Zobrazeno 1 - 10
of 64
pro vyhledávání: '"H. P. Neumann"'
Autor:
Maximilian Strunz, Lukas M. Simon, Meshal Ansari, Jaymin J. Kathiriya, Ilias Angelidis, Christoph H. Mayr, George Tsidiridis, Marius Lange, Laura F. Mattner, Min Yee, Paulina Ogar, Arunima Sengupta, Igor Kukhtevich, Robert Schneider, Zhongming Zhao, Carola Voss, Tobias Stoeger, Jens H. L. Neumann, Anne Hilgendorff, Jürgen Behr, Michael O’Reilly, Mareike Lehmann, Gerald Burgstaller, Melanie Königshoff, Harold A. Chapman, Fabian J. Theis, Herbert B. Schiller
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-20 (2020)
Injury repair is characterized by the generation of transient cell states important for tissue recovery. Here, the authors present a single cell RNA-seq map of recovery from bleomycin lung injury in mice and uncover a Krt8+ transitional stem cell sta
Externí odkaz:
https://doaj.org/article/c56bf52cb142499c98ef8cc384553dbe
Publikováno v:
Brain Pathology. 5:181-193
After a decade of intensive clinical and molecular genetic efforts the von Hippel-Lindau (VHL) gene was cloned in 1993. The open reading frame encodes the putative protein of 284 amino acids. A large number of different mutations have been identified
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8a016a3af47dd13018e919573620456
https://doi.org/10.1111/j.1750-3639.1995.tb00592.x
https://doi.org/10.1111/j.1750-3639.1995.tb00592.x
Publikováno v:
Liebigs Annalen der Chemie. 1993:1313-1317
(+)-(1R,4R)-Bicyclo[2.2.1]hept-5-en-2-one (7) was prepared in 78.5% yield by oxidative degradation of (+)-(1R)-endo-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid (4) by using an improved procedure for the oxidation of the dianion of 4 with dioxygen. Dih
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a562f0efc1801596c12095d02bd776be
https://doi.org/10.1002/jlac.1993199301213
https://doi.org/10.1002/jlac.1993199301213
Publikováno v:
ChemInform. 25
(+)-(1R,4R)-Bicyclo[2.2.1]hept-5-en-2-one (7) was prepared in 78.5% yield by oxidative degradation of (+)-(1R)-endo-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid (4) by using an improved procedure for the oxidation of the dianion of 4 with dioxygen. Dih
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7b5b1ce784eb4f989ac9f35a2b4cda4
https://doi.org/10.1002/chin.199414280
https://doi.org/10.1002/chin.199414280
Publikováno v:
Klinische Monatsblatter fur Augenheilkunde. 226(11)
The aim of this study was to characterise the results of a screening for von Hippel-Lindau disease (VHL), angiomatosis retinae (AR) and further VHL lesions in at-risk relatives of ophthalmological VHL index patients.A retrospective analysis of 20 VHL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e5aba89da8adac69ad1af68b87dec94
https://pubmed.ncbi.nlm.nih.gov/19916152
https://pubmed.ncbi.nlm.nih.gov/19916152
Autor:
M, Cybulla, K, Walter, H P, Neumann, U, Widmer, M, Schärer, G, Sunder-Plassmann, T, Jansen, A, Rolfs, M, Beck
Publikováno v:
Deutsche medizinische Wochenschrift (1946). 132(28-29)
Fabry's disease is a rare, X-chromosome linked recessive lysosomal storage disorder. In its course multiple organ damage occurs, e.g. in skin, nerves, kidneys and heart. The disease not only markedly impairs the quality of life but also shortens life
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ba4adff5d8d0fb600b220da0d5876a03
https://pubmed.ncbi.nlm.nih.gov/17607649
https://pubmed.ncbi.nlm.nih.gov/17607649
Publikováno v:
Laryngo- rhino- otologie. 83(9)
Paragangliomas of the head and neck represent rare tumors of neural crest origin that arise from chemoreceptors. They are highly vascular neoplasms that are benign in the majority of cases. There are controversial discussions concerning the different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2aa2dfc901f2d000c01fd29de55874c9
https://pubmed.ncbi.nlm.nih.gov/15372340
https://pubmed.ncbi.nlm.nih.gov/15372340
Autor:
H. P. Neumann
Publikováno v:
JAMA: The Journal of the American Medical Association. 274:1149-1151
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bc8037a3c1502d3a3fc48dfbfe18c8b
https://doi.org/10.1001/jama.274.14.1149
https://doi.org/10.1001/jama.274.14.1149
Publikováno v:
Cancer research. 60(24)
Most pheochromocytomas are sporadic but about 10% are though to be hereditary. Although the etiology of most inherited pheochromocytoma is well known, little is known about the etiology of the more common sporadic tumor. Recently, germ-line mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5ac3da185bccf2cc1e6e59a59514bcd2
https://pubmed.ncbi.nlm.nih.gov/11156372
https://pubmed.ncbi.nlm.nih.gov/11156372
Publikováno v:
The Journal of clinical endocrinology and metabolism. 85(12)
Pheochromocytomas arise sporadically and as a component tumor of the inherited cancer syndromes von Hippel-Lindau disease (VHL), multiple endocrine neoplasia type 2 (MEN 2), and type 1 neurofibromatosis. Germline mutations of the VHL tumor suppressor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b8e4cd07356e691da65144f53a769dc
https://pubmed.ncbi.nlm.nih.gov/11134110
https://pubmed.ncbi.nlm.nih.gov/11134110