-
1
-
-
0009464836
-
On the chemical composition of meat broth
-
Chevreul E. Sur la composition chimique du bouillon de viandes. J. Pharm. Sci. Access. 1835, 21:231-242.
-
(1835)
J. Pharm. Sci. Access.
, vol.21
, pp. 231-242
-
-
Chevreul, E.1
-
2
-
-
0028050667
-
Creatine in humans with special reference to creatine supplementation
-
Balsom P., Söderland K., Ekbolm B. Creatine in humans with special reference to creatine supplementation. Sports Med. 1994, 18:268-280.
-
(1994)
Sports Med.
, vol.18
, pp. 268-280
-
-
Balsom, P.1
Söderland, K.2
Ekbolm, B.3
-
3
-
-
0033935979
-
Creatine and creatinine metabolism
-
Wyss M., Kaddurah-Daouk R. Creatine and creatinine metabolism. Physiol. Rev. 2000, 80:1107-1219.
-
(2000)
Physiol. Rev.
, vol.80
, pp. 1107-1219
-
-
Wyss, M.1
Kaddurah-Daouk, R.2
-
4
-
-
0037129967
-
Health implications of creatine: can oral creatine supplementation protect against neurological and atherosclerotic disease?
-
Wyss M., Schulze A. Health implications of creatine: can oral creatine supplementation protect against neurological and atherosclerotic disease?. Neuroscience 2002, 112:243-260.
-
(2002)
Neuroscience
, vol.112
, pp. 243-260
-
-
Wyss, M.1
Schulze, A.2
-
5
-
-
0001461389
-
Muscle contraction without formation of lactic acid
-
Lundsgaard E. Unter suchungenüber Muskel kontraktion en ohne Milchsäure bildung. Biochem. Z. 1930, 217:162-177.
-
(1930)
Biochem. Z.
, vol.217
, pp. 162-177
-
-
Lundsgaard, E.1
-
6
-
-
0001461390
-
Further investigation on muscle contraction without lactate formation
-
Lundsgaard E. Weitere Untersuchungen fiber Muskel kontraktion en ohne Milchsäure bildung. Biochem. Z. 1930, 227:51-83.
-
(1930)
Biochem. Z.
, vol.227
, pp. 51-83
-
-
Lundsgaard, E.1
-
7
-
-
0009502136
-
Über die enzymatische aufspaltung der keratin phosphorsaure; zugleich ein beitragzum chemismus der muskel kontraktion. (On the enzymic cleavage of creatinephosphate; also a contribution to the chemistry of the muscle contraction)
-
Lohman K. Über die enzymatische aufspaltung der keratin phosphorsaure; zugleich ein beitragzum chemismus der muskel kontraktion. (On the enzymic cleavage of creatinephosphate; also a contribution to the chemistry of the muscle contraction). Biochem. Z. 1934, 271.
-
(1934)
Biochem. Z.
, vol.271
-
-
Lohman, K.1
-
8
-
-
0000720406
-
Myosin and adenosine triphosphatase
-
Engelhardt W.A., Lyubimova M.N. Myosin and adenosine triphosphatase. Nature 1939, 144:668-669.
-
(1939)
Nature
, vol.144
, pp. 668-669
-
-
Engelhardt, W.A.1
Lyubimova, M.N.2
-
9
-
-
43849087699
-
Functions and effects of creatine in the central nervous system
-
Andres R.H., Ducray A.D., Schlattner U., Wallimannb T., Widmer H.F. Functions and effects of creatine in the central nervous system. Brain Res. Bull. 2008, 76:329-343.
-
(2008)
Brain Res. Bull.
, vol.76
, pp. 329-343
-
-
Andres, R.H.1
Ducray, A.D.2
Schlattner, U.3
Wallimannb, T.4
Widmer, H.F.5
-
10
-
-
43149113670
-
AGAT, GAMT and SLC6A8 distribution in the central nervous system, in relation to creatine deficiency syndromes: A review
-
Braissant O., Henry H. AGAT, GAMT and SLC6A8 distribution in the central nervous system, in relation to creatine deficiency syndromes: A review. J. Inherit. Metab. Dis. 2008, 31:230-239.
