key player in tooth enamel formation. Am J Pathol 174:91-100
-
(2009)
Am J Pathol
, vol.174
, pp. 91-100
-
-
Asaka, T.1
Akiyama, M.2
Domon, T.3
-
7
-
-
22544456862
-
Compound genetic ablation of nidogen 1 and 2 causes basement membrane defects and perinatal lethality in mice
-
Bader BL, Smyth N, Nedbal S et al. (2005) Compound genetic ablation of nidogen 1 and 2 causes basement membrane defects and perinatal lethality in mice. Mol Cell Biol 25:6846-6856
-
(2005)
Mol Cell Biol
, vol.25
, pp. 6846-6856
-
-
Bader, B.L.1
Smyth, N.2
Nedbal, S.3
-
8
-
-
0002349725
-
Ultrastructural evaluation of mouse mutations
-
(Sundberg JP, Boggess D, eds). Boca Raton: CRC Press
-
Bechtold LS (2000) Ultrastructural evaluation of mouse mutations. In: Systematic Characterization of Mouse Mutations. (Sundberg JP, Boggess D, eds). Boca Raton: CRC Press, 121-129
-
(2000)
Systematic Characterization of Mouse Mutations
, pp. 121-129
-
-
Bechtold, L.S.1
-
9
-
-
0036129838
-
Generation of a new congenic mouse strain to test the relationships among serum insulin-like growth factor I, bone mineral density, and skeletal morphology in vivo
-
Bouxsein ML, Rosen CJ, Turner CH et al. (2002) Generation of a new congenic mouse strain to test the relationships among serum insulin-like growth factor I, bone mineral density, and skeletal morphology in vivo. J Bone Miner Res 17:570-579
-
(2002)
J Bone Miner Res
, vol.17
, pp. 570-579
-
-
Bouxsein, M.L.1
Rosen, C.J.2
Turner, C.H.3
-
10
-
-
0035809198
-
An inducible mouse model for epidermolysis bullosa simplex: Implications for gene therapy
-
Cao T, Longley MA, Wang XJ et al. (2001) An inducible mouse model for epidermolysis bullosa simplex: implications for gene therapy. J Cell Biol 152:651-656
-
(2001)
J Cell Biol
, vol.152
, pp. 651-656
-
-
Cao, T.1
Longley, M.A.2
Wang, X.J.3
-
11
-
-
15044358758
-
Inherited junctional epidermolysis bullosa in the German Pointer: Establishment of a large animal model
-
Capt A, Spirito F, Guaguere E et al. (2005) Inherited junctional epidermolysis bullosa in the German Pointer: establishment of a large animal model. J Invest Dermatol 124:530-535
-
(2005)
J Invest Dermatol
, vol.124
, pp. 530-535
-
-
Capt, A.1
Spirito, F.2
Guaguere, E.3
-
12
-
-
0034792542
-
Novel mutations in the LAMC2 gene in non-Herlitz junctional epidermolysis bullosa: Effects of laminin-5 assembly, secretion, and deposition
-
Castiglia D, Posteraro P, Spirito F et al. (2001) Novel mutations in the LAMC2 gene in non-Herlitz junctional epidermolysis bullosa: effects of laminin-5 assembly, secretion, and deposition. J Invest Dermatol 117:731-739
-
(2001)
J Invest Dermatol
, vol.117
, pp. 731-739
-
-
Castiglia, D.1
Posteraro, P.2
Spirito, F.3
-
13
-
-
25444507445
-
The "goldilocks effect" in cystic fibrosis: Identification of a lung phenotype in the cftr knockout and heterozygous mouse
-
Cohen JC, Lundblad LK, Bates JH et al. (2004) The "Goldilocks effect" in cystic fibrosis: identification of a lung phenotype in the cftr knockout and heterozygous mouse. BMC Genetics 5:21
