-
1
-
-
0025838034
-
Management of gestational diabetes
-
Coustan D.R. Management of gestational diabetes. Clin. Obstet. Gynecol. 34:1991;558-564.
-
(1991)
Clin. Obstet. Gynecol.
, vol.34
, pp. 558-564
-
-
Coustan, D.R.1
-
2
-
-
0029560649
-
Gestational diabetes mellitus: Is it a clinical entity?
-
Hod M., Rabinerson D. Gestational diabetes mellitus: is it a clinical entity? Diab. Rev. 3:1995;605-620.
-
(1995)
Diab. Rev.
, vol.3
, pp. 605-620
-
-
Hod, M.1
Rabinerson, D.2
-
3
-
-
2642648616
-
Etiology and pathogenesis of gestational diabetes
-
Kuhl C. Etiology and pathogenesis of gestational diabetes. Diab. Care. 21(suppl 2):1998;B19-26.
-
(1998)
Diab. Care
, vol.21
, Issue.SUPPL. 2
, pp. 19-26
-
-
Kuhl, C.1
-
4
-
-
0021997016
-
Frequency of diabetes mellitus in mothers of probands with gestational diabetes mellitus: Possible maternal influence on the predisposition to gestational diabetes
-
Martin A.O., Simpson J.L., Ober C., Frienkel N. Frequency of diabetes mellitus in mothers of probands with gestational diabetes mellitus: possible maternal influence on the predisposition to gestational diabetes. Am. J. Obstet. Gynecol. 151:1985;471-475.
-
(1985)
Am. J. Obstet. Gynecol.
, vol.151
, pp. 471-475
-
-
Martin, A.O.1
Simpson, J.L.2
Ober, C.3
Frienkel, N.4
-
5
-
-
0027287964
-
Identification of glucokinase mutations in subjects with gestational diabetes mellitus
-
Stoffel M., Bell K.L., Blackburn C.L. et al. Identification of glucokinase mutations in subjects with gestational diabetes mellitus. Diabetes. 42:1993;937-940.
-
(1993)
Diabetes
, vol.42
, pp. 937-940
-
-
Stoffel, M.1
Bell, K.L.2
Blackburn, C.L.3
-
6
-
-
0030983176
-
A novel point mutation in the insulin gene giving rise to hyperproinsulinemia
-
Warren-Perry M.G., Mansley S.E., Ostrega D. et al. A novel point mutation in the insulin gene giving rise to hyperproinsulinemia. J. Clin. Endocrinol. 82:1997;1629-1631.
-
(1997)
J. Clin. Endocrinol.
, vol.82
, pp. 1629-1631
-
-
Warren-Perry, M.G.1
Mansley, S.E.2
Ostrega, D.3
-
7
-
-
0023908084
-
Molecular genetic analysis and assessment of insulin action and pancreatic beta cell function
-
Elbein S.C., Ward W.K., Beard J.C., Permutt M.A. Molecular genetic analysis and assessment of insulin action and pancreatic beta cell function. Diabetes. 37:1988;377-382.
-
(1988)
Diabetes
, vol.37
, pp. 377-382
-
-
Elbein, S.C.1
Ward, W.K.2
Beard, J.C.3
Permutt, M.A.4
-
8
-
-
0028209092
-
Variability of the pancreatic islet beta cell/liver (GLUT2) glucose transporter gene in NIDDM patients
-
Tanizawa Y., Riggs A.C., Chiu K.C. et al. Variability of the pancreatic islet beta cell/liver (GLUT2) glucose transporter gene in NIDDM patients. Diabetologia. 37:1994;420-427.
-
(1994)
Diabetologia
, vol.37
, pp. 420-427
-
-
Tanizawa, Y.1
Riggs, A.C.2
Chiu, K.C.3
-
9
-
-
0026723385
-
Gene expression of GLUT4 in skeletal muscle from insulin-resistant patients with obesity, IGT, GDM and NIDDM
-
Garvey W.T., Maianu L., Hancock J.A., Golichowski A.M., Baron A. Gene expression of GLUT4 in skeletal muscle from insulin-resistant patients with obesity, IGT, GDM and NIDDM. Diabetes. 41:1992;465-475.
-
(1992)
Diabetes
, vol.41
, pp. 465-475
-
-
Garvey, W.T.1
Maianu, L.2
Hancock, J.A.3
Golichowski, A.M.4
Baron, A.5
-
10
-
-
0026906885
-
Mutation in mitochondrial tRNA (Leu)(UUR) gene in a large pedigree with maternally transmitted type 2 diabetes mellitus and deafness
-
Van den Ouweland J.M., Lemkes H.H., Ruitenbeek W. et al. Mutation in mitochondrial tRNA (Leu)(UUR) gene in a large pedigree with maternally transmitted type 2 diabetes mellitus and deafness. Nat. Genet. 1:1992;368-371.
