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词条 Israel Hanukoglu
释义

  1. Education

  2. Contributions to science

     Structures of keratins  Steroid hormone synthesis  Epithelial sodium channel (ENaC) 

  3. Awards

  4. Academic and Civic activities

  5. Obama Birth Certificate Controversy

  6. References

  7. External links

{{Infobox scientist
| name = Israel Hanukoglu
| image =
| image_size =
| alt =
| caption =
| birth_date =
| birth_place = Istanbul, Turkey
| nationality = Israeli
| fields = Biochemistry, molecular biology
| workplaces = Ariel University
| alma_mater = Hebrew University of Jerusalem
| thesis_title = Mechanism of electron transport to cytochrome P-450 in adrenal cortex mitochondrial monooxygenase systems
| thesis_year = 1980
| doctoral_advisor = Colin Jefcoate
| academic_advisors = Neal L. First, David Nelson, W.W. Cleland
| known_for = Keratin structure, steroidogenic enzymes, Epithelial sodium channels
| awards = Lindner Prize
| website =
}}Israel Hanukoglu ({{lang-tr|İsrael Hanukoğlu}}) is a Turkish-born Israeli scientist. He is a full professor of biochemistry and molecular biology[1] at Ariel University and former Science and Technology Adviser to the Prime Minister of Israel (1996–1999). He is founder of Israel Science and Technology Homepage.[2]

Education

Israel Hanukoglu received his undergraduate degree cum laude with double majors in biology and psychology and a minor in political science from the Hebrew University of Jerusalem. He then went to the University of Wisconsin–Madison for graduate studies and received his M.Sc. degree in 1976 in an inter-disciplinary Endocrinology-Reproductive physiology program. His Ph.D. thesis was on the "Mechanism of electron transport to cytochrome P-450 in adrenal cortex mitochondrial steroid monooxygenase systems" carried out under the supervision of Prof. Colin R. Jefcoate.

Contributions to science

Prof. Hanukoglu's scientific work concentrated in three different areas outlined below.

Structures of keratins

Hanukoglu's career in molecular biology started at the Department of Biochemistry of the University of Chicago (1980-1983 with Elaine Fuchs), where he cloned and sequenced cDNAs coding for cytoskeletal proteins, actin[3] and alpha keratins.[4][5] He elucidated the first structures of cytoskeletal keratin families, and predicted the long helical domains of these proteins. By computerized analysis of amino acid sequences he predicted that the central rod domain of intermediate filament proteins is composed of four helical segments separated by three short linker sequences. Later crystallographic studies have confirmed this as a general model for intermediate filament protein structure.[6][7]

Steroid hormone synthesis

During his Ph.D. thesis research, Israel isolated the mitochondrial enzymes that catalyze the first step in the synthesis of steroid hormones in all steroidogenic tissues, including the adrenal cortex, and the reproductive organs.[8] The first step of steroidogenesis is dependent on the transfer of electrons from NADPH to a P450 type enzyme (P450scc) via an electron-transfer chain that includes two additional proteins.[9] These proteins are located on the inner mitochondrial membrane.[10] Israel reconstituted this system using proteins he purified, characterized the process of electron transfer between the proteins, and built a kinetic model that simulated precisely the dynamic behavior of this complex system.[11][8]

In his first academic position at the Department of Biology at the Technion-Israel Institute of Technology, he first determined the molar stoichiometry of the mitochondrial P450 system proteins using specific antibodies that he generated.[12] He then set out to clone the cDNAs and the genes that code for these enzymes. His lab was the first to clone the cDNAs and the gene coding for adrenodoxin reductase - the first enzyme in the electron transfer chain of the mitochondrial P450 system.[13][14][15]

By sequence and structural analyses of adrenodoxin reductase, Israel identified its binding sites for the electron donor and acceptor coenzymes, NADPH and FAD.[14] By sequence analyses of the large oxidoreductase type of enzyme families, he noted that the FAD-binding site is a classical Rossmann fold, but the NADPH binding site has a different consensus sequence that could be responsible for NAD vs. NADP coenzyme specificity. The importance of the motifs he identified was confirmed by re-engineering of coenzyme specificities of different enzymes.[16] Elucidation of the crystal structure of adrenodoxin reductase further verified Israel's identification of the coenzyme binding sites.[17] Analysis of the phylogeny of this enzyme in eukaryotes showed that the NADP binding site sequence is strictly conserved.[18]

