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Items: 1 to 50 of 130

1.

Spin-momentum locked spin manipulation in a two-dimensional Rashba system.

Kohda M, Okayasu T, Nitta J.

Sci Rep. 2019 Feb 13;9(1):1909. doi: 10.1038/s41598-018-37967-9.

2.

If a fish can pass the mark test, what are the implications for consciousness and self-awareness testing in animals?

Kohda M, Hotta T, Takeyama T, Awata S, Tanaka H, Asai JY, Jordan AL.

PLoS Biol. 2019 Feb 7;17(2):e3000021. doi: 10.1371/journal.pbio.3000021. eCollection 2019 Feb.

3.

Cardiomyopathy in children with mitochondrial disease: Prognosis and genetic background.

Imai-Okazaki A, Kishita Y, Kohda M, Mizuno Y, Fushimi T, Matsunaga A, Yatsuka Y, Hirata T, Harashima H, Takeda A, Nakaya A, Sakata Y, Kogaki S, Ohtake A, Murayama K, Okazaki Y.

Int J Cardiol. 2019 Mar 15;279:115-121. doi: 10.1016/j.ijcard.2019.01.017. Epub 2019 Jan 5.

PMID:
30642647
4.

Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome.

Borna NN, Kishita Y, Kohda M, Lim SC, Shimura M, Wu Y, Mogushi K, Yatsuka Y, Harashima H, Hisatomi Y, Fushimi T, Ichimoto K, Murayama K, Ohtake A, Okazaki Y.

Neurogenetics. 2019 Jan 3. doi: 10.1007/s10048-018-0561-9. [Epub ahead of print]

PMID:
30607703
5.

Does a cichlid fish process face holistically? Evidence of the face inversion effect.

Kawasaka K, Hotta T, Kohda M.

Anim Cogn. 2019 Mar;22(2):153-162. doi: 10.1007/s10071-018-01231-4. Epub 2019 Jan 2.

PMID:
30603930
6.
7.

Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.

Martin CA, Sarlós K, Logan CV, Thakur RS, Parry DA, Bizard AH, Leitch A, Cleal L, Ali NS, Al-Owain MA, Allen W, Altmüller J, Aza-Carmona M, Barakat BAY, Barraza-García J, Begtrup A, Bogliolo M, Cho MT, Cruz-Rojo J, Dhahrabi HAM, Elcioglu NH; GOSgene, Gorman GS, Jobling R, Kesterton I, Kishita Y, Kohda M, Le Quesne Stabej P, Malallah AJ, Nürnberg P, Ohtake A, Okazaki Y, Pujol R, Ramirez MJ, Revah-Politi A, Shimura M, Stevens P, Taylor RW, Turner L, Williams H, Wilson C, Yigit G, Zahavich L, Alkuraya FS, Surralles J, Iglesias A, Murayama K, Wollnik B, Dattani M, Heath KE, Hickson ID, Jackson AP.

Am J Hum Genet. 2018 Sep 6;103(3):456. doi: 10.1016/j.ajhg.2018.08.012. No abstract available.

8.

Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.

Martin CA, Sarlós K, Logan CV, Thakur RS, Parry DA, Bizard AH, Leitch A, Cleal L, Ali NS, Al-Owain MA, Allen W, Altmüller J, Aza-Carmona M, Barakat BAY, Barraza-García J, Begtrup A, Bogliolo M, Cho MT, Cruz-Rojo J, Dhahrabi HAM, Elcioglu NH; GOSgene, Gorman GS, Jobling R, Kesterton I, Kishita Y, Kohda M, Le Quesne Stabej P, Malallah AJ, Nürnberg P, Ohtake A, Okazaki Y, Pujol R, Ramirez MJ, Revah-Politi A, Shimura M, Stevens P, Taylor RW, Turner L, Williams H, Wilson C, Yigit G, Zahavich L, Alkuraya FS, Surralles J, Iglesias A, Murayama K, Wollnik B, Dattani M, Heath KE, Hickson ID, Jackson AP.

Am J Hum Genet. 2018 Aug 2;103(2):221-231. doi: 10.1016/j.ajhg.2018.07.001. Epub 2018 Jul 26. Erratum in: Am J Hum Genet. 2018 Sep 6;103(3):456.

