Results 101 to 110 of about 3,935,207 (294)
Golgi enzymes are retrieved from the plasma membrane to the trans‐Golgi network
FEBS Letters, EarlyView.Golgi enzymes are traditionally considered resident proteins retained within the Golgi apparatus. Here, we demonstrate that a subset transiently reaches the cell surface and is subsequently retrieved to the trans‐Golgi network via retrograde transport. Using a nanobody‐based toolkit, we uncover a dynamic trafficking cycle of several Golgi enzymes.
Dominik P. Buser, Tina Junne
wiley +1 more source
Ligand‐dependent transcriptional heterogeneity in cell cycle gene expression delays G1/S entry
FEBS Letters, EarlyView.EGF and HRG induce distinct G1/S progression programs in ErbB2‐amplified BT474 breast cancer cells. Despite activating the potent ErbB2–ErbB3 heterodimer, HRG does not accelerate cell‐cycle entry. Instead, EGF promotes earlier restriction‐point passage via ERK–FOS signaling, whereas HRG activates the AKT–MYC axis, driving transcriptional heterogeneity ...
Ririn Rahmala Febri +5 more
wiley +1 more source
, 1985 This is the 1985 edition of the Index. The Index is written by student editors, and it is the college’s yearbook. It includes an annual record of events at Wooster. This specific Index is divided into different sections including college life, activities,
Editors, Index, Index Editors,
core
Subgroups of finite index in an additive group of a ring
International Journal of Mathematics and Mathematical Sciences, 2001 If K is an infinite field and G⫅K is a subgroup of finite index in an additive group, then K∗=G∗G∗−1 where G∗ denotes the set of all invertible elements in G and G∗−1 denotes all inverses of elements of G∗.
Doostali Mojdeh, S. Hassan Hashemi
doaj +1 more source
Small Entire Functions with Infinite Growth Index
Journal of Mathematical Analysis and Applications, 2002 Let \(H(\mathbb C)\) denote the space of all entire functions, endowed with the compact-open topology. For \(f \in H(\mathbb C)\) and \(r>0\) let \(M_f(r):=\max\{|f(z)|: |z|=r\}\). Then the growth of \(m\)-order of \(f\) is defined by \[ \rho_m(f) := \limsup_{r\to\infty}{\frac{\log_{m+1}{M_f(r)}}{\log{r}}} , \] where \(\log_m\) denotes the \(m\)-times ...
openaire +2 more sources
FEBS Letters, EarlyView.Encapsulins are protein nanocompartments that play an important role in iron storage. In the Myxococcus xanthus encapsulin system, two cargo proteins called EncB and EncC contribute to iron mineralization. Here, we show that EncB and EncC generate iron‐containing minerals with distinct chemical compositions, suggesting that the composition of stored ...
Harry B. McDowell +2 more
wiley +1 more source
Field indices and common index divisors of generalized eisenstein trinomial fields
Mathematics OpenLet [Formula: see text] be a prime number and let [Formula: see text], where [Formula: see text] is a root of the generalized Eisenstein trinomial f(X)=Xp+pa1cp−2X+pa1cp−1, with [Formula: see text] and [Formula: see text]. The arithmetic study of indices,
Mohammed Yacine Djedidi +1 more
doaj +1 more source
‘Guide and Prejudice’— How Argonautes recognize targets across domains of life
FEBS Letters, EarlyView.Argonaute proteins use short nucleic‐acid guides to locate and regulate specific targets across all domains of life. Despite striking diversity—from human gene silencing to bacterial immune defence—all Argonautes share a conserved three‐stage recognition logic: guide‐directed sampling, progressive target pairing with a conformational checkpoint and ...
Jack P. K. Bravo
wiley +1 more source
Subgroups of infinite index in the modular group [PDF]
Glasgow Mathematical Journal, 1978 The modular group Г is the group of integral bilinear transformations of the extended complex plane which preserve the upper half-plane. It has the presentation 〈x, y:x2 = y3 = 1〉, and the generators can be chosen so that u = xy maps z to z + 1.
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