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Commentary: The beginning of the end of the 'modern synthesis'? Commentary on Jablonka E, Lamb MJ. The inheritance of acquired epigenetic variations.

International journal of epidemiology

Pembrey M.
PMID: 25855718
Int J Epidemiol. 2015 Aug;44(4):1112-6. doi: 10.1093/ije/dyv025. Epub 2015 Apr 07.

No abstract available.

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Pembrey M. Commentary: The beginning of the end of the 'modern synthesis'? Commentary on Jablonka E, Lamb MJ. The inheritance of acquired epigenetic variations. Int J Epidemiol. 2015;44(4):1112-6doi: 10.1093/ije/dyv025.
Pembrey, M. (2015). Commentary: The beginning of the end of the 'modern synthesis'? Commentary on Jablonka E, Lamb MJ. The inheritance of acquired epigenetic variations. International journal of epidemiology, 44(4), 1112-6. https://doi.org/10.1093/ije/dyv025
Pembrey, Marcus. "Commentary: The beginning of the end of the 'modern synthesis'? Commentary on Jablonka E, Lamb MJ. The inheritance of acquired epigenetic variations." International journal of epidemiology vol. 44,4 (2015): 1112-6. doi: https://doi.org/10.1093/ije/dyv025
Pembrey M. Commentary: The beginning of the end of the 'modern synthesis'? Commentary on Jablonka E, Lamb MJ. The inheritance of acquired epigenetic variations. Int J Epidemiol. 2015 Aug;44(4):1112-6. doi: 10.1093/ije/dyv025. Epub 2015 Apr 07. PMID: 25855718.
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Exploring the role of nongenetic inheritance in the etiology of human disease.

Biology of reproduction

Escher J, Corces V, Mansuy I, Yan W.
PMID: 34373898
Biol Reprod. 2021 Sep 14;105(3):567-569. doi: 10.1093/biolre/ioab151.

No abstract available.

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Escher J, Corces V, Mansuy I, et al. Exploring the role of nongenetic inheritance in the etiology of human disease. Biol Reprod. 2021;105(3):567-569doi: 10.1093/biolre/ioab151.
Escher, J., Corces, V., Mansuy, I., & Yan, W. (2021). Exploring the role of nongenetic inheritance in the etiology of human disease. Biology of reproduction, 105(3), 567-569. https://doi.org/10.1093/biolre/ioab151
Escher, Jill, et al. "Exploring the role of nongenetic inheritance in the etiology of human disease." Biology of reproduction vol. 105,3 (2021): 567-569. doi: https://doi.org/10.1093/biolre/ioab151
Escher J, Corces V, Mansuy I, Yan W. Exploring the role of nongenetic inheritance in the etiology of human disease. Biol Reprod. 2021 Sep 14;105(3):567-569. doi: 10.1093/biolre/ioab151. PMID: 34373898.
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[Mitochondrial inherited diseases].

Nihon rinsho. Japanese journal of clinical medicine

Goto Y.
PMID: 20979265
Nihon Rinsho. 2010 Aug;68:27-32.

No abstract available.

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Goto Y. [Mitochondrial inherited diseases]. Nihon Rinsho. 2010;68:27-32
Goto, Y. (2010). [Mitochondrial inherited diseases]. Nihon rinsho. Japanese journal of clinical medicine, 6827-32.
Goto, Yu-ichi. "[Mitochondrial inherited diseases]." Nihon rinsho. Japanese journal of clinical medicine vol. 68 (2010): 27-32.
Goto Y. [Mitochondrial inherited diseases]. Nihon Rinsho. 2010 Aug;68:27-32. Japanese. PMID: 20979265.
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The Mendelian colorectal cancer syndromes.

Annals of clinical biochemistry

Tomlinson I.
PMID: 26169059
Ann Clin Biochem. 2015 Nov;52:690-2. doi: 10.1177/0004563215597944. Epub 2015 Jul 13.

A small minority of colorectal cancers (CRCs) (≤5%) are caused by a single, inherited faulty gene. These diseases, the Mendelian colorectal cancer (CRC) syndromes, have been central to our understanding of colorectal carcinogenesis in general. Most of the approximately...

