| Year |
Citation |
Score |
| 2018 |
Soma S, Latimer AJ, Chun H, Vicary AC, Timbalia SA, Boulet A, Rahn JJ, Chan SSL, Leary SC, Kim BE, Gitlin JD, Gohil VM. Elesclomol restores mitochondrial function in genetic models of copper deficiency. Proceedings of the National Academy of Sciences of the United States of America. PMID 30038027 DOI: 10.1073/Pnas.1806296115 |
0.459 |
|
| 2018 |
Kumar D, Thomason RT, Yankova M, Gitlin JD, Mains RE, Eipper BA, King SM. Microvillar and ciliary defects in zebrafish lacking an actin-binding bioactive peptide amidating enzyme. Scientific Reports. 8: 4547. PMID 29540787 DOI: 10.1038/S41598-018-22732-9 |
0.688 |
|
| 2017 |
Thomason RT, Pettiglio MA, Herrera C, Kao C, Gitlin JD, Bartnikas TB. Characterization of trace metal content in the developing zebrafish embryo. Plos One. 12: e0179318. PMID 28617866 DOI: 10.1371/Journal.Pone.0179318 |
0.693 |
|
| 2015 |
Hodgkinson VL, Zhu S, Wang Y, Ladomersky E, Nickelson K, Weisman GA, Lee J, Gitlin JD, Petris MJ. Autonomous requirements of the Menkes disease protein in the nervous system. American Journal of Physiology. Cell Physiology. ajpcell.00130.2015. PMID 26269458 DOI: 10.1152/Ajpcell.00130.2015 |
0.404 |
|
| 2015 |
Hodgkinson VL, Dale JM, Garcia ML, Weisman GA, Lee J, Gitlin JD, Petris MJ. X-linked spinal muscular atrophy in mice caused by autonomous loss of ATP7A in the motor neuron. The Journal of Pathology. 236: 241-50. PMID 25639447 DOI: 10.1002/Path.4511 |
0.365 |
|
| 2015 |
Kao C, Messerli MA, Gitlin JD, Mehta SB. Adaptation of Actin Cytoskeleton during Suspended Animation Biophysical Journal. 108: 453. DOI: 10.1016/J.Bpj.2014.11.2473 |
0.327 |
|
| 2014 |
Gitlin JD. Copper homeostasis: specialized functions of the late secretory pathway. Developmental Cell. 29: 631-2. PMID 24960690 DOI: 10.1016/J.Devcel.2014.06.002 |
0.373 |
|
| 2012 |
Wang Y, Zhu S, Hodgkinson V, Prohaska JR, Weisman GA, Gitlin JD, Petris MJ. Maternofetal and neonatal copper requirements revealed by enterocyte-specific deletion of the Menkes disease protein. American Journal of Physiology. Gastrointestinal and Liver Physiology. 303: G1236-44. PMID 23064757 DOI: 10.1152/Ajpgi.00339.2012 |
0.456 |
|
| 2012 |
Wang Y, Zhu S, Weisman GA, Gitlin JD, Petris MJ. Conditional knockout of the Menkes disease copper transporter demonstrates its critical role in embryogenesis. Plos One. 7: e43039. PMID 22900086 DOI: 10.1371/Journal.Pone.0043039 |
0.457 |
|
| 2011 |
van Boxtel AL, Gansner JM, Hakvoort HW, Snell H, Legler J, Gitlin JD. Lysyl oxidase-like 3b is critical for cartilage maturation during zebrafish craniofacial development. Matrix Biology : Journal of the International Society For Matrix Biology. 30: 178-87. PMID 21244857 DOI: 10.1016/J.Matbio.2010.12.002 |
0.326 |
|
| 2010 |
Ishizaki H, Spitzer M, Wildenhain J, Anastasaki C, Zeng Z, Dolma S, Shaw M, Madsen E, Gitlin J, Marais R, Tyers M, Patton EE. Combined zebrafish-yeast chemical-genetic screens reveal gene-copper-nutrition interactions that modulate melanocyte pigmentation. Disease Models & Mechanisms. 3: 639-51. PMID 20713646 DOI: 10.1242/Dmm.005769 |
0.438 |
|
| 2010 |
