Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 37 entries
Sorted by: Best Match Show Resources per page
Feasibility of Increased Navy Bean Powder Consumption for Primary and Secondary Colorectal Cancer Prevention.

Current nutrition and food science

Borresen EC, Gundlach KA, Wdowik M, Rao S, Brown RJ, Ryan EP.
PMID: 25009453
Curr Nutr Food Sci. 2014 May;10(2):112-119. doi: 10.2174/1573401310666140306005934.

INTRODUCTION: Emerging evidence supports that increased consumption of dry beans (METHODS: Seven meals and six snacks were developed for both the absence and inclusion of cooked navy bean powder (35grams/day). Sixteen healthy adults (7 non-cancer and 9 CRC survivors)...

Cite
Borresen EC, Gundlach KA, Wdowik M, et al. Feasibility of Increased Navy Bean Powder Consumption for Primary and Secondary Colorectal Cancer Prevention. Curr Nutr Food Sci. 2014;10(2):112-119doi: 10.2174/1573401310666140306005934.
Borresen, E. C., Gundlach, K. A., Wdowik, M., Rao, S., Brown, R. J., & Ryan, E. P. (2014). Feasibility of Increased Navy Bean Powder Consumption for Primary and Secondary Colorectal Cancer Prevention. Current nutrition and food science, 10(2), 112-119. https://doi.org/10.2174/1573401310666140306005934
Borresen, Erica C, et al. "Feasibility of Increased Navy Bean Powder Consumption for Primary and Secondary Colorectal Cancer Prevention." Current nutrition and food science vol. 10,2 (2014): 112-119. doi: https://doi.org/10.2174/1573401310666140306005934
Borresen EC, Gundlach KA, Wdowik M, Rao S, Brown RJ, Ryan EP. Feasibility of Increased Navy Bean Powder Consumption for Primary and Secondary Colorectal Cancer Prevention. Curr Nutr Food Sci. 2014 May;10(2):112-119. doi: 10.2174/1573401310666140306005934. PMID: 25009453; PMCID: PMC4082309.
Copy Download .nbib Format: NLM
Metabolomics and metabolic pathway networks from human colorectal cancers, adjacent mucosa, and stool.

Cancer & metabolism

Brown DG, Rao S, Weir TL, O'Malia J, Bazan M, Brown RJ, Ryan EP.
PMID: 27275383
Cancer Metab. 2016 Jun 06;4:11. doi: 10.1186/s40170-016-0151-y. eCollection 2016.

BACKGROUND: Colorectal cancers (CRC) are associated with perturbations in cellular amino acids, nucleotides, pentose-phosphate pathway carbohydrates, and glycolytic, gluconeogenic, and tricarboxylic acid intermediates. A non-targeted global metabolome approach was utilized for exploring human CRC, adjacent mucosa, and stool. In...

Cite
Brown DG, Rao S, Weir TL, et al. Metabolomics and metabolic pathway networks from human colorectal cancers, adjacent mucosa, and stool. Cancer Metab. 2016;4:11doi: 10.1186/s40170-016-0151-y.
Brown, D. G., Rao, S., Weir, T. L., O'Malia, J., Bazan, M., Brown, R. J., & Ryan, E. P. (2016). Metabolomics and metabolic pathway networks from human colorectal cancers, adjacent mucosa, and stool. Cancer & metabolism, 411. https://doi.org/10.1186/s40170-016-0151-y
Brown, Dustin G, et al. "Metabolomics and metabolic pathway networks from human colorectal cancers, adjacent mucosa, and stool." Cancer & metabolism vol. 4 (2016): 11. doi: https://doi.org/10.1186/s40170-016-0151-y
Brown DG, Rao S, Weir TL, O'Malia J, Bazan M, Brown RJ, Ryan EP. Metabolomics and metabolic pathway networks from human colorectal cancers, adjacent mucosa, and stool. Cancer Metab. 2016 Jun 06;4:11. doi: 10.1186/s40170-016-0151-y. eCollection 2016. PMID: 27275383; PMCID: PMC4893840.
Copy Download .nbib Format: NLM
[No title available]

Open forum infectious diseases

Peterson MS, Joyner CJ, Cordy RJ, Salinas JL, Machiah D, Lapp SA, Meyer EVS, Gumber S, Galinski MR.
PMID: 30937329
Open Forum Infect Dis. 2019 Jan 19;6(3):ofz021. doi: 10.1093/ofid/ofz021. eCollection 2019 Mar.