-
(2008)
J. Inherit. Metab. Dis.
, vol.31
, pp. 230-239
-
-
Braissant, O.1
Henry, H.2
-
11
-
-
72749117347
-
Dissociation of AGAT, GAMT and SLC6A8 in CNS: relevance to creatine deficiency syndromes
-
Braissant O., Béard E., Torrent C., Henry H. Dissociation of AGAT, GAMT and SLC6A8 in CNS: relevance to creatine deficiency syndromes. Neurobiol. Dis. 2010, 37:423-433.
-
(2010)
Neurobiol. Dis.
, vol.37
, pp. 423-433
-
-
Braissant, O.1
Béard, E.2
Torrent, C.3
Henry, H.4
-
12
-
-
78651274358
-
Synthesis and transport of creatine in the CNS: importance for cerebral functions
-
Béard E., Braissant O. Synthesis and transport of creatine in the CNS: importance for cerebral functions. J. Neurochem. 2010, 115:297-313.
-
(2010)
J. Neurochem.
, vol.115
, pp. 297-313
-
-
Béard, E.1
Braissant, O.2
-
13
-
-
43849095420
-
Cerebral creatine deficiency syndromes: clinical aspects, treatment and pathophysiology
-
Stockler S., Schutz P.W., Salomons G.S. Cerebral creatine deficiency syndromes: clinical aspects, treatment and pathophysiology. Subcell. Biochem. 2007, 46:149-166.
-
(2007)
Subcell. Biochem.
, vol.46
, pp. 149-166
-
-
Stockler, S.1
Schutz, P.W.2
Salomons, G.S.3
-
14
-
-
0038497516
-
Clinical characteristics and diagnostic clues in inborn errors of creatine metabolism
-
Stromberger C., Bodamer O.A., Stöckler-Ipsiroglu S. Clinical characteristics and diagnostic clues in inborn errors of creatine metabolism. J. Inherit. Metab. Dis. 2003, 26:299-308.
-
(2003)
J. Inherit. Metab. Dis.
, vol.26
, pp. 299-308
-
-
Stromberger, C.1
Bodamer, O.A.2
Stöckler-Ipsiroglu, S.3
-
15
-
-
13244259284
-
Biochemical and clinical characteristics of creatine deficiency syndromes
-
Sykut-Cegielska J., Gradowska W., Mercimek-Mahmutoglu S., Stöckler-Ipsiroglu S. Biochemical and clinical characteristics of creatine deficiency syndromes. Acta Biochim. Pol. 2004, 51:875-882.
-
(2004)
Acta Biochim. Pol.
, vol.51
, pp. 875-882
-
-
Sykut-Cegielska, J.1
Gradowska, W.2
Mercimek-Mahmutoglu, S.3
Stöckler-Ipsiroglu, S.4
-
16
-
-
71849103775
-
Are cerebral creatine deficiency syndromes on the radar screen?
-
Almeida L.S., Rosenberg E.H., Verhoeven N.M., Jakobs C. Are cerebral creatine deficiency syndromes on the radar screen?. Futur. Neurol. 2006, 1:637-649.
-
(2006)
Futur. Neurol.
, vol.1
, pp. 637-649
-
-
Almeida, L.S.1
Rosenberg, E.H.2
Verhoeven, N.M.3
Jakobs, C.4
-
17
-
-
84887611367
-
Creatine deficiency syndromes
-
Seattle (WA): Univ Washington, Seattle, (1993-2010), R.A. Pagon, T.C. Bird, C.R. Dolan, K. Stephens (Eds.)
-
Mercimek-Mahmutoglu S., Stöckler-Ipsiroglu S. Creatine deficiency syndromes. GeneReviews 2009, Seattle (WA): Univ Washington, Seattle, (1993-2010, http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=creatine). R.A. Pagon, T.C. Bird, C.R. Dolan, K. Stephens (Eds.).
-
(2009)
GeneReviews
-
-
Mercimek-Mahmutoglu, S.1
Stöckler-Ipsiroglu, S.2
-
18
-
-
35248884675
-
Creatine transporter deficiency: prevalence among patients with mental retardation and pitfalls in metabolite screening
-
Arias A., Corbella M., Fons C., Sempere A., García-Villoria J., Ormazabal A., Poo P., Pineda M., Vilaseca M.A., Campistol J., Briones P., Pàmpols T., Salomons G.S., Ribes A., Artuch R. Creatine transporter deficiency: prevalence among patients with mental retardation and pitfalls in metabolite screening. Clin. Biochem. 2007, 40:1328-1331.
