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Search Results - Tüngler, V
Search Results - Tüngler, V
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Inherited or de novo mutation affecting aspartate 18 of TREX1 results in either familial chilblain lupus or Aicardi-Goutières syndrome
by
Tüngler, V.
,
Silver, R.M.
,
Walkenhorst, H.
,
Günther, C.
,
Lee-Kirsch, M.A.
Published in
British journal of dermatology (1951)
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Progesterone attenuates demyelination and microglial reaction in the lysolecithin-injured spinal cord
by
Garay, L
,
Tüngler, V
,
Deniselle, M.C.G
,
Lima, A
,
Roig, P
,
De Nicola, A.F
Published in
Neuroscience
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Defective removal of ribonucleotides from DNA promotes systemic lupus erythematosus
by
Günther, C
,
Kind, B
,
Reijns, MAM
,
Berndt, N
,
Martinez-Bueno, M
,
Wolf, C
,
Tüngler, V
,
Chara, O
,
Lee, YA
,
Hübner, N
,
Bicknell, L
,
Blum, S
,
Krug, C
,
Schmidt, F
,
Kretschmer, S
,
Koss, S
,
Astell, KR
,
Ramantani, G
,
Bauerfeind, A
,
Morris, DL
,
Graham, DS Cunninghame
,
Bubeck, D
,
Leitch, A
,
Ralston, SH
,
Blackburn, EA
,
Gahr, M
,
Witte, T
,
Vyse, TJ
,
Melchers, I
,
Mangold, E
,
Nöthen, MM
,
Aringer, M
,
Kuhn, A
,
Lüthke, K
,
Unger, L
,
Bley, A
,
Lorenzi, A
,
Isaacs, JD
,
Alexopoulou, D
,
Conrad, K
,
Dahl, A
,
Roers, A
,
Alarcon-Riquelme, ME
,
Jackson, AP
,
Lee-Kirsch, MA
Published in
Pediatric rheumatology online journal
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Inherited or de novo mutation affecting aspartate 18 of TREX1 results in either familial chilblain lupus or Aicardi-Goutières syndrome: Correspondence
by
Tüngler, V.
,
Silver, R.M.
,
Walkenhorst, H.
,
Günther, C.
,
Lee-Kirsch, M.A.
Published in
British journal of dermatology (1951)
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Genetic methods for analysis of autoinflammatory diseases
by
Bienias, M
,
König, N
,
Wolf, C
,
Kretschmer, S
,
Rösen-Wolff, A
,
Berner, R
,
Tüngler, V
,
Lee-Kirsch, M A
Published in
Zeitschrift für Rheumatologie
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Genetische Methoden für die Analyse autoinflammatorischer Erkrankungen
by
Bienias, M.
,
König, N.
,
Wolf, C.
,
Kretschmer, S.
,
Rösen-Wolff, A.
,
Berner, R.
,
Tüngler, V.
,
Lee-Kirsch, M. A.
Published in
Zeitschrift für Rheumatologie
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Klinische Symptome und Pathogenese der Typ-1-Interferonopathien
by
Diesterheft, M.
,
Schuster, M.
,
Rösen-Wolff, A.
,
Berner, R.
,
Tüngler, V.
,
Lee-Kirsch, M.
Published in
Monatsschrift Kinderheilkunde
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Thymulin-Based Gene Therapy and Pituitary Function in Animal Models of Aging
by
Reggiani, Paula C.
,
Poch, Brenda
,
Cónsole, Gloria M.
,
Rimoldi, Omar J.
,
Schwerdt, Jose I.
,
Tüngler, Victoria
,
Garcia-Bravo, Margarita M.
,
Dardenne, Mireille
,
Goya, Rodolfo G.
Published in
Neuroimmunomodulation
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Inherited or de novo mutation affecting aspartate 18 of TREX1 results in either familial chilblain lupus or Aicardi-Goutières syndrome
by
Tüngler, V
,
Silver, R M
,
Walkenhorst, H
,
Günther, C
,
Lee-Kirsch, M A
Published in
The British journal of dermatology
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Wet oxidation properties of process waste waters of fine chemical and pharmaceutical origin
by
Hosseini, A. M.
,
Tungler, A.
,
Bakos, V.
Published in
Reaction kinetics, mechanisms and catalysis
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Enantioselective hydrogenations with highly mesoporous carbon supported Pd catalysts
by
Sı́pos, É
,
Fogassy, G
,
Tungler, A
,
Samant, P.V
,
Figueiredo, J.L
Published in
Journal of molecular catalysis. A, Chemical
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Diastereoselective heterogeneous catalytic hydrogenation of N-heterocycles. Part I. Hydrogenation of pyridines
by
Hegedűs, László
,
Háda, Viktor
,
Tungler, Antal
,
Máthé, Tibor
,
Szepesy, László
Published in
Applied catalysis. A, General
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