-
(2004)
BMC Genetics
, vol.5
, pp. 21
-
-
Cohen, J.C.1
Lundblad, L.K.2
Bates, J.H.3
-
14
-
-
0023679117
-
A disease resembling junctional epidermolysis bullosa in a toy poodle
-
Dunstan RW, Sills RC, Wilkinson JE et al. (1988) A disease resembling junctional epidermolysis bullosa in a toy poodle. Am J Dermatopath 10:442-447
-
(1988)
Am J Dermatopath
, vol.10
, pp. 442-447
-
-
Dunstan, R.W.1
Sills, R.C.2
Wilkinson, J.E.3
-
15
-
-
22044435548
-
Gene therapy approaches for epidermolysis bullosa
-
Ferrari S, Pellegrini G, Mavilio F et al. (2005) Gene therapy approaches for epidermolysis bullosa. Clin Dermatol 23:430-436
-
(2005)
Clin Dermatol
, vol.23
, pp. 430-436
-
-
Ferrari, S.1
Pellegrini, G.2
Mavilio, F.3
-
16
-
-
33645815303
-
Bone mineralization in children with epidermolysis bullosa
-
Fewtrell MS, Allgrove J, Gordon I et al. (2006) Bone mineralization in children with epidermolysis bullosa. Br J Dermatol 154:959-962
-
(2006)
Br J Dermatol
, vol.154
, pp. 959-962
-
-
Fewtrell, M.S.1
Allgrove, J.2
Gordon, I.3
-
17
-
-
70450232212
-
-
New York: Springer, Wien, xix
-
Fine J-D, Hintner H (2009) Life with Epidermolysis Bullosa (EB): Etiology, Diagnosis, Multidisciplinary Care, and Therapy. New York: Springer, Wien, xix, 338 p
-
(2009)
Life with Epidermolysis Bullosa (EB): Etiology, Diagnosis, Multidisciplinary Care, and Therapy
, pp. 338
-
-
Fine, J.-D.1
Hintner, H.2
-
18
-
-
43449084027
-
The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB
-
Fine JD, Eady RA, Bauer EA et al. (2008a) The classification of inherited epidermolysis bullosa (EB): report of the Third International Consensus Meeting on Diagnosis and Classification of EB. J Am Acad Dermatol 58:931-950
-
(2008)
J Am Acad Dermatol
, vol.58
, pp. 931-950
-
-
Fine, J.D.1
Eady, R.A.2
Bauer, E.A.3
-
19
-
-
34548383444
-
Tracheolaryngeal complications of inherited epidermolysis bullosa: Cumulative experience of the national epidermolysis bullosa registry
-
Fine JD, Johnson LB, Weiner M et al. (2007) Tracheolaryngeal complications of inherited epidermolysis bullosa: cumulative experience of the national epidermolysis bullosa registry. Laryngoscope 117:1652-1660
-
(2007)
Laryngoscope
, vol.117
, pp. 1652-1660
-
-
Fine, J.D.1
Johnson, L.B.2
Weiner, M.3
-
20
-
-
38149099101
-
Cause-specific risks of childhood death in inherited epidermolysis bullosa
-
Fine JD, Johnson LB, Weiner M et al. (2008b) Cause-specific risks of childhood death in inherited epidermolysis bullosa. J Pediatr 152:276-280
-
(2008)
J Pediatr
, vol.152
, pp. 276-280
-
-
Fine, J.D.1
Johnson, L.B.2
Weiner, M.3
-
21
-
-
0024220724
-
Hereditary junctional mechanobullous disease in a foal
-
Frame SR, Harrington DD, Fessler J et al. (1988) Hereditary junctional mechanobullous disease in a foal. J Am Vet Med Assoc 193:1420-1424
-
(1988)
J Am Vet Med Assoc
, vol.193
, pp. 1420-1424
-
-
Frame, S.R.1
Harrington, D.D.2
Fessler, J.3
-
23
-
-
43049093343
-
A hypomorphic mouse model of dystrophic epidermolysis bullosa reveals mechanisms of disease and response to fibroblast therapy
