المؤلفون: Elżbieta Rudolphi-Szydło, Barbara Dyba, Anna Janeczko, Dariusz Latowski, Iwona Sadura, Maria Filek

المصدر: BMC Plant Biology, Vol 22, Iss 1, Pp 1-16 (2022)

مصطلحات موضوعية: Brassinosteroids, Homocastasterone, Castasterone, Cell membrane, Langmuir technic, plant, EPR method, electrokinetic potential, Botany, QK1-989

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1471-2229

URL الوصول: https://doaj.org/article/001216e473324844935a59beff6efeee

المؤلفون: V. A. Khripach, V. N. Zhabinskii, E. V. Sikorov, S. I. Lazarev, В. А. Хрипач, В. Н. Жабинский, Е. В. Сикоров, С. И. Лазарев

المساهمون: The work was financially supported by the Belarusian Republican Foundation for Fundamental Research (grant agreement no. X23RNF-087)., Работа выполнена при финансовой поддержке Белорусского республиканского фонда фундаментальных исследований (проект Х23РНФ-087).

المصدر: Proceedings of the National Academy of Sciences of Belarus, Chemical Series; Том 59, № 3 (2023); 202-210 ; Известия Национальной академии наук Беларуси. Серия химических наук; Том 59, № 3 (2023); 202-210 ; 2524-2342 ; 1561-8331 ; 10.29235/1561-8331-2023-59-3

مصطلحات موضوعية: дебромирование, homocastasterone, epoxides, debromination, гомокастастерон, эпоксиды

وصف الملف: application/pdf

Relation: https://vestichem.belnauka.by/jour/article/view/826/711; Khripach, V. A. Brassinosteroids. A New Class of Plant Hormones / V. A. Khripach, V. N. Zhabinskii, A. E. de Groot. – San Diego: Academic Press, 1999. – 456 c.; Bajguz, A. Brassinosteroids – Occurence and Chemical Structures in Plants / A. Bajguz // Brassinosteroids: A Class of Plant Hormone / eds.: S. Hayat, Aqil Ahmad. – Dordrecht, 2011. – P. 1–27. https://doi.org/10.1007/978-94-007-0189-2_1; Wei, Z. Regulation of brassinosteroid homeostasis in higher plants / Z. Wei, J. Li // Front. Plant Sci. – 2020. – Vol. 11. – № 583622. https://doi.org/10.3389/fpls.2020.583622; The DWF4 gene of Arabidopsis encodes a cytochrome P450 that mediates multiple 22a-hydroxylation steps in bras sinosteroid biosynthesis / S. W. Choe [et al.] // Plant Cell. – 1998. – Vol. 10, № 2. – P. 231–243. https://doi.org/10.1105/tpc.10.2.231; Arabidopsis CYP90B1 catalyses the early C-22 hydroxylation of C27, C28 and C29 sterols / S. Fujita [et al.] // Plant J. – 2006. – Vol. 45, № 5. – P. 765–774. https://doi.org/10.1111/j.1365-313X.2005.02639.x; CYP724B2 and CYP90B3 function in the early C-22 hydroxylation steps of brassinosteroid biosynthetic pathway in tomato / T. Ohnishi [et al.] // Biosci. Biotechnol. Biochem. – 2006. – Vol. 70, № 9. – P. 2071–2080. https://doi.org/10.1271/bbb.60034; Khripach, V. A. Synthetic Aspects of Brassinosteroids / V. A. Khripach, V. N. Zhabinskii, Y. V. Ermolovich // Studies in Natural Products Chemistry / ed. Atta-ur-Rahman. – Amsterdam, 2015. – P. 309–352. https://doi.org/10.1016/B978-0-444-63460-3.00006-7; Synthesis of hexadeuterated 23-dehydroxybrassinosteroids / V. A. Khripach [et al.] // Steroids. – 2002. – Vol. 67, № 13–14. – P. 1101–1108. https://doi.org/10.1016/S0039-128X(02)00071-5; Synthesis of [26,27-2H6]brassinosteroids from 23,24-bisnorcholenic acid methyl ester / A. P. Antonchick [et al.] // Steroids. – 2004. – Vol. 69, № 10. – P. 617–628. https://doi.org/10.1016/j.steroids.2004.05.014; Hurski, A. L. A new approach to the side chain formation of 24-alkyl-22-hydroxy steroids: application to the preparation of early brassinolide biosynthetic precursors / A. L. Hurski, V. N. Zhabinskii, V. A. Khripach // Steroids. – 2012. – Vol. 77, № 7. – P. 780–790. https://doi.org/10.1016/j.steroids.2012.03.010; A convenient synthesis of (22S)-22-hydroxycampesterol and some related steroids / S. Takatsuto [et al.] // J. Chem. Res. (S). – 1998. – № 4. – P. 176–177. https://doi.org/10.1039/A707201E; A concise and stereoselective synthesis of the cathasterone’s side chain / T. S. Mei [et al.] // Chin. Chem. Lett. – 2004. – Vol. 15. – P. 762–764.; Synthesis of cathasterone and its related putative intermediates in brassinolide biosynthesis / S. Takatsuto [et al.] // J. Chem. Res. (S). – 1997. – № 11. – P. 418–419. https://doi.org/10.1039/A704788F; Synthesis of 24-epicathasterone and related brassinosteroids with modified side chain / B. Voigt [et al.] // Tetrahedron. – 1997. – Vol. 53, № 50. – P. 17039–17054. https://doi.org/10.1016/S0040-4020(97)10146-6; Новый синтез (22S,23S)-28-гомокастастерона / А. А. Ахрем [и др.] // Докл. Акад. наук СССР. – 1984. – Т. 275, № 5. – С. 1089–1091.; Fuentes-Figuerо E. Burgueno-Tapia // Chirality. – 2022. – Vol. 34, № 2. – P. 396–420. https://doi.org/10.1002/chir.23390; Configurational assignment of epimeric 22,23-epoxides of steroids by C-13 NMR-spectroscopy / M. G. Sierra [et al.] // Tetrahedron. – 1986. – Vol. 42, № 2. – P. 755–758. https://doi.org/10.1016/S0040-4020(01)87482-2; Nakane, M. Stereoselectivity in the electrophilic addition reactions of stigmast-22(23)-ene derivatives / M. Nakane, M. Morisaki, N. Ikekawa // Tetrahedron. – 1975. – Vol. 31, № 22. – P. 2755–2760. https://doi.org/10.1016/0040-4020(75)80285-7; https://vestichem.belnauka.by/jour/article/view/826