-
(1992)
Nat. Genet.
, vol.1
, pp. 368-371
-
-
Van Den Ouweland, J.M.1
Lemkes, H.H.2
Ruitenbeek, W.3
-
12
-
-
0031695496
-
Noninsulin-dependent diabetes mellitus as a mitochondrial genomeic disease
-
Mathews C.E., Berdianier C.D. Noninsulin-dependent diabetes mellitus as a mitochondrial genomeic disease. Pro. Soc. Exp. Biol. Med. 219:1998;97-108.
-
(1998)
Pro. Soc. Exp. Biol. Med.
, vol.219
, pp. 97-108
-
-
Mathews, C.E.1
Berdianier, C.D.2
-
14
-
-
0029966749
-
Mitochondrial DNA is required for regulation of glucose-stimulated insulin secretion in a mouse pancreatic beta cell line; MIN6
-
Soejima A., Inoue K., Takai D. et al. Mitochondrial DNA is required for regulation of glucose-stimulated insulin secretion in a mouse pancreatic beta cell line; MIN6. J. Biol. Chem. 271:1996;261-294.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 261-294
-
-
Soejima, A.1
Inoue, K.2
Takai, D.3
-
15
-
-
0029040769
-
Mitochondrial DNA, diabetes and pancreatic pathology in Kearn-Sayre syndrome
-
Poulton J., O'Rahilly S., Morten K., Clark A. Mitochondrial DNA, diabetes and pancreatic pathology in Kearn-Sayre syndrome. Diabetologia. 38:1995;868-871.
-
(1995)
Diabetologia
, vol.38
, pp. 868-871
-
-
Poulton, J.1
O'Rahilly, S.2
Morten, K.3
Clark, A.4
-
16
-
-
15644370476
-
A common mitochondrial DNA variant is associated with insulin resistance in adult life
-
Poulton J., Brown M.S., Cooper A., Marchington D.R., Phillips D.I.W. A common mitochondrial DNA variant is associated with insulin resistance in adult life. Diabetologia. 41:1998;54-58.
-
(1998)
Diabetologia
, vol.41
, pp. 54-58
-
-
Poulton, J.1
Brown, M.S.2
Cooper, A.3
Marchington, D.R.4
Phillips, D.I.W.5
-
17
-
-
0029772109
-
Identification of seven novel mutations in LH β-subunit gene by SSCP
-
Roy A.C., Liao W.X., Chen Y., Arulkumaran S., Ratnam S.S. Identification of seven novel mutations in LH β-subunit gene by SSCP. Mol. Cell. Biochem. 165:1996;151-153.
-
(1996)
Mol. Cell. Biochem.
, vol.165
, pp. 151-153
-
-
Roy, A.C.1
Liao, W.X.2
Chen, Y.3
Arulkumaran, S.4
Ratnam, S.S.5
-
18
-
-
0019423856
-
Sequence and organization of human mitochondrial genome
-
Anderson S., Bankier A.T., Barrell B.G. et al. Sequence and organization of human mitochondrial genome. Nature. 290:1981;457-465.
-
(1981)
Nature
, vol.290
, pp. 457-465
-
-
Anderson, S.1
Bankier, A.T.2
Barrell, B.G.3
-
19
-
-
0031929585
-
A new molecular variant of luteinizing hormone associated with female infertility
-
Liao W.X., Roy A.C., Chan C., Arulkumaran S., Ratnam S.S. A new molecular variant of luteinizing hormone associated with female infertility. Fertil. Steril. 69:1998;102-106.
-
(1998)
Fertil. Steril.
, vol.69
, pp. 102-106
-
-
Liao, W.X.1
Roy, A.C.2
Chan, C.3
Arulkumaran, S.4
Ratnam, S.S.5
-
20
-
-
0028935878
-
A new mitochondrial DNA mutation associated with non-insulin-dependent diabetes mellitus
-
Nakawa Y., Ikegami H., Yamato E. et al. A new mitochondrial DNA mutation associated with non-insulin-dependent diabetes mellitus. Biochem. Biophys. Res. Comm. 209:1995;664-668.
-
(1995)
Biochem. Biophys. Res. Comm.
, vol.209
, pp. 664-668
-
-
Nakawa, Y.1
Ikegami, H.2
Yamato, E.3
-
21
-
-
0030004883
-
Mitochondrial DNA 3394 mutation in the NADH dehydrogenase subunit 1 associated with non-insulin-dependent diabetes mellitus
-
Hirai M., Suzuki S., Ouoda M. et al. Mitochondrial DNA 3394 mutation in the NADH dehydrogenase subunit 1 associated with non-insulin-dependent diabetes mellitus. Biochem. Biophys. Res. Comm. 219:1996;951-955.