9.

Identification of the Coiled-Coil Domain as an Essential Methyl-CpG-Binding Domain Protein 3 Element for Preserving Lineage Commitment Potential of Embryonic Stem Cells.

Hirasaki M, Ueda A, Asaka MN, Uranishi K, Suzuki A, Kohda M, Mizuno Y, Okazaki Y, Nishimoto M, Sharif J, Koseki H, Okuda A.

Stem Cells. 2018 Sep;36(9):1355-1367. doi: 10.1002/stem.2849. Epub 2018 Jul 15.

PMID:
29761578
10.

Leigh syndrome with spinal cord involvement due to a hemizygous NDUFA1 mutation.

Miyauchi A, Osaka H, Nagashima M, Kuwajima M, Monden Y, Kohda M, Kishita Y, Okazaki Y, Murayama K, Ohtake A, Yamagata T.

Brain Dev. 2018 Jun;40(6):498-502. doi: 10.1016/j.braindev.2018.02.007. Epub 2018 Mar 3.

PMID:
29506883
11.

Characteristics of MUTYH variants in Japanese colorectal polyposis patients.

Takao M, Yamaguchi T, Eguchi H, Tada Y, Kohda M, Koizumi K, Horiguchi SI, Okazaki Y, Ishida H.

Int J Clin Oncol. 2018 Jun;23(3):497-503. doi: 10.1007/s10147-017-1234-7. Epub 2018 Jan 12.

PMID:
29330641
12.

Barth Syndrome: Different Approaches to Diagnosis.

Imai-Okazaki A, Kishita Y, Kohda M, Yatsuka Y, Hirata T, Mizuno Y, Harashima H, Hirono K, Ichida F, Noguchi A, Yoshida M, Tokorodani C, Nishiuchi R, Takeda A, Nakaya A, Sakata Y, Murayama K, Ohtake A, Okazaki Y.

J Pediatr. 2018 Feb;193:256-260. doi: 10.1016/j.jpeds.2017.09.075. Epub 2017 Dec 15.

PMID:
29249525
13.

Drift-Induced Enhancement of Cubic Dresselhaus Spin-Orbit Interaction in a Two-Dimensional Electron Gas.

Kunihashi Y, Sanada H, Tanaka Y, Gotoh H, Onomitsu K, Nakagawara K, Kohda M, Nitta J, Sogawa T.

Phys Rev Lett. 2017 Nov 3;119(18):187703. doi: 10.1103/PhysRevLett.119.187703. Epub 2017 Oct 31.

PMID:
29219564
14.

A social cichlid fish failed to pass the mark test.

Hotta T, Komiyama S, Kohda M.

Anim Cogn. 2018 Jan;21(1):127-136. doi: 10.1007/s10071-017-1146-y. Epub 2017 Nov 17.

PMID:
29150813
15.

Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies.

Feichtinger RG, Oláhová M, Kishita Y, Garone C, Kremer LS, Yagi M, Uchiumi T, Jourdain AA, Thompson K, D'Souza AR, Kopajtich R, Alston CL, Koch J, Sperl W, Mastantuono E, Strom TM, Wortmann SB, Meitinger T, Pierre G, Chinnery PF, Chrzanowska-Lightowlers ZM, Lightowlers RN, DiMauro S, Calvo SE, Mootha VK, Moggio M, Sciacco M, Comi GP, Ronchi D, Murayama K, Ohtake A, Rebelo-Guiomar P, Kohda M, Kang D, Mayr JA, Taylor RW, Okazaki Y, Minczuk M, Prokisch H.

Am J Hum Genet. 2017 Oct 5;101(4):525-538. doi: 10.1016/j.ajhg.2017.08.015. Epub 2017 Sep 21.

16.

Laterality is Universal Among Fishes but Increasingly Cryptic Among Derived Groups.

Hori M, Nakajima M, Hata H, Yasugi M, Takahashi S, Nakae M, Yamaoka K, Kohda M, Kitamura JI, Maehata M, Tanaka H, Okada N, Takeuchi Y.

Zoolog Sci. 2017 Aug;34(4):267-274. doi: 10.2108/zs160196.

PMID:
28770681
17.

HDR-del: A tool based on Hamming distance for prioritizing pathogenic chromosomal deletions in exome sequencing.

