This is a Validated Antibody Database (VAD) review about cow STAT5A, based on 48 published articles (read how Labome selects the articles), using STAT5A antibody in all methods. It is aimed to help Labome visitors find the most suited STAT5A antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
STAT5A synonym: STAT5A/MGF; STATA5; signal transducer and activator of transcription 5A; STAT5A, Mammary Gland Factor; mammary gland factor; signal transducer and activator of transcription factor 5A

Invitrogen
rabbit polyclonal
  • immunohistochemistry - paraffin section; mouse; 1:100; loading ...; fig 4g
  • western blot; mouse; 1:1000; loading ...; fig 4a
In order to investigate estrogen receptor alpha positive breast cancer, Invitrogen STAT5A antibody (Invitrogen, 71-6900) was used in immunohistochemistry - paraffin section on mouse samples at 1:100 (fig 4g) and in western blot on mouse samples at 1:1000 (fig 4a). Breast Cancer Res (2017) ncbi
rabbit polyclonal
  • western blot; human; loading ...; fig 1a
In order to determine the molecular mechanisms that enable JAK2/signal transducer and activator of transcription 5 to access promoters of genes implicated in breast cancer pathogenesis, Invitrogen STAT5A antibody (Invitrogen, 71-6900) was used in western blot on human samples (fig 1a). J Biol Chem (2017) ncbi
rabbit polyclonal
  • western blot; human; loading ...; fig 2c
In order to explore the extracellular matrix features that control prolactin signals, Invitrogen STAT5A antibody (Invitrogen, 71-6900) was used in western blot on human samples (fig 2c). Oncotarget (2016) ncbi
rabbit polyclonal
  • immunohistochemistry - free floating section; rat; 1:100
In order to examine the daily rhythm of STAT3 protein, Invitrogen STAT5A antibody (Invitrogen, 71-6900) was used in immunohistochemistry - free floating section on rat samples at 1:100. J Neurosci Res (2016) ncbi
rabbit polyclonal
  • immunohistochemistry - paraffin section; mouse; 1:100; fig 5
  • western blot; mouse; 1:10000; fig 5
In order to elucidate the molecular mechanisms involved in the upregulation of ABCG2 during lactation, Invitrogen STAT5A antibody (Invitrogen, 71-6900) was used in immunohistochemistry - paraffin section on mouse samples at 1:100 (fig 5) and in western blot on mouse samples at 1:10000 (fig 5). Am J Physiol Endocrinol Metab (2014) ncbi
rabbit polyclonal
  • chromatin immunoprecipitation; mouse
In order to study the regulation of growth hormone stimulated genes, Invitrogen STAT5A antibody (Invitrogen, 71-6900) was used in chromatin immunoprecipitation on mouse samples . Mol Cell Endocrinol (2014) ncbi
rabbit polyclonal
  • immunohistochemistry - paraffin section; mouse
  • western blot; mouse; 1:1000
In order to report that image analysis decreased inter-observer variability when scoring immunohistologically stained human hepatocellular patient samples, Invitrogen STAT5A antibody (Invitrogen, #71-6900) was used in immunohistochemistry - paraffin section on mouse samples and in western blot on mouse samples at 1:1000. PLoS ONE (2014) ncbi
rabbit polyclonal
  • western blot; human
In order to study the involvement of collagen matrices in tumorigenic prolactin signaling in breast cancer cells, Invitrogen STAT5A antibody (Invitrogen, 71-6900) was used in western blot on human samples . J Biol Chem (2013) ncbi
rabbit polyclonal
  • western blot; human; 1:4000; fig 3