METHODS: We present quantitative parasitological and histopathological analyses of tissue sections from a cohort of naive, mostly splenectomized RESULTS: The lung, liver, and kidney showed the most tissue injury, with pathological presentations similar to observations reported from autopsies. Parasite...

Cite
Peterson MS, Joyner CJ, Cordy RJ, et al. . Open Forum Infect Dis. 2019;6(3):ofz021doi: 10.1093/ofid/ofz021.
Peterson, M. S., Joyner, C. J., Cordy, R. J., Salinas, J. L., Machiah, D., Lapp, S. A., Meyer, E. V. S., Gumber, S., & Galinski, M. R. (2019). . Open forum infectious diseases, 6(3), ofz021. https://doi.org/10.1093/ofid/ofz021
Peterson, Mariko S, et al. "." Open forum infectious diseases vol. 6,3 (2019): ofz021. doi: https://doi.org/10.1093/ofid/ofz021
Peterson MS, Joyner CJ, Cordy RJ, Salinas JL, Machiah D, Lapp SA, Meyer EVS, Gumber S, Galinski MR. . Open Forum Infect Dis. 2019 Jan 19;6(3):ofz021. doi: 10.1093/ofid/ofz021. eCollection 2019 Mar. PMID: 30937329; PMCID: PMC6436601.
Copy Download .nbib Format: NLM
[No title available]

Zeitschrift fur Orthopadie und Unfallchirurgie

Sitte-Zöllner A, Walcher F, Geginat G, Piatek S.
PMID: 28683498
Z Orthop Unfall. 2017 Jun;155(3):344-345. doi: 10.1055/s-0043-103015. Epub 2017 Jul 06.

No abstract available.

Cite
Sitte-Zöllner A, Walcher F, Geginat G, et al. Letter to the Editor: A. Probst, N. Reimers, A. Hecht, R. Langenhan: Geriatrische proximale Femurfraktur und Harnwegsinfekt – Überlegungen zur perioperativen Infektionsprophylaxe. . Z Orthop Unfall. 2017;155(3):344-345doi: 10.1055/s-0043-103015.
Sitte-Zöllner, A., Walcher, F., Geginat, G., & Piatek, S. (2017). Letter to the Editor: A. Probst, N. Reimers, A. Hecht, R. Langenhan: Geriatrische proximale Femurfraktur und Harnwegsinfekt – Überlegungen zur perioperativen Infektionsprophylaxe. . Zeitschrift fur Orthopadie und Unfallchirurgie, 155(3), 344-345. https://doi.org/10.1055/s-0043-103015
Sitte-Zöllner, Albrecht, et al. "Letter to the Editor: A. Probst, N. Reimers, A. Hecht, R. Langenhan: Geriatrische proximale Femurfraktur und Harnwegsinfekt – Überlegungen zur perioperativen Infektionsprophylaxe." . Zeitschrift fur Orthopadie und Unfallchirurgie vol. 155,3 (2017): 344-345. doi: https://doi.org/10.1055/s-0043-103015
Sitte-Zöllner A, Walcher F, Geginat G, Piatek S. Letter to the Editor: A. Probst, N. Reimers, A. Hecht, R. Langenhan: Geriatrische proximale Femurfraktur und Harnwegsinfekt – Überlegungen zur perioperativen Infektionsprophylaxe. . Z Orthop Unfall. 2017 Jun;155(3):344-345. doi: 10.1055/s-0043-103015. Epub 2017 Jul 06. German. PMID: 28683498.
Copy Download .nbib Format: NLM
Unusually Long-Lived Photocharges in Helical Organic Semiconductor Nanostructures.

ACS nano

Hafner RJ, Tian L, Brauer JC, Schmaltz T, Sienkiewicz A, Balog S, Flauraud V, Brugger J, Frauenrath H.
PMID: 30138559
ACS Nano. 2018 Sep 25;12(9):9116-9125. doi: 10.1021/acsnano.8b03165. Epub 2018 Sep 05.