Imai-Okazaki A, Kohda M, Kobayashi K, Hirata T, Sakata Y, Murayama K, Ohtake A, Okazaki Y, Nakaya A, Ott J.

Hum Mutat. 2017 Dec;38(12):1796-1800. doi: 10.1002/humu.23298. Epub 2017 Sep 21.

PMID:
28722338
18.

ATAD3 gene cluster deletions cause cerebellar dysfunction associated with altered mitochondrial DNA and cholesterol metabolism.

Desai R, Frazier AE, Durigon R, Patel H, Jones AW, Dalla Rosa I, Lake NJ, Compton AG, Mountford HS, Tucker EJ, Mitchell ALR, Jackson D, Sesay A, Di Re M, van den Heuvel LP, Burke D, Francis D, Lunke S, McGillivray G, Mandelstam S, Mochel F, Keren B, Jardel C, Turner AM, Ian Andrews P, Smeitink J, Spelbrink JN, Heales SJ, Kohda M, Ohtake A, Murayama K, Okazaki Y, Lombès A, Holt IJ, Thorburn DR, Spinazzola A.

Brain. 2017 Jun 1;140(6):1595-1610. doi: 10.1093/brain/awx094.

19.

Clinical validity of biochemical and molecular analysis in diagnosing Leigh syndrome: a study of 106 Japanese patients.

Ogawa E, Shimura M, Fushimi T, Tajika M, Ichimoto K, Matsunaga A, Tsuruoka T, Ishige M, Fuchigami T, Yamazaki T, Mori M, Kohda M, Kishita Y, Okazaki Y, Takahashi S, Ohtake A, Murayama K.

J Inherit Metab Dis. 2017 Sep;40(5):685-693. doi: 10.1007/s10545-017-0042-6. Epub 2017 Apr 20.

20.

A novel mutation in TAZ causes mitochondrial respiratory chain disorder without cardiomyopathy.

Borna NN, Kishita Y, Ishikawa K, Nakada K, Hayashi JI, Tokuzawa Y, Kohda M, Nyuzuki H, Yamashita-Sugahara Y, Nasu T, Takeda A, Murayama K, Ohtake A, Okazaki Y.

J Hum Genet. 2017 Apr;62(5):539-547. doi: 10.1038/jhg.2016.165. Epub 2017 Jan 26.

PMID:
28123175
21.

DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burst.

Zaha K, Matsumoto H, Itoh M, Saitsu H, Kato K, Kato M, Ogata S, Murayama K, Kishita Y, Mizuno Y, Kohda M, Nishino I, Ohtake A, Okazaki Y, Matsumoto N, Nonoyama S.

Clin Genet. 2016 Nov;90(5):472-474. doi: 10.1111/cge.12805. Epub 2016 Jun 14. No abstract available.

PMID:
27301544
22.

Dried blood spots for newborn screening allows easy determination of a high heteroplasmy rate in severe infantile cardiomyopathy.

Imai A, Kishita Y, Nakayama Y, Fujita S, Futatani T, Kohda M, Yatsuka Y, Nakaya A, Sakata Y, Murayama K, Ohtake A, Okazaki Y.

Int J Cardiol. 2016 Oct 15;221:446-9. doi: 10.1016/j.ijcard.2016.06.287. Epub 2016 Jun 29. No abstract available.

PMID:
27409572
23.

Observation of the D'yakonov-Perel' Spin Relaxation in Single-Crystalline Pt Thin Films.

Ryu J, Kohda M, Nitta J.

Phys Rev Lett. 2016 Jun 24;116(25):256802. doi: 10.1103/PhysRevLett.116.256802. Epub 2016 Jun 22.

PMID:
27391739
24.

HDR: a statistical two-step approach successfully identifies disease genes in autosomal recessive families.

Imai A, Kohda M, Nakaya A, Sakata Y, Murayama K, Ohtake A, Lathrop M, Okazaki Y, Ott J.

J Hum Genet. 2016 Nov;61(11):959-963. doi: 10.1038/jhg.2016.85. Epub 2016 Jun 30.

25.

Current-Controlled Spin Precession of Quasistationary Electrons in a Cubic Spin-Orbit Field.