As the steroidogenic tissues have very high levels of antioxidants, Israel suspected that the P450 systems may leak electrons producing oxygen radicals. He examined this issue and showed that indeed, electrons that leak during the action mitochondrial P450 systems generate reactive oxygen species.[19][20][21] His studies also showed that in bovine ovary, levels of antioxidants are coordinately regulated with steroidogenesis.[22]

His other work in this field includes elucidation of the mechanism of action of corticotropin (ACTH) in regulating steroid hormone synthesis in the adrenal cortex,[23][24] regulation of adrenal steroidogenic capacity in disease states,[25] and the cloning and elucidation of the structure of ACTH receptor.[26]

In this field, Israel organized the first International Symposium in Molecular Steroidogenesis in Jerusalem in 1991 which served as the cornerstone for a continuing series of international symposia for scientists who specialize in this field.[27]

Epithelial sodium channel (ENaC)

In his clinical work as an endocrinologist, Israel's older brother, Prof. Aaron Hanukoglu (Tel Aviv University, Sackler Medical School and E. Wolfson Medical Center), identified that a hereditary disease named pseudohypoaldosteronism (PHA) type I encompasses two independent syndromes.[28] Following this discovery the two brothers continued their collaboration to understand the molecular basis of the severe form of PHA.

By their collaborative work that also included additional labs, the Hanukoglu brothers discovered that the severe forms of pseudohypoaldosteronism type I result from mutations in three genes (SCNN1A, SCNN1B, and SCNN1B) that encode for protein subunits of the Epithelial sodium (Na+) channel (ENaC).[29][30][31][32] These studies also helped establish that ENaC is the principal channel involved in blood volume and blood pressure regulation in humans.[33]

Following these studies, the Hanukoglu brothers directed their attention to understand the structure and function of ENaC assembled from normal and mutated subunits. Their analyses showed that the phenotypic variations in the severity of pseudohypoaldosteronism are associated with the types of genetic mutations.[34][35] Their work on the structure of ENaC subunits led to the identification of charged residues and regions responsible for transport of the protein to membrane and for regulation of extracellular Na+ ions.[36][37]

In an extensive review of studies on ASIC and ENaC, Prof. Hanukoglu has summarized the major similarities between ASIC and ENaC type channels.[38]

To define the sites of localization of ENaC in tissues and within cells, Hanukoglu's laboratory generated polyclonal antibodies against extracellular ENaC subunits. These antibodies for the first time permitted visualization of intracellular localization of ENaC at high resolution and led to the discovery that in all cells with motile cilia ENaC is located on cilia.[39] These studies establish that ENaC is an important regulator of fluid level in the luminal side of cells with motile cilia in the female reproductive and respiratory tract.[39] More recently, they showed that these sodium channels are also located in the seminiferous tubules in the testis and in the tail and head region of sperm.[40]

Systemic pseudohypoaldosteronism patients with mutated ENaC subunits may lose significant amount salt in sweat especially at hot climates.[28] To identify the sites of salt loss, Hanukoglu brothers examined the localization of ENaC in the human skin.[41] In a comprehensive study examining all the layers of skin and epidermal appendages, they found a widespread distribution of ENaC in keratinocytes in the epidermal layers. Yet, in the eccrine sweat glands, ENaC was localized on the apical cell membrane exposed to the duct of these sweat glands. Based on additional observations, they concluded that the ENaC located on the eccrine gland sweat ducts is responsible for the uptake of Na+ ions from sweat secretions. This recycling of Na+ reduces the concentration of salt in perspiration and prevents the loss of salt at hot climates via perspiration.[41]

Awards

  • American Field Service International Scholarship (from Turkey to the USA) (1969).
  • Ford Foundation Fellowship in Endocrinology (1975).
  • Damon Runyon Cancer Research Foundation Fellowship Award in Biochemistry (1981).
  • National Cancer Institute, National Research Service Award for Postdoctoral Fellowship in Biochemistry (1982).
  • Technion V.P.R. Fund-Henri Gutwirth Award for Excellence in Research (1984).
  • Delta Research Career Development Award at Weizmann Institute of Science (1987).
  • The first Hans Lindner Prize in Endocrinology, Israel Endocrine Society (1988).
  • Lubell Prize for outstanding young scientist at the Weizmann Institute of Science (1991).
  • [https://publons.com/author/305419/israel-hanukoglu#profile Sentinel of Science Award for peer review in Biochemistry, Genetics and Molecular Biology by Publons] (1st place among Israeli Scientists - 2016)

In addition to the personal prizes above, the research presentations from the laboratory of Prof. Hanukoglu received four awards at national and international meetings.

