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Seite 30 für „Gene“ · Literaturverweise aus öffentlichen Artikeln
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Onasemnogene Abeparvovec is Safe in Hemolytic Disease of the Newborn: A Case Report
pubmed · 39689850
Literaturverweis öffnenCanine and Feline Pemphigus Foliaceus—an Update on Pathogenesis and Treatment
pubmed · 39725576
Literaturverweis öffnenCase Report: Association of a rare single nucleotide variant in the KCNH2 gene with drug-induced QT prolongation
pubmed · 41816791
Literaturverweis öffnenAlopecia Areata: an Update on Etiopathogenesis, Diagnosis, and Management
pubmed · 34403083
Literaturverweis öffnenInteraction between dietary cholesterol intake and genetic variants for cholesterol absorption in relation to coronary artery disease mortality: a prospective analysis in the Singapore Chinese Health Study
pubmed · 40935150
Literaturverweis öffnen[Sense and nonsense with respect to the gene for dyslexia].
pubmed · 10028322
Literaturverweis öffnenGenetic analysis of the SRD5A2 gene in Indian patients with 5alpha-reductase deficiency
pubmed · 19492581
Literaturverweis öffnenCorrelation between tricuspid regurgitation and fetal cardiac structure or signs and prenatal genetic testing abnormalities in fetuses at 12+ 0 to 16+ 0 weeks of gestation
pubmed · 42210096
Literaturverweis öffnenHBV PreS/S gene mutations in patients with chronic hepatitis B
pubmed · 42498832
Literaturverweis öffnenDepression in neurodegenerative disease: neurobiological mechanisms and emerging treatments
pubmed · 42410083
Literaturverweis öffnenEvolution of biotechnological advances and regenerative therapies for endometrial disorders: a systematic review
pubmed · 38796750
Literaturverweis öffnenEngineering a functional tendon-bone interface: mechanisms and prospects of magnesium alloys in promoting neurotized regeneration via modulating stem cell-nerve interplay
pubmed · 42245934
Literaturverweis öffnen[Detection of pathogenic gene mutations in thirteen cases of congenital bilateral absence of vas deferens infertility patients]
pubmed · 39397452
Literaturverweis öffnenBlood-based RBBP7 and RIBC1 methylation as a candidate epigenetic biomarker for ovarian cancer epigenetic markers RBBP7 and RIBC1 in ovarian cancer.
pubmed · 42525292
Literaturverweis öffnenHaemolacria: etiopathogenesis, diagnosis, treatment
pubmed · 34965079
Literaturverweis öffnenPulmonary Nocardiosis Diagnosed by Plasma Metagenomic Next-Generation Sequencing in a Patient With Recurrent Febrile Neutropenia
pubmed · 42465527
Literaturverweis öffnenScrotal flap phalloplasty as temporary neophallus in infants and children with penile agenesis: Multi-institutional experience and long-term follow-up
pubmed · 36272933
Literaturverweis öffnenInherited epidermolysis bullosa: update on the clinical and genetic aspects
pubmed · 32732072
Literaturverweis öffnenGenetic Analysis of Isolated Hepatic Ductal Plate Malformation Reveals Novel Variants and Insights into Phenotypic Correlation
pubmed · 42365546
Literaturverweis öffnenFamilial erythrocytosis and phenotypic heterogeneity associated with different defects in alpha globin genes: a significant new case of Hb Wroclaw (α88(F9) Ala>Glu; HBA1: c.266C>A)
pubmed · 41622866
Literaturverweis öffnenA Rare Case of Childhood Glaucoma Resulting from Anterior Segment Dysgenesis Associated with a Homozygous Mutation in the CPAMD8 Gene
pubmed · 42074612
Literaturverweis öffnenErgebnisse der lungenvolumenreduzierenden Operation bei diffusem Lungenemphysem
pubmed · 10460285
Literaturverweis öffnenMolecular and biochemical correlates of urinary composition in kidney stone pathogenesis
pubmed · 42320707
Literaturverweis öffnenSTAC3D Against the Odds: Characterizing the Musculoskeletal Phenotype of STAC3 Gene Disorder
pubmed · 42490135
Literaturverweis öffnenAcrokeratosis verruciformis of Hopf: Genetic, clinicopathologic and therapeutic features (Review)
pubmed · 42205461
Literaturverweis öffnenPrevalence and Genetic Spectrum of Inherited Kidney Diseases: A Chinese Cohort Study
pubmed · 41920701
Literaturverweis öffnenPolymorphism of the FSHB Gene Is Associated with Endometrial Hyperplasia
pubmed · 42195338
Literaturverweis öffnen