Altmann P, Hernandez FG, Ferreira GJ, Kohda M, Reichl C, Wegscheider W, Salis G.

Phys Rev Lett. 2016 May 13;116(19):196802. doi: 10.1103/PhysRevLett.116.196802. Epub 2016 May 9.

PMID:
27232032
26.

Facial Recognition in a Discus Fish (Cichlidae): Experimental Approach Using Digital Models.

Satoh S, Tanaka H, Kohda M.

PLoS One. 2016 May 18;11(5):e0154543. doi: 10.1371/journal.pone.0154543. eCollection 2016.

27.

Drift transport of helical spin coherence with tailored spin-orbit interactions.

Kunihashi Y, Sanada H, Gotoh H, Onomitsu K, Kohda M, Nitta J, Sogawa T.

Nat Commun. 2016 Mar 8;7:10722. doi: 10.1038/ncomms10722.

28.

Rapid detection of germline mutations for hereditary gastrointestinal polyposis/cancers using HaloPlex target enrichment and high-throughput sequencing technologies.

Kohda M, Kumamoto K, Eguchi H, Hirata T, Tada Y, Tanakaya K, Akagi K, Takenoshita S, Iwama T, Ishida H, Okazaki Y.

Fam Cancer. 2016 Oct;15(4):553-62. doi: 10.1007/s10689-016-9872-x.

PMID:
26837502
29.

Rapidly progressive infantile cardiomyopathy with mitochondrial respiratory chain complex V deficiency due to loss of ATPase 6 and 8 protein.

Imai A, Fujita S, Kishita Y, Kohda M, Tokuzawa Y, Hirata T, Mizuno Y, Harashima H, Nakaya A, Sakata Y, Takeda A, Mori M, Murayama K, Ohtake A, Okazaki Y.

Int J Cardiol. 2016 Mar 15;207:203-5. doi: 10.1016/j.ijcard.2016.01.026. Epub 2016 Jan 7. No abstract available.

PMID:
26803244
30.

A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies.

Kohda M, Tokuzawa Y, Kishita Y, Nyuzuki H, Moriyama Y, Mizuno Y, Hirata T, Yatsuka Y, Yamashita-Sugahara Y, Nakachi Y, Kato H, Okuda A, Tamaru S, Borna NN, Banshoya K, Aigaki T, Sato-Miyata Y, Ohnuma K, Suzuki T, Nagao A, Maehata H, Matsuda F, Higasa K, Nagasaki M, Yasuda J, Yamamoto M, Fushimi T, Shimura M, Kaiho-Ichimoto K, Harashima H, Yamazaki T, Mori M, Murayama K, Ohtake A, Okazaki Y.

PLoS Genet. 2016 Jan 7;12(1):e1005679. doi: 10.1371/journal.pgen.1005679. eCollection 2016 Jan.

31.

The social and ecological costs of an 'over-extended' phenotype.

Jordan LA, Maguire SM, Hofmann HA, Kohda M.

Proc Biol Sci. 2016 Jan 13;283(1822). pii: 20152359. doi: 10.1098/rspb.2015.2359.

32.

Identification of a Japanese Lynch syndrome patient with large deletion in the 3' region of the EPCAM gene.

Eguchi H, Kumamoto K, Suzuki O, Kohda M, Tada Y, Okazaki Y, Ishida H.

Jpn J Clin Oncol. 2016 Feb;46(2):178-84. doi: 10.1093/jjco/hyv172. Epub 2015 Nov 27.

PMID:
26613680
33.

Facial Recognition in a Group-Living Cichlid Fish.

Kohda M, Jordan LA, Hotta T, Kosaka N, Karino K, Tanaka H, Taniyama M, Takeyama T.

PLoS One. 2015 Nov 25;10(11):e0142552. doi: 10.1371/journal.pone.0142552. eCollection 2015.

34.

Depth segregation and diet disparity revealed by stable isotope analyses in sympatric herbivorous cichlids in Lake Tanganyika.

Hata H, Shibata J, Omori K, Kohda M, Hori M.

Zoological Lett. 2015 May 14;1:15. doi: 10.1186/s40851-015-0016-1. eCollection 2015.

35.

Developmental origin of abnormal dendritic growth in the mouse brain induced by in utero disruption of aryl hydrocarbon receptor signaling.