الاتاحة: https://vestichem.belnauka.by/jour/article/view/826
https://doi.org/10.29235/1561-8331-2023-59-3-202-210

المؤلفون: Julia Stachurska, Magdalena Rys, Ewa Pociecha, Hazem M. Kalaji, Piotr Dąbrowski, Jana Oklestkova, Barbara Jurczyk, Anna Janeczko

المصدر: International Journal of Molecular Sciences; Volume 23; Issue 9; Pages: 5224

مصطلحات موضوعية: brassinosteroids, brassinosteroid insensitive 1, dehardening, delayed chlorophyll fluorescence, frost tolerance, homocastasterone, photosystem I, photosystem II, prompt chlorophyll fluorescence, stress tolerance

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Molecular Plant Sciences; https://dx.doi.org/10.3390/ijms23095224

الاتاحة: https://doi.org/10.3390/ijms23095224

المؤلفون: N. A. Laman, K. R. Kem, V. I. Anikeev, V. N. Zhabinskii, N. B. Khripach, Н. А. Ламан, К. Р. Кем, В. И. Аникеев, В. Н. Жабинский, Н. Б. Хрипач

المصدر: Doklady of the National Academy of Sciences of Belarus; Том 66, № 2 (2022); 199-205 ; Доклады Национальной академии наук Беларуси; Том 66, № 2 (2022); 199-205 ; 2524-2431 ; 1561-8323 ; 10.29235/1561-8323-2022-66-2

مصطلحات موضوعية: ингибирование, winter wheat, fiber flax, salinization, salt stress, brassinosteroids, brassinolide, epibrassinolide, homobrassinolide, homocastasterone, incrustation, inhibition, озимая пшеница, лен-долгунец, засоление, солевой стресс, брассиностероиды, брассинолид, эпибрассинолид, гомобрассинолид, гомокастастерон, инкрустация

