-
1
-
-
0025854490
-
Importance of maternal history of non-insulin dependent diabetic patients
-
Alcolado JC, Alcolado R: Importance of maternal history of non-insulin dependent diabetic patients. BMJ 302:1178-1180, 1991
-
(1991)
BMJ
, vol.302
, pp. 1178-1180
-
-
Alcolado, J.C.1
Alcolado, R.2
-
2
-
-
0028011772
-
Maternal effect and familial aggregation in NIDDM: The CODIAB Study
-
Thomas F, Balkau B, Vauzelle-Kervroedan F, Papoz L, CODiAB-INSERM-Zeneca Study Group: Maternal effect and familial aggregation in NIDDM: the CODIAB Study. Diabetes 43:63-67, 1994
-
(1994)
Diabetes
, vol.43
, pp. 63-67
-
-
Thomas, F.1
Balkau, B.2
Vauzelle-Kervroedan, F.3
Papoz, L.4
-
3
-
-
0000204255
-
Maternal inheritance of human mitochondrial DNA
-
Giles RE, Blanc H, Cann HM, Wallace DC: Maternal inheritance of human mitochondrial DNA. Proc Natl Acad Sci USA 77:6715-6719, 1980
-
(1980)
Proc Natl Acad Sci USA
, vol.77
, pp. 6715-6719
-
-
Giles, R.E.1
Blanc, H.2
Cann, H.M.3
Wallace, D.C.4
-
4
-
-
0026463740
-
Does the mitochondrial DNA play a role in the development of diabetes?
-
Gerbitz KD: Does the mitochondrial DNA play a role in the development of diabetes? Diabetologia 35:1181-1186, 1992
-
(1992)
Diabetologia
, vol.35
, pp. 1181-1186
-
-
Gerbitz, K.D.1
-
5
-
-
0028258021
-
Leu(UUR) gene mutation in Japanese patients
-
Leu(UUR) gene mutation in Japanese patients. Diabetologia 37:504-510, 1994
-
(1994)
Diabetologia
, vol.37
, pp. 504-510
-
-
Katagiri, H.1
Asano, T.2
Ishihara, H.3
Inukai, K.4
Anai, M.5
Yamanouchi, T.6
Tsukuda, K.7
Kikuchi, M.8
Kitaoka, H.9
Ohsawa, N.10
Yazaki, Y.11
Oka, Y.12
-
7
-
-
0029978295
-
A mass screening device of genome by polymerase chain reaction-restriction fragment-single-strand conformation polymorphism analysis
-
Tawata M, Iwase E, Aida K, Onaya T: A mass screening device of genome by polymerase chain reaction-restriction fragment-single-strand conformation polymorphism analysis. Genet Anal Biomol Eng 12:125-127, 1996
-
(1996)
Genet Anal Biomol Eng
, vol.12
, pp. 125-127
-
-
Tawata, M.1
Iwase, E.2
Aida, K.3
Onaya, T.4
-
8
-
-
0030965762
-
Mitochondrial DNA mutations in Japanese detected by polymerase chain reaction-restriction fragment-single-strand conformation polymorphism analysis
-
Tawata M, Ikegishi Y, Iwase E, Aida K, Onaya T: Mitochondrial DNA mutations in Japanese detected by polymerase chain reaction-restriction fragment-single-strand conformation polymorphism analysis. Genet Anal Biomol Eng 14:17-19, 1997
-
(1997)
Genet Anal Biomol Eng
, vol.14
, pp. 17-19
-
-
Tawata, M.1
Ikegishi, Y.2
Iwase, E.3
Aida, K.4
Onaya, T.5
-
9
-
-
0019423856
-
Sequence and organization of the human mitochondrial genome
-
Anderson S, Bankier AT, Barrell BG, de Bruijn MHL, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJH, Staden R, Young IG: Sequence and organization of the human mitochondrial genome. Nature 290:457-465, 1981