-
(2007)
Clin. Biochem.
, vol.40
, pp. 1328-1331
-
-
Arias, A.1
Corbella, M.2
Fons, C.3
Sempere, A.4
García-Villoria, J.5
Ormazabal, A.6
Poo, P.7
Pineda, M.8
Vilaseca, M.A.9
Campistol, J.10
Briones, P.11
Pàmpols, T.12
Salomons, G.S.13
Ribes, A.14
Artuch, R.15
-
19
-
-
46149112586
-
Detection of low-level somatic and germline mosaicism by denaturing high-performance liquid chromatography in a EURO-MRX family with SLC6A8 deficiency
-
Betsalel O.T., van de Kamp J.M., Martínez-Muñoz C., Rosenberg E.H., de Brouwer A.P., Pouwels P.J., van der Knaap M.S., Mancini G.M., Jakobs C., Hamel B.C., Salomons G.S. Detection of low-level somatic and germline mosaicism by denaturing high-performance liquid chromatography in a EURO-MRX family with SLC6A8 deficiency. Neurogenetics 2008, 9:183-190.
-
(2008)
Neurogenetics
, vol.9
, pp. 183-190
-
-
Betsalel, O.T.1
van de Kamp, J.M.2
Martínez-Muñoz, C.3
Rosenberg, E.H.4
de Brouwer, A.P.5
Pouwels, P.J.6
van der Knaap, M.S.7
Mancini, G.M.8
Jakobs, C.9
Hamel, B.C.10
Salomons, G.S.11
-
20
-
-
33744473608
-
X-linked creatine transporter (SLC6A8) mutations in about 1% of males with mental retardation of unknown etiology
-
Clark A.J., Rosenberg E.H., Almeida L.S., Wood T.C., Jakobs C., Stevenson R.E., Schwartz C.E., Salomons G.S. X-linked creatine transporter (SLC6A8) mutations in about 1% of males with mental retardation of unknown etiology. Hum. Genet. 2006, 119:604-610.
-
(2006)
Hum. Genet.
, vol.119
, pp. 604-610
-
-
Clark, A.J.1
Rosenberg, E.H.2
Almeida, L.S.3
Wood, T.C.4
Jakobs, C.5
Stevenson, R.E.6
Schwartz, C.E.7
Salomons, G.S.8
-
21
-
-
33750972301
-
High frequency of creatine deficiency syndromes in patients with unexplained mental retardation
-
Lion-François L., Cheillan D., Pitelet G., Acquaviva-Bourdain C., Bussy G., Cotton F., Guibaud L., Gérard D., Rivier C., Vianey-Saban C., Jakobs C., Salomons G.S., des Portes V. High frequency of creatine deficiency syndromes in patients with unexplained mental retardation. Neurology 2006, 67:1713-1714.
-
(2006)
Neurology
, vol.67
, pp. 1713-1714
-
-
Lion-François, L.1
Cheillan, D.2
Pitelet, G.3
Acquaviva-Bourdain, C.4
Bussy, G.5
Cotton, F.6
Guibaud, L.7
Gérard, D.8
Rivier, C.9
Vianey-Saban, C.10
Jakobs, C.11
Salomons, G.S.12
des Portes, V.13
-
22
-
-
79951701408
-
Disorders of creatine transport and metabolism
-
Longo N., Ardon O., Vanzo R., Schwartz E., Pasquali M. Disorders of creatine transport and metabolism. Am. J. Med. Genet. C: Semin. Med. Genet. 2011, 157:72-78.
-
(2011)
Am. J. Med. Genet. C: Semin. Med. Genet.
, vol.157
, pp. 72-78
-
-
Longo, N.1
Ardon, O.2
Vanzo, R.3
Schwartz, E.4
Pasquali, M.5
-
23
-
-
24644493709
-
Incidence of brain creatine transporter deficiency in males with developmental delay referred for brain magnetic resonance imaging
-
Newmeyer A., Cecil K.M., Schapiro M., Clark J.F., Degrauw T.J. Incidence of brain creatine transporter deficiency in males with developmental delay referred for brain magnetic resonance imaging. J. Dev. Behav. Pediatr. 2005, 26:276-282.