وصف الملف: application/pdf

Relation: https://doklady.belnauka.by/jour/article/view/1055/1051; Khripach, V. A. Brassinosteroids – A New Class of Plant Hormones / V. A. Khripach, V. N. Zhabinskii, Ae. De Groot. – Academic Press, 1999. – 456 p. https://doi.org/10.1016/b978-0-12-406360-0.x5000-x; Brassinosteroids: multidimensional regulators of plant growth, development, and stress responses / T. M. Nolan [et al.] // Plant Cell. – 2020. – Vol. 32, N 2. – P. 295–318. https://doi.org/10.1105/tpc.19.00335; The physiological and molecular mechanism of brassinosteroid in response to stress: a review / A. Anwar [et al.] // Biological Research. – 2018. – Vol. 51, N 1. – Art. 46. https://doi.org/10.1186/s40659-018-0195-2; Ability of lactone- and ketone-containing brassinosteroids to induce priming in rapeseed plants to salt stress / L. V. Kolomeichuk [et al.] // Russian Journal of Plant Physiology. – 2021. – Vol. 68, N 3. – P. 499–509. https://doi.org/10.1134/s1021443721020084; Nolan, T. Cross-talk of brassinosteroid signaling in controlling growth and stress responses / T. Nolan, J. Chen, Y. Yin // Biochemical Journal. – 2017. – Vol. 474, N 16. – P. 2641–2661. https://doi.org/10.1042/bcj20160633; Understanding brassinosteroid-regulated mechanisms to improve stress tolerance in plants: a critical review / F. Nawaz [et al.] // Environmental Science and Pollution Research. – 2017. – Vol. 24, N 19. – P. 15959–15975. https://doi.org/10.1007/s11356-017-9163-6; Влияние инкрустации семян смесями N-фосфонометилглицина и эпибрассинолида на рост растений / Н. А. Ламан [и др.] // Докл. Нац. акад. наук Беларуси. – 2016. – Т. 60, № 6. – С. 84–90.; Ламан, Н. А. Ростовые реакции проростков отдельных видов и сортов сельскохозяйственных растений на обработку семян глифосатом (N-фосфонометилглицином) / Н. А. Ламан, К. Р. Кем, А. Ф. Судник // Вес. Нац. акад. навук Беларусi. Сер. бiял. навук. – 2016. – № 4. – С. 7–13.; Hasanuzzaman, M. Plant response to salt stress and role of exogenous protectants to mitigate salt-induced damages / M. Hasanuzzaman, K. Nahar, M. Fujita // Ecophysiology and Responses of Plants Under Salt Stress. – New York, 2013. – P. 25–87. https://doi.org/10.1007/978-1-4614-4747-4_2; Effect of brassinosteroids on protein synthesis and plant-cell ultrastructure under stress conditions / O. N. Kulaeva [et al.] // ACS Symposium Series. – 1999. – Vol. 474 (Brassinosteroids). – P. 141–155. https://doi.org/10.1021/bk-1991-0474.ch012; Role of nitric oxide in hydrogen peroxide-dependent induction of abiotic stress tolerance by brassinosteroids in cucumber / J.-X. Cui [et al.] // Plant, Cell and Environment. – 2011. – Vol. 34, N 2. – P. 347–358. https://doi.org/10.1111/j.1365-3040.2010.02248.x; Влияние лактон- и кетонсодержащих брассиностероидов на фотосинтетическую активность листьев ячменя при старении / И. С. Ковтун [и др.] // Физиология растений. – 2021. – Т. 68, № 3. – C. 268–278.; Laman, N. A. The sprouting of small, flat and long germinating seeds by roll method using a synthetic ventilation grid / N. A. Laman, S. I. Budai, O. E. Barnatovich // Proceedings of the Academy Agrarian Sciences of Republic of Belarus. – 2000. – Vol. 4. – P. 57–61.; Особенности действия брассиностероидов в составе инсекто-фунгицидных композиций на рост проростков рапса (Brassica napus L.) в условиях низкотемпературного стресса / А. Ф. Судник [и др.] // Ботаника (исследования). – Минск, 2011. – Вып. 40. – С. 560–574.; Альмиклафи, Ж. А. К. Х. Исследование стресс-протекторного действия брассиностероидов на растения рапса: дис. … канд. биол. наук / Ж. А. К. Х. Альмиклафи. – М., 2014. – 108 с.; https://doklady.belnauka.by/jour/article/view/1055

