These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

86 related articles for article (PubMed ID: 29938988)

  • 21. Congenital lymphatic malformations.
    Blei F
    Ann N Y Acad Sci; 2008; 1131():185-94. PubMed ID: 18519970
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [A neonate with the heart in the right hemithorax].
    van der Feen C; van Oort AM; Pelleboer RA
    Ned Tijdschr Geneeskd; 2006 Dec; 150(49):2681-5. PubMed ID: 17194001
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Vegfd modulates both angiogenesis and lymphangiogenesis during zebrafish embryonic development.
    Bower NI; Vogrin AJ; Le Guen L; Chen H; Stacker SA; Achen MG; Hogan BM
    Development; 2017 Feb; 144(3):507-518. PubMed ID: 28087639
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Comparison of molecular determinants of angiogenesis and lymphangiogenesis in lymph node metastases and in primary tumours of patients with breast cancer.
    Van den Eynden GG; Van der Auwera I; Van Laere SJ; Trinh XB; Colpaert CG; van Dam P; Dirix LY; Vermeulen PB; Van Marck EA
    J Pathol; 2007 Sep; 213(1):56-64. PubMed ID: 17674348
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Lysyl oxidase expression is decreased in the developing diaphragm and lungs of nitrofen-induced congenital diaphragmatic hernia.
    Takahashi T; Friedmacher F; Takahashi H; Daniel Hofmann A; Puri P
    Eur J Pediatr Surg; 2015 Feb; 25(1):15-9. PubMed ID: 25111273
    [TBL] [Abstract][Full Text] [Related]  

  • 26. PELVIS Syndrome.
    Girard C; Bigorre M; Guillot B; Bessis D
    Arch Dermatol; 2006 Jul; 142(7):884-8. PubMed ID: 16847205
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Abnormal lung development in congenital diaphragmatic hernia.
    Ameis D; Khoshgoo N; Keijzer R
    Semin Pediatr Surg; 2017 Jun; 26(3):123-128. PubMed ID: 28641748
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Trisomy 18 syndrome with incomplete Cantrell syndrome.
    Hou YJ; Chen FL; Ng YY; Hu JM; Chen SJ; Chen JY; Su PH
    Pediatr Neonatol; 2008 Jun; 49(3):84-7. PubMed ID: 18947004
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Congenital diaphragmatic hernia: where and what is the evidence?
    Losty PD
    Semin Pediatr Surg; 2014 Oct; 23(5):278-82. PubMed ID: 25459012
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Congenital diaphragmatic hernia. A cause of persistent pulmonary hypertension of the newborn which lacks an effective therapy.
    Thébaud B; Mercier JC; Dinh-Xuan AT
    Biol Neonate; 1998 Nov; 74(5):323-36. PubMed ID: 9742261
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Possible responsibility of EDNRA gene triplication, coding for the endothelin 1 ET-A receptor in a case of congenital diaphragmatic hernia].
    Masson L; Houfflin-Debarge V; Petit F; Vaast P; Coulon C
    J Gynecol Obstet Biol Reprod (Paris); 2015 Apr; 44(4):387-90. PubMed ID: 24842646
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Maspin overexpression correlates with increased expression of vascular endothelial growth factors A, C, and D in human ovarian carcinoma.
    Bolat F; Gumurdulu D; Erkanli S; Kayaselcuk F; Zeren H; Ali Vardar M; Kuscu E
    Pathol Res Pract; 2008; 204(6):379-87. PubMed ID: 18343598
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Increased fetal nuchal translucency as a predictor of Cantrell's pentology--case report].
    Staboulidou I; Wüstemann M; Schmidt P; Günter HH; Scharf A
    Z Geburtshilfe Neonatol; 2005 Dec; 209(6):231-4. PubMed ID: 16395641
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genome-wide enrichment of damaging de novo variants in patients with isolated and complex congenital diaphragmatic hernia.
    Longoni M; High FA; Qi H; Joy MP; Hila R; Coletti CM; Wynn J; Loscertales M; Shan L; Bult CJ; Wilson JM; Shen Y; Chung WK; Donahoe PK
    Hum Genet; 2017 Jun; 136(6):679-691. PubMed ID: 28303347
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Baller-Gerold syndrome associated with dextrocardia.
    Ceylan A; Peker E; Dogan M; Tuncer O; Kirimi E
    Genet Couns; 2011; 22(1):69-74. PubMed ID: 21614991
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The relationship of diaphragmatic defect, liver growth, and lung hypoplasia in nitrofen-induced congenital diaphragmatic hernia in the rat.
    Langwieler T; Fiegel HC; Alaamian M; Mann O; Beshir I; Izbicki JR; Kluth D
    Pediatr Surg Int; 2004 Jul; 20(7):509-14. PubMed ID: 15221367
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Tie2Cre-mediated inactivation of plexinD1 results in congenital heart, vascular and skeletal defects.
    Zhang Y; Singh MK; Degenhardt KR; Lu MM; Bennett J; Yoshida Y; Epstein JA
    Dev Biol; 2009 Jan; 325(1):82-93. PubMed ID: 18992737
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Congenital diaphragmatic hernia.
    Bell MJ
    J Maine Med Assoc; 1973 Sep; 64(9):211-4. PubMed ID: 4747210
    [No Abstract]   [Full Text] [Related]  

  • 39. [Hydrometrocolpos, polydactylia and congenital heart defect (the McKusick-Dungy-Kaufman syndrome)].
    Hamel BC; ter Haar BG
    Tijdschr Kindergeneeskd; 1984 Aug; 52(4):129-33. PubMed ID: 6495304
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Muscle connective tissue controls development of the diaphragm and is a source of congenital diaphragmatic hernias.
    Merrell AJ; Ellis BJ; Fox ZD; Lawson JA; Weiss JA; Kardon G
    Nat Genet; 2015 May; 47(5):496-504. PubMed ID: 25807280
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.