-
Fritsch A, Loeckermann S, Kern JS et al. (2008) A hypomorphic mouse model of dystrophic epidermolysis bullosa reveals mechanisms of disease and response to fibroblast therapy. J Clin Invest 118:1669-1679
-
(2008)
J Clin Invest
, vol.118
, pp. 1669-1679
-
-
Fritsch, A.1
Loeckermann, S.2
Kern, J.S.3
-
24
-
-
27144512476
-
The Tetratricopeptide repeat domain 7 gene is mutated in flaky skin mice: A model for psoriasis, autoimmunity, and anemia
-
Maywood, NJ
-
Helms C, Pelsue S, Cao L et al. (2005) The Tetratricopeptide repeat domain 7 gene is mutated in flaky skin mice: a model for psoriasis, autoimmunity, and anemia. Exp Biol Med (Maywood, NJ) 230:659-667
-
(2005)
Exp Biol Med
, vol.230
, pp. 659-667
-
-
Helms, C.1
Pelsue, S.2
Cao, L.3
-
25
-
-
0034115701
-
The chemical composition of tooth enamel in junctional epidermolysis bullosa
-
Kirkham J, Robinson C, Strafford SM et al. (2000) The chemical composition of tooth enamel in junctional epidermolysis bullosa. Arch Oral Biol 45:377-386
-
(2000)
Arch Oral Biol
, vol.45
, pp. 377-386
-
-
Kirkham, J.1
Robinson, C.2
Strafford, S.M.3
-
26
-
-
0031229599
-
IAP insertion in the murine LamB3 gene results in junctional epidermolysis bullosa
-
Kuster JE, Guarnieri MH, Ault JG et al. (1997) IAP insertion in the murine LamB3 gene results in junctional epidermolysis bullosa. Mamm Genome 8:673-681
-
(1997)
Mamm Genome
, vol.8
, pp. 673-681
-
-
Kuster, J.E.1
Guarnieri, M.H.2
Ault, J.G.3
-
27
-
-
0035981217
-
Alternative transcriptional initiation and splicing of mouse Lamc2 message
-
Lee G, Kim MG, Yim JB et al. (2001) Alternative transcriptional initiation and splicing of mouse Lamc2 message. Mol Cells 12:380-390
-
(2001)
Mol Cells
, vol.12
, pp. 380-390
-
-
Lee, G.1
Kim, M.G.2
Yim, J.B.3
-
28
-
-
33845524625
-
Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells
-
Mavilio F, Pellegrini G, Ferrari S et al. (2006) Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells. Nat Med 12:1397-1402
-
(2006)
Nat Med
, vol.12
, pp. 1397-1402
-
-
Mavilio, F.1
Pellegrini, G.2
Ferrari, S.3
-
30
-
-
0141887524
-
Targeted inactivation of murine laminin gamma2-chain gene recapitulates human junctional epidermo-lysis bullosa
-
Meng X, Klement JF, Leperi DA et al. (2003) Targeted inactivation of murine laminin gamma2-chain gene recapitulates human junctional epidermo-lysis bullosa. J Invest Dermatol 121:720-731
-
(2003)
J Invest Dermatol
, vol.121
, pp. 720-731
-
-
Meng, X.1
Klement, J.F.2
Leperi, D.A.3
-
31
-
-
0030840389
-
Nonlethal junctional epidermolysis bullosa in a dog
-
Nagata M, Iwasaki T, Masuda H et al. (1997) Non-lethal junctional epidermolysis bullosa in a dog. Br J Dermatol 137:445-449
-
(1997)
Br J Dermatol
, vol.137
, pp. 445-449
-
-
Nagata, M.1
Iwasaki, T.2
Masuda, H.3
-
32
-
-
0029591562
-
Dystrophic form of inherited epidermolysis bullosa in a dog (Akita Inu)
-
Nagata M, Shimizu H, Masunaga T et al. (1995) Dystrophic form of inherited epidermolysis bullosa in a dog (Akita Inu). Br J Dermatol 133:1000-1003
-
(1995)
Br J Dermatol
, vol.133
