Gezielt nachschlagen
Suche
Suche startet nach einer kurzen Eingabepause.
Hier finden Sie Quellen, die öffentliche HealthOS-Artikel zitieren. Im lokalen PubMed-Bestand recherchieren →
Seite 31 für „Gene“ · Literaturverweise aus öffentlichen Artikeln
Suchtreffer
Quellen in Artikeln
Sertoli cell-only syndrome: advances, challenges, and perspectives in genetics and mechanisms
pubmed · 36814036
Literaturverweis öffnenGenotype-phenotype correlation in alpha-thalassemia: predicting genetic subgroups via laboratory parameters
pubmed · 42239965
Literaturverweis öffnenA case of epilepsy with myoclonic atonic seizures caused by SLC6A1 gene mutation due to balanced chromosomal translocation
pubmed · 36966012
Literaturverweis öffnenGenetic and Environmental Contributions to Antisocial Personality Disorder
doi · 10.20944/preprints202601.2358.v1
Literaturverweis öffnenClassifying the structural heterogeneity of peritoneal adhesions by histopathological extracellular matrix characteristics
pubmed · 42426329
Literaturverweis öffnenMüllerian Agenesis Presenting as Primary Amenorrhea in a 16-Year-Old Girl From a Low-Resource Setting in Bangladesh: Psychological Impact and Multidisciplinary Management
pubmed · 42434533
Literaturverweis öffnenPathogenesis of Melasma Explained
pubmed · 40022484
Literaturverweis öffnenInternational Consensus Definition and Diagnostic Criteria for Generalized Pustular Psoriasis From the International Psoriasis Council
pubmed · 38691347
Literaturverweis öffnenFamilial lymphoma and genetic predisposition: an updated review
pubmed · 42316213
Literaturverweis öffnenIndirect Exposure to Topical Minoxidil Causing Generalized Hypertrichosis in Children: A Report of Two Cases
pubmed · 41772750
Literaturverweis öffnenImmunopathogenesis and immunoregulatory mechanisms in allergic contact dermatitis
pubmed · 42212145
Literaturverweis öffnenDie paroxysmale nächtliche Hämoglobinurie - ein erworbener genetischer Defekt der hämatopoietischen Stammzelle<sup>*</sup>
pubmed · 7821202
Literaturverweis öffnenSMPD4 deficiency disrupts indirect neurogenesis and neuronal migration in gyrencephalic cortex
pubmed · 42389936
Literaturverweis öffnenCongenital Bilateral Complete Agenesis of the Hallucal Sesamoids: A Case Report
pubmed · 42152882
Literaturverweis öffnenFamily with probable achondrogenesis and lipid inclusions in fibroblasts
pubmed · 4120916
Literaturverweis öffnenAkutes kardiogenes Lungenödem: Stellenwert der nicht-invasiven Beatmung
pubmed · 17187320
Literaturverweis öffnen[Legasthenia from the genetic viewpoint].
pubmed · 6358770
Literaturverweis öffnenOverview of skin diseases linked to connexin gene mutations
pubmed · 23675785
Literaturverweis öffnenRegenerative Nanoscaffolds for Chronic Tympanic Membrane Perforation: From Bench to Clinical Translation
pubmed · 42363864
Literaturverweis öffnenTranscranial alternating current stimulation at 10 Hz promotes oligodendrogenesis and reduces g-ratio after cuprizone-induced demyelination
pubmed · 41907448
Literaturverweis öffnenA Novel Variant of CORO1A Gene Contributing to the Development of Primary Immunodeficiency in Children
pubmed · 42318436
Literaturverweis öffnenConnective tissue proteinases and inhibitors in abdominal aortic aneurysms. Involvement of the vasa vasorum in the pathogenesis of aortic aneurysms
pubmed · 1931869
Literaturverweis öffnenSkin Barrier Dysfunction in Acne Vulgaris: Pathogenesis and Therapeutic Approaches
pubmed · 39668545
Literaturverweis öffnenCurrarino syndrome: a comprehensive genetic review of a rare congenital disorder
pubmed · 33836786
Literaturverweis öffnenApigenin restores macrophage homeostasis and angiogenesis via Fgr/IL10 axis in recurrent spontaneous abortion.
pubmed · 42462890
Literaturverweis öffnenHypericum perforatum: a comprehensive review on pharmacognosy, preclinical studies, putative molecular mechanism, and clinical studies in neurodegenerative diseases
pubmed · 38175276
Literaturverweis öffnenInfektionen mit den humanpathogenen Mykoplasmenspezies M. genitalium und M. pneumoniae
pubmed · 40355732
Literaturverweis öffnenCongenital Hypoglossia With Craniofacial Anomalies Without Limb Defects: A Rare Phenotypic Variant of Oromandibular-Limb Hypogenesis Syndrome
pubmed · 42440826
Literaturverweis öffnen[Cat-scratch disease: historical, clinical, phylogenetic and taxonomic aspects].
pubmed · 9198973
Literaturverweis öffnenExome and Genome Sequencing to Diagnose the Genetic Basis of Neonatal Hypotonia: An International Consortium Study
pubmed · 39700446
Literaturverweis öffnen