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Results of search for 'au:"Bäumer, A"', page 5 of 6
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Authors
BAUMER, A
Backmann, L
Balmer, D
Baumer, A
Binkert, F
Brinkmann, A
Bäumer, A
Bäumer, A T
Böhm, M
Dutly, F
Kornhuber, J
Linnane, A W
Nickenig, G
Riederer, P
Riegel, M
Rösler, M
Schinzel, A
Strehlow, K
Thome, J
Wassmann, S
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Topics
Abnormalities, Multiple
Adolescent
Adult
Aged
Animals
Base Sequence
Child
Child, Preschool
Chromosome Deletion
Female
Humans
In Situ Hybridization, Fluorescence
Male
Middle Aged
Molecular Sequence Data
Mutation
Pedigree
blood
genetics
metabolism
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Undetermined
Your search returned 119 results.
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81.
Antioxidative enzymes in human hearts with idiopathic dilated cardiomyopathy.
[electronic resource]
by
Bäumer, A T
Flesch, M
Wang, X
Shen, Q
Feuerstein, G Z
Böhm, M
Producer:
20000418
In:
Journal of molecular and cellular cardiology
vol. 32
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82.
Meiotic origin of two ring chromosomes 18 in a girl with developmental delay.
[electronic resource]
by
Baumer, A
Giovannucci Uzielli, M L
Guarducci, S
Lapi, E
Röthlisberger, B
Schinzel, A
Producer:
20030326
In:
American journal of medical genetics
vol. 113
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83.
Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.
[electronic resource]
by
Riegel, M
Baumer, A
Jamar, M
Delbecque, K
Herens, C
Verloes, A
Schinzel, A
Producer:
20011207
In:
Human genetics
vol. 109
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84.
Initial maternal meiotic I error leading to the formation of a maternal i(2q) and a paternal i(2p) in a healthy male.
[electronic resource]
by
Baumer, A
Basaran, S
Taralczak, M
Cefle, K
Ozturk, S
Palanduz, S
Schinzel, A
Producer:
20071011
In:
Cytogenetic and genome research
vol. 118
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85.
Mitochondrial gene mutation: the ageing process and degenerative diseases.
[electronic resource]
by
Linnane, A W
Baumer, A
Maxwell, R J
Preston, H
Zhang, C F
Marzuki, S
Producer:
19910528
In:
Biochemistry international
vol. 22
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86.
De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21.
[electronic resource]
by
Riegel, M
Baumer, A
Piram, A
Ortolan, D
Peres, L C
Pina-Neto, J M
Producer:
20010726
In:
Genetic counseling (Geneva, Switzerland)
vol. 12
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87.
Seven cases of Wiedmann-Beckwith syndrome, including the first reported case of mosaic paternal isodisomy along the whole chromosome 11.
[electronic resource]
by
Dutly, F
Baumer, A
Kayserili, H
Yüksel-Apak, M
Zerova, T
Hebisch, G
Schinzel, A
Producer:
19990602
In:
American journal of medical genetics
vol. 79
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88.
A case with de novo interstitial deletion of chromosome 7q21.1-q22.
[electronic resource]
by
Manguoğlu, E
Berker-Karaüzüm, S
Baumer, A
Mihçi, E
Taçoy, S
Lüleci, G
Schinzel, A
Producer:
20060111
In:
Genetic counseling (Geneva, Switzerland)
vol. 16
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89.
Differential effects of estrogen and progesterone on AT(1) receptor gene expression in vascular smooth muscle cells.
[electronic resource]
by
Nickenig, G
Strehlow, K
Wassmann, S
Bäumer, A T
Albory, K
Sauer, H
Böhm, M
Producer:
20001107
In:
Circulation
vol. 102
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90.
Negative feedback regulation of reactive oxygen species on AT1 receptor gene expression.
[electronic resource]
by
Nickenig, G
Strehlow, K
Bäumer, A T
Baudler, S
Wassmann, S
Sauer, H
Böhm, M
Producer:
20001205
In:
British journal of pharmacology
vol. 131
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91.
Down-regulation of intrinsic P-glycoprotein expression in multicellular prostate tumor spheroids by reactive oxygen species.
[electronic resource]
by
Wartenberg, M
Ling, F C
Schallenberg, M
Bäumer, A T
Petrat, K
Hescheler, J
Sauer, H
Producer:
20010705
In:
The Journal of biological chemistry
vol. 276
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92.
High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions.
[electronic resource]
by
Baumer, A
Dutly, F
Balmer, D
Riegel, M
Tükel, T
Krajewska-Walasek, M
Schinzel, A A
Producer:
19980826
In:
Human molecular genetics
vol. 7
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93.
Long-term tooth retention in periodontitis patients in four German university centres.
[electronic resource]
by
Graetz, C
Bäumer, A
Eickholz, P
Kocher, T
Petsos, H
Pretzl, B
Schwendicke, F
Holtfreter, B
Producer:
20201022
In:
Journal of dentistry
vol. 94
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94.
Exploring the role of oxygen in Fanconi's anemia.
[electronic resource]
by
Liebetrau, W
Rünge, T M
Baumer, A
Henning, C
Gross, O
Schindler, D
Poot, M
Hoehn, H
Producer:
19970218
In:
Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer
vol. 143
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95.
Method for in situ investigation of mitochondrial DNA deletions.
[electronic resource]
by
Kovalenko, S A
Harms, P J
Tanaka, M
Baumer, A
Kelso, J
Ozawa, T
Linnane, A W
Producer:
19980102
In:
Human mutation
vol. 10
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96.
Isolated central form of tetrahydrobiopterin deficiency associated with hemizygosity on chromosome 11q and a mutant allele of PTPS.
[electronic resource]
by
Blau, N
Scherer-Oppliger, T
Baumer, A
Riegel, M
Matasovic, A
Schinzel, A
Jaeken, J
Thöny, B
Producer:
20000822
In:
Human mutation
vol. 16
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97.
Inhibition of geranylgeranylation reduces angiotensin II-mediated free radical production in vascular smooth muscle cells: involvement of angiotensin AT1 receptor expression and Rac1 GTPase.
[electronic resource]
by
Wassmann, S
Laufs, U
Bäumer, A T
Müller, K
Konkol, C
Sauer, H
Böhm, M
Nickenig, G
Producer:
20010322
In:
Molecular pharmacology
vol. 59
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98.
The Gly/Glu polymorphism of the neurotrophin 3 gene: allele frequencies in a Caucasian population and relevance for psychiatric disorders.
[electronic resource]
by
Thome, J
Baumer, A
Harsányi, A
Foley, P
Kornhuber, J
Wiesbeck, G A
Rösler, M
Riederer, P
Producer:
19970212
In:
Neuroreport
vol. 7
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99.
Reduction of oxidative stress and AT1 receptor expression by the selective oestrogen receptor modulator idoxifene.
[electronic resource]
by
Bäumer, A T
Wassmann, S
Ahlbory, K
Strehlow, K
Müller, C
Sauer, H
Böhm, M
Nickenig, G
Producer:
20011205
In:
British journal of pharmacology
vol. 134
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100.
Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 gene.
[electronic resource]
by
Bartholdi, D
Klein, A
Weissert, M
Koenig, N
Baumer, A
Boltshauser, E
Schinzel, A
Berger, W
Mátyás, G
Producer:
20060628
In:
Clinical genetics
vol. 69
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