-
(2005)
J. Dev. Behav. Pediatr.
, vol.26
, pp. 276-282
-
-
Newmeyer, A.1
Cecil, K.M.2
Schapiro, M.3
Clark, J.F.4
Degrauw, T.J.5
-
24
-
-
57749176618
-
Prevalence of the fragile X syndrome among Estonian mentally retarded and the entire children's population
-
Puusepp H., Kahre T., Sibul H., Soo V., Lind I., Raukas E., Ounap K. Prevalence of the fragile X syndrome among Estonian mentally retarded and the entire children's population. J. Child Neurol. 2008, 23:1400-1405.
-
(2008)
J. Child Neurol.
, vol.23
, pp. 1400-1405
-
-
Puusepp, H.1
Kahre, T.2
Sibul, H.3
Soo, V.4
Lind, I.5
Raukas, E.6
Ounap, K.7
-
25
-
-
84897956170
-
The screening of SLC6A8 deficiency among Estonian families with X-linked mental retardation
-
(Online DOI 10.1007/s10545-008-1063-y)
-
Puusepp H., Kall K., Salomons G.S., Talvik I., Männamaa M., Rein R., Jakobs C., Õunap K. The screening of SLC6A8 deficiency among Estonian families with X-linked mental retardation. JIMD Short Report #147 2008, (Online DOI 10.1007/s10545-008-1063-y).
-
(2008)
JIMD Short Report #147
-
-
Puusepp, H.1
Kall, K.2
Salomons, G.S.3
Talvik, I.4
Männamaa, M.5
Rein, R.6
Jakobs, C.7
Õunap, K.8
-
26
-
-
3042544793
-
High prevalence of SLC6A8 deficiency in X-linked mental retardation
-
Rosenberg E.H., Almeida L.S., Kleefstra T., deGrauw R.S., Yntema H.G., Bahi N., Moraine C., Ropers H.H., Fryns J.P., deGrauw T.J., Jakobs C., Salomons G.S. High prevalence of SLC6A8 deficiency in X-linked mental retardation. Am. J. Hum. Genet. 2004, 75:97-105.
-
(2004)
Am. J. Hum. Genet.
, vol.75
, pp. 97-105
-
-
Rosenberg, E.H.1
Almeida, L.S.2
Kleefstra, T.3
deGrauw, R.S.4
Yntema, H.G.5
Bahi, N.6
Moraine, C.7
Ropers, H.H.8
Fryns, J.P.9
deGrauw, T.J.10
Jakobs, C.11
Salomons, G.S.12
-
27
-
-
84870890213
-
Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms
-
Cheillan D., Joncquel-Chevalier Curt M., Briand G., Salomons G.S., Mention-Mulliez K., Dobbelaere D., Cuisset J.M., Lion-François L., des Portes V., Chabli A., Valayannopoulos V., Benoist J.F., Pinard J.M., Simard G., Douay O., Deiva K., Afenjar A., Héron D., Rivier F., Chabrol B., Prieur F., Cartault F., Pitelet G., Goldenberg A., Bekri S., Gerard M., Delorme R., Tardieu M., Porchet N., Vianey-Saban C., Vamecq J. Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms. Orphanet J. Rare Dis. 2012, 7:96.
-
(2012)
Orphanet J. Rare Dis.
, vol.7
, pp. 96
-
-
Cheillan, D.1
Joncquel-Chevalier Curt, M.2
Briand, G.3
Salomons, G.S.4
Mention-Mulliez, K.5
Dobbelaere, D.6
Cuisset, J.M.7
Lion-François, L.8
des Portes, V.9
Chabli, A.10
Valayannopoulos, V.11
Benoist, J.F.12
Pinard, J.M.13
Simard, G.14
Douay, O.15
Deiva, K.16
Afenjar, A.17
Héron, D.18
Rivier, F.19
Chabrol, B.20
Prieur, F.21
Cartault, F.22
Pitelet, G.23
Goldenberg, A.24
Bekri, S.25
Gerard, M.26
Delorme, R.27
Tardieu, M.28
Porchet, N.29
Vianey-Saban, C.30
Vamecq, J.31
more..
