Results 111 to 120 of about 14,685,767 (350)

Tumor Necrosis Factor-α −308G>A Allelic Variant Modulates Iron Accumulation in Patients with Hereditary Hemochromatosis [PDF]

, 2006
Pierre‐Alexandre Krayenbuehl, Friedrich E. Maly, Martin Hersberger, Peter Wiesli, Andreas Himmelmann, Karim Eid, P Greminger, W. Vetter, Georg Schulthess   +8 more
openalex   +1 more source

Factors associated with rapid improvement in visual acuity in patients with Leber's hereditary optic neuropathy after gene therapy [PDF]

, 2020
Hongli Liu, Jiajia Yuan, Yong Zhang, Zhen Tian, Xin Li, Dan Wang, Yangyang Du, Lin Song, Bin Li   +8 more
openalex   +1 more source

Biophysical approaches for studying viral entry

FEBS Letters, EarlyView.
Viruses infect all living organisms and have been responsible for major epidemics and pandemics. Their ongoing evolutionary battle with host defenses creates a constant need for improved tools to study viral behavior. Advancing methods to probe viral attachment, fusion, and genome release deepen our understanding of how infections begin and support the
Inbar Yosibash, Raya Sorkin
wiley   +1 more source

Hereditary risk factors for thrombophilia and probability of venous thromboembolism during pregnancy and the puerperium.

Blood, 2016
A. Gerhardt, R. Scharf, I. Greer, R. Zotz   +3 more
semanticscholar   +1 more source

Càncer colorectal hereditari: Aplicacions diagnòstiques de l'estudi de la dosi dels gens APC, MLH1 i MSH2 [PDF]

, 2009
[cat] Les síndromes de càncer colorectal (CCR) hereditari representen entre un 3% i un 5% de tots els casos de CCR i inclouen tots aquells individus amb un elevat grau d'agregació familiar.
Castellsagué Torrents, Ester
core  

Hereditary thrombophilic risk factors and venous thromboembolism in Istanbul, Turkey: The role in different clinical manifestations of venous thromboembolism

, 2008
The aim of this study was to investigate the hereditary thrombophilic risk factors in patients with venous thromboembolism (NIT E) and whether these risk factors play a different role in patients with isolated pulmonary embolism (PE) as compared with ...
Uenaltuna, Nihan Erginel, Okumus, Gulfer, Unlucerci, Yesim, Kiyan, Esen, Abaci, Neslihan, Diz-Kucukkaya, Reyhan, Arseven, Orhan, Tabak, Levent, Issever, Halim   +8 more
core   +1 more source

The human gut microbiome across the life course

FEBS Letters, EarlyView.
Despite significant individual variation and continuous change throughout life, the human gut microbiome follows some life stage‐specific trends. This article provides a brief overview of how gut microbiome composition shifts across different phases of life. Created in BioRender. Özkurt, E. (2026) https://BioRender.com/8q4nrnc.
Alise J. Ponsero, Basak Bahcivanci, Antonietta Hayhoe, Animesh Acharjee, Ezgi Özkurt   +4 more
wiley   +1 more source

Septin 9 PB domains coordinate centrosome positioning and microtubule acetylation to control epithelial polarity

FEBS Letters, EarlyView.
Septin 9 polybasic domains couple phosphoinositide‐rich membrane binding to centrosome positioning, Golgi organization, and microtubule acetylation to control epithelial polarity. Their loss disrupts this axis, causing centrosome mispositioning, Golgi fragmentation, reduced microtubule acetylation, and polarity inversion via upregulation of the ...
Ting ting Cai, Mohyeddine Omrane, Nassima Benzoubir, Didier Samuel, Ama Gassama‐Diagne   +4 more
wiley   +1 more source

Plasma‐derived human factor X concentrate for the treatment of patients with hereditary factor X deficiency [PDF]

, 2023
Miguel A. Escobar, Kaan Kavaklı
openalex   +1 more source

Hereditary methemoglobinemia manifesting in adolescence

, 2016
Methemoglobinemia is an uncommon cause of cyanosis that may present at any age. Although acquired methemoglobinemia secondary to exposure to oxidative stressors is the most common cause of methemoglobinemia in adults, hereditary methemoglobinemia has to ...
Siraj O Wali, Rajaa Z Alsaggaf, Mazen A Badawi, Maha A Badawi   +3 more
core   +1 more source