Academic and Civic activities

Besides a scientific career Hanukoglu has maintained an active academic and civic leadership role. In 2003, Hanukoglu founded Israel's first Molecular Biology B.Sc. degree program in the Ariel University Center of Samaria[42] and served as the Chairman of the Molecular Biology Department there from 2003 to 2008.[43]

Prof. Hanukoglu is currently on the editorial board of three journals.[44] He is one of the top reviewers of scientific articles in the life sciences (ranked to be in the top 98 percentile according to the [https://publons.com/author/305419/israel-hanukoglu#stats Publons registry]).

In 1995 Prof. Hanukoglu was elected as the Chairman of the Professors for a Strong Israel, a self-described "non-partisan organization of academics united by a shared concern for the security and the Jewish character of the State of Israel." From 1996 to 1999 he served as the Science Adviser to the Prime Minister of Israel Benjamin Netanyahu. Hanukoglu was placed as an honorary candidate on the Herut – The National Movement list.[45]

In 2003 he was appointed as the scientific adviser to the Mayor of Rishon-Lezion for establishing the Jewish Nobel Prize Laureate Boulevard Outdoor Museum. Since 1996 he has served as a founding member of the Ariel Center for Policy Research executive board.[43]

Obama Birth Certificate Controversy

Hanukoglu's website, the Israel Science and Technology Homepage, includes the page, "Long-Form Birth Certificate of Obama is a Forged Document."[46] The analyses presented assert that "without a doubt that the Long-Form Birth Certificate of Mr. Obama is a fabricated, fake and forged document."