In order to elucidate the role of the lactogenic hormone prolactin in the regulation of ABCG2, Invitrogen STAT5A antibody (Invitrogen, 71-6900) was used in western blot on human samples at 1:4000 (fig 3). Mol Pharmacol (2013) ncbi
rabbit polyclonal
  • western blot; mouse; fig 2
In order to determine the roles of growth hormone and STAT5 in metabolism and liver cancer onset, Invitrogen STAT5A antibody (Invitrogen, 71-6900) was used in western blot on mouse samples (fig 2). Hepatology (2011) ncbi
rabbit polyclonal
  • western blot; mouse; fig 7
In order to test if Jak2 contributes to Ang II-mediated neointima formation following vascular injury, Invitrogen STAT5A antibody (Invitrogen, 716900) was used in western blot on mouse samples (fig 7). J Mol Cell Cardiol (2011) ncbi
rabbit polyclonal
  • western blot; human; fig 1
In order to study the role of Stat5 serine phosphorylation in oncogenesis, Invitrogen STAT5A antibody (Zymed, 71-6900) was used in western blot on human samples (fig 1). Blood (2010) ncbi
rabbit polyclonal
  • western blot; mouse
In order to determine the role of STAT5 in liver fibrogenesis, Invitrogen STAT5A antibody (Invitrogen, 71-6900) was used in western blot on mouse samples . Hepatology (2010) ncbi
rabbit polyclonal
In order to determine the extent to which JAK2 and Src family kinases mediate GH-mediated activation of STAT1, 3, and 5a/b, ERKs 1 and 2, and Akt, Invitrogen STAT5A antibody (Zymed Laboratories, 71-6900) was used . Mol Endocrinol (2008) ncbi
rabbit polyclonal
In order to assess the role of FAK in mammary epithelial cells in vivo, Invitrogen STAT5A antibody (Zymed Laboratories, 71-6900) was used . J Biol Chem (2007) ncbi
rabbit polyclonal
In order to examine the consequences of Stat5 crosstalk with the glucocorticoid receptor in hepatocytes, Invitrogen STAT5A antibody (Zymed, 71-6900) was used . Genes Dev (2007) ncbi
rabbit polyclonal
In order to examine STAT3 following resistance exercise in human skeletal muscle, Invitrogen STAT5A antibody (Zymed, 71-6900) was used . J Appl Physiol (1985) (2007) ncbi
rabbit polyclonal
In order to propose that Stat5 tetramers are associated with leukemogenesis, Invitrogen STAT5A antibody (Zymed, 71-6900) was used . Cancer Cell (2005) ncbi
rabbit polyclonal
In order to assess GH receptor expression and signal transduction and the effect of GH and IGF-I exposure on cell proliferation and hormone secretion in nonfunctioning pituitary adenomas, Invitrogen STAT5A antibody (ZYMED, 71-6900) was used . Clin Endocrinol (Oxf) (2004) ncbi
rabbit polyclonal
In order to examine the expression, tyrosine phosphorylation status and nuclear localization of Stat5a in human breast cancers, Invitrogen STAT5A antibody (Zymed, 71-6900) was used . Int J Cancer (2004) ncbi
rabbit polyclonal
In order to study T cell responses in the presence of IL-2 and IL-15, Invitrogen STAT5A antibody (Zymed, 71-6900) was used . Proc Natl Acad Sci U S A (2003) ncbi
rabbit polyclonal
In order to test if a mimic of phosphorylated human prolactin, S179D-PRL, initiates signaling in mammary tumor cells alone and in combination with unmodified prolactin, Invitrogen STAT5A antibody (Zymed, 71-6900) was used . Endocrinology (2003) ncbi
rabbit polyclonal
In order to study the role of p21-activated kinase in the mammary gland, Invitrogen STAT5A antibody (Zymed, 71?C6900) was used . J Cell Biol (2003) ncbi
rabbit polyclonal
