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Seite 37 für „Gene“ · Literaturverweise aus öffentlichen Artikeln
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Vitiligo: Mechanisms of Pathogenesis and Treatment.
pubmed · 32017656
Literaturverweis öffnenMeasles: An Updated Literature Review of the Host Response, Pathogenesis, Complications, Prevention Measures, and Recent Outbreaks
pubmed · 41751468
Literaturverweis öffnenImpact of Genetics on Endocrine Manifestations of Cystic Fibrosis
pubmed · 42162871
Literaturverweis öffnenMicroglial ITAM & ITIM Signaling in Neurodegenerative Disease and Brain Aging
pubmed · 42269855
Literaturverweis öffnenEpidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta‐analysis
pubmed · 37086676
Literaturverweis öffnenEmerging Genetic Therapy for Sickle Cell Disease
pubmed · 30355263
Literaturverweis öffnenSickle Cell Disease—Genetics, Pathophysiology, Clinical Presentation and Treatment
pubmed · 33072979
Literaturverweis öffnenComplication Profiles of Corpectomy-Containing Versus Non-Corpectomy Anterior Cervical Surgery for Degenerative Cervical Myelopathy: A Multicenter Study of 1,024 Cases
pubmed · 42479634
Literaturverweis öffnenAortic aneurysms: current pathogenesis and therapeutic targets.
pubmed · 38036736
Literaturverweis öffnenWhat is Intervertebral Disc Degeneration, and What Causes It?
pubmed · 16915105
Literaturverweis öffnenNovel Filamin genes variants implicated in skeletal dysplasias: integrated structural modeling and in silico functional characterization
pubmed · 41086097
Literaturverweis öffnen[STAT3 gene-related hyper-IgE syndrome complicated by pulmonary aspergillosis: a case report]
pubmed · 42236459
Literaturverweis öffnenGenetic drivers of etiologic heterogeneity in thyroid cancer
pubmed · 42431967
Literaturverweis öffnenThe evaluation of gene polymorphisms associated with autoinflammatory syndrome in patients with palindromic rheumatism complicated by intermittent hydrarthrosis
pubmed · 31897954
Literaturverweis öffnenGenetic variation at the glycosaminoglycan metabolism pathway contributes to the risk of psoriatic arthritis but not psoriasis
pubmed · 30552173
Literaturverweis öffnenA Cannabinoid 2-Selective Agonist Inhibits Allogeneic Skin Graft Rejection In Vivo
pubmed · 35185546
Literaturverweis öffnenLate effects after allogeneic hematopoietic stem cell transplantation in patients with primary immunodeficiency
pubmed · 42459651
Literaturverweis öffnenHypoxie beim Zervixkarzinom: Pathogenese, Charakterisierung und biologische/klinische Konsequenzen 1
pubmed · 11370526
Literaturverweis öffnenCharacteristics, Epigenetics, and Management of Non-Infectious Preterm Birth-Sterile Intrauterine Inflammation and Idiopathic Preterm Birth
pubmed · 42355410
Literaturverweis öffnenSecond-/Third-Line Therapie nach Versagen eine Next-Generation-Hormontherapie (NHA) und ggf. Second-Line-Therapie mit Abirateron bei metasta
pubmed · 34020501
Literaturverweis öffnenDiagnostic yield of targeted next-generation sequencing for pediatric hereditary hemolytic anemia
pubmed · 37697358
Literaturverweis öffnenFive Pathogenetic Classifications for Alloimmune Hemolytic Disease of the Fetus And Newborn
pubmed · 41520492
Literaturverweis öffnenA Case of Listeria monocytogenes Meningitis (Complicated) with Hydrocephalus and Occipital Lobe Infarction
pubmed · 42473611
Literaturverweis öffnenExpanding the Genetic Landscape of Congenital Stationary Night Blindness Through the Analysis of Consanguineous Pakistani Families
pubmed · 42194996
Literaturverweis öffnenStable Gastric Pentadecapeptide BPC 157 as a Therapy and Safety Key: A Special Beneficial Pleiotropic Effect Controlling and Modulating Angiogenesis and the NO-System
pubmed · 40573323
Literaturverweis öffnenNiacin accelerates skeletal muscle regeneration and enhances C2C12 differentiation by activating the PI3K/Akt signaling pathway
pubmed · 42082121
Literaturverweis öffnenNovel biallelic multi-exon duplication in the PIGN gene associated with multiple congenital anomalies-hypotonia-seizures syndrome 1
pubmed · 42420894
Literaturverweis öffnenImmunopathogenesis and immunoregulatory mechanisms in allergic contact dermatitis
pubmed · 42212145
Literaturverweis öffnenIdentification of a novel hereditary spherocytosis gene mutation in a Chinese child with α-globin gene triplication
pubmed · 42467362
Literaturverweis öffnenSpatial Analysis Reveals Gene Expression and Microenvironmental Changes in the Transition of Nevus to Melanoma
pubmed · 42258703
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