References

1. ^http://www.inn.co.il/Besheva/Article.aspx/1541
2. ^https://www.science.co.il/About.php
3. ^{{cite journal | vauthors = Hanukoglu I, Tanese N, Fuchs E | title = Complementary DNA sequence of a human cytoplasmic actin. Interspecies divergence of 3' non-coding regions | journal = Journal of Molecular Biology | volume = 163 | issue = 4 | pages = 673–8 | date = Feb 1983 | pmid = 6842590 | doi = 10.1016/0022-2836(83)90117-1 }}
4. ^{{cite journal | vauthors = Hanukoglu I, Fuchs E | title = The cDNA sequence of a human epidermal keratin: divergence of sequence but conservation of structure among intermediate filament proteins. | journal = Cell | volume = 31 | issue = 1 | pages = 243–252 | date=Nov 1982 | doi = 10.1016/0092-8674(82)90424-X | pmid = 6186381 |url=https://zenodo.org/record/890743}}
5. ^{{cite journal | vauthors = Hanukoglu I, Fuchs E | title = The cDNA sequence of a Type II cytoskeletal keratin reveals constant and variable structural domains among keratins. | journal = Cell | volume = 33 | issue = 3 | pages = 915–924 |date=Jul 1983 | doi = 10.1016/0092-8674(83)90034-X | PMID = 6191871 |url=https://zenodo.org/record/890739}}
6. ^{{cite journal | vauthors = Lee CH, Kim MS, Chung BM, Leahy DJ, Coulombe PA | title = Structural basis for heteromeric assembly and perinuclear organization of keratin filaments | journal = Nature Structural & Molecular Biology | volume = 19 | issue = 7 | pages = 707–15 | date = Jul 2012 | pmid = 22705788 | doi = 10.1038/nsmb.2330 | pmc=3864793}}
7. ^{{Cite journal | vauthors = Hanukoglu I, Ezra L | title = Proteopedia: Coiled-coil structure of keratins. | journal = Biochem Mol Biol Educ | volume = 42 | issue = 1 | pages = 93–94 |date=Jan 2014 | doi = 10.1002/bmb.20746 | PMID = 24265184}}
8. ^1 {{cite journal | vauthors = Hanukoglu I, Spitsberg V, Bumpus JA, Dus KM, Jefcoate CR | title = Adrenal mitochondrial cytochrome P-450scc. Cholesterol and adrenodoxin interactions at equilibrium and during turnover | journal = The Journal of Biological Chemistry | volume = 256 | issue = 9 | pages = 4321–8 | date = May 1981 | pmid = 7217084 | doi = }}
9. ^{{cite journal | vauthors = Hanukoglu I | title = Steroidogenic enzymes: structure, function, and role in regulation of steroid hormone biosynthesis | journal = The Journal of Steroid Biochemistry and Molecular Biology | volume = 43 | issue = 8 | pages = 779–804 | date = Dec 1992 | pmid = 22217824 | doi = 10.1016/0960-0760(92)90307-5 |url=https://zenodo.org/record/890723}}
10. ^{{cite journal | vauthors = Hanukoglu I, Suh BS, Himmelhoch S, Amsterdam A | title = Induction and mitochondrial localization of cytochrome P450scc system enzymes in normal and transformed ovarian granulosa cells | journal = The Journal of Cell Biology | volume = 111 | issue = 4 | pages = 1373–81 | date = October 1990 | pmid = 2170421 | pmc = 2116250 | doi = 10.1083/jcb.111.4.1373 }}
11. ^{{cite journal | vauthors = Hanukoglu I, Jefcoate CR | title = Mitochondrial cytochrome P-450scc. Mechanism of electron transport by adrenodoxin | journal = The Journal of Biological Chemistry | volume = 255 | issue = 7 | pages = 3057–61 | date = Apr 1980 | pmid = 6766943 | doi = | url = http://www.jbc.org/content/255/7/3057.full.pdf }}
12. ^{{cite journal | vauthors = Hanukoglu I, Hanukoglu Z | title = Stoichiometry of mitochondrial cytochromes P-450, adrenodoxin and adrenodoxin reductase in adrenal cortex and corpus luteum. Implications for membrane organization and gene regulation | journal = European Journal of Biochemistry | volume = 157 | issue = 1 | pages = 27–31 | date = May 1986 | pmid = 3011431 | doi = 10.1111/j.1432-1033.1986.tb09633.x | url = https://zenodo.org/record/890737 }}
13. ^{{cite journal | vauthors = Hanukoglu I, Gutfinger T, Haniu M, Shively JE | title = Isolation of a cDNA for adrenodoxin reductase (ferredoxin-NADP+ reductase). Implications for mitochondrial cytochrome P-450 systems. | journal = European Journal of Biochemistry | volume = 169 | issue = 3 | pages = 449–455 |date=Dec 1987 | doi = 10.1111/j.1432-1033.1987.tb13632.x | pmid = 3691502 | url=https://zenodo.org/record/890735 }}