Brady GF, Galbán S, Liu X, Basrur V, Gitlin JD, Elenitoba-Johnson KS, Wilson TE, Duckett CS. Regulation of the copper chaperone CCS by XIAP-mediated ubiquitination. Molecular and Cellular Biology. 30: 1923-36. PMID 20154138 DOI: 10.1128/Mcb.00900-09 |
0.432 |
|
| 2009 |
Mendelsohn BA, Malone JP, Townsend RR, Gitlin JD. Proteomic analysis of anoxia tolerance in the developing zebrafish embryo. Comparative Biochemistry and Physiology. Part D, Genomics & Proteomics. 4: 21-31. PMID 20403745 DOI: 10.1016/J.Cbd.2008.09.003 |
0.329 |
|
| 2008 |
Gansner JM, Gitlin JD. Essential role for the alpha 1 chain of type VIII collagen in zebrafish notochord formation. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 237: 3715-26. PMID 19035365 DOI: 10.1002/Dvdy.21779 |
0.379 |
|
| 2008 |
Madsen EC, Gitlin JD. Zebrafish mutants calamity and catastrophe define critical pathways of gene-nutrient interactions in developmental copper metabolism. Plos Genetics. 4: e1000261. PMID 19008952 DOI: 10.1371/Journal.Pgen.1000261 |
0.427 |
|
| 2008 |
Gansner JM, Madsen EC, Mecham RP, Gitlin JD. Essential role for fibrillin-2 in zebrafish notochord and vascular morphogenesis. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 237: 2844-61. PMID 18816837 DOI: 10.1002/Dvdy.21705 |
0.395 |
|
| 2008 |
Mendelsohn BA, Kassebaum BL, Gitlin JD. The zebrafish embryo as a dynamic model of anoxia tolerance. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 237: 1780-8. PMID 18521954 DOI: 10.1002/Dvdy.21581 |
0.305 |
|
| 2008 |
Mendelsohn BA, Gitlin JD. Coordination of development and metabolism in the pre-midblastula transition zebrafish embryo. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 237: 1789-98. PMID 18521947 DOI: 10.1002/Dvdy.21584 |
0.325 |
|
| 2008 |
Madsen EC, Morcos PA, Mendelsohn BA, Gitlin JD. In vivo correction of a Menkes disease model using antisense oligonucleotides. Proceedings of the National Academy of Sciences of the United States of America. 105: 3909-14. PMID 18316734 DOI: 10.1073/Pnas.0710865105 |
0.429 |
|
| 2007 |
de Bie P, van de Sluis B, Burstein E, van de Berghe PV, Muller P, Berger R, Gitlin JD, Wijmenga C, Klomp LW. Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B. Gastroenterology. 133: 1316-26. PMID 17919502 DOI: 10.1053/J.Gastro.2007.07.020 |
0.399 |
|
| 2007 |
Gansner JM, Mendelsohn BA, Hultman KA, Johnson SL, Gitlin JD. Essential role of lysyl oxidases in notochord development. Developmental Biology. 307: 202-13. PMID 17543297 DOI: 10.1016/J.Ydbio.2007.04.029 |
0.45 |
|
| 2007 |
Madsen E, Gitlin JD. Copper and iron disorders of the brain. Annual Review of Neuroscience. 30: 317-37. PMID 17367269 DOI: 10.1146/Annurev.Neuro.30.051606.094232 |
0.399 |
|
| 2007 |
Madsen E, Gitlin JD. Copper deficiency. Current Opinion in Gastroenterology. 23: 187-92. PMID 17268249 DOI: 10.1097/MOG.0b013e32801421bb |
0.302 |
|
| 2007 |
Anderson C, Bartlett SJ, Gansner JM, Wilson D, He L, Gitlin JD, Kelsh RN, Dowden J. Chemical genetics suggests a critical role for lysyl oxidase in zebrafish notochord morphogenesis. Molecular Biosystems. 3: 51-9. PMID 17216056 DOI: 10.1039/B613673G |
0.359 |
|
| 2007 |
Wang J, Caruano-Yzermans A, Rodriguez A, Scheurmann JP, Slunt HH, Cao X, Gitlin J, Hart PJ, Borchelt DR. Disease-associated mutations at copper ligand histidine residues of superoxide dismutase 1 diminish the binding of copper and compromise dimer stability. The Journal of Biological Chemistry. 282: 345-52. PMID 17092942 DOI: 10.1074/Jbc.M604503200 |
