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  1. 1.   Fgf8 promotes survival of nephron progenitors by regulating BAX/BAK-mediated apoptosis
  2. Anderson,Matthew; Misaghian, Salvia; Sharma,Nirmala; Perantoni,Alan; Lewandoski,Mark
  3. Differentiation; research in biological diversity. 2022, Dec 06; 130: 7-15.
  1. 2.   Inactivation of Fgf3 and Fgf4 within the Fgf3/Fgf4/Fgf15 gene cluster reveals their redundant requirement for mouse inner ear induction and embryonic survival
  2. Zelarayan, Laura; Vendrell, Victor; Domínguez-Frutos, Elena; López-Hernández, Iris; Schimmang-Alonso, Kiril; Alonso, María Teresa; Alvarez, Yolanda; Maier, Hannes; Anderson,Matthew; Lewandoski,Mark; Schimmang, Thomas
  3. Developmental dynamics : an official publication of the American Association of Anatomists. 2021, Nov 12;
  1. 3.   The Fgf8 subfamily (Fgf8, Fgf17 and Fgf18) is required for closure of the embryonic ventral body wall
  2. Boylan,Michael; Anderson,Matthew; Ornitz, David M; Lewandoski,Mark
  3. Development (Cambridge, England). 2020, NOV; 147(21): pii: dev.189506.
  1. 4.   The G-Protein-Coupled Chemoattractant Receptor Fpr2 Exacerbates High Glucose-Mediated Proinflammatory Responses of Müller Glial Cells
  2. Yu, Ying; Bao, Zhiyao; Wang, Xiaofei; Gong, Wang; Chen, Hui; Guan, Huaijin; Le, Yingying; Su, Shaobo; Chen, Keqiang; Wang, Jiming
  3. Frontiers in Immunology. 2017, Dec 19; 8: 1852.
  1. 5.   Examination of Potential Modifiers of the Association of APOL1 Alleles with CKD Progression.
  2. Chen, Teresa K; Choi, Michael J; Kao, W H Linda; Astor, Brad C; Scialla, Julia J; Appel, Lawrence J; Li, Liang; Lipkowitz, Michael S; Wolf, Myles; Parekh, Rulan S; Winkler, Cheryl; Estrella, Michelle M; Crews, Deidra C
  3. Clinical journal of the American Society of Nephrology : CJASN. 2015, Dec 7; 10(12): 2128-35.
  1. 6.   Oncogenic met receptor induces cell-cycle progression in Xenopus oocytes independent of direct Grb2 and shc binding or Mos synthesis, but requires phosphatidylinositol 3-kinase and Raf signaling
  2. Mood, K.; Saucier, C.; Ishimura, A.; Bong, Y. S.; Lee, H. S.; Park, M.; Daar, I. O.
  3. Journal of Cellular Physiology. 2006, APR; 207(1): 271-285.
  1. 7.   Adrenomedullin is a cross-talk molecule that regulates tumor and mast cell function during human carcinogenesis
  2. Zudaire, E.; Martinez, A.; Garayoa, M.; Pio, R.; Kaur, G.; Woolhiser, M. R.; Metcalfe, D. D.; Hook, W. A.; Siraganian, R. P.; Guise, T. A.; Chirgwin, J. M.; Cuttitta, F.
  3. American Journal of Pathology. 2006, JAN; 168(1): 280-291.
  1. 8.   FGFR1 function at the earliest stages of mouse limb development plays an indispensable role in subsequent autopod morphogenesis
  2. Li, C. L.; Xu, X. L.; Nelson, D. K.; Williams, T.; Kuehn, M. R.; Deng, C. X.
  3. Development. 2005, NOV; 132(21): 4755-4764.
  1. 9.   Conditional inactivation of Fgfr1 in mouse defines its role in limb bud establishment, outgrowth and digit patterning
  2. Verheyden, J. M.; Lewandoski, M.; Deng, C. X.; Harfe, B. D.; Sun, X.
  3. Development. 2005, OCT; 132(19): 4235-4245.
  1. 10.   Tyr-298 in ephrinB1 is critical for an interaction with the Grb4 adaptor protein
  2. Bong, Y. S.; Park, Y. H.; Lee, H. S.; Mood, K.; Ishimura, A.; Daar, I. O.
  3. Biochemical Journal. 2004 377(Part 2): 499-507.
  1. 11.   Inhibition of FGF signaling causes expansion of the endoderm in Xenopus
  2. Cha, S. W.; Hwang, Y. S.; Chae, J. P.; Lee, S. Y.; Lee, H. S.; Daar, I.; Park, M. J.; Kim, J.
  3. Biochemical and Biophysical Research Communications. 2004 315(1): 100-106.
  1. 12.   Docking protein SNT1 is a critical mediator of fibroblast growth factor signaling during Xenopus embryonic development
  2. Akagi, K.; Park, E. K.; Mood, K.; Daar, I. O.
  3. Developmental Dynamics. 2002 223(2): 216-228.
  1. 13.   Involvement of BMP-4/msx-1 and FGF pathways in neural induction in the Xenopus embryo
  2. Ishimura, A.; Maeda, R.; Takeda, M.; Kikkawa, M.; Daar, I. O.; Maeno, M.
  3. Development Growth & Differentiation. 2000 42(4): 307-316.
  1. 14.   Comparisons of genomic structures and chromosomal locations of the mouse aldose reductase and aldose reductase-like genes
  2. Ho, H. T. B.; Jenkins, N. A.; Copeland, N. G.; Gilbert, D. J.; Winkles, J. A.; Louie, H. W. Y.; Lee, F. K.; Chung, S. S. M.; Chung, S. K.
  3. European Journal of Biochemistry. 1999 259(3): 726-730.
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