In order to investigate the role of STATs and PRL receptors in TGFalpha-induced mammary epithelial abnormalities in vivo, Invitrogen STAT5A antibody (Zymed Labs, 71-6900) was used . Mol Cell Endocrinol (2001) ncbi
Cell Signaling Technology
rabbit monoclonal (D47E7)
  • western blot; mouse; loading ...; fig 5b
Cell Signaling Technology STAT5A antibody (Cell Signaling, 4322) was used in western blot on mouse samples (fig 5b). Blood (2018) ncbi
rabbit monoclonal (D47E7)
  • western blot; mouse; 1:1000; loading ...; fig s1h
Cell Signaling Technology STAT5A antibody (Cell Signaling, 4322T) was used in western blot on mouse samples at 1:1000 (fig s1h). Nat Commun (2018) ncbi
rabbit monoclonal (D47E7)
  • western blot; human; 1:1000; loading ...; fig 1d
Cell Signaling Technology STAT5A antibody (Cell Signaling Technologies, 4322) was used in western blot on human samples at 1:1000 (fig 1d). Nat Commun (2018) ncbi
rabbit monoclonal (D47E7)
  • western blot; human; loading ...; fig 3h, 3i
Cell Signaling Technology STAT5A antibody (Cell Signaling, 4322P) was used in western blot on human samples (fig 3h, 3i). J Exp Med (2018) ncbi
rabbit monoclonal (D47E7)
  • western blot; mouse; 1:1000; loading ...; fig 2a
Cell Signaling Technology STAT5A antibody (Cell signaling, 4322) was used in western blot on mouse samples at 1:1000 (fig 2a). Biochem Biophys Res Commun (2018) ncbi
rabbit monoclonal (D47E7)
  • western blot; mouse; fig s9c
In order to investigate the effect of lymphatic endothelial S1P on mitochondrial function and naive T cell survival, Cell Signaling Technology STAT5A antibody (Cell Signaling, D47E7) was used in western blot on mouse samples (fig s9c). Nature (2017) ncbi
rabbit monoclonal (D47E7)
  • western blot; mouse; 1:400; loading ...; fig 3c
Cell Signaling Technology STAT5A antibody (Cell Signaling Technology, D47E7) was used in western blot on mouse samples at 1:400 (fig 3c). J Clin Invest (2017) ncbi
rabbit monoclonal (D47E7)
  • western blot; mouse; loading ...
In order to assess if aerobic glycolysis and glutaminolysis co-operatively reduce UDP-GlcNAc biosynthesis and N-glycan branching in mouse T cell blasts, Cell Signaling Technology STAT5A antibody (Cell Signaling, D47E7) was used in western blot on mouse samples . elife (2017) ncbi
rabbit monoclonal (D47E7)
  • western blot; human; loading ...; fig 4
Cell Signaling Technology STAT5A antibody (Cell Signaling Technology, D47E7) was used in western blot on human samples (fig 4). Oncotarget (2016) ncbi
rabbit monoclonal (D47E7)
  • western blot; mouse; fig 3h
  • western blot; human; fig s4b
In order to test if modulation of Rho-associated kinase 2 alters the generation of T follicular helper cells, Cell Signaling Technology STAT5A antibody (Cell Signaling, 4322S) was used in western blot on mouse samples (fig 3h) and in western blot on human samples (fig s4b). Sci Signal (2016) ncbi
rabbit monoclonal (D47E7)
  • western blot; human; fig s3a
In order to investigate the role of growth hormone in colon cancer, Cell Signaling Technology STAT5A antibody (Cell Signaling, 4322) was used in western blot on human samples (fig s3a). Proc Natl Acad Sci U S A (2016) ncbi
rabbit monoclonal (D47E7)
  • western blot; mouse; fig 1
In order to characterize induction of lactation-specific tight junctions concurrent with beta-casein expression in mammary epithelial cells due to prolactin and glucocorticoid signaling, Cell Signaling Technology STAT5A antibody (Cell Signalling, 4322) was used in western blot on mouse samples (fig 1). Biochim Biophys Acta (2016) ncbi