0.431 |
|
| 2006 |
Schlief ML, West T, Craig AM, Holtzman DM, Gitlin JD. Role of the Menkes copper-transporting ATPase in NMDA receptor-mediated neuronal toxicity. Proceedings of the National Academy of Sciences of the United States of America. 103: 14919-24. PMID 17003121 DOI: 10.1073/Pnas.0605390103 |
0.364 |
|
| 2006 |
Samuel TK, Gitlin JD. Copper and nitric oxide meet in the plasma. Nature Chemical Biology. 2: 452-3. PMID 16921354 DOI: 10.1038/Nchembio0906-452 |
0.32 |
|
| 2006 |
Mendelsohn BA, Yin C, Johnson SL, Wilm TP, Solnica-Krezel L, Gitlin JD. Atp7a determines a hierarchy of copper metabolism essential for notochord development. Cell Metabolism. 4: 155-62. PMID 16890543 DOI: 10.1016/J.Cmet.2006.05.001 |
0.451 |
|
| 2006 |
Schlief ML, Gitlin JD. Copper homeostasis in the CNS: a novel link between the NMDA receptor and copper homeostasis in the hippocampus. Molecular Neurobiology. 33: 81-90. PMID 16603790 DOI: 10.1385/Mn:33:2:81 |
0.393 |
|
| 2006 |
Jensen PJ, Gitlin JD, Carayannopoulos MO. GLUT1 deficiency links nutrient availability and apoptosis during embryonic development. The Journal of Biological Chemistry. 281: 13382-7. PMID 16543226 DOI: 10.1074/Jbc.M601881200 |
0.364 |
|
| 2006 |
Caruano-Yzermans AL, Bartnikas TB, Gitlin JD. Mechanisms of the copper-dependent turnover of the copper chaperone for superoxide dismutase. The Journal of Biological Chemistry. 281: 13581-7. PMID 16531609 DOI: 10.1074/Jbc.M601580200 |
0.456 |
|
| 2006 |
Gitlin JD, Lill R. Special issue: Cell biology of metals Biochimica Et Biophysica Acta. 1763: 1405. DOI: 10.1016/J.Bbamcr.2006.06.011 |
0.329 |
|
| 2005 |
Schlief ML, Craig AM, Gitlin JD. NMDA receptor activation mediates copper homeostasis in hippocampal neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 239-46. PMID 15634787 DOI: 10.1523/Jneurosci.3699-04.2005 |
0.369 |
|
| 2004 |
Nittis T, Gitlin JD. Role of copper in the proteosome-mediated degradation of the multicopper oxidase hephaestin. The Journal of Biological Chemistry. 279: 25696-702. PMID 15087449 DOI: 10.1074/Jbc.M401151200 |
0.425 |
|
| 2004 |
Harris ZL, Davis-Kaplan SR, Gitlin JD, Kaplan J. A fungal multicopper oxidase restores iron homeostasis in aceruloplasminemia. Blood. 103: 4672-3. PMID 14739215 DOI: 10.1182/Blood-2003-11-4060 |
0.401 |
|
| 2003 |
Tao TY, Liu F, Klomp L, Wijmenga C, Gitlin JD. The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein. The Journal of Biological Chemistry. 278: 41593-6. PMID 12968035 DOI: 10.1074/Jbc.C300391200 |
0.457 |
|
| 2003 |
Bartnikas TB, Gitlin JD. Mechanisms of biosynthesis of mammalian copper/zinc superoxide dismutase. The Journal of Biological Chemistry. 278: 33602-8. PMID 12815046 DOI: 10.1074/Jbc.M305435200 |
0.461 |
|
| 2003 |
Tao TY, Gitlin JD. Hepatic copper metabolism: insights from genetic disease. Hepatology (Baltimore, Md.). 37: 1241-7. PMID 12773998 DOI: 10.1053/Jhep.2003.50281 |
0.34 |
|
| 2003 |
Hamza I, Prohaska J, Gitlin JD. Essential role for Atox1 in the copper-mediated intracellular trafficking of the Menkes ATPase. Proceedings of the National Academy of Sciences of the United States of America. 100: 1215-20. PMID 12538877 DOI: 10.1073/Pnas.0336230100 |