-
(1996)
Biochem. Biophys. Res. Comm.
, vol.219
, pp. 951-955
-
-
Hirai, M.1
Suzuki, S.2
Ouoda, M.3
-
22
-
-
0029965430
-
MITOMAP: A human mitochondrial genome database
-
Kogelnik M.A., Lott M.T., Brown M.D., Navathe S.B., Wallace D.C. MITOMAP: a human mitochondrial genome database. Nucleic Acids. Res. 24:1996;177-179.
-
(1996)
Nucleic Acids. Res.
, vol.24
, pp. 177-179
-
-
Kogelnik, M.A.1
Lott, M.T.2
Brown, M.D.3
Navathe, S.B.4
Wallace, D.C.5
-
23
-
-
0023652658
-
Photolabelling of a mitochondrially encoded subunit of NADH dehydrogenase with [3H] dihydrorotenone
-
Earley F.G., Patel S.D., Ragan I., Attardi G. Photolabelling of a mitochondrially encoded subunit of NADH dehydrogenase with [3H] dihydrorotenone. FEBS Lett. 219:1987;108-112.
-
(1987)
FEBS Lett.
, vol.219
, pp. 108-112
-
-
Earley, F.G.1
Patel, S.D.2
Ragan, I.3
Attardi, G.4
-
24
-
-
0032434102
-
Molecular timing of primate divergences as estimated by two nonprimate calibration points
-
Arnason U., Gullberg A., Janke A. Molecular timing of primate divergences as estimated by two nonprimate calibration points. J. Mol. Evol. 47(6):1998;718-727.
-
(1998)
J. Mol. Evol.
, vol.47
, Issue.6
, pp. 718-727
-
-
Arnason, U.1
Gullberg, A.2
Janke, A.3
-
25
-
-
0019983804
-
Complete sequence of bovine mitochondrial DNA: Conserved features of the mammalian mitochondrial genome
-
Anderson S., deBruijn M.H., Coulson A.R., Eperon I.C., Sanger F., Young I.G. Complete sequence of bovine mitochondrial DNA: conserved features of the mammalian mitochondrial genome. J. Mol. Biol. 56(4):1982;683-717.
-
(1982)
J. Mol. Biol.
, vol.56
, Issue.4
, pp. 683-717
-
-
Anderson, S.1
Debruijn, M.H.2
Coulson, A.R.3
Eperon, I.C.4
Sanger, F.5
Young, I.G.6
-
26
-
-
0028132144
-
The complete mitochondrial DNA sequence of the horse, Equus caballus: Extensive heteroplasmy of the control region
-
Xu X., Arnason U. The complete mitochondrial DNA sequence of the horse, Equus caballus: extensive heteroplasmy of the control region. Gene. 148(2):1994;357-362.
-
(1994)
Gene
, vol.148
, Issue.2
, pp. 357-362
-
-
Xu, X.1
Arnason, U.2
-
27
-
-
0025995774
-
Electron transfer properties of NADH: Ubiquinone reductase in the ND1/3460 and ND4/11778 mutations of LHON
-
Majander A., Huoponen K., Savontaus M.L., Nikoskelainen E., Wikstrom M. Electron transfer properties of NADH: ubiquinone reductase in the ND1/3460 and ND4/11778 mutations of LHON. FEBS Lett. 292:1991;289-292.
-
(1991)
FEBS Lett.
, vol.292
, pp. 289-292
-
-
Majander, A.1
Huoponen, K.2
Savontaus, M.L.3
Nikoskelainen, E.4
Wikstrom, M.5
-
28
-
-
0029045299
-
Mitochondrial DNA variation in human evolution, degenerative diseases and aging
-
Wallace D.C. Mitochondrial DNA variation in human evolution, degenerative diseases and aging. Am. J. Hum. Genet. 57:1995;202-223.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 202-223
-
-
Wallace, D.C.1
-
29
-
-
0030879372
-
Mitochondrial DNA and diseases
-
Suomalainen A. Mitochondrial DNA and diseases. Ann. Med. 29:1997;235-246.
-
(1997)
Ann. Med.
, vol.29
, pp. 235-246
-
-
Suomalainen, A.1
-
32
-
-
0025845270
-
Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies
-
Hess J.F., Parisi M.A., Bennett J.L., Clayton D.A. Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature. 351:1991;236-239.
-
(1991)
Nature
, vol.351
, pp. 236-239
-
-
Hess, J.F.1
Parisi, M.A.2
Bennett, J.L.3
Clayton, D.A.4
-
33
-
-
0030799693
-
A new mitochondrial DNA mutation associated with mitochondrial myopathy: TRNA-Leu (UUR) 3254C-to-G
-
Kawarai T., Kawakami H., Kozuka K. et al. A new mitochondrial DNA mutation associated with mitochondrial myopathy: tRNA-Leu (UUR) 3254C-to-G. Neurology. 49:1997;598-600.