Photocharge generation and formation of long-lived charge carriers are relevant in photosynthesis, photocatalysis, photovoltaics, and organic electronics. A better understanding of the factors that determine these processes in synthetic polymer semiconductors is crucial, but difficult due to their morphological...

Cite
Hafner RJ, Tian L, Brauer JC, et al. Unusually Long-Lived Photocharges in Helical Organic Semiconductor Nanostructures. ACS Nano. 2018;12(9):9116-9125doi: 10.1021/acsnano.8b03165.
Hafner, R. J., Tian, L., Brauer, J. C., Schmaltz, T., Sienkiewicz, A., Balog, S., Flauraud, V., Brugger, J., & Frauenrath, H. (2018). Unusually Long-Lived Photocharges in Helical Organic Semiconductor Nanostructures. ACS nano, 12(9), 9116-9125. https://doi.org/10.1021/acsnano.8b03165
Hafner, Regina J, et al. "Unusually Long-Lived Photocharges in Helical Organic Semiconductor Nanostructures." ACS nano vol. 12,9 (2018): 9116-9125. doi: https://doi.org/10.1021/acsnano.8b03165
Hafner RJ, Tian L, Brauer JC, Schmaltz T, Sienkiewicz A, Balog S, Flauraud V, Brugger J, Frauenrath H. Unusually Long-Lived Photocharges in Helical Organic Semiconductor Nanostructures. ACS Nano. 2018 Sep 25;12(9):9116-9125. doi: 10.1021/acsnano.8b03165. Epub 2018 Sep 05. PMID: 30138559.
Copy Download .nbib Format: NLM
Different Protein Sources in the Maternal Diet of the Rat during Gestation and Lactation Affect Milk Composition and Male Offspring Development during Adulthood.

Reproductive sciences (Thousand Oaks, Calif.)

Bautista CJ, Reyes-Castro LA, Bautista RJ, Ramirez V, Elias-López AL, Hernández-Pando R, Zambrano E.
PMID: 34159572
Reprod Sci. 2021 Sep;28(9):2481-2494. doi: 10.1007/s43032-021-00492-8. Epub 2021 Jun 22.

Protein sources in maternal diet are important for mammary gland differentiation and milk protein; however, few studies have examined the metabolic and cellular adaptations of mothers based on protein source diets during pregnancy and lactation, and leptin concentration in...

Cite
Bautista CJ, Reyes-Castro LA, Bautista RJ, et al. Different Protein Sources in the Maternal Diet of the Rat during Gestation and Lactation Affect Milk Composition and Male Offspring Development during Adulthood. Reprod Sci. 2021;28(9):2481-2494doi: 10.1007/s43032-021-00492-8.
Bautista, C. J., Reyes-Castro, L. A., Bautista, R. J., Ramirez, V., Elias-López, A. L., Hernández-Pando, R., & Zambrano, E. (2021). Different Protein Sources in the Maternal Diet of the Rat during Gestation and Lactation Affect Milk Composition and Male Offspring Development during Adulthood. Reproductive sciences (Thousand Oaks, Calif.), 28(9), 2481-2494. https://doi.org/10.1007/s43032-021-00492-8
Bautista, Claudia J, et al. "Different Protein Sources in the Maternal Diet of the Rat during Gestation and Lactation Affect Milk Composition and Male Offspring Development during Adulthood." Reproductive sciences (Thousand Oaks, Calif.) vol. 28,9 (2021): 2481-2494. doi: https://doi.org/10.1007/s43032-021-00492-8
Bautista CJ, Reyes-Castro LA, Bautista RJ, Ramirez V, Elias-López AL, Hernández-Pando R, Zambrano E. Different Protein Sources in the Maternal Diet of the Rat during Gestation and Lactation Affect Milk Composition and Male Offspring Development during Adulthood. Reprod Sci. 2021 Sep;28(9):2481-2494. doi: 10.1007/s43032-021-00492-8. Epub 2021 Jun 22. PMID: 34159572.
Copy Download .nbib Format: NLM
Corrigendum to: Immunological Variables Associated With Clinical and Endoscopic Response to Vedolizumab in Patients With Inflammatory Bowel Diseases.

Journal of Crohn's & colitis

Coletta M, Paroni M, Alvisi MF, De Luca M, Rulli E, Mazza S, Facciotti F, Lattanzi G, Strati F, Abrignani S, Claudio