14. ^1 {{cite journal | vauthors = Hanukoglu I, Gutfinger T | title = cDNA sequence of adrenodoxin reductase. Identification of NADP-binding sites in oxidoreductases | journal = European Journal of Biochemistry / FEBS | volume = 180 | issue = 2 | pages = 479–84 | date = Mar 1989 | pmid = 2924777 | doi = 10.1111/j.1432-1033.1989.tb14671.x|url=https://zenodo.org/record/890733 }}
15. ^{{cite journal | vauthors = Solish SB, Picado-Leonard J, Morel Y, Kuhn RW, Mohandas TK, Hanukoglu I, Miller WL | title = Human adrenodoxin reductase: two mRNAs encoded by a single gene on chromosome 17cen----q25 are expressed in steroidogenic tissues | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 85 | issue = 19 | pages = 7104–7108 | date = Oct 1988 | pmid = 2845396 | pmc = 282132 | doi = 10.1073/pnas.85.19.7104 }}
16. ^{{cite journal | vauthors = Scrutton NS, Berry A, Perham RN | title = Redesign of the coenzyme specificity of a dehydrogenase by protein engineering | journal = Nature | volume = 343 | issue = 6253 | pages = 38–43 | date = Jan 1990 | pmid = 2296288 | doi = 10.1038/343038a0 }}
17. ^{{cite journal | vauthors = Ziegler GA, Vonrhein C, Hanukoglu I, Schulz GE | title = The structure of adrenodoxin reductase of mitochondrial P450 systems: electron transfer for steroid biosynthesis | journal = Journal of Molecular Biology | volume = 289 | issue = 4 | pages = 981–90 | date = Jun 1999 | pmid = 10369776 | doi = 10.1006/jmbi.1999.2807 }}
18. ^{{cite journal | vauthors = Hanukoglu I | title = Conservation of the Enzyme-Coenzyme Interfaces in FAD and NADP Binding Adrenodoxin Reductase-A Ubiquitous Enzyme | journal = Journal of Molecular Evolution | volume = 85 | issue= 5 | pages= 205–218 | year= 2017 | pmid= 29177972 | doi= 10.1007/s00239-017-9821-9 | url=}}
19. ^{{cite journal | vauthors = Hanukoglu I, Rapoport R, Weiner L, Sklan D | title = Electron leakage from the mitochondrial NADPH-adrenodoxin reductase-adrenodoxin-P450scc (cholesterol side chain cleavage) system | journal = Archives of Biochemistry and Biophysics | volume = 305 | issue = 2 | pages = 489–98 | date = September 1993 | pmid = 8396893 | doi = 10.1006/abbi.1993.1452 }}
20. ^{{cite journal | vauthors = Rapoport R, Sklan D, Hanukoglu I | title=Electron leakage from the adrenal cortex mitochondrial P450scc and P450c11 systems: NADPH and steroid dependence.|journal=Archives of Biochemistry and Biophysics|date=10 March 1995|volume=317|issue=2|pages=412–6|pmid=7893157 | doi= 10.1006/abbi.1995.1182}}
21. ^{{cite journal | vauthors = Hanukoglu I | title = Antioxidant protective mechanisms against reactive oxygen species (ROS) generated by mitochondrial P450 systems in steroidogenic cells | journal = Drug Metabolism Reviews | volume = 38 | issue = 1-2 | pages = 171–96 | year = 2006 | pmid = 16684656 | doi = 10.1080/03602530600570040|url=https://zenodo.org/record/890701 }}
22. ^{{cite journal | vauthors = Rapoport R, Sklan D, Wolfenson D, Shaham-Albalancy A, Hanukoglu I | title = Antioxidant capacity is correlated with steroidogenic status of the corpus luteum during the bovine estrous cycle | journal = Biochim. Biophys. Acta | volume = 1380 | issue = 1 | pages = 133–40 |date=March 1998 | pmid = 9545562 | doi = 10.1016/S0304-4165(97)00136-0|url=https://zenodo.org/record/890705 }}
23. ^{{cite journal | vauthors = Hanukoglu I, Feuchtwanger R, Hanukoglu A | title = Mechanism of corticotropin and cAMP induction of mitochondrial cytochrome P450 system enzymes in adrenal cortex cells | journal = The Journal of Biological Chemistry | volume = 265 | issue = 33 | pages = 20602–8 | date = Nov 1990 | pmid = 2173715 | doi = | url = https://zenodo.org/record/890729 }}
24. ^{{cite journal | vauthors = Raikhinstein M, Hanukoglu I | title = Mitochondrial-genome-encoded RNAs: differential regulation by corticotropin in bovine adrenocortical cells | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 90 | issue = 22 | pages = 10509–13 | date = Nov 1993 | pmid = 7504267 | pmc = 47806 | doi = 10.1073/pnas.90.22.10509 }}