-
(1997)
Neurology
, vol.49
, pp. 598-600
-
-
Kawarai, T.1
Kawakami, H.2
Kozuka, K.3
-
34
-
-
0031761155
-
Gestational diabetes mellitus and subsequent development of overt diabetes mellitus
-
Damm P. Gestational diabetes mellitus and subsequent development of overt diabetes mellitus. Dan. Med. Bull. 45(5):1998;495-509.
-
(1998)
Dan. Med. Bull.
, vol.45
, Issue.5
, pp. 495-509
-
-
Damm, P.1
-
35
-
-
0029588599
-
Non-insulin-dependent diabetes mellitus and gestational diabetes mellitus: Same disease, another name?
-
Pendergrass M., Fazioni E., DeFronzo R.A. Non-insulin-dependent diabetes mellitus and gestational diabetes mellitus: same disease, another name? Diab. Rev. 3(4):1995;566-583.
-
(1995)
Diab. Rev.
, vol.3
, Issue.4
, pp. 566-583
-
-
Pendergrass, M.1
Fazioni, E.2
Defronzo, R.A.3
-
36
-
-
0028978105
-
Mutation in the mitochondrial tRNALeu at position 3243 and spontaneous abortions in Japanese women attending a clinic for diabetic pregnancies
-
Yanagisawa K., Uchigata Y., Sanaka M. et al. Mutation in the mitochondrial tRNALeu at position 3243 and spontaneous abortions in Japanese women attending a clinic for diabetic pregnancies. Diabetologia. 38:1995;809-815.
-
(1995)
Diabetologia
, vol.38
, pp. 809-815
-
-
Yanagisawa, K.1
Uchigata, Y.2
Sanaka, M.3
-
37
-
-
0029886392
-
Mitochondrial gene mutations in patients with insulin-dependent diabetes mellitus in Taiwan
-
Chuang L.M., Wu H.P., Tsai W.Y., Lai C.S., Tai T.Y., Lin B.J. Mitochondrial gene mutations in patients with insulin-dependent diabetes mellitus in Taiwan. Pancreas. 12(3):1996;243-247.
-
(1996)
Pancreas
, vol.12
, Issue.3
, pp. 243-247
-
-
Chuang, L.M.1
Wu, H.P.2
Tsai, W.Y.3
Lai, C.S.4
Tai, T.Y.5
Lin, B.J.6
-
38
-
-
0030871929
-
Gestational diabetes mellitus and gene mutations which affect insulin secretion
-
Allan C.J., Argyropoulos G., Bowker M. et al. Gestational diabetes mellitus and gene mutations which affect insulin secretion. Diab. Res. Clin. Pract. 36:1997;135-141.
-
(1997)
Diab. Res. Clin. Pract.
, vol.36
, pp. 135-141
-
-
Allan, C.J.1
Argyropoulos, G.2
Bowker, M.3
-
39
-
-
0030030748
-
Molecular scanning of candidate mitochondrial tRNA genes in type 2 (non-insulin-dependent) diabetes mellitus
-
Thomas A.W., Edwards A., Sherratt E.J., Majid A., Gagg J., Alcolado J.C. Molecular scanning of candidate mitochondrial tRNA genes in type 2 (non-insulin-dependent) diabetes mellitus. J. Med. Genet. 33:1996;253-255.
-
(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
-
40
-
-
0031024114
-
UKPDS 21: Low prevalence of the mitochondrial transfer RNA gene (tRNA(Leu(UUR))) mutation at position 3243 bp in UK Caucasian type 2 diabetes patients
-
Saker P.J., Hattersley A.T., Barrow B. et al. UKPDS 21: Low prevalence of the mitochondrial transfer RNA gene (tRNA(Leu(UUR))) mutation at position 3243 bp in UK Caucasian type 2 diabetes patients. Dia. Med. 14(1):1997;42-45.
-
(1997)
Dia. Med.
, vol.14
, Issue.1
, pp. 42-45
-
-
Saker, P.J.1
Hattersley, A.T.2
Barrow, B.3
-
41
-
-
8044255246
-
Mitochondrial gene transfer ribonucleic acid tRNA-Leu (UUR) 3243 and tRNA-Lys 8344 mutation and diabetes mellitus in Korea
-
Lee H.C., Song Y.D., Li H.R. et al. Mitochondrial gene transfer ribonucleic acid tRNA-Leu (UUR) 3243 and tRNA-Lys 8344 mutation and diabetes mellitus in Korea. J. Clin. Endocrinol. Metab. 82:1997;372-374.
-
(1997)
J. Clin. Endocrinol. Metab.
, vol.82
, pp. 372-374
-
-
Lee, H.C.1
Song, Y.D.2
Li, H.R.3
|