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  1. 2641
    “…As the pancreas and gut share the same embryological origin and produce insulin, we will also discuss the possible application of gut organoids for diabetes therapy. …”
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    Recent advances in organoid culture for insulin production and diabetes therapy: methods and challenges
  2. 2642
    “…Retrorectal cystic hamartomas, or tailgut cysts, are complex congenital cystic lesions which arise from embryologic tissues. Fewer than 200 cases have been reported worldwide, with women outnumbering men by 3:1. …”
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    Laparoscopic approach to tailgut cyst (retrorectal cystic hamartoma)
  3. 2643
    “…The urachus is the embryological remnant of the allantois, which connects the apex of the bladder to the umbilicus, and usually fully obliterates to become the median umbilical ligament. …”
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    The primary considerations and image guided diagnosis of an infected urachal cyst in a pediatric patient
  4. 2644
    por Sarkar, Taranika, Jagroop, Sophia
    Publicado 2020
    “…Pancreatic Divisum (PD) is the most common congenital variation of pancreatic duct anatomy, arising when embryological ventral and dorsal endodermal buds fail to fuse (“classic” PD) or only fuse partially (“incomplete” PD). …”
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    A Case of Late Presentation of Pancreatic Divisum in a Patient with Recurrent Pancreatitis
  5. 2645
    “…We found that these more efficient schemes complete reliable cell fate decisions within the short embryological timescales. We discuss the influence of promoter architectures on decision times and error rates, present concrete examples that rapidly readout the morphogen, and predictions for new experiments. …”
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    A mechanism for hunchback promoters to readout morphogenetic positional information in less than a minute
  6. 2646
    “…BACKGROUND: Congenital portosystemic shunts are embryological malformations in which portal venous flow is diverted to the systemic circulation. …”
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    Congenital portosystemic shunt occlusion with an Amplatzer PFO occlusion device: a case report
  7. 2647
    “…Here, we highlight and review developmental and genetic aspects of the cranial base, including its transition from cartilage to bone, dual embryological origins, and vignettes of transcription factors controlling its formation.…”
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    The Skull’s Girder: A Brief Review of the Cranial Base
  8. 2648
    “…Also, significant discoveries including new embryological molecular genetic transcription factors, the role of active placental mineral transport, and hormone regulation factors have changed the understanding of calcium and phosphate homeostasis in the fetus and the newborn. …”
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    Endocrine Diseases of Newborn: Epidemiology, Pathogenesis, Therapeutic Options, and Outcome “Current Insights Into Disorders of Calcium and Phosphate in the Newborn”
  9. 2649
    “…Neurovascular surgeons need to understand the variations of the NRILN associated with congenital cardiovascular anomalies and effective use of intraoperative nerve monitoring (IONM). We discuss the embryological origin, IONM, and surgical pitfalls of this case.…”
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    Carotid Endarterectomy for a Patient with a Right-sided Aortic Arch and Aberrant Left Subclavian Artery Predicting a Left Non-recurrent Inferior Laryngeal Nerve: A Case Report and Literature Review
  10. 2650
    “…Classic embryological experiments have established that the early mouse embryo develops via sequential lineage bifurcations. …”
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    Human naive epiblast cells possess unrestricted lineage potential
  11. 2651
    “…Persistent embryological connections between the anterior and posterior circulations are rare entities. …”
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    Endovascular management of dissecting posterior cerebral artery aneurysm associated with persistent hypoglossal artery: A case report
  12. 2652
    “…Although PPL has been shown to be different from classical primary central nervous system lymphoma because of the embryological origin of structures, individual and precise treatment of PPL remains unknown. …”
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    Case Report: Identification of Potential Prognosis-Related TP53 Mutation and BCL6-LPP Fusion in Primary Pituitary Lymphoma by Next Generation Sequencing: Two Cases
  13. 2653
    “…The Cattell–Braasch–Valdoni maneuver (right-sided medial visceral mobilization and intestinal derotation maneuver) restores the embryological twist of the duodenojejunal junction, which demystifies the distorted peripancreatic vascular anatomy and facilitates a safe and radical “mesopancreas-first” pancreatic head cancer resection. …”
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    “Mesopancreas-first” radical resection of pancreatic head cancer following the Cattell–Braasch–Valdoni maneuver: Appreciating the legacy of pioneers in visceral surgery
  14. 2654
    “…As we will demonstrate in this article, shared anomalies are influenced, and in some cases solely and sequentially explained, by interaction aplasia and neo‐axial orientation; two embryological mechanisms to which each set of conjoined twins is subjected and are responsible for their ultimate phenotypical fate. …”
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    Characterizing the coalescence area of conjoined twins to elucidate congenital disorders in singletons
  15. 2655
    “…Fibropolycystic liver disease encompasses a spectrum of related liver and biliary tract lesions caused by abnormal embryologic development of the ductal plates. These disorders include congenital hepatic fibrosis, biliary hamartomas, polycystic liver disease (PCLD), choledochal cysts, and Carolis disease. …”
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    Apixaban Causing Hepatic Cystic Bleeding: A Rare but a Life-Threatening Complication
  16. 2656
    “…Tailgut cysts are rare developmental cysts arising from remnants of the embryological postnatal gut. Despite being frequently located in the presacral space, isolated cases of aberrant locations have been reported, including, perirenal, perianal, and subcutaneous sites, with only two cases of subdural tailgut cysts reported to date. …”
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    Isolated lumbar intradural tailgut cyst: A case report and review of the literature
  17. 2657
    “…In this review, the outcomes from the published literature in the past 10 years on the effects of AFB1 pathophysiological mechanisms on embryological and fetal development are discussed. In several animal species, including humans, AFB1 has a teratogenic effect(,) resulting in bone malformations, visceral anomalies, lesions in several organs, and behavioral and reproductive changes, in addition to low birth weight. …”
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    Effects of Prenatal Exposure to Aflatoxin B1: A Review
  18. 2658
    “…In this review, we summarize recent findings on the embryological development of the cardiovascular system and the pathogenesis and treatment of cardiovascular disease, as revealed by scRNA-seq technology. …”
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    Applications of Single-Cell RNA Sequencing in Cardiovascular Research
  19. 2659
    “…Kommerell’s Diverticulum (KD) is a rare congenital anomaly caused by a persistent remnant of the fourth primitive dorsal arch during embryological development. Although the prevalence of KD is rare, it is important to identify and diagnose this condition to provide definitive care.…”
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    No Pain and No Gain: Kommerell’s Diverticulum with a Right-Sided Aortic Arch, and an Aberrant Left Subclavian Artery Presenting in a Body Builder with Muscle Bulk Imbalance
  20. 2660
    “…The eustachian valve (EV) is a vestigial structure found at the junction of the inferior vena cava and the right atrium, a remnant of the embryological sinus venosus that may persist throughout life. …”
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    A Rare Case of Eustachian Valve Endocarditis in a Young Male With Poorly Controlled Type 1 Diabetes Mellitus
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