rabbit monoclonal (D47E7)
  • western blot; human; loading ...; fig 5a
Cell Signaling Technology STAT5A antibody (Ozyme, 4322) was used in western blot on human samples (fig 5a). Oncotarget (2016) ncbi
rabbit monoclonal (D47E7)
  • western blot; human; fig 2
In order to test whether the CCL20-CCR6 interaction is functional in metastatic cutaneous T cell lymphoma cells, Cell Signaling Technology STAT5A antibody (Cell Signaling, 4322) was used in western blot on human samples (fig 2). Oncotarget (2016) ncbi
rabbit monoclonal (D47E7)
  • western blot; mouse; 1:1000; fig 2
Cell Signaling Technology STAT5A antibody (cell Signaling Tech, 4322) was used in western blot on mouse samples at 1:1000 (fig 2). Sci Rep (2016) ncbi
rabbit monoclonal (D47E7)
  • western blot; mouse; fig 6
In order to characterize prolactin receptor signaling for mammary gland development by a novel nectin-mediated cell adhesion apparatus, Cell Signaling Technology STAT5A antibody (Cell signaling, 4322) was used in western blot on mouse samples (fig 6). J Biol Chem (2016) ncbi
rabbit monoclonal (D47E7)
  • western blot; mouse; fig 4
Cell Signaling Technology STAT5A antibody (Cell Signaling, 4322) was used in western blot on mouse samples (fig 4). J Biol Chem (2015) ncbi
rabbit monoclonal (D47E7)
  • western blot; human; fig 5d
In order to identify factors that contribute to mycosis fungoides pathogenesis, Cell Signaling Technology STAT5A antibody (Cell Signaling, 4322) was used in western blot on human samples (fig 5d). Blood (2015) ncbi
rabbit monoclonal (D47E7)
  • western blot; human; 1:1000; fig 4
Cell Signaling Technology STAT5A antibody (Cell signaling, 4322) was used in western blot on human samples at 1:1000 (fig 4). Front Microbiol (2015) ncbi
rabbit monoclonal (D47E7)
  • flow cytometry; mouse; fig s11a
In order to assess the effects of Hspa9 haploinsufficiency on hematopoiesis using zebrafish, Cell Signaling Technology STAT5A antibody (Cell Sig Tech, 4322) was used in flow cytometry on mouse samples (fig s11a). Exp Hematol (2015) ncbi
rabbit monoclonal (D47E7)
  • western blot; human; loading ...; fig 4b
In order to investigate the role of GNB1 and GNB2 in cancer cells., Cell Signaling Technology STAT5A antibody (Cell signaling, 4322) was used in western blot on human samples (fig 4b). Nat Med (2015) ncbi
rabbit monoclonal (D47E7)
  • western blot; mouse
In order to study the role of prolactin and STAT5 during early prostate tumorigenesis, Cell Signaling Technology STAT5A antibody (Cell Signaling Technology, 4322) was used in western blot on mouse samples . Am J Pathol (2014) ncbi
EMD Millipore
rabbit monoclonal (A11W)
  • western blot; human; tbl s3
EMD Millipore STAT5A antibody (Millipore, A11W) was used in western blot on human samples (tbl s3). Cell Death Dis (2015) ncbi
rabbit monoclonal (A11W)
  • western blot; human
EMD Millipore STAT5A antibody (Upstate / Millipore, 05-886) was used in western blot on human samples . Leukemia (2013) ncbi
Articles Reviewed
  1. Chorzalska A, Morgan J, Ahsan N, Treaba D, Olszewski A, Petersen M, et al. Bone marrow-specific loss of ABI1 induces myeloproliferative neoplasm with features resembling human myelofibrosis. Blood. 2018;: pubmed publisher
  2. Zhang C, Wang C, Jiang M, Gu C, Xiao J, Chen X, et al. Act1 is a negative regulator in T and B cells via direct inhibition of STAT3. Nat Commun. 2018;9:2745 pubmed publisher