0.462 |
|
| 2002 |
Hamza I, Gitlin JD. Copper chaperones for cytochrome c oxidase and human disease. Journal of Bioenergetics and Biomembranes. 34: 381-8. PMID 12539965 DOI: 10.1023/A:1021254104012 |
0.419 |
|
| 2002 |
Nittis T, Gitlin JD. The copper-iron connection: hereditary aceruloplasminemia. Seminars in Hematology. 39: 282-9. PMID 12382203 DOI: 10.1053/Shem.2002.35633 |
0.355 |
|
| 2002 |
Hellman NE, Kono S, Mancini GM, Hoogeboom AJ, De Jong GJ, Gitlin JD. Mechanisms of copper incorporation into human ceruloplasmin. The Journal of Biological Chemistry. 277: 46632-8. PMID 12351628 DOI: 10.1074/Jbc.M206246200 |
0.451 |
|
| 2002 |
Hellman NE, Gitlin JD. Ceruloplasmin metabolism and function. Annual Review of Nutrition. 22: 439-58. PMID 12055353 DOI: 10.1146/Annurev.Nutr.22.012502.114457 |
0.45 |
|
| 2002 |
Subramaniam JR, Lyons WE, Liu J, Bartnikas TB, Rothstein J, Price DL, Cleveland DW, Gitlin JD, Wong PC. Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading. Nature Neuroscience. 5: 301-7. PMID 11889469 DOI: 10.1038/Nn823 |
0.392 |
|
| 2002 |
Hellman NE, Kono S, Miyajima H, Gitlin JD. Biochemical analysis of a missense mutation in aceruloplasminemia. The Journal of Biological Chemistry. 277: 1375-80. PMID 11689569 DOI: 10.1074/Jbc.M109123200 |
0.405 |
|
| 2001 |
Bartnikas TB, Gitlin JD. How to make a metalloprotein. Nature Structural Biology. 8: 733-4. PMID 11524666 DOI: 10.1038/Nsb0901-733 |
0.441 |
|
| 2001 |
Hamza I, Faisst A, Prohaska J, Chen J, Gruss P, Gitlin JD. The metallochaperone Atox1 plays a critical role in perinatal copper homeostasis. Proceedings of the National Academy of Sciences of the United States of America. 98: 6848-52. PMID 11391006 DOI: 10.1073/Pnas.111058498 |
0.45 |
|
| 2001 |
McLoughlin DM, Standen CL, Lau KF, Ackerley S, Bartnikas TP, Gitlin JD, Miller CC. The neuronal adaptor protein X11alpha interacts with the copper chaperone for SOD1 and regulates SOD1 activity. The Journal of Biological Chemistry. 276: 9303-7. PMID 11115513 DOI: 10.1074/Jbc.M010023200 |
0.373 |
|
| 2000 |
Bartnikas TB, Waggoner DJ, Casareno RL, Gaedigk R, White RA, Gitlin JD. Chromosomal localization of CCS, the copper chaperone for Cu/Zn superoxide dismutase. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 409-11. PMID 10790544 DOI: 10.1007/S003350010078 |
0.351 |
|
| 2000 |
Waggoner DJ, Drisaldi B, Bartnikas TB, Casareno RL, Prohaska JR, Gitlin JD, Harris DA. Brain copper content and cuproenzyme activity do not vary with prion protein expression level. The Journal of Biological Chemistry. 275: 7455-8. PMID 10713045 DOI: 10.1074/Jbc.275.11.7455 |
0.398 |
|
| 2000 |
Wong PC, Waggoner D, Subramaniam JR, Tessarollo L, Bartnikas TB, Culotta VC, Price DL, Rothstein J, Gitlin JD. Copper chaperone for superoxide dismutase is essential to activate mammalian Cu/Zn superoxide dismutase. Proceedings of the National Academy of Sciences of the United States of America. 97: 2886-91. PMID 10694572 DOI: 10.1073/Pnas.040461197 |
0.399 |
|
| 2000 |
Hamza I, Klomp LW, Gaedigk R, White RA, Gitlin JD. Structure, expression, and chromosomal localization of the mouse Atox1 gene. Genomics. 63: 294-7. PMID 10673341 DOI: 10.1006/Geno.1999.6046 |