-
(1981)
Nature
, vol.290
, pp. 457-465
-
-
Anderson, S.1
Bankier, A.T.2
Barrell, B.G.3
De Bruijn, M.H.L.4
Coulson, A.R.5
Drouin, J.6
Eperon, I.C.7
Nierlich, D.P.8
Roe, B.A.9
Sanger, F.10
Schreier, P.H.11
Smith, A.J.H.12
Staden, R.13
Young, I.G.14
-
10
-
-
0028607254
-
Variant forms of glucokinase gene in Japanese patients with late-onset type 2 diabetes
-
Tawata M, Kurihara A, Gan N, Iwase E, Ohtaka M, Inoue M, Onaya T: Variant forms of glucokinase gene in Japanese patients with late-onset type 2 diabetes. Acta Diabetol 31:238-241, 1994
-
(1994)
Acta Diabetol
, vol.31
, pp. 238-241
-
-
Tawata, M.1
Kurihara, A.2
Gan, N.3
Iwase, E.4
Ohtaka, M.5
Inoue, M.6
Onaya, T.7
-
11
-
-
0024756969
-
Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
-
Orita M, Suzuki Y, Sekiya T, Hayashi K: Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. Genomics 5:874-879, 1989
-
(1989)
Genomics
, vol.5
, pp. 874-879
-
-
Orita, M.1
Suzuki, Y.2
Sekiya, T.3
Hayashi, K.4
-
12
-
-
0026906885
-
Leu(UUR) gene in a large pedigree with maternally transmitted type 2 diabetes mellitus and deafness
-
Leu(UUR) gene in a large pedigree with maternally transmitted type 2 diabetes mellitus and deafness. Nat Genet 1:368-371, 1992
-
(1992)
Nat Genet
, vol.1
, pp. 368-371
-
-
Van den Ouweland, J.M.1
Lemkes, H.H.2
Ruitenbeek, W.3
Sandkuijl, L.A.4
De Vijlder, M.F.5
Struyvenberg, P.A.6
Van de Kamp, J.J.7
Maassen, J.A.8
-
13
-
-
0026849690
-
Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial deletion
-
Ballinger SW, Shoffner JM, Hedaya EV, Trounce I, Polak MA, Koontz DA, Wallace DC: Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial deletion. Nat Genet 1:11-15, 1992
-
(1992)
Nat Genet
, vol.1
, pp. 11-15
-
-
Ballinger, S.W.1
Shoffner, J.M.2
Hedaya, E.V.3
Trounce, I.4
Polak, M.A.5
Koontz, D.A.6
Wallace, D.C.7
-
15
-
-
0025863393
-
Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease
-
Ozawa T, Tanaka M, Ino H, Ohno K, Sano T, Wada Y, Yoneda M, Tanno Y, Miyatake T, Tanaka T, Itoyama S, Ikebe S, Hattori N, Mizuno Y: Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease. Biochem Biophys Res Commun 176:938-946, 1991
-
(1991)
Biochem Biophys Res Commun
, vol.176
, pp. 938-946
-
-
Ozawa, T.1
Tanaka, M.2
Ino, H.3
Ohno, K.4
Sano, T.5
Wada, Y.6
Yoneda, M.7
Tanno, Y.8
Miyatake, T.9
Tanaka, T.10
Itoyama, S.11
Ikebe, S.12
Hattori, N.13
Mizuno, Y.14
-
16
-
-
0030030748
-
Molecular scanning of candidate mitochondrial tRNA genes in type 2 (non-insulin dependent) diabetes mellitus
-
Thomas AW, Edwards A, Sherratt EJ, Majid A, Gagg J, Alcolado JC: Molecular scanning of candidate mitochondrial tRNA genes in type 2 (non-insulin dependent) diabetes mellitus. J Med Genet 33:253-255, 1996
-
(1996)
J Med Genet
, vol.33
, pp. 253-255
-
-
Thomas, A.W.1
Edwards, A.2
Sherratt, E.J.3
Majid, A.4
Gagg, J.5
Alcolado, J.C.6
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