  3. Ng S, Yoshida N, Christie A, Ghandi M, Dharia N, Dempster J, et al. Targetable vulnerabilities in T- and NK-cell lymphomas identified through preclinical models. Nat Commun. 2018;9:2024 pubmed publisher
  4. Khalil S, Delehanty L, Grado S, Holy M, White Z, Freeman K, et al. Iron modulation of erythropoiesis is associated with Scribble-mediated control of the erythropoietin receptor. J Exp Med. 2018;215:661-679 pubmed publisher
  5. Kim H, Kim H, Kim K, German M, Kim H. Ectopic serotonin production in β-cell specific transgenic mice. Biochem Biophys Res Commun. 2018;495:1986-1991 pubmed publisher
  6. Mendoza A, Fang V, Chen C, Serasinghe M, Verma A, Muller J, et al. Lymphatic endothelial S1P promotes mitochondrial function and survival in naive T cells. Nature. 2017;546:158-161 pubmed publisher
  7. Barcus C, O Leary K, Brockman J, Rugowski D, Liu Y, Garcia N, et al. Elevated collagen-I augments tumor progressive signals, intravasation and metastasis of prolactin-induced estrogen receptor alpha positive mammary tumor cells. Breast Cancer Res. 2017;19:9 pubmed publisher
  8. Hirai M, Arita Y, McGlade C, Lee K, Chen J, Evans S. Adaptor proteins NUMB and NUMBL promote cell cycle withdrawal by targeting ERBB2 for degradation. J Clin Invest. 2017;127:569-582 pubmed publisher
  9. Araujo L, Khim P, Mkhikian H, Mortales C, Demetriou M. Glycolysis and glutaminolysis cooperatively control T cell function by limiting metabolite supply to N-glycosylation. elife. 2017;6: pubmed publisher
  10. Schauwecker S, Kim J, Licht J, Clevenger C. Histone H1 and Chromosomal Protein HMGN2 Regulate Prolactin-induced STAT5 Transcription Factor Recruitment and Function in Breast Cancer Cells. J Biol Chem. 2017;292:2237-2254 pubmed publisher
  11. Ma Y, Chen L, Xie G, Zhou Y, Yue C, Yuan X, et al. Elevated level of interleukin-35 in colorectal cancer induces conversion of T cells into iTr35 by activating STAT1/STAT3. Oncotarget. 2016;7:73003-73015 pubmed publisher
  12. Weiss J, Chen W, Nyuydzefe M, Trzeciak A, Flynn R, Tonra J, et al. ROCK2 signaling is required to induce a subset of T follicular helper cells through opposing effects on STATs in autoimmune settings. Sci Signal. 2016;9:ra73 pubmed publisher
  13. Barcus C, Keely P, Eliceiri K, Schuler L. Prolactin signaling through focal adhesion complexes is amplified by stiff extracellular matrices in breast cancer cells. Oncotarget. 2016;7:48093-48106 pubmed publisher
  14. Chesnokova V, Zonis S, Zhou C, Recouvreux M, Ben Shlomo A, Araki T, et al. Growth hormone is permissive for neoplastic colon growth. Proc Natl Acad Sci U S A. 2016;113:E3250-9 pubmed publisher
  15. Kobayashi K, Tsugami Y, Matsunaga K, Oyama S, Kuki C, Kumura H. Prolactin and glucocorticoid signaling induces lactation-specific tight junctions concurrent with ?-casein expression in mammary epithelial cells. Biochim Biophys Acta. 2016;1863:2006-16 pubmed publisher
  16. Derangère V, Fumet J, Boidot R, Bengrine L, Limagne E, Chevriaux A, et al. Does bevacizumab impact anti-EGFR therapy efficacy in metastatic colorectal cancer?. Oncotarget. 2016;7:9309-21 pubmed publisher
  17. Ikeda S, Kitadate A, Ito M, Abe F, Nara M, Watanabe A, et al. Disruption of CCL20-CCR6 interaction inhibits metastasis of advanced cutaneous T-cell lymphoma. Oncotarget. 2016;7:13563-74 pubmed publisher
  18. Watari K, Shibata T, Nabeshima H, Shinoda A, Fukunaga Y, Kawahara A, et al. Impaired differentiation of macrophage lineage cells attenuates bone remodeling and inflammatory angiogenesis in Ndrg1 deficient mice. Sci Rep. 2016;6:19470 pubmed publisher