0.409 |
|
| 1999 |
Hamza I, Schaefer M, Klomp LW, Gitlin JD. Interaction of the copper chaperone HAH1 with the Wilson disease protein is essential for copper homeostasis. Proceedings of the National Academy of Sciences of the United States of America. 96: 13363-8. PMID 10557326 DOI: 10.1073/Pnas.96.23.13363 |
0.447 |
|
| 1999 |
Harris ZL, Durley AP, Man TK, Gitlin JD. Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux. Proceedings of the National Academy of Sciences of the United States of America. 96: 10812-7. PMID 10485908 DOI: 10.1073/Pnas.96.19.10812 |
0.343 |
|
| 1999 |
Waggoner DJ, Bartnikas TB, Gitlin JD. The role of copper in neurodegenerative disease. Neurobiology of Disease. 6: 221-30. PMID 10448050 DOI: 10.1006/Nbdi.1999.0250 |
0.454 |
|
| 1999 |
Culotta VC, Lin SJ, Schmidt P, Klomp LW, Casareno RL, Gitlin J. Intracellular pathways of copper trafficking in yeast and humans. Advances in Experimental Medicine and Biology. 448: 247-54. PMID 10079832 DOI: 10.1007/978-1-4615-4859-1_22 |
0.453 |
|
| 1999 |
Schaefer M, Hopkins RG, Failla ML, Gitlin JD. Hepatocyte-specific localization and copper-dependent trafficking of the Wilson's disease protein in the liver. The American Journal of Physiology. 276: G639-46. PMID 10070040 DOI: 10.1152/Ajpgi.1999.276.3.G639 |
0.388 |
|
| 1999 |
Schaefer M, Gitlin JD. Genetic disorders of membrane transport. IV. Wilson's disease and Menkes disease. The American Journal of Physiology. 276: G311-4. PMID 9950803 DOI: 10.1152/Ajpgi.1999.276.2.G311 |
0.341 |
|
| 1999 |
Borjigin J, Payne AS, Deng J, Li X, Wang MM, Ovodenko B, Gitlin JD, Snyder SH. A Novel Pineal Night-Specific ATPase Encoded by the Wilson Disease Gene The Journal of Neuroscience. 19: 1018-1026. DOI: 10.1523/Jneurosci.19-03-01018.1999 |
0.377 |
|
| 1998 |
Casareno RL, Waggoner D, Gitlin JD. The copper chaperone CCS directly interacts with copper/zinc superoxide dismutase. The Journal of Biological Chemistry. 273: 23625-8. PMID 9726962 DOI: 10.1074/Jbc.273.37.23625 |
0.423 |
|
| 1998 |
Payne AS, Kelly EJ, Gitlin JD. Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutation. Proceedings of the National Academy of Sciences of the United States of America. 95: 10854-9. PMID 9724794 DOI: 10.1073/Pnas.95.18.10854 |
0.444 |
|
| 1998 |
Harris ZL, Klomp LW, Gitlin JD. Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis. The American Journal of Clinical Nutrition. 67: 972S-977S. PMID 9587138 DOI: 10.1093/Ajcn/67.5.972S |
0.426 |
|
| 1998 |
Payne AS, Gitlin JD. Functional expression of the menkes disease protein reveals common biochemical mechanisms among the copper-transporting P-type ATPases. The Journal of Biological Chemistry. 273: 3765-70. PMID 9452509 DOI: 10.1074/Jbc.273.6.3765 |
0.434 |
|
| 1998 |
Hung IH, Casareno RL, Labesse G, Mathews FS, Gitlin JD. HAH1 is a copper-binding protein with distinct amino acid residues mediating copper homeostasis and antioxidant defense. The Journal of Biological Chemistry. 273: 1749-54. PMID 9430722 DOI: 10.1074/Jbc.273.3.1749 |
0.453 |
|
| 1997 |
Culotta VC, Klomp LW, Strain J, Casareno RL, Krems B, Gitlin JD. The copper chaperone for superoxide dismutase. The Journal of Biological Chemistry. 272: 23469-72. PMID 9295278 DOI: 10.1074/Jbc.272.38.23469 |