, pp. 1000-1003
-
-
Nagata, M.1
Shimizu, H.2
Masunaga, T.3
-
33
-
-
0036553471
-
Junctional epidermolysis bullosa in the Middle East: Clinical and genetic studies in a series of consanguineous families
-
Nakano A, Lestringant GG, Paperna T et al. (2002) Junctional epidermolysis bullosa in the Middle East: clinical and genetic studies in a series of consanguineous families. J Am Acad Dermatol 46:510-516
-
(2002)
J Am Acad Dermatol
, vol.46
, pp. 510-516
-
-
Nakano, A.1
Lestringant, G.G.2
Paperna, T.3
-
34
-
-
33644620397
-
Lung development in laminin gamma2 deficiency: Abnormal tracheal hemidesmosomes with normal branching morphogenesis and epithelial differentiation
-
Nguyen NM, Pulkkinen L, Schlueter JA et al. (2006) Lung development in laminin gamma2 deficiency: abnormal tracheal hemidesmosomes with normal branching morphogenesis and epithelial differentiation. Respir Res 7:28
-
(2006)
Respir Res
, vol.7
, pp. 28
-
-
Nguyen, N.M.1
Pulkkinen, L.2
Schlueter, J.A.3
-
35
-
-
33847725511
-
Humanization of autoantigen
-
Nishie W, Sawamura D, Goto M et al. (2007) Humanization of autoantigen. Nat Med 13:378-383
-
(2007)
Nat Med
, vol.13
, pp. 378-383
-
-
Nishie, W.1
Sawamura, D.2
Goto, M.3
-
36
-
-
0037794315
-
A comparative study of immunohistochemistry and electron microscopy used in the diagnosis of epidermolysis bullosa
-
Petronius D, Bergman R, Ben Izhak O et al. (2003) A comparative study of immunohistochemistry and electron microscopy used in the diagnosis of epidermolysis bullosa. Am J Dermatopathol 25:198-203
-
(2003)
Am J Dermatopathol
, vol.25
, pp. 198-203
-
-
Petronius, D.1
Bergman, R.2
Ben Izhak, O.3
-
37
-
-
0028180092
-
Mutations in the gamma 2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa
-
Pulkkinen L, Christiano AM, Airenne T et al. (1994) Mutations in the gamma 2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa. Nat Genet 6:293-297
-
(1994)
Nat Genet
, vol.6
, pp. 293-297
-
-
Pulkkinen, L.1
Christiano, A.M.2
Airenne, T.3
-
38
-
-
1642357093
-
Immunohistochemical and immunofluorescence methods
-
(Sundberg JP, Boggess D, eds). Boca Raton, FL: CRC Press
-
Relyea MJ, Sundberg JP, Ward JM (2000) Immunohistochemical and immunofluorescence methods. In: Systematic Approach to Evaluation of Mouse Mutations. (Sundberg JP, Boggess D, eds). Boca Raton, FL: CRC Press, 131-144
-
(2000)
Systematic Approach to Evaluation of Mouse Mutations
, pp. 131-144
-
-
Relyea, M.J.1
Sundberg, J.P.2
Ward, J.M.3
-
39
-
-
0033553883
-
Targeted disruption of the LAMA3 gene in mice reveals abnormalities in survival and late stage differentiation of epithelial cells
-
Ryan MC, Lee K, Miyashita Y et al. (1999) Targeted disruption of the LAMA3 gene in mice reveals abnormalities in survival and late stage differentiation of epithelial cells. J Cell Biol 145:1309-1323
-
(1999)
J Cell Biol
, vol.145
, pp. 1309-1323
-
-
Ryan, M.C.1
Lee, K.2
Miyashita, Y.3
-
40
-
-
0003019810
-
An analysis of pressure-volume characteristics of the lungs
-
