Zobrazeno 1 - 10
of 129
pro vyhledávání: '"E. Schoenle"'
Publikováno v:
Diabetic Medicine. 24:27-34
Aims This study compared the effect of insulin detemir on glycaemic control (HbA1c, fasting plasma glucose and variability thereof) with that of Neutral Protamine Hagedorn human isophane (NPH) insulin, both combined with insulin aspart, in children w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35bae716d3ef5b68be627fee9ed08e67
https://doi.org/10.1111/j.1464-5491.2007.02024.x
https://doi.org/10.1111/j.1464-5491.2007.02024.x
Publikováno v:
Endocrinology. 141:1446-1454
CYP17 is a microsomal enzyme embodying two distinct activities, 17alpha-hydroxylase and 17,20-lyase, essential for the synthesis of cortisol and sex hormone precursors, respectively. The two activities are differentially regulated in a tissue and dev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6a15f9b0d05b536475b53fef4c14b8b
https://doi.org/10.1210/endo.141.4.7402
https://doi.org/10.1210/endo.141.4.7402
Autor:
Krystyna H. Chrzanowska, Iosif W. Lurie, Barto J. Otten, Ben C.J. Hamel, H. Ilyina, M. Krajewska-Walasek, Damina Balmer, E. Schoenle, Gholamali Tariverdian, Dieter Kotzot, Albert Schinzel, Alessandra Baumer
Publikováno v:
European Journal of Pediatrics, 159, pp. 247-256
European Journal of Pediatrics, 159, 247-256
European Journal of Pediatrics, 159, 247-256
Uniparental disomy (UPD) is defined as the inheritance of both homologous chromosomes from only one parent. So far, maternal UPD 7 has been described in 28 cases. Here, we report 4 new cases, present clinical information of 5 cases previously reporte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1c0fe35f74044a07d88b5f62a095912
https://doi.org/10.1007/s004310050064
https://doi.org/10.1007/s004310050064
Autor:
K. P. Koopmans, E Schoenle, Jacques Rahier, Timo Otonkoski, Klaus Mohnike, Khalid Hussain, Wolfgang Mohnike, Heikki Minn, C Fekete, Maria-Joao Ribeiro, J De Lonlay, A Mutair, Oliver Blankenstein, Henrik Thybo Christesen
Publikováno v:
Hormone Research in Paediatrics. 66:40-42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e1e4139b6b1aa423deb2d4f203d2ce0
https://doi.org/10.1159/000093471
https://doi.org/10.1159/000093471
Autor:
Helena G. Ilyina, Albert Schinzel, F. Bernasconi, Ben C.J. Hamel, Iosif W. Lurie, Dieter Kotzot, E A Werder, Martin Hergersberg, Barto J. Otten, E. Schoenle, Wendy P. Robinson, Károly Méhes, Silke Schmitt
Publikováno v:
Human Molecular Genetics. 4:583-587
Maternal uniparental disomy for the entire chromosome 7 has so far been reported in three patients with intrauterine and postnatal growth retardation. Two were detected because they were homozygous for a cystic fibrosis mutation for which only the mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65bd525f57d8a8df74bb7b252677062f
https://doi.org/10.1093/hmg/4.4.583
https://doi.org/10.1093/hmg/4.4.583
Publikováno v:
Ciba Foundation Symposium 116-Growth Factors in Biology and Medicine
Insulin-like growth factors (IGF) I and II produce acute insulin-like effects or promote growth indices in hypophysectomized rats, depending on their mode of administration. Intravenous bolus injections of IGF I and II, like insulin, lower the blood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85321d8a6baa59df7832c0d0a539d99c
https://doi.org/10.1002/9780470720974.ch11
https://doi.org/10.1002/9780470720974.ch11
Publikováno v:
Biochemical and biophysical research communications. 274(1)
Lhx3 is a LIM-homeobox protein essential for pituitary development in mice. The human homologue gene spans 7.2 kb and contains 7 exons, including two alternatively spliced first exons. This structure encodes two distinct protein isoforms, LHX3a and L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a62a86299ecd9afc89609dfb94228f33
https://pubmed.ncbi.nlm.nih.gov/10903894
https://pubmed.ncbi.nlm.nih.gov/10903894
Publikováno v:
Pediatric research. 39(1)
Wilms tumor is a common embryonic tumor in childhood. Two Wilms tumor-suppressor genes, WT1 and WT2, are located on chromosome 11p, WT2 at 11p15.5 close to the IGF-II gene, which is highly expressed in some Wilms tumors. We established Wilms tumor ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b96069b3b3f6eb14426796c80deff944
https://pubmed.ncbi.nlm.nih.gov/8825403
https://pubmed.ncbi.nlm.nih.gov/8825403
Publikováno v:
The Journal of clinical endocrinology and metabolism. 80(2)
Removal of a craniopharyngioma usually results in panhypopituitarism. Some children, however, grow normally or even excessively after extirpation of the tumor despite a proven lack of GH and have so far not been treated with hGH. We studied the effec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7b804715b80250951c9c3d747feb9ce
https://pubmed.ncbi.nlm.nih.gov/7852493
https://pubmed.ncbi.nlm.nih.gov/7852493
Publikováno v:
European journal of pediatrics. 152(2)
The concentration of mRNA of insulin-like growth factor-II is (IGF-II) much elevated in some embryonic tumours such as Wilms tumour (nephroblastoma). In order to prove whether or not IGF-II is produced by the tumour tisue, IGF-II was extracted from f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f13b06b3236755de3dc3f9be7ab124f1
https://pubmed.ncbi.nlm.nih.gov/8383050
https://pubmed.ncbi.nlm.nih.gov/8383050