Papers associated with hif1a

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	Characterization of a hypoxia-inducible factor (HIF-1alpha ) from rainbow trout. Accumulation of protein occurs at normal venous oxygen tension., Soitamo AJ, Rabergh CM, Gassmann M, Sistonen L, Nikinmaa M., J Biol Chem. June 8, 2001; 276 (23): 19699-705.
	Short upstream region drives dynamic expression of hypoxia-inducible factor 1alpha during Xenopus development., Sipe CW, Gruber EJ, Saha MS., Dev Dyn. June 1, 2004; 230 (2): 229-38.
	Kidney development and gene expression in the HIF2alpha knockout mouse., Steenhard BM, Freeburg PB, Isom K, Stroganova L, Borza DB, Hudson BG, St John PL, Zelenchuk A, Abrahamson DR., Dev Dyn. April 1, 2007; 236 (4): 1115-25.
	Molecular cloning and characterization of the Xenopus hypoxia-inducible factor 1alpha (xHIF1alpha)., de Beaucourt A, Coumailleau P., J Cell Biochem. December 15, 2007; 102 (6): 1542-52.
	HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus., Nagao K, Taniyama Y, Kietzmann T, Doi T, Komuro I, Morishita R., J Biol Chem. April 25, 2008; 283 (17): 11841-9.
	Faulty old ideas about translational regulation paved the way for current confusion about how microRNAs function., Kozak M., Gene. November 1, 2008; 423 (2): 108-15.
	Gene expression profiles in Rana pirica tadpoles following exposure to a predation threat., Mori T, Yanagisawa Y, Kitani Y, Sugiyama M, Kishida O, Nishimura K., BMC Genomics. April 2, 2015; 16 258.
	Nutrient-Deprived Retinal Progenitors Proliferate in Response to Hypoxia: Interaction of the HIF-1 and mTOR Pathway., Khaliullina H, Love NK, Harris WA., J Dev Biol. June 1, 2016; 4 (2):
	Aberrant regulation of Wnt signaling in hepatocellular carcinoma., Liu LJ, Xie SX, Chen YT, Xue JL, Zhang CJ, Zhu F., World J Gastroenterol. September 7, 2016; 22 (33): 7486-99.
	Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors., Kaminski MM, Tosic J, Kresbach C, Engel H, Klockenbusch J, Müller AL, Pichler R, Grahammer F, Kretz O, Huber TB, Walz G, Arnold SJ, Lienkamp SS., Nat Cell Biol. December 1, 2016; 18 (12): 1269-1280.
	The myeloid lineage is required for the emergence of a regeneration-permissive environment following Xenopus tail amputation., Aztekin C, Hiscock TW, Butler R, De Jesús Andino F, Robert J, Gurdon JB, Jullien J., Development. February 5, 2020; 147 (3):
	Predation threats for a 24-h period activated the extension of axons in the brains of Xenopus tadpoles., Mori T, Kitani Y, Hatakeyama D, Machida K, Goto-Inoue N, Hayakawa S, Yamamoto N, Kashiwagi K, Kashiwagi A., Sci Rep. July 16, 2020; 10 (1): 11737.
	Transcriptional regulatory elements of hif1α in a distal locus of islet1 in Xenopus laevis., Miyakawa M, Katada T, Numa Y, Kinoshita T., Comp Biochem Physiol B Biochem Mol Biol. January 1, 2021; 255 110598.
	Hif1α and Wnt are required for posterior gene expression during Xenopus tropicalis tail regeneration., Patel JH, Schattinger PA, Takayoshi EE, Wills AE., Dev Biol. March 1, 2022; 483 157-168.
	Identification of pharmacological inducers of a reversible hypometabolic state for whole organ preservation., Sperry MM, Charrez B, Fotowat H, Gardner E, Pilobello K, Izadifar Z, Lin T, Kuelker A, Kaki S, Lewandowski M, Lightbown S, Martinez R, Marquez S, Moore J, Plaza-Oliver M, Sesay AM, Shcherbina K, Sheehan K, Takeda T, Del Campo D, Andrijauskaite K, Cisneros E, Lopez R, Cano I, Maxwell Z, Jessop I, Veraza R, Bunegin L, Percival TJ, Yracheta J, Pena JJ, Wood DM, Homas ZT, Hinshaw CJ, Cox-Hinshaw J, Parry OG, Sleeter JJ, Weitzel EK, Levin M, Super M, Novak R, Ingber DE., Elife. September 24, 2024; 13
	Deletion of sf3b4 causes splicing defects and gene dysregulation that disrupt craniofacial development and survival., Griffin C, Coppenrath K, Khan D, Lin Z, Horb M, Saint-Jeannet JP., Dis Model Mech. March 1, 2025; 18 (3):

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