Salazar E, Knowles JH (1964) An analysis of pressure-volume characteristics of the lungs. J Appl Physiol 19:97-104
-
(1964)
J Appl Physiol
, vol.19
, pp. 97-104
-
-
Salazar, E.1
Knowles, J.H.2
-
41
-
-
0029056416
-
Retroviral sequences located within an intron of the dilute gene alter dilute expression in a tissue-specific manner
-
Seperack PK, Mercer JA, Strobel MC et al. (1995) Retroviral sequences located within an intron of the dilute gene alter dilute expression in a tissue-specific manner. EMBO J 14:2326-2332
-
(1995)
EMBO J
, vol.14
, pp. 2326-2332
-
-
Seperack, P.K.1
Mercer, J.A.2
Strobel, M.C.3
-
42
-
-
84941618983
-
Necropsy methods
-
(Hedrich HJ, ed). London: Academic Press
-
Seymour R, Ichiki T, Mikaelian I et al. (2004) Necropsy methods. In: Laboratory Mouse. (Hedrich HJ, ed). London: Academic Press, 495-516
-
(2004)
Laboratory Mouse
, pp. 495-516
-
-
Seymour, R.1
Ichiki, T.2
Mikaelian, I.3
-
43
-
-
0033545239
-
Absence of basement membranes after targeting the LAMC1 gene results in embryonic lethality due to failure of endoderm differentiation
-
Smyth N, Vatansever HS, Murray P et al. (1999) Absence of basement membranes after targeting the LAMC1 gene results in embryonic lethality due to failure of endoderm differentiation. J Cell Biol 144:151-160
-
(1999)
J Cell Biol
, vol.144
, pp. 151-160
-
-
Smyth, N.1
Vatansever, H.S.2
Murray, P.3
-
44
-
-
0036379397
-
Animal models for skin blistering conditions: Absence of laminin 5 causes hereditary junctional mechanobullous disease in the Belgian horse
-
Spirito F, Charlesworth A, Linder K et al. (2002) Animal models for skin blistering conditions: absence of laminin 5 causes hereditary junctional mechanobullous disease in the Belgian horse. J Invest Dermatol 119:684-691
-
(2002)
J Invest Dermatol
, vol.119
, pp. 684-691
-
-
Spirito, F.1
Charlesworth, A.2
Linder, K.3
-
45
-
-
0023802496
-
Role of endogenous retroviruses as mutagens: The hairless mutation of mice
-
Stoye JP, Fenner S, Greenoak GE et al. (1988) Role of endogenous retroviruses as mutagens: the hairless mutation of mice. Cell 54:383-391
-
(1988)
Cell
, vol.54
, pp. 383-391
-
-
Stoye, J.P.1
Fenner, S.2
Greenoak, G.E.3
-
46
-
-
0028365880
-
PCR-amplification of simple sequence repeat variants from pooled DNA samples for rapidly mapping new mutations of the mouse
-
Taylor BA, Navin A, Phillips SJ (1994) PCR-amplification of simple sequence repeat variants from pooled DNA samples for rapidly mapping new mutations of the mouse. Genomics 21:626-632
-
(1994)
Genomics
, vol.21
, pp. 626-632
-
-
Taylor, B.A.1
Navin, A.2
Phillips, S.J.3
-
47
-
-
60849091919
-
Amelioration of epidermolysis bullosa by transfer of wild-type bone marrow cells
-
Tolar J, Ishida-Yamamoto A, Riddle M et al. (2009) Amelioration of epidermolysis bullosa by transfer of wild-type bone marrow cells. Blood 113:1167-1174
-
(2009)
Blood
, vol.113
, pp. 1167-1174
-
-
Tolar, J.1
Ishida-Yamamoto, A.2
Riddle, M.3
-
48
-
-
0033922371
-
Preparation of PCR-quality mouse genomic DNA with hot sodium hydroxide and tris (HotSHOT)
-
54
-