0.462 |
|
| 1997 |
Hung IH, Suzuki M, Yamaguchi Y, Yuan DS, Klausner RD, Gitlin JD. Biochemical characterization of the Wilson disease protein and functional expression in the yeast Saccharomyces cerevisiae. The Journal of Biological Chemistry. 272: 21461-6. PMID 9261163 DOI: 10.1074/Jbc.272.34.21461 |
0.447 |
|
| 1997 |
Klomp LW, Lin SJ, Yuan DS, Klausner RD, Culotta VC, Gitlin JD. Identification and functional expression of HAH1, a novel human gene involved in copper homeostasis. The Journal of Biological Chemistry. 272: 9221-6. PMID 9083055 DOI: 10.1074/Jbc.272.14.9221 |
0.4 |
|
| 1997 |
Miyajima H, Takahashi Y, Kamata T, Shimizu H, Sakai N, Gitlin JD. Use of desferrioxamine in the treatment of aceruloplasminemia. Annals of Neurology. 41: 404-7. PMID 9066364 DOI: 10.1002/Ana.410410318 |
0.314 |
|
| 1996 |
Klomp LW, Gitlin JD. Expression of the ceruloplasmin gene in the human retina and brain: implications for a pathogenic model in aceruloplasminemia. Human Molecular Genetics. 5: 1989-96. PMID 8968753 DOI: 10.1093/Hmg/5.12.1989 |
0.366 |
|
| 1996 |
Yamaguchi Y, Heiny ME, Suzuki M, Gitlin JD. Biochemical characterization and intracellular localization of the Menkes disease protein. Proceedings of the National Academy of Sciences of the United States of America. 93: 14030-5. PMID 8943055 DOI: 10.1073/Pnas.93.24.14030 |
0.392 |
|
| 1996 |
Takahashi Y, Miyajima H, Shirabe S, Nagataki S, Suenaga A, Gitlin JD. Characterization of a nonsense mutation in the ceruloplasmin gene resulting in diabetes and neurodegenerative disease. Human Molecular Genetics. 5: 81-84. PMID 8789443 DOI: 10.1093/Hmg/5.1.81 |
0.335 |
|
| 1996 |
Miyajima H, Takahashi Y, Serizawa M, Kaneko E, Gitlin JD. Increased plasma lipid peroxidation in patients with aceruloplasminemia. Free Radical Biology & Medicine. 20: 757-60. PMID 8721620 DOI: 10.1016/0891-5849(95)02178-7 |
0.311 |
|
| 1996 |
Harris ZL, Gitlin JD. Genetic and molecular basis for copper toxicity. The American Journal of Clinical Nutrition. 63: 836S-41S. PMID 8615371 DOI: 10.1093/Ajcn/63.5.836 |
0.455 |
|
| 1995 |
Hackett BP, Brody SL, Liang M, Zeitz ID, Bruns LA, Gitlin JD. Primary structure of hepatocyte nuclear factor/forkhead homologue 4 and characterization of gene expression in the developing respiratory and reproductive epithelium. Proceedings of the National Academy of Sciences of the United States of America. 92: 4249-53. PMID 7753791 DOI: 10.1073/Pnas.92.10.4249 |
0.314 |
|
| 1995 |
Harris ZL, Takahashi Y, Miyajima H, Serizawa M, MacGillivray RT, Gitlin JD. Aceruloplasminemia: molecular characterization of this disorder of iron metabolism. Proceedings of the National Academy of Sciences of the United States of America. 92: 2539-43. PMID 7708681 DOI: 10.1073/Pnas.92.7.2539 |
0.385 |
|
| 1992 |
Hackett BP, Gitlin JD. Cell-specific expression of a Clara cell secretory protein-human growth hormone gene in the bronchiolar epithelium of transgenic mice. Proceedings of the National Academy of Sciences of the United States of America. 89: 9079-83. PMID 1409605 DOI: 10.1073/Pnas.89.19.9079 |
0.32 |
|
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