الاتاحة: https://doklady.belnauka.by/jour/article/view/1055
https://doi.org/10.29235/1561-8323-2022-66-2-199-205

المؤلفون: Andrés Martin, Bellido, Ayelén Mariana, Distéfano, Nicolás, Setzes, María Milagros, Cascallares, Jana, Oklestkova, Ondrej, Novak, Javier Alberto, Ramirez, Eduardo J, Zabaleta, Diego F, Fiol, Gabriela C, Pagnussat

المصدر: Proceedings of the National Academy of Sciences of the United States of America

مصطلحات موضوعية: endocrine system, homocastasterone, Adrenodoxin, Arabidopsis, Embryonic Development, Phytosterols, Plant Biology, Biological Sciences, Gametogenesis, Mitochondria, Electron Transport, Ferredoxin-NADP Reductase, Cytochrome P-450 Enzyme System, Electron Transport Chain Complex Proteins, Mitochondrial Membranes, embryogenesis, Amino Acid Sequence, Germ Cells, Plant, gametophyte, plant reproduction, hormones, hormone substitutes, and hormone antagonists, Protein Binding, P450

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::81ff8a84fa1e4dd1fafe07522b21f1dc
https://pubmed.ncbi.nlm.nih.gov/35046016

المؤلفون: Elżbieta Rudolphi-Szydło, Barbara Dyba, Anna Janeczko, Dariusz Latowski, Iwona Sadura, Maria Filek

المصدر: BMC plant biology. 22(1)

مصطلحات موضوعية: Cold Temperature, brassinosteroids, homocastasterone, EPR method, Brassinosteroids, Temperature, Langmuir technic, plant, Plant Science, electrokinetic potential, castasterone, cell membrane

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5269922f95a95c4f0bc59018d3b83449
https://pubmed.ncbi.nlm.nih.gov/35585507

المؤلفون: Wendy A. Stirk, Miroslav Strnad, Danuše Tarkowská, Johannes Van Staden, Vince Ördög, Péter Bálint

المصدر: European Journal of Phycology
riUAL. Repositorio Institucional de la Universidad de Almería
Universidad de Almería

مصطلحات موضوعية: 0106 biological sciences, 0301 basic medicine, chemistry.chemical_classification, endocrine system, Salt (chemistry), Endogeny, Plant Science, Aquatic Science, Biology, Homocastasterone, 01 natural sciences, Temperature stress, 03 medical and health sciences, chemistry.chemical_compound, 030104 developmental biology, chemistry, Biochemistry, 010606 plant biology & botany, Brassinolide

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b183ccd7511c1371926e05a16577a805
https://doi.org/10.1080/09670262.2018.1441447

المؤلفون: Mahadeo R. Patil, Aleš Marek, Tomáš Elbert

المصدر: Journal of Labelled Compounds and Radiopharmaceuticals. 60:176-182

مصطلحات موضوعية: 010405 organic chemistry, Chemistry, Organic Chemistry, Radiochemistry, Stereoisomerism, Tritium, 010402 general chemistry, Homocastasterone, 01 natural sciences, Biochemistry, Catalysis, Cholestanones, 0104 chemical sciences, Analytical Chemistry, Isotope Labeling, Yield (chemistry), Drug Discovery, Radiology, Nuclear Medicine and imaging, Specific activity, Spectroscopy

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e29b65b0b0754116d76d0b9d6d85fd4
https://doi.org/10.1002/jlcr.3488

المؤلفون: D. Vijayalakshmi, Kotteazeth Srikumar, Velan Athithan

المصدر: Chemico-Biological Interactions. 331:109215

مصطلحات موضوعية: medicine.medical_specialty, Endocrinology, Chemistry, Internal medicine, medicine, General Medicine, Toxicology, Homocastasterone, Liver X receptor, Chem biol, Cholesterol triglycerides

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::34a1285f5add898730bf4e711d3a9284
https://doi.org/10.1016/j.cbi.2020.109215