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Tomlinson I. The Mendelian colorectal cancer syndromes. Ann Clin Biochem. 2015;52:690-2doi: 10.1177/0004563215597944.
Tomlinson, I. (2015). The Mendelian colorectal cancer syndromes. Annals of clinical biochemistry, 52690-2. https://doi.org/10.1177/0004563215597944
Tomlinson, Ian. "The Mendelian colorectal cancer syndromes." Annals of clinical biochemistry vol. 52 (2015): 690-2. doi: https://doi.org/10.1177/0004563215597944
Tomlinson I. The Mendelian colorectal cancer syndromes. Ann Clin Biochem. 2015 Nov;52:690-2. doi: 10.1177/0004563215597944. Epub 2015 Jul 13. PMID: 26169059; PMCID: PMC4611988.
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Commentary: Reflections on: Jablonka E, Lamb MJ. The inheritance of acquired epigenetic variations.

International journal of epidemiology

Jablonka E, Lamb MJ.
PMID: 25855715
Int J Epidemiol. 2015 Aug;44(4):1103-5. doi: 10.1093/ije/dyv023. Epub 2015 Apr 07.

No abstract available.

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Jablonka E, Lamb MJ. Commentary: Reflections on: Jablonka E, Lamb MJ. The inheritance of acquired epigenetic variations. Int J Epidemiol. 2015;44(4):1103-5doi: 10.1093/ije/dyv023.
Jablonka, E., & Lamb, M. J. (2015). Commentary: Reflections on: Jablonka E, Lamb MJ. The inheritance of acquired epigenetic variations. International journal of epidemiology, 44(4), 1103-5. https://doi.org/10.1093/ije/dyv023
Jablonka, Eva, and Lamb, Marion J. "Commentary: Reflections on: Jablonka E, Lamb MJ. The inheritance of acquired epigenetic variations." International journal of epidemiology vol. 44,4 (2015): 1103-5. doi: https://doi.org/10.1093/ije/dyv023
Jablonka E, Lamb MJ. Commentary: Reflections on: Jablonka E, Lamb MJ. The inheritance of acquired epigenetic variations. Int J Epidemiol. 2015 Aug;44(4):1103-5. doi: 10.1093/ije/dyv023. Epub 2015 Apr 07. PMID: 25855715.
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The social transmission of metacontrol policies: Mechanisms underlying the interpersonal transfer of persistence and flexibility.

Neuroscience and biobehavioral reviews

Hommel B, Colzato LS.
PMID: 28088534
Neurosci Biobehav Rev. 2017 Oct;81:43-58. doi: 10.1016/j.neubiorev.2017.01.009. Epub 2017 Jan 11.

Humans often face binary cognitive-control dilemmas, with the choice between persistence and flexibility being a crucial one. Tackling these dilemmas requires metacontrol, i.e., the control of the current cognitive-control policy. As predicted from functional, psychometric, neuroscientific, and modeling approaches,...

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Hommel B, Colzato LS. The social transmission of metacontrol policies: Mechanisms underlying the interpersonal transfer of persistence and flexibility. Neurosci Biobehav Rev. 2017;81:43-58doi: 10.1016/j.neubiorev.2017.01.009.
Hommel, B., & Colzato, L. S. (2017). The social transmission of metacontrol policies: Mechanisms underlying the interpersonal transfer of persistence and flexibility. Neuroscience and biobehavioral reviews, 8143-58. https://doi.org/10.1016/j.neubiorev.2017.01.009
Hommel, Bernhard, and Colzato, Lorenza S. "The social transmission of metacontrol policies: Mechanisms underlying the interpersonal transfer of persistence and flexibility." Neuroscience and biobehavioral reviews vol. 81 (2017): 43-58. doi: https://doi.org/10.1016/j.neubiorev.2017.01.009
Hommel B, Colzato LS. The social transmission of metacontrol policies: Mechanisms underlying the interpersonal transfer of persistence and flexibility. Neurosci Biobehav Rev. 2017 Oct;81:43-58. doi: 10.1016/j.neubiorev.2017.01.009. Epub 2017 Jan 11. PMID: 28088534.
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Molecular mechanisms of epigenetic inheritance: Possible evolutionary implications.

Seminars in cell & developmental biology

Sarkies P.
PMID: 31228598
Semin Cell Dev Biol. 2020 Jan;97:106-115. doi: 10.1016/j.semcdb.2019.06.005. Epub 2019 Jun 21.

Recently interest in multi-generational epigenetic phenomena have been fuelled by highly reproducible intergenerational and transgenerational inheritance paradigms in several model organisms. Such paradigms are essential in order to begin to use genetics to unpick the mechanistic bases of how...