25. ^{{cite journal | vauthors = Hanukoglu A, Fried D, Nakash I, Hanukoglu I | title = Selective increases in adrenal steroidogenic capacity during acute respiratory disease in infants. | journal = Eur J Endocrinol | volume = 133 | issue = 5 | pages = 552–6 |date=Nov 1995 | doi = 10.1530/eje.0.1330552 | PMID = 7581984 }}
26. ^{{cite journal | vauthors = Raikhinstein M, Zohar M, Hanukoglu I | title = cDNA cloning and sequence analysis of the bovine adrenocorticotropic hormone (ACTH) receptor | journal = Biochimica et Biophysica Acta | volume = 1220 | issue = 3 | pages = 329–32 | date = Feb 1994 | pmid = 8305507 | doi = 10.1016/0167-4889(94)90157-0 |url=https://zenodo.org/record/890717}}
27. ^{{Cite journal | last1 = Hanukoglu | first1 = I. | title = Current research on steroid metabolism: transition from biochemistry to molecular-cell biology. | journal = J Steroid Biochem Mol Biol | volume = 43 | issue = 8 | pages = 745–9 |date=Dec 1992 | doi = 10.1016/0960-0760(92)90304-2 | PMID = 22217821 }}
28. ^1 {{cite journal | vauthors = Hanukoglu A | title = Type I pseudohypoaldosteronism includes two clinically and genetically distinct entities with either renal or multiple target organ defects | journal = The Journal of Clinical Endocrinology and Metabolism | volume = 73 | issue = 5 | pages = 936–44 | date = November 1991 | pmid = 1939532 | doi = 10.1210/jcem-73-5-936 }}
29. ^{{cite journal | vauthors = Strautnieks SS, Thompson RJ, Hanukoglu A, Dillon MJ, Hanukoglu I, Kuhnle U, Seckl J, Gardiner RM, Chung E | title = Localisation of pseudohypoaldosteronism genes to chromosome 16p12.2-13.11 and 12p13.1-pter by homozygosity mapping | journal = Human Molecular Genetics | volume = 5 | issue = 2 | pages = 293–9 | date = February 1996 | pmid = 8824886 | doi = 10.1093/hmg/5.2.293 }}
30. ^{{cite journal | vauthors = Chang SS, Grunder S, Hanukoglu A, Rösler A, Mathew PM, Hanukoglu I, Schild L, Lu Y, Shimkets RA, Nelson-Williams C, Rossier BC, Lifton RP | title = Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1 | journal = Nature Genetics | volume = 12 | issue = 3 | pages = 248–53 | date = March 1996 | pmid = 8589714 | doi = 10.1038/ng0396-248 }}
31. ^{{cite journal | vauthors = Saxena A, Hanukoglu I, Saxena D, Thompson RJ, Gardiner RM, Hanukoglu A | title = Novel mutations responsible for autosomal recessive multisystem pseudohypoaldosteronism and sequence variants in epithelial sodium channel alpha-, beta-, and gamma-subunit genes | journal = The Journal of Clinical Endocrinology and Metabolism | volume = 87 | issue = 7 | pages = 3344–50 | date = July 2002 | pmid = 12107247 | doi = 10.1210/jcem.87.7.8674 }}
32. ^{{cite journal | vauthors = Edelheit O, Hanukoglu I, Gizewska M, Kandemir N, Tenenbaum-Rakover Y, Yurdakök M, Zajaczek S, Hanukoglu A | title = Novel mutations in epithelial sodium channel (ENaC) subunit genes and phenotypic expression of multisystem pseudohypoaldosteronism | journal = Clinical Endocrinology | volume = 62 | issue = 5 | pages = 547–53 | date = May 2005 | pmid = 15853823 | doi = 10.1111/j.1365-2265.2005.02255.x }}
33. ^{{cite journal | vauthors = Hanukoglu I, Hanukoglu A | title = Epithelial sodium channel (ENaC) family: Phylogeny, structure-function, tissue distribution, and associated inherited diseases | journal = Gene | volume = 579 | issue = 2 | pages = 95–132 | date = April 2016 | pmid = 26772908 | pmc = 4756657 | doi = 10.1016/j.gene.2015.12.061 }}
34. ^{{cite journal | vauthors = Hanukoglu A, Edelheit O, Shriki Y, Gizewska M, Dascal N, Hanukoglu I | title = Renin-aldosterone response, urinary Na/K ratio and growth in pseudohypoaldosteronism patients with mutations in epithelial sodium channel (ENaC) subunit genes | journal = The Journal of Steroid Biochemistry and Molecular Biology | volume = 111 | issue = 3-5 | pages = 268–74 | date = September 2008 | pmid = 18634878 | doi = 10.1016/j.jsbmb.2008.06.013 }}
35. ^{{cite journal | vauthors = Edelheit O, Hanukoglu I, Shriki Y, Tfilin M, Dascal N, Gillis D, Hanukoglu A | title = Truncated beta epithelial sodium channel (ENaC) subunits responsible for multi-system pseudohypoaldosteronism support partial activity of ENaC | journal = The Journal of Steroid Biochemistry and Molecular Biology | volume = 119 | issue = 1-2 | pages = 84–8 | date = March 2010 | pmid = 20064610 | doi = 10.1016/j.jsbmb.2010.01.002 }}