المؤلفون: Javier A. Ramírez, Lydia R. Galagovsky, Adaucto Bellarmino Pereira-Netto

المصدر: Scientia Horticulturae. 181:13-17

مصطلحات موضوعية: 28-HOMOCASTASTERONE, Mutant, Stimulation, Horticulture, Biology, Homocastasterone, behavioral disciplines and activities, Ciencias Biológicas, Plantlet, chemistry.chemical_compound, Nutrient, Biosynthesis, LYCOPERSICUM ESCULENTUM, mental disorders, Botany, ROOTING, Ciencias de las Plantas, Botánica, BRASSINOSTEROIDS, fungi, chemistry, embryonic structures, Shoot, sense organs, Elongation, CIENCIAS NATURALES Y EXACTAS

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::118fd07f0af261d152043565ee600c63
https://doi.org/10.1016/j.scienta.2014.10.048

المؤلفون: M. E. Raiman, R. P. Litvinovskaya, Vladimir A. Khripach

المصدر: Russian Journal of Organic Chemistry. 44:1614-1618

مصطلحات موضوعية: chemistry.chemical_compound, Hydrolysis, Acetic acid, Chemistry, Boiling, Organic Chemistry, Organic chemistry, chemistry.chemical_element, Osmium, Homocastasterone, Derivative (chemistry), Boron trifluoride

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::48fa2fd57dd42a4f43eb8b341d023be5
https://doi.org/10.1134/s1070428008110080

المؤلفون: D. K. Buslov, Vladimir A. Khripach, V. N. Zhabinsky, N. A. Borisevich

المصدر: Journal of Applied Spectroscopy. 75:637-643

مصطلحات موضوعية: Group (periodic table), Chemistry, Analytical chemistry, Side chain, Infrared spectroscopy, Optical density, Condensed Matter Physics, Homocastasterone, Maxima, Spectroscopy, Spectral line

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::a936fe5f8107ede91d90868e5b2d05ed
https://doi.org/10.1007/s10812-008-9111-9

المؤلفون: V, Athithan, R, Premalatha, Mukherjee, Victor, N, Mani, K, Srikumar

المصدر: International Journal of Pharmacy and Pharmaceutical Sciences; Vol 7, Issue 7, 2015; 125-128 ; 0975-1491 ; 2656-0097

مصطلحات موضوعية: Homocastasterone, Oxysterol, Haematological parameters, Blood glucose, Lipid peroxidation, Pharmacology

وصف الملف: application/pdf; text/html

Relation: https://journals.innovareacademics.in/index.php/ijpps/article/view/5980/pdf_917; https://journals.innovareacademics.in/index.php/ijpps/article/view/5980/7097; https://journals.innovareacademics.in/index.php/ijpps/article/view/5980

الاتاحة: https://journals.innovareacademics.in/index.php/ijpps/article/view/5980

المؤلفون: Srikumar Kotteazeth, Athithan Velan

المصدر: International Journal of Clinical and Experimental Physiology. 5:48

مصطلحات موضوعية: Hexokinase, chemistry.chemical_compound, Biochemistry, chemistry, Oxysterol, Mrna expression, Homocastasterone, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::80c1fe45231b4f1701ed1ce9e31427a7
https://doi.org/10.4103/ijcep.ijcep_12_18

المؤلفون: Ramírez, J.A., Brosa, C., Galagovsky, L.R.

مصطلحات موضوعية: Bioactivity, Brassinosteroids, Gramineae, Oryza sativa, Synthesis of fluorinated analogues, 6 deoxo 28 homocastasterone stigmasta 2alpha,3alpha,22,23 tetraol, 6alpha fluorostigmasta 2alpha,3alpha,22,23 tetraol, 6alpha hydroxy 28 homocastasterone stigmasta 2alpha,3alpha,6alpha,22,23 pentaol, 6beta hydroxy 28 homocastasterone stigmasta 2alpha,3alpha,6beta,22,23 pentaol, brassinosteroid, functional group, hexamethonium bromide, hydroxyl group, phytohormone, unclassified drug, article, drug activity, hormone action, Poaceae, rice, synthesis