  19. Kitayama M, Mizutani K, Maruoka M, Mandai K, Sakakibara S, Ueda Y, et al. A Novel Nectin-mediated Cell Adhesion Apparatus That Is Implicated in Prolactin Receptor Signaling for Mammary Gland Development. J Biol Chem. 2016;291:5817-31 pubmed publisher
  20. Moravcová S, Červená K, Pačesová D, Bendová Z. Identification of STAT3 and STAT5 proteins in the rat suprachiasmatic nucleus and the Day/Night difference in astrocytic STAT3 phosphorylation in response to lipopolysaccharide. J Neurosci Res. 2016;94:99-108 pubmed publisher
  21. Seto D, Kandarian S, Jackman R. A Key Role for Leukemia Inhibitory Factor in C26 Cancer Cachexia. J Biol Chem. 2015;290:19976-86 pubmed publisher
  22. McGirt L, Jia P, Baerenwald D, Duszynski R, Dahlman K, Zic J, et al. Whole-genome sequencing reveals oncogenic mutations in mycosis fungoides. Blood. 2015;126:508-19 pubmed publisher
  23. Cheng H, Liang Y, Kuo Y, Chuu C, Lin C, Lee M, et al. Identification of thioridazine, an antipsychotic drug, as an antiglioblastoma and anticancer stem cell agent using public gene expression data. Cell Death Dis. 2015;6:e1753 pubmed publisher
  24. Suzuki M, Takeda T, Nakagawa H, Iwata S, Watanabe T, Siddiquey M, et al. The heat shock protein 90 inhibitor BIIB021 suppresses the growth of T and natural killer cell lymphomas. Front Microbiol. 2015;6:280 pubmed publisher
  25. Krysiak K, Tibbitts J, Shao J, Liu T, Ndonwi M, Walter M. Reduced levels of Hspa9 attenuate Stat5 activation in mouse B cells. Exp Hematol. 2015;43:319-30.e10 pubmed publisher
  26. Yoda A, Adelmant G, Tamburini J, Chapuy B, Shindoh N, Yoda Y, et al. Mutations in G protein β subunits promote transformation and kinase inhibitor resistance. Nat Med. 2015;21:71-5 pubmed publisher
  27. Sackmann Sala L, Chiche A, Mosquera Garrote N, Boutillon F, Cordier C, Pourmir I, et al. Prolactin-induced prostate tumorigenesis links sustained Stat5 signaling with the amplification of basal/stem cells and emergence of putative luminal progenitors. Am J Pathol. 2014;184:3105-19 pubmed publisher
  28. Wu A, Yang M, Dalvi P, Turinsky A, Wang W, Butcher D, et al. Role of STAT5 and epigenetics in lactation-associated upregulation of multidrug transporter ABCG2 in the mammary gland. Am J Physiol Endocrinol Metab. 2014;307:E596-610 pubmed publisher
  29. Lin G, LaPensee C, Qin Z, Schwartz J. Reciprocal occupancy of BCL6 and STAT5 on Growth Hormone target genes: contrasting transcriptional outcomes and promoter-specific roles of p300 and HDAC3. Mol Cell Endocrinol. 2014;395:19-31 pubmed publisher
  30. Schlederer M, Mueller K, Haybaeck J, Heider S, Huttary N, Rosner M, et al. Reliable quantification of protein expression and cellular localization in histological sections. PLoS ONE. 2014;9:e100822 pubmed publisher
  31. Barcus C, Keely P, Eliceiri K, Schuler L. Stiff collagen matrices increase tumorigenic prolactin signaling in breast cancer cells. J Biol Chem. 2013;288:12722-32 pubmed publisher
  32. Caldarelli A, Muller J, Paskowski Rogacz M, Herrmann K, Bauer R, Koch S, et al. A genome-wide RNAi screen identifies proteins modulating aberrant FLT3-ITD signaling. Leukemia. 2013;27:2301-10 pubmed publisher
  33. Wu A, Dalvi P, Lu X, Yang M, Riddick D, Matthews J, et al. Induction of multidrug resistance transporter ABCG2 by prolactin in human breast cancer cells. Mol Pharmacol. 2013;83:377-88 pubmed publisher