Kimura E, Kubo K, Matsuyoshi C, Benner S, Hosokawa M, Endo T, Ling W, Kohda M, Yokoyama K, Nakajima K, Kakeyama M, Tohyama C.

Neurotoxicol Teratol. 2015 Nov-Dec;52(Pt A):42-50. doi: 10.1016/j.ntt.2015.10.005. Epub 2015 Oct 23.

36.

Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26.

Kishita Y, Pajak A, Bolar NA, Marobbio CM, Maffezzini C, Miniero DV, Monné M, Kohda M, Stranneheim H, Murayama K, Naess K, Lesko N, Bruhn H, Mourier A, Wibom R, Nennesmo I, Jespers A, Govaert P, Ohtake A, Van Laer L, Loeys BL, Freyer C, Palmieri F, Wredenberg A, Okazaki Y, Wedell A.

Am J Hum Genet. 2015 Nov 5;97(5):761-8. doi: 10.1016/j.ajhg.2015.09.013. Epub 2015 Oct 29.

37.

Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement.

Haack TB, Jackson CB, Murayama K, Kremer LS, Schaller A, Kotzaeridou U, de Vries MC, Schottmann G, Santra S, Büchner B, Wieland T, Graf E, Freisinger P, Eggimann S, Ohtake A, Okazaki Y, Kohda M, Kishita Y, Tokuzawa Y, Sauer S, Memari Y, Kolb-Kokocinski A, Durbin R, Hasselmann O, Cremer K, Albrecht B, Wieczorek D, Engels H, Hahn D, Zink AM, Alston CL, Taylor RW, Rodenburg RJ, Trollmann R, Sperl W, Strom TM, Hoffmann GF, Mayr JA, Meitinger T, Bolognini R, Schuelke M, Nuoffer JM, Kölker S, Prokisch H, Klopstock T.

Ann Clin Transl Neurol. 2015 May;2(5):492-509. doi: 10.1002/acn3.189. Epub 2015 Mar 13.

38.

Loophole in K→πνν Search and New Weak Leptonic Forces.

Fuyuto K, Hou WS, Kohda M.

Phys Rev Lett. 2015 May 1;114(17):171802. Epub 2015 Apr 29.

PMID:
25978226
39.

Correction: A Genome-Wide Association Study for Diabetic Retinopathy in a Japanese Population: Potential Association with a Long Intergenic Non-Coding RNA.

Awata T, Yamashita H, Kurihara S, Morita-Ohkubo T, Miyashita Y, Katayama S, Mori K, Yoneya S, Kohda M, Okazaki Y, Maruyama T, Shimada A, Yasuda K, Nishida N, Tokunaga K, Koike A.

PLoS One. 2015 Apr 24;10(4):e0126789. doi: 10.1371/journal.pone.0126789. eCollection 2015. No abstract available.

40.

COQ4 mutations cause a broad spectrum of mitochondrial disorders associated with CoQ10 deficiency.

Brea-Calvo G, Haack TB, Karall D, Ohtake A, Invernizzi F, Carrozzo R, Kremer L, Dusi S, Fauth C, Scholl-Bürgi S, Graf E, Ahting U, Resta N, Laforgia N, Verrigni D, Okazaki Y, Kohda M, Martinelli D, Freisinger P, Strom TM, Meitinger T, Lamperti C, Lacson A, Navas P, Mayr JA, Bertini E, Murayama K, Zeviani M, Prokisch H, Ghezzi D.

Am J Hum Genet. 2015 Feb 5;96(2):309-17. doi: 10.1016/j.ajhg.2014.12.023.

41.

Shot noise induced by nonequilibrium spin accumulation.

Arakawa T, Shiogai J, Ciorga M, Utz M, Schuh D, Kohda M, Nitta J, Bougeard D, Weiss D, Ono T, Kobayashi K.

Phys Rev Lett. 2015 Jan 9;114(1):016601. Epub 2015 Jan 7.

PMID:
25615488
42.

Myocerebrohepatopathy spectrum disorder due to POLG mutations: A clinicopathological report.

Montassir H, Maegaki Y, Murayama K, Yamazaki T, Kohda M, Ohtake A, Iwasa H, Yatsuka Y, Okazaki Y, Sugiura C, Nagata I, Toyoshima M, Saito Y, Itoh M, Nishino I, Ohno K.