Relation: http://hdl.handle.net/20.500.12110/paper_00319422_v66_n5_p581_Ramirez

الاتاحة: https://hdl.handle.net/20.500.12110/paper_00319422_v66_n5_p581_Ramirez

المؤلفون: Bellido, Andres, Distefano, Ayelen Mariana, Setzes, Nicolás, Cascallares, María Milagros, Oklestkova, Jana, Novak, Ondrej, Ramirez, Javier Alberto, Zabaleta, Eduardo Julian, Fiol, Diego Fernando, Pagnussat, Gabriela Carolina

مصطلحات موضوعية: EMBRYOGENESIS, GAMETOPHYTE, HOMOCASTASTERONE, P450, PLANT REPRODUCTION, https://purl.org/becyt/ford/1.6, https://purl.org/becyt/ford/1

وصف الملف: application/pdf

Relation: http://hdl.handle.net/11336/210629; CONICET Digital; CONICET

الاتاحة: http://hdl.handle.net/11336/210629

المؤلفون: Acebedo, S.L., Alonso, F., Galagovsky, L.R., Ramírez, J.A.

مصطلحات موضوعية: Brassinosteroids, Difluorinated steroids, Plant hormones, 28 homocastasterone, 2alpha, 3alpha difluoro 22,23 dihydroxy 5alpha stigmastan 6 one, 2alpha,3alpha difluoro 5alpha stigmast 22 en 6 one, 3,3 difluoro 22,23 dihydroxy 5alpha stigmastan 6 one, 3,3 difluoro 5alpha stigmast 22 en 6 one, brassinosteroid, unclassified drug, article, biological activity, controlled study, fluorination, receptor binding, synthesis, Cholestanols, Magnetic Resonance Spectroscopy, Molecular Structure, Steroids, Heterocyclic, Structure-Activity Relationship

Relation: http://hdl.handle.net/20.500.12110/paper_0039128X_v76_n10-11_p1016_Acebedo

الاتاحة: https://hdl.handle.net/20.500.12110/paper_0039128X_v76_n10-11_p1016_Acebedo

المؤلفون: Galagovsky, L.R., Gros, E.G., Ramírez, J.A.

مصطلحات موضوعية: 28-Homobrassinolide, Bioactivity, Biosynthesis, Brassinosteroids, C-3 Fluorinated analogs, 22,23 dihydroxy 3alpha fluorostigmastan 6 one, 22,23 dihydroxy 3beta fluorostigmastan 6 one, 24 ethylbrassinosteroid derivative, 24 methylbrassinosteroid derivative, 28 homobrassinolide, 28 homocastasterone, 28 homoteasterone, 28 homotyphasterol, brassinolide, cholestane derivative, fluorine, homobrassinolide, unclassified drug, article, bioassay, chemical structure, chemistry, fluorination, mass spectrometry, methodology, nuclear magnetic resonance spectroscopy, plant growth, rice, synthesis, Cholestanones

Relation: http://hdl.handle.net/20.500.12110/paper_00319422_v58_n6_p973_Galagovsky

الاتاحة: https://hdl.handle.net/20.500.12110/paper_00319422_v58_n6_p973_Galagovsky

المؤلفون: Pereira-Netto, A.B., Cruz-Silva, C.T.A., Schaefer, S., Ramírez, J.A., Galagovsky, L.R.

مصطلحات موضوعية: 28-Homocastasterone, 5F-HCTS, Ethylene, Malus prunifolia, Carboxylic acids, Hormones, Wood, Brassinosteroids, Homocastasterone, Micropropagation techniques, Rootstock, Plants (botany), Branches, Brass, Elongation, Malus, Plants, Embryophyta, Malus x domestica

Relation: http://hdl.handle.net/20.500.12110/paper_09311890_v20_n3_p286_PereiraNetto

الاتاحة: https://hdl.handle.net/20.500.12110/paper_09311890_v20_n3_p286_PereiraNetto

المؤلفون: Athithan V, Premalatha R, Srikumar K

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://arjournals.org/index.php/ijdd/article/viewFile/1460/pdf/.

مصطلحات موضوعية: Homocastasterone, ketosteroid, plasma lipid, blood glucose, marker enzyme

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.654.8691; http://arjournals.org/index.php/ijdd/article/viewFile/1460/pdf/

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.654.8691
http://arjournals.org/index.php/ijdd/article/viewFile/1460/pdf/