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Sarkies P. Molecular mechanisms of epigenetic inheritance: Possible evolutionary implications. Semin Cell Dev Biol. 2019;97:106-115doi: 10.1016/j.semcdb.2019.06.005.
Sarkies, P. (2020). Molecular mechanisms of epigenetic inheritance: Possible evolutionary implications. Seminars in cell & developmental biology, 97106-115. https://doi.org/10.1016/j.semcdb.2019.06.005
Sarkies, Peter. "Molecular mechanisms of epigenetic inheritance: Possible evolutionary implications." Seminars in cell & developmental biology vol. 97 (2020): 106-115. doi: https://doi.org/10.1016/j.semcdb.2019.06.005
Sarkies P. Molecular mechanisms of epigenetic inheritance: Possible evolutionary implications. Semin Cell Dev Biol. 2020 Jan;97:106-115. doi: 10.1016/j.semcdb.2019.06.005. Epub 2019 Jun 21. PMID: 31228598; PMCID: PMC6945114.
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[Inheritance patterns].

Munchener medizinische Wochenschrift (1950)

STENGEL VON RUTKOWSKI L.
PMID: 13025448
Munch Med Wochenschr. 1952 Dec 19;94(51):2588-90.

No abstract available.

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STENGEL VON RUTKOWSKI L. Uber Vererbungsschemata. [Inheritance patterns]. Munch Med Wochenschr. 1952;94(51):2588-90
STENGEL VON RUTKOWSKI, L. (1952). Uber Vererbungsschemata. [Inheritance patterns]. Munchener medizinische Wochenschrift (1950), 94(51), 2588-90.
STENGEL VON RUTKOWSKI, L. "Uber Vererbungsschemata." [Inheritance patterns]. Munchener medizinische Wochenschrift (1950) vol. 94,51 (1952): 2588-90.
STENGEL VON RUTKOWSKI L. Uber Vererbungsschemata. [Inheritance patterns]. Munch Med Wochenschr. 1952 Dec 19;94(51):2588-90. Undetermined. PMID: 13025448.
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Nonadditive Effects of Genes in Human Metabolomics.

Genetics

Tsepilov YA, Shin SY, Soranzo N, Spector TD, Prehn C, Adamski J, Kastenmüller G, Wang-Sattler R, Strauch K, Gieger C, Aulchenko YS, Ried JS.
PMID: 25977471
Genetics. 2015 Jul;200(3):707-18. doi: 10.1534/genetics.115.175760. Epub 2015 May 14.

Genome-wide association studies (GWAS) are widely applied to analyze the genetic effects on phenotypes. With the availability of high-throughput technologies for metabolite measurements, GWAS successfully identified loci that affect metabolite concentrations and underlying pathways. In most GWAS, the effect...

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Tsepilov YA, Shin SY, Soranzo N, et al. Nonadditive Effects of Genes in Human Metabolomics. Genetics. 2015;200(3):707-18doi: 10.1534/genetics.115.175760.
Tsepilov, Y. A., Shin, S. Y., Soranzo, N., Spector, T. D., Prehn, C., Adamski, J., Kastenmüller, G., Wang-Sattler, R., Strauch, K., Gieger, C., Aulchenko, Y. S., & Ried, J. S. (2015). Nonadditive Effects of Genes in Human Metabolomics. Genetics, 200(3), 707-18. https://doi.org/10.1534/genetics.115.175760
Tsepilov, Yakov A, et al. "Nonadditive Effects of Genes in Human Metabolomics." Genetics vol. 200,3 (2015): 707-18. doi: https://doi.org/10.1534/genetics.115.175760
Tsepilov YA, Shin SY, Soranzo N, Spector TD, Prehn C, Adamski J, Kastenmüller G, Wang-Sattler R, Strauch K, Gieger C, Aulchenko YS, Ried JS. Nonadditive Effects of Genes in Human Metabolomics. Genetics. 2015 Jul;200(3):707-18. doi: 10.1534/genetics.115.175760. Epub 2015 May 14. PMID: 25977471; PMCID: PMC4512538.
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Transgenerational genomics: the profession should enhance its role as advocate for the health of the next generation.

BJOG : an international journal of obstetrics and gynaecology

Braude PR, Morris EP.
PMID: 33314570
BJOG. 2021 Jun;128(7):1171-1173. doi: 10.1111/1471-0528.16626. Epub 2021 Jan 06.