-
28
-
-
3242812051
-
Determination of guanidinoacetate and creatine in urine and plasma by liquid chromatography-tandem mass spectrometry
-
Cognat S., Cheillan D., Piraud M., Roos B., Jakobs C., Vianey-Saban C. Determination of guanidinoacetate and creatine in urine and plasma by liquid chromatography-tandem mass spectrometry. Clin. Chem. 2004, 50:1459-1461.
-
(2004)
Clin. Chem.
, vol.50
, pp. 1459-1461
-
-
Cognat, S.1
Cheillan, D.2
Piraud, M.3
Roos, B.4
Jakobs, C.5
Vianey-Saban, C.6
-
29
-
-
0000841697
-
Uber den niederschlag, welchenpikrinsaure in normalen ham erzeugt und ubereineneue reaction des kreatinins
-
Jaffe M. Uber den niederschlag, welchenpikrinsaure in normalen ham erzeugt und ubereineneue reaction des kreatinins. Z. Physiol. Chem. 1886, 10:391-400.
-
(1886)
Z. Physiol. Chem.
, vol.10
, pp. 391-400
-
-
Jaffe, M.1
-
30
-
-
77956875677
-
GC-MS determination of creatinine in human biological fluids as pentafluorobenzyl derivative in clinical studies and biomonitoring: inter-laboratory comparison in urine with Jaffé, HPLC and enzymatic assays
-
Tsikas D., Wolf A., Mitschke A., Gutzki F.M., Will W., Bader M. GC-MS determination of creatinine in human biological fluids as pentafluorobenzyl derivative in clinical studies and biomonitoring: inter-laboratory comparison in urine with Jaffé, HPLC and enzymatic assays. J. Chromatogr. B: Analyt. Technol. Biomed. Life Sci. 2010, 878:2582-2595.
-
(2010)
J. Chromatogr. B: Analyt. Technol. Biomed. Life Sci.
, vol.878
, pp. 2582-2595
-
-
Tsikas, D.1
Wolf, A.2
Mitschke, A.3
Gutzki, F.M.4
Will, W.5
Bader, M.6
-
31
-
-
33747190052
-
Methods for the diagnosis of creatine deficiency syndromes: a comparative study
-
Arias A., Ormazabal A., Moreno J., González B., Vilaseca M.A., García-Villoria J., Pàmpols T., Briones P., Artuch R., Ribes A. Methods for the diagnosis of creatine deficiency syndromes: a comparative study. J. Neurosci. Methods 2006, 156:305-309.
-
(2006)
J. Neurosci. Methods
, vol.156
, pp. 305-309
-
-
Arias, A.1
Ormazabal, A.2
Moreno, J.3
González, B.4
Vilaseca, M.A.5
García-Villoria, J.6
Pàmpols, T.7
Briones, P.8
Artuch, R.9
Ribes, A.10
-
32
-
-
0030759324
-
GC-MS determination of guanidinoacetate in urine and plasma
-
Hunneman D.H., Hanefeld F. GC-MS determination of guanidinoacetate in urine and plasma. J. Inherit. Metab. Dis. 1997, 20:450-452.
-
(1997)
J. Inherit. Metab. Dis.
, vol.20
, pp. 450-452
-
-
Hunneman, D.H.1
Hanefeld, F.2
-
33
-
-
77957371580
-
GC/MS determination of guanidinoacetate and creatine in urine: a routine method for creatine deficiency syndrome diagnosis
-
Nasrallah F., Feki M., Briand G., Kaabachi N. GC/MS determination of guanidinoacetate and creatine in urine: a routine method for creatine deficiency syndrome diagnosis. Clin. Biochem. 2010, 43:1356-1361.
-
(2010)
Clin. Biochem.
, vol.43
, pp. 1356-1361
-
-
Nasrallah, F.1
Feki, M.2
Briand, G.3
Kaabachi, N.4
-
34
-
-
0032446322
-
An accurate stable isotope dilution gas chromatographic-mass spectrometric approach to the diagnosis of guanidinoacetate methyltransferase deficiency
-
Struys E.A., Jansen E.E., ten Brink H.J., Verhoeven N.M., Van der Knaap M.S., Jakobs C. An accurate stable isotope dilution gas chromatographic-mass spectrometric approach to the diagnosis of guanidinoacetate methyltransferase deficiency. J. Pharm. Biomed. Anal. 1998, 18:659-665.
