ライフサイエンスコーパス: Tamm

1 Tamm states can exist with zero in-plane wavevector comp

2 Tamm-Horsfall protein (THP) is a glycoprotein uniquely e

3 Tamm-Horsfall protein (THP), also known as uromodulin, i

4 ge band structure and can be classified as a Tamm-like state lacking any surface defect.

5 Here, we implement a Tamm-plasmon-polariton structure and study the coupling

6 Uromodulin (also known as Tamm-Horsfall protein) is a kidney-specific glycoprotein

7 teractions between urinary proteins, such as Tamm-Horsfall protein, and TLR-4 add to the complexity o

8 Tamm state under the metal film and display Tamm state-coupled emission (TSCE).

9 nt of mild cysts that were positive only for Tamm-Horsfall protein (THP), a loop of Henle marker, whi

10 ules tested inhibited aggregation, including Tamm-Horsfall protein, which did not inhibit growth.

11 er loading reduced aquaporin-2 but increased Tamm-Horsfall protein (THP) and particle detection by NT

12 ies of articles from the laboratory of Lukas Tamm, the spontaneous orientation of the SNARE motif of

13 xpress COX-2, bNOS, NKCC2, and ROMK, but not Tamm-Horsfall protein, and showed rapid (86)Rb(+) uptake

14 Here we show that elimination of Tamm-Horsfall protein (THP) expression from mouse kidney

15 stably expressing human-relevant mutants of Tamm-Horsfall protein in polarized Madin-Darby canine ki

16 thod to understand the optical properties of Tamm states and localization of the modes or electric fi

17 t prevent adhesion of bacteria by release of Tamm-Horsfall protein, lactoferrin, lipocalin, and const

18 ive to wavelength, which suggests the use of Tamm structures to provide both directional emission and

19 ltered light chains bind to a common site on Tamm-Horsfall protein (THP), which is produced by cells

20 inant glutathione-S-transferase-OPN (G-OPN), Tamm-Horsfall protein, chondroitin sulfate, human serum

21 Our structure is designed to support optical Tamm states, which are trapped electromagnetic modes bet

22 tecture to exploit hybrid plasmonic-photonic Tamm plasmon modes.

23 This removed Tamm-Horsfall protein, the major contaminant, and subfra

24 gene under the direction of the TAL-specific Tamm-Horsfall protein promoter was generated.

25 Here we show that Tamm-Horsfall protein (THP) is the principal urinary pro

26 In contrast to SPCE, the Tamm states can display either S or P polarization.

27 top of the metal film can interact with the Tamm state under the metal film and display Tamm state-c

28 to specifically bind and trap the wild-type Tamm-Horsfall protein (THP) and prevent it from exiting

29 Uromodulin (UMOD)/Tamm-Horsfall protein, the most abundant human urinary p

30 odes the most common protein in human urine, Tamm-Horsfall protein, and rare mutations in UMOD cause

31 of the UMOD gene, which encodes uromodulin (Tamm-Horsfall protein), associate with chronic kidney di

32 revalent soluble urinary protein uromodulin (Tamm-Horsfall protein), potently inhibited growth of pat

33 ar, because the encoded protein, uromodulin (Tamm-Horsfall protein), is exclusively produced by the k

34 Uromodulin/Tamm-Horsfall protein is not immunostimulatory in the tu

35 t that pathologic accumulation of uromodulin/Tamm-Horsfall glycoprotein (THP) occurs in the endoplasm

36 theory (TDDFT), both within a commonly used Tamm-Dancoff approximation (TDA).

37 s well as an assessment of the commonly used Tamm-Dancoff approximation to the GW-BSE approach.

38 lar dynamics simulations are performed using Tamm-Dancoff time-dependent density functional theory.

39 s to demonstrate the utility of the in vitro Tamm-Horsfall protein (THP)-1 human monocyte cell cultur

40 The gene neither codistributed with Tamm-Horsfall protein nor aquaporin-2.

41 ight chains (FLCs), which coprecipitate with Tamm-Horsfall glycoprotein (THP) in the lumen of the dis

42 immunoglobulin free light chains (FLCs) with Tamm-Horsfall glycoprotein (THP).

43 f filtered monoclonal light chains (LC) with Tamm-Horsfall glycoprotein (THP) triggers heterotypic ag