No abstract available.

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Braude PR, Morris EP. Transgenerational genomics: the profession should enhance its role as advocate for the health of the next generation. BJOG. 2021;128(7):1171-1173doi: 10.1111/1471-0528.16626.
Braude, P. R., & Morris, E. P. (2021). Transgenerational genomics: the profession should enhance its role as advocate for the health of the next generation. BJOG : an international journal of obstetrics and gynaecology, 128(7), 1171-1173. https://doi.org/10.1111/1471-0528.16626
Braude, P R, and Morris, E P. "Transgenerational genomics: the profession should enhance its role as advocate for the health of the next generation." BJOG : an international journal of obstetrics and gynaecology vol. 128,7 (2021): 1171-1173. doi: https://doi.org/10.1111/1471-0528.16626
Braude PR, Morris EP. Transgenerational genomics: the profession should enhance its role as advocate for the health of the next generation. BJOG. 2021 Jun;128(7):1171-1173. doi: 10.1111/1471-0528.16626. Epub 2021 Jan 06. PMID: 33314570.
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Epigenetic inheritance and the responsibility for health in society.

The lancet. Diabetes & endocrinology

Hanson M, Müller R.
PMID: 28010782
Lancet Diabetes Endocrinol. 2017 Jan;5(1):11-12. doi: 10.1016/S2213-8587(16)30400-4.

No abstract available.

Cite
Hanson M, Müller R. Epigenetic inheritance and the responsibility for health in society. Lancet Diabetes Endocrinol. 2017;5(1):11-12doi: 10.1016/S2213-8587(16)30400-4.
Hanson, M., & Müller, R. (2017). Epigenetic inheritance and the responsibility for health in society. The lancet. Diabetes & endocrinology, 5(1), 11-12. https://doi.org/10.1016/S2213-8587(16)30400-4
Hanson, Mark, and Müller, Ruth. "Epigenetic inheritance and the responsibility for health in society." The lancet. Diabetes & endocrinology vol. 5,1 (2017): 11-12. doi: https://doi.org/10.1016/S2213-8587(16)30400-4
Hanson M, Müller R. Epigenetic inheritance and the responsibility for health in society. Lancet Diabetes Endocrinol. 2017 Jan;5(1):11-12. doi: 10.1016/S2213-8587(16)30400-4. PMID: 28010782.
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Understanding the impact of genetic testing for inherited retinal dystrophy.

European journal of human genetics : EJHG

Combs R, McAllister M, Payne K, Lowndes J, Devery S, Webster AR, Downes SM, Moore AT, Ramsden S, Black G, Hall G.
PMID: 23403902
Eur J Hum Genet. 2013 Nov;21(11):1209-13. doi: 10.1038/ejhg.2013.19. Epub 2013 Feb 13.

The capability of genetic technologies is expanding rapidly in the field of inherited eye disease. New genetic testing approaches will deliver a step change in the ability to diagnose and extend the possibility of targeted treatments. However, evidence is...

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Combs R, McAllister M, Payne K, et al. Understanding the impact of genetic testing for inherited retinal dystrophy. Eur J Hum Genet. 2013;21(11):1209-13doi: 10.1038/ejhg.2013.19.
Combs, R., McAllister, M., Payne, K., Lowndes, J., Devery, S., Webster, A. R., Downes, S. M., Moore, A. T., Ramsden, S., Black, G., & Hall, G. (2013). Understanding the impact of genetic testing for inherited retinal dystrophy. European journal of human genetics : EJHG, 21(11), 1209-13. https://doi.org/10.1038/ejhg.2013.19
Combs, Ryan, et al. "Understanding the impact of genetic testing for inherited retinal dystrophy." European journal of human genetics : EJHG vol. 21,11 (2013): 1209-13. doi: https://doi.org/10.1038/ejhg.2013.19
Combs R, McAllister M, Payne K, Lowndes J, Devery S, Webster AR, Downes SM, Moore AT, Ramsden S, Black G, Hall G. Understanding the impact of genetic testing for inherited retinal dystrophy. Eur J Hum Genet. 2013 Nov;21(11):1209-13. doi: 10.1038/ejhg.2013.19. Epub 2013 Feb 13. PMID: 23403902; PMCID: PMC3798830.
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Showing 1 to 12 of 14 entries