-
1
-
-
0028097109
-
Molecular cloning, expression and chromosomal localization of human AMP-activated protein kinase
-
Beri RK, Marley AE, See CG, Sopwith WF, Aguan K, Carling D, Scott J, et al (1994) Molecular cloning, expression and chromosomal localization of human AMP-activated protein kinase. FEES Lett 356:117-121
-
(1994)
FEES Lett
, vol.356
, pp. 117-121
-
-
Beri, R.K.1
Marley, A.E.2
See, C.G.3
Sopwith, W.F.4
Aguan, K.5
Carling, D.6
Scott, J.7
-
3
-
-
0024427198
-
A simple and efficient non-organic procedure for the isolation of genomic DNA from blood
-
Grimberg J, Nawoschik S, Belluscio L, McKee R, Turck A, Eisenberg A (1989) A simple and efficient non-organic procedure for the isolation of genomic DNA from blood. Nucleic Acids Res 17:8390
-
(1989)
Nucleic Acids Res
, vol.17
, pp. 8390
-
-
Grimberg, J.1
Nawoschik, S.2
Belluscio, L.3
McKee, R.4
Turck, A.5
Eisenberg, A.6
-
4
-
-
0028231090
-
The 1993-94 Généthon human genetic linkage map
-
Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Millasseau P, Marc S, et al (1994) The 1993-94 Généthon human genetic linkage map. Nat Genet 7:246-339
-
(1994)
Nat Genet
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
Millasseau, P.6
Marc, S.7
-
5
-
-
0027938872
-
Characterization by cDNA of two new human protein kinases: Evidence by sequence comparison of a new family of mammalian protein kinases
-
Hanes J, von der Kammer H, Klaudiny J, Scheit KH (1994) Characterization by cDNA of two new human protein kinases: evidence by sequence comparison of a new family of mammalian protein kinases. J Mol Biol 244:665-672
-
(1994)
J Mol Biol
, vol.244
, pp. 665-672
-
-
Hanes, J.1
Von der Kammer, H.2
Klaudiny, J.3
Scheit, K.H.4
-
7
-
-
0019826715
-
Primary familial amyloidosis of the cornea
-
Mondino BJ, Rapp MF, Sugar J, Sundar Raj CV, Brown SI (1981) Primary familial amyloidosis of the cornea. Am J Ophthalmol 92:732-736
-
(1981)
Am J Ophthalmol
, vol.92
, pp. 732-736
-
-
Mondino, B.J.1
Rapp, M.F.2
Sugar, J.3
Sundar Raj, C.V.4
Brown, S.I.5
-
8
-
-
0031020733
-
Kerato-epirhelin mutations in four 5q31-linked corneal dystrophies
-
Munier FL, Korvatska E, Djemai A, Paslier DL, Zografos L, Pescia G, Schordert DF (1997) Kerato-epirhelin mutations in four 5q31-linked corneal dystrophies. Nat Genet 15: 247-251
-
(1997)
Nat Genet
, vol.15
, pp. 247-251
-
-
Munier, F.L.1
Korvatska, E.2
Djemai, A.3
Paslier, D.L.4
Zografos, L.5
Pescia, G.6
Schordert, D.F.7
-
9
-
-
0001001932
-
A rare case of corneal dystrophy
-
Nakaizumi G (1914) A rare case of corneal dystrophy. Acta Soc Ophthalmol Jpn 18:949-950
-
(1914)
Acta Soc Ophthalmol Jpn
, vol.18
, pp. 949-950
-
-
Nakaizumi, G.1
-
10
-
-
0015318852
-
Localized corneal amyloidosis: Case report with electron microscopic observations
-
Ramsey MS, Fine BS, Cohen SW (1972) Localized corneal amyloidosis: case report with electron microscopic observations. Am J Ophthalmol 73:560-565
-
(1972)
Am J Ophthalmol
, vol.73
, pp. 560-565
-
-
Ramsey, M.S.1
Fine, B.S.2
Cohen, S.W.3
-
11
-
-
0026783009
-
CDNA cloning and sequence analysis of βig-h3, a novel gene induced in a human adenocarcinoma cell line after treatment with transforming growth factor beta
-
Skonier J, Neubauer M, Madisen L, Bennett K, Plowman GD, Purchio AF (1992) cDNA cloning and sequence analysis of βig-h3, a novel gene induced in a human adenocarcinoma cell line after treatment with transforming growth factor beta, DNA Cell Biol 11:511-522
-
(1992)
DNA Cell Biol
, vol.11
, pp. 511-522
-
-
Skonier, J.1
Neubauer, M.2
Madisen, L.3
Bennett, K.4
Plowman, G.D.5
Purchio, A.F.6
-
12
-
-
0002522755
-
Corneal dystrophies and degenerations
-
Smolin G, Thoft RA (eds). Little, Brown, Boston
-
Smolin G (1994) Corneal dystrophies and degenerations. In: Smolin G, Thoft RA (eds) Cornea, 3d ed. Little, Brown, Boston, pp 499-533
-
(1994)
Cornea, 3d Ed.
, pp. 499-533
-
-
Smolin, G.1
-
13
-
-
0029963126
-
Linkage of a gene for macular corneal dystrophy to chromosome 16
-
Vance JM, Jonasson F, Lennon F, Sarrica J, Damji KF, Stauffer J, Pericak-Vance MA, et al (1996) Linkage of a gene for macular corneal dystrophy to chromosome 16. Am J Hum Genet 58:757-762
-
(1996)
Am J Hum Genet
, vol.58
, pp. 757-762
-
-
Vance, J.M.1
Jonasson, F.2
Lennon, F.3
Sarrica, J.4
Damji, K.F.5
Stauffer, J.6
Pericak-Vance, M.A.7
-
14
-
-
0018904839
-
Gelatinous drop-like dystrophy: A form of primary corneal amyloidosis
-
Weber FL, Babel J (1980) Gelatinous drop-like dystrophy: a form of primary corneal amyloidosis. Arch Ophthalmol 98: 144-148
-
(1980)
Arch Ophthalmol
, vol.98
, pp. 144-148
-
-
Weber, F.L.1
Babel, J.2
-
15
-
-
0026446099
-
A second-generation linkage map of the human genome
-
Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseix G, et al (1992) A second-generation linkage map of the human genome. Nature 359:794-801
-
(1992)
Nature
, vol.359
, pp. 794-801
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
Vignal, A.4
Morissette, J.5
Millasseau, P.6
Vaysseix, G.7
-
16
-
-
0023734170
-
Molecular genetics of mouse serum amyloid P component (SAP): Cloning and gene mapping
-
Whitehead AS, Rits M, Michaelson J (1988) Molecular genetics of mouse serum amyloid P component (SAP): cloning and gene mapping. Immunogenetics 28:388-390
-
(1988)
Immunogenetics
, vol.28
, pp. 388-390
-
-
Whitehead, A.S.1
Rits, M.2
Michaelson, J.3
|