Brain Dev. 2015 Aug;37(7):719-24. doi: 10.1016/j.braindev.2014.10.013. Epub 2014 Nov 18.

PMID:
25466440
43.

Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy.

Kopajtich R, Nicholls TJ, Rorbach J, Metodiev MD, Freisinger P, Mandel H, Vanlander A, Ghezzi D, Carrozzo R, Taylor RW, Marquard K, Murayama K, Wieland T, Schwarzmayr T, Mayr JA, Pearce SF, Powell CA, Saada A, Ohtake A, Invernizzi F, Lamantea E, Sommerville EW, Pyle A, Chinnery PF, Crushell E, Okazaki Y, Kohda M, Kishita Y, Tokuzawa Y, Assouline Z, Rio M, Feillet F, Mousson de Camaret B, Chretien D, Munnich A, Menten B, Sante T, Smet J, Régal L, Lorber A, Khoury A, Zeviani M, Strom TM, Meitinger T, Bertini ES, Van Coster R, Klopstock T, Rötig A, Haack TB, Minczuk M, Prokisch H.

Am J Hum Genet. 2014 Dec 4;95(6):708-20. doi: 10.1016/j.ajhg.2014.10.017. Epub 2014 Nov 26.

44.

A genome-wide association study for diabetic retinopathy in a Japanese population: potential association with a long intergenic non-coding RNA.

Awata T, Yamashita H, Kurihara S, Morita-Ohkubo T, Miyashita Y, Katayama S, Mori K, Yoneya S, Kohda M, Okazaki Y, Maruyama T, Shimada A, Yasuda K, Nishida N, Tokunaga K, Koike A.

PLoS One. 2014 Nov 3;9(11):e111715. doi: 10.1371/journal.pone.0111715. eCollection 2014. Erratum in: PLoS One. 2015;10(4):e0126789.

45.

Diet disparity among sympatric herbivorous cichlids in the same ecomorphs in Lake Tanganyika: amplicon pyrosequences on algal farms and stomach contents.

Hata H, Tanabe AS, Yamamoto S, Toju H, Kohda M, Hori M.

BMC Biol. 2014 Oct 29;12:90. doi: 10.1186/s12915-014-0090-4.

46.

New MT-ND6 and NDUFA1 mutations in mitochondrial respiratory chain disorders.

Uehara N, Mori M, Tokuzawa Y, Mizuno Y, Tamaru S, Kohda M, Moriyama Y, Nakachi Y, Matoba N, Sakai T, Yamazaki T, Harashima H, Murayama K, Hattori K, Hayashi J, Yamagata T, Fujita Y, Ito M, Tanaka M, Nibu K, Ohtake A, Okazaki Y.

Ann Clin Transl Neurol. 2014 May;1(5):361-9. doi: 10.1002/acn3.59. Epub 2014 Apr 28.

47.

Bower-building behaviour is associated with increased sperm longevity in Tanganyikan cichlids.

Morita M, Awata S, Yorifuji M, Ota K, Kohda M, Ochi H.

J Evol Biol. 2014 Dec;27(12):2629-43. doi: 10.1111/jeb.12522. Epub 2014 Oct 20.

48.

Duration of memory of dominance relationships in a group living cichlid.

Hotta T, Takeyama T, Jordan LA, Kohda M.

Naturwissenschaften. 2014 Sep;101(9):745-51. doi: 10.1007/s00114-014-1213-z. Epub 2014 Jul 24.

PMID:
25057095
49.

Direct determination of spin-orbit interaction coefficients and realization of the persistent spin helix symmetry.

Sasaki A, Nonaka S, Kunihashi Y, Kohda M, Bauernfeind T, Dollinger T, Richter K, Nitta J.

Nat Nanotechnol. 2014 Sep;9(9):703-9. doi: 10.1038/nnano.2014.128. Epub 2014 Jul 13.

PMID:
25017310
50.

Maternal food provisioning in a substrate-brooding African cichlid.

Ota K, Kohda M.

PLoS One. 2014 Jun 9;9(6):e99094. doi: 10.1371/journal.pone.0099094. eCollection 2014.

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