Zobrazeno 1 - 10
of 89
pro vyhledávání: '"M, Rutz"'
Publikováno v:
Molecules, Vol 28, Iss 17, p 6191 (2023)
The unsymmetrical diborane(4) derivative [(d(CH2P(iPr)2)abB)–Bpin] (1) proved to be a versatile PBP boryl pincer ligand precursor for Co(I) (2a, 4a), Rh(I) (2–3b) and Ir(I/III) (2–3c, 5–6c) complexes, in particular of the types [(d(CH2P(iPr)2
Externí odkaz:
https://doaj.org/article/e1e77209b96747018aca16a050f52cfb
Publikováno v:
Organometallics. 41:3044-3054
Autor:
Puneet Kumar, Janis Louie, Judah L. Evangelista, Philipp M. Rutz, Ashish Thakur, Jacob M. Cowley, Matthew B. Prater, Jonas Renner, Ryan M. Stolley
Publikováno v:
Organic Letters. 22:924-928
A Ni-catalyzed (4 + 2) cycloaddition of alkynes and azetidinones toward piperidinones was used as key reaction in the enantioselective synthesis of naturally occurring indolizidine alkaloids. The reaction benefits from the use of an easily accessible
Publikováno v:
British Journal of Dermatology. 175:988-993
BACKGROUND Direct immunofluorescence microscopy (DIF) studies constitute the gold standard for diagnosis of bullous pemphigoid (BP) but depend on the availability of specialized laboratories and often on an additional skin biopsy specimen. OBJECTIVES
Publikováno v:
Journal of autism and developmental disorders. 49(2)
Despite current guidelines, few children with autism spectrum disorder (ASD) receive genetic evaluations. We surveyed Utah pediatricians to characterize the knowledge, beliefs, current practices and perceived barriers of pediatricians regarding genet
Publikováno v:
European journal of medical genetics. 62(1)
De novo variants of ASH1L, which encodes a histone methyltransferase, have been reported in a few patients with intellectual disability and autistic features. Here, we identified a novel de novo frame-shift variant, c.2422_2423delAAinsT which predict
Autor:
Grace S. Kurian, Irene Lunghi, Gaël C.-T. Nguyen Tang, Christel L. Roth, Federico M. Rutz, Cecilia Schweblin, Jade Leiba, Priscilla Soulié
Publikováno v:
Revue Médicale Suisse. 14:712-713
Autor:
Eman E.A. Mohammed, Franklin D. Echevarria, Rafi Simon Awedikian, N. Matthew Ellinwood, Michelle M. Rutz-Mendicino, Elizabeth M. Whitley, Elizabeth M. Snella
Publikováno v:
Molecular Genetics and Metabolism. 107:129-135
Mucopolysaccharidosis type IIIB (MPS IIIB) is a neuropathic lysosomal storage disorder (LSD) resulting from an inherited deficiency of N -acetyl-α-d-glucosaminidase (Naglu) activity, an enzyme required to degrade the glycosaminoglycan heparan sulfat
Publikováno v:
Journal of Power Sources. 207:173-182
In cooperation with the industrial project partners ACCUREC Recycling and UVR-FIA a recycling process specially dedicated to portable Li-ion batteries was developed combining a mechanical pretreatment with hydro- and pyrometallurgical process steps.
Publikováno v:
Das Gesundheitswesen. 77