Truett GE, Heeger P, Mynatt RL et al. (2000) Preparation of PCR-quality mouse genomic DNA with hot sodium hydroxide and tris (HotSHOT). BioTechniques 29:52, 54
-
(2000)
BioTechniques
, vol.29
, pp. 52
-
-
Truett, G.E.1
Heeger, P.2
Mynatt, R.L.3
-
49
-
-
0030767241
-
Epidermolysis bullosa: A spectrum of clinical phenotypes explained by molecular heterogeneity
-
Uitto J, Pulkkinen L, McLean WH (1997) Epidermolysis bullosa: a spectrum of clinical phenotypes explained by molecular heterogeneity. Mol Med Today 3:457-465
-
(1997)
Mol Med Today
, vol.3
, pp. 457-465
-
-
Uitto, J.1
Pulkkinen, L.2
McLean, W.H.3
-
50
-
-
7444248879
-
Progress in epidermolysis bullosa: Genetic classification and clinical implications
-
Uitto J, Richard G (2004) Progress in epidermolysis bullosa: genetic classification and clinical implications. Am J Med Genet C Semin Med Genet 131C:61-74
-
(2004)
Am J Med Genet C Semin Med Genet
, vol.131 C
, pp. 61-74
-
-
Uitto, J.1
Richard, G.2
-
51
-
-
33747877557
-
The Kindlins: Subcellular localization and expression during murine development
-
Ussar S, Wang HV, Linder S et al. (2006) The Kindlins: subcellular localization and expression during murine development. Exp Cell Res 312:3142-3151
-
(2006)
Exp Cell Res
, vol.312
, pp. 3142-3151
-
-
Ussar, S.1
Wang, H.V.2
Linder, S.3
-
52
-
-
0036333442
-
Specific ablation of the nidogen-binding site in the laminin gamma1 chain interferes with kidney and lung development
-
Willem M, Miosge N, Halfter W et al. (2002) Specific ablation of the nidogen-binding site in the laminin gamma1 chain interferes with kidney and lung development. Development 129:2711-2722
-
(2002)
Development
, vol.129
, pp. 2711-2722
-
-
Willem, M.1
Miosge, N.2
Halfter, W.3
-
53
-
-
0030437293
-
Structural and compositional alteration of tooth enamel in hereditary epidermolysis bullosa
-
Wright JT, Hall KI, Deaton TG et al. (1996) Structural and compositional alteration of tooth enamel in hereditary epidermolysis bullosa. Connect Tissue Res 34:271-279
-
(1996)
Connect Tissue Res
, vol.34
, pp. 271-279
-
-
Wright, J.T.1
Hall, K.I.2
Deaton, T.G.3
-
54
-
-
0027689006
-
Development defects of enamel in humans with hereditary epidermolysis bullosa
-
Wright JT, Johnson LB, Fine JD (1993) Development defects of enamel in humans with hereditary epidermolysis bullosa. Arch Oral Biol 38:945-955
-
(1993)
Arch Oral Biol
, vol.38
, pp. 945-955
-
-
Wright, J.T.1
Johnson, L.B.2
Fine, J.D.3
-
55
-
-
0031939643
-
Expression and localization of laminin-5 subunits in the mouse incisor
-
Yoshiba N, Yoshiba K, Aberdam D et al. (1998) Expression and localization of laminin-5 subunits in the mouse incisor. Cell Tissue Res 292:143-149
-
(1998)
Cell Tissue Res
, vol.292
, pp. 143-149
-
-
Yoshiba, N.1
Yoshiba, K.2
Aberdam, D.3
-
56
-
-
25144520251
-
Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiP
-
Zhao L, Longo-Guess C, Harris BS et al. (2005) Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiP. Nat Genet 37:974-979
-
(2005)
Nat Genet
, vol.37
, pp. 974-979
-
-
Zhao, L.1
Longo-Guess, C.2
Harris, B.S.3
|