-
(1998)
J. Pharm. Biomed. Anal.
, vol.18
, pp. 659-665
-
-
Struys, E.A.1
Jansen, E.E.2
ten Brink, H.J.3
Verhoeven, N.M.4
Van der Knaap, M.S.5
Jakobs, C.6
-
35
-
-
4444293116
-
Age related reference values for urine creatine and guanidinoacetic acid concentration in children and adolescents by gas chromatography-mass spectrometry
-
Valongo C., Cardoso M.L., Domingues P., Almeida L., Verhoeven N., Salomons G., Jakobs C., Vilarinho L. Age related reference values for urine creatine and guanidinoacetic acid concentration in children and adolescents by gas chromatography-mass spectrometry. Clin. Chim. Acta 2004, 348:155.
-
(2004)
Clin. Chim. Acta
, vol.348
, pp. 155
-
-
Valongo, C.1
Cardoso, M.L.2
Domingues, P.3
Almeida, L.4
Verhoeven, N.5
Salomons, G.6
Jakobs, C.7
Vilarinho, L.8
-
36
-
-
25644446103
-
Laboratory diagnosis of defects of creatine biosynthesis and transport
-
Verhoeven N.M., Salomons G.S., Jakobs C. Laboratory diagnosis of defects of creatine biosynthesis and transport. Clin. Chim. Acta 2005, 361:1-9.
-
(2005)
Clin. Chim. Acta
, vol.361
, pp. 1-9
-
-
Verhoeven, N.M.1
Salomons, G.S.2
Jakobs, C.3
-
37
-
-
34548730771
-
Investigations of the effects of gender, diurnal variation, and age in human urinary metabolomic profiles
-
Slupsky C.M., Rankin K.N., Wagner J., Fu H., Chang D., Weljie A.M., Saude E.J., Lix B., Adamko D.J., Shah S., Greiner R., Sykes B.D., Marrie T.J. Investigations of the effects of gender, diurnal variation, and age in human urinary metabolomic profiles. Anal. Chem. 2007, 79:6995-7004.
-
(2007)
Anal. Chem.
, vol.79
, pp. 6995-7004
-
-
Slupsky, C.M.1
Rankin, K.N.2
Wagner, J.3
Fu, H.4
Chang, D.5
Weljie, A.M.6
Saude, E.J.7
Lix, B.8
Adamko, D.J.9
Shah, S.10
Greiner, R.11
Sykes, B.D.12
Marrie, T.J.13
-
38
-
-
84857789699
-
Metabolic profiling of gender: headspace-SPME/GC-MS and 1H NMR analysis of urine
-
Zhang S., Liu L., Steffen D., Ye T., Raftery D. Metabolic profiling of gender: headspace-SPME/GC-MS and 1H NMR analysis of urine. Metabolomics 2012, 8:323-334.
-
(2012)
Metabolomics
, vol.8
, pp. 323-334
-
-
Zhang, S.1
Liu, L.2
Steffen, D.3
Ye, T.4
Raftery, D.5
-
39
-
-
0013984971
-
Influence of sex hormones on amidinotransferase levels. Metabolic control of creatine biosynthesis
-
Kriskó I., Walker J.B. Influence of sex hormones on amidinotransferase levels. Metabolic control of creatine biosynthesis. Acta Endocrinol. (Copenh) 1966, 53:655-662.
-
(1966)
Acta Endocrinol. (Copenh)
, vol.53
, pp. 655-662
-
-
Kriskó, I.1
Walker, J.B.2
-
40
-
-
0035351264
-
Estrogen modulates the expression of l-arginine:glycine amidinotransferase in chick liver
-
Zhu Y., Evans M.I. Estrogen modulates the expression of l-arginine:glycine amidinotransferase in chick liver. Mol. Cell. Biochem. 2001, 221:139-145.
-
(2001)
Mol. Cell. Biochem.