36. ^{{cite journal | vauthors = Edelheit O, Hanukoglu I, Dascal N, Hanukoglu A | title = Identification of the roles of conserved charged residues in the extracellular domain of an epithelial sodium channel (ENaC) subunit by alanine mutagenesis | journal = American Journal of Physiology. Renal Physiology | volume = 300 | issue = 4 | pages = F887-97 | date = April 2011 | pmid = 21209000 | doi = 10.1152/ajprenal.00648.2010 }}
37. ^{{cite journal | vauthors = Edelheit O, Ben-Shahar R, Dascal N, Hanukoglu A, Hanukoglu I | title = Conserved charged residues at the surface and interface of epithelial sodium channel subunits--roles in cell surface expression and the sodium self-inhibition response | journal = The FEBS Journal | volume = 281 | issue = 8 | pages = 2097–111 | date = April 2014 | pmid = 24571549 | doi = 10.1111/febs.12765 }}
38. ^{{cite journal | vauthors = Hanukoglu I | title = ASIC and ENaC type sodium channels: Conformational states and the structures of the ion selectivity filters | journal = The FEBS Journal | volume = | issue = | date = August 2016 | pmid = 27580245 | doi = 10.1111/febs.13840 }}
39. ^1 {{cite journal | vauthors = Enuka Y, Hanukoglu I, Edelheit O, Vaknine H, Hanukoglu A | title = Epithelial sodium channels (ENaC) are uniformly distributed on motile cilia in the oviduct and the respiratory airways | journal = Histochemistry and Cell Biology | volume = 137 | issue = 3 | pages = 339–53 | date = March 2012 | pmid = 22207244 | doi = 10.1007/s00418-011-0904-1 }}
40. ^{{cite journal| author=Sharma S, Hanukoglu A, Hanukoglu I| title=Localization of epithelial sodium channel (ENaC) and CFTR in the germinal epithelium of the testis, Sertoli cells, and spermatozoa. | journal=Journal of Molecular Histology | year= 2018 | volume= 49 | issue= 2 | pages= 195–208 | pmid=29453757 | doi=10.1007/s10735-018-9759-2 }}
41. ^1 {{cite journal | vauthors = Hanukoglu I, Boggula VR, Vaknine H, Sharma S, Kleyman T, Hanukoglu A | title = Expression of epithelial sodium channel (ENaC) and CFTR in the human epidermis and epidermal appendages | journal = Histochemistry and Cell Biology | volume = 147 | issue = 6 | pages = 733–748 | date = January 2017 | pmid = 28130590 | doi = 10.1007/s00418-016-1535-3 |url=https://zenodo.org/record/890756}}
42. ^Israel Hanukoglu. [https://www.science.co.il/hi/cv-brief.php Brief Biography]
43. ^1 Israel Hanukoglu. [https://www.science.co.il/hi/CV.php Curriculum Vitae]
44. ^{{cite journal| vauthors = Tsueng G, Good BM, Ping P, Golemis E, Hanukoglu I, van Wijnen AJ, Su AI |title=Gene Wiki Reviews-Raising the quality and accessibility of information about the human genome.|journal=Gene|date=5 November 2016|volume=592|issue=2|pages=235–8|doi=10.1016/j.gene.2016.04.053|pmid=27150585|url=https://zenodo.org/record/890749}}
45. ^Candidates for the 16th Knesset {{webarchive|url=https://web.archive.org/web/20150627111958/http://www.mfa.gov.il/mfa/aboutisrael/history/pages/candidates%20for%20the%2016th%20knesset.aspx |date=2015-06-27 }} Israel Ministry of Foreign Affairs
46. ^{{Cite web|url=https://www.science.co.il/Obama-Birth-Certificate.htm|title=Long-Form Birth Certificate of Obama is a Forged Document|website=www.science.co.il|access-date=2016-12-16}}

External links

  • [https://www.science.co.il/hi/cv-brief.php BRIEF BIOGRAPHY]
  • [https://www.science.co.il/hi/ Home page of Professor Israel Hanukoglu]
  • [https://www.science.co.il/hi/pub/1999-JMB-99299392.pdf Crystal Structure of NADP binding enzyme that details the structural properties of NADP binding motif]
  • [https://scholar.google.com/citations?user=fr1qJwQAAAAJ Google Scholar profile of citations of Prof. Hanukoglu's publications]
{{Authority control}}{{DEFAULTSORT:Hanukoglu, Israel}}

10 : Israeli Jews|Israeli biochemists|Molecular biologists|Ariel University|Hebrew University of Jerusalem alumni|University of Wisconsin–Madison alumni|Israeli people of Turkish-Jewish descent|Turkish emigrants to Israel|Living people|Year of birth missing (living people)
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