  34. Mueller K, Kornfeld J, Friedbichler K, Blaas L, Egger G, Esterbauer H, et al. Impairment of hepatic growth hormone and glucocorticoid receptor signaling causes steatosis and hepatocellular carcinoma in mice. Hepatology. 2011;54:1398-409 pubmed publisher
  35. Kirabo A, Oh S, Kasahara H, Wagner K, Sayeski P. Vascular smooth muscle Jak2 deletion prevents angiotensin II-mediated neointima formation following injury in mice. J Mol Cell Cardiol. 2011;50:1026-34 pubmed publisher
  36. Friedbichler K, Kerenyi M, Kovacic B, Li G, Hoelbl A, Yahiaoui S, et al. Stat5a serine 725 and 779 phosphorylation is a prerequisite for hematopoietic transformation. Blood. 2010;116:1548-58 pubmed publisher
  37. Blaas L, Kornfeld J, Schramek D, Musteanu M, Zollner G, Gumhold J, et al. Disruption of the growth hormone--signal transducer and activator of transcription 5--insulinlike growth factor 1 axis severely aggravates liver fibrosis in a mouse model of cholestasis. Hepatology. 2010;51:1319-26 pubmed publisher
  38. Jin H, Lanning N, Carter Su C. JAK2, but not Src family kinases, is required for STAT, ERK, and Akt signaling in response to growth hormone in preadipocytes and hepatoma cells. Mol Endocrinol. 2008;22:1825-41 pubmed publisher
  39. Nagy T, Wei H, Shen T, Peng X, Liang C, Gan B, et al. Mammary epithelial-specific deletion of the focal adhesion kinase gene leads to severe lobulo-alveolar hypoplasia and secretory immaturity of the murine mammary gland. J Biol Chem. 2007;282:31766-76 pubmed
  40. Engblom D, Kornfeld J, Schwake L, Tronche F, Reimann A, Beug H, et al. Direct glucocorticoid receptor-Stat5 interaction in hepatocytes controls body size and maturation-related gene expression. Genes Dev. 2007;21:1157-62 pubmed
  41. Trenerry M, Carey K, Ward A, Cameron Smith D. STAT3 signaling is activated in human skeletal muscle following acute resistance exercise. J Appl Physiol (1985). 2007;102:1483-9 pubmed
  42. Moriggl R, Sexl V, Kenner L, Duntsch C, Stangl K, Gingras S, et al. Stat5 tetramer formation is associated with leukemogenesis. Cancer Cell. 2005;7:87-99 pubmed
  43. Clausen L, Kristiansen M, Rasmussen L, Billestrup N, Blaabjerg O, Ledet T, et al. Growth hormone receptor expression and function in pituitary adenomas. Clin Endocrinol (Oxf). 2004;60:576-83 pubmed
  44. Cotarla I, Ren S, Zhang Y, Gehan E, Singh B, Furth P. Stat5a is tyrosine phosphorylated and nuclear localized in a high proportion of human breast cancers. Int J Cancer. 2004;108:665-71 pubmed
  45. Dubois S, Shou W, Haneline L, Fleischer S, Waldmann T, Müller J. Distinct pathways involving the FK506-binding proteins 12 and 12.6 underlie IL-2-versus IL-15-mediated proliferation of T cells. Proc Natl Acad Sci U S A. 2003;100:14169-74 pubmed
  46. Schroeder M, Brockman J, Walker A, Schuler L. Inhibition of prolactin (PRL)-induced proliferative signals in breast cancer cells by a molecular mimic of phosphorylated PRL, S179D-PRL. Endocrinology. 2003;144:5300-7 pubmed
  47. Wang R, Vadlamudi R, Bagheri Yarmand R, Beuvink I, Hynes N, Kumar R. Essential functions of p21-activated kinase 1 in morphogenesis and differentiation of mammary glands. J Cell Biol. 2003;161:583-92 pubmed
  48. Schroeder M, Rose Hellekant T, Sandgren E, Schuler L. Dysregulation of mammary Stats 1,3 and 5 and PRL receptors by overexpression of TGFalpha. Mol Cell Endocrinol. 2001;175:173-83 pubmed