, vol.221
, pp. 139-145
-
-
Zhu, Y.1
Evans, M.I.2
-
41
-
-
34547901382
-
Estrogenic effects in the immature rat uterus after dietary exposure to ethinylestradiol and zearalenone using a systems biology approach
-
Heneweer M., Houtman R., Poortman J., Groot M., Maliepaard C., Peijnenburg A. Estrogenic effects in the immature rat uterus after dietary exposure to ethinylestradiol and zearalenone using a systems biology approach. Toxicol. Sci. 2007, 99:303-314.
-
(2007)
Toxicol. Sci.
, vol.99
, pp. 303-314
-
-
Heneweer, M.1
Houtman, R.2
Poortman, J.3
Groot, M.4
Maliepaard, C.5
Peijnenburg, A.6
-
42
-
-
79959423192
-
Gender differences in serum and glucocorticoid regulated kinase-1 (SGK-1) expression during renal ischemia/reperfusion injury
-
Rusai K., Prókai A., Szebeni B., Mészáros K., Fekete A., Szalay B., Vannay Á., Degrell P., Müller V., Tulassay T., Szabó A.J. Gender differences in serum and glucocorticoid regulated kinase-1 (SGK-1) expression during renal ischemia/reperfusion injury. Cell. Physiol. Biochem. 2011, 27:727-738.
-
(2011)
Cell. Physiol. Biochem.
, vol.27
, pp. 727-738
-
-
Rusai, K.1
Prókai, A.2
Szebeni, B.3
Mészáros, K.4
Fekete, A.5
Szalay, B.6
Vannay, Á.7
Degrell, P.8
Müller, V.9
Tulassay, T.10
Szabó, A.J.11
-
43
-
-
22744453219
-
Stimulation of the creatine transporter SLC6A8 by the protein kinases SGK1 and SGK3
-
Shojaiefard M., Christie D.L., Lang F. Stimulation of the creatine transporter SLC6A8 by the protein kinases SGK1 and SGK3. Biochem. Biophys. Res. Commun. 2005, 334:742-746.
-
(2005)
Biochem. Biophys. Res. Commun.
, vol.334
, pp. 742-746
-
-
Shojaiefard, M.1
Christie, D.L.2
Lang, F.3
-
44
-
-
35848935450
-
PIKfyve in the SGK1 mediated regulation of the creatine transporter SLC6A8
-
Strutz-Seebohm N., Shojaiefard M., Christie D., Tavare J., Seebohm G., Lang F. PIKfyve in the SGK1 mediated regulation of the creatine transporter SLC6A8. Cell. Physiol. Biochem. 2007, 20:729-734.
-
(2007)
Cell. Physiol. Biochem.
, vol.20
, pp. 729-734
-
-
Strutz-Seebohm, N.1
Shojaiefard, M.2
Christie, D.3
Tavare, J.4
Seebohm, G.5
Lang, F.6
-
45
-
-
0031120087
-
The role of estrogen in bone growth and maturation during childhood and adolescence
-
Cutler Jr G.B. The role of estrogen in bone growth and maturation during childhood and adolescence. J. Steroid Biochem. Mol. Biol. 1997, 61:141-144.
-
(1997)
J. Steroid Biochem. Mol. Biol.
, vol.61
, pp. 141-144
-
-
Cutler Jr, G.B.1
-
46
-
-
0028007173
-
Estrogen levels in childhood determined by an ultrasensitive recombinant cell bioassay
-
Klein K.O., Baron J., Colli M.J., McDonnell D.P., Cutler Jr G.B. Estrogen levels in childhood determined by an ultrasensitive recombinant cell bioassay. J. Clin. Invest. 1994, 94:2475-2480.
-
(1994)
J. Clin. Invest.
, vol.94
, pp. 2475-2480
-
-
Klein, K.O.1
Baron, J.2
Colli, M.J.3
McDonnell, D.P.4
Cutler Jr, G.B.5
-
47
-
-
84856764276
-
Seaweed intake and urinary sex hormone levels in preschool Japanese children
-
Wada K., Nakamura K., Tamai Y., Tsuji M., Watanabe K., Ando K., Nagata C. Seaweed intake and urinary sex hormone levels in preschool Japanese children. Cancer Causes Control 2012, 23:239-244.
-
(2012)
Cancer Causes Control
, vol.23
, pp. 239-244
-
-
Wada, K.1
Nakamura, K.2
Tamai, Y.3
Tsuji, M.4
Watanabe, K.5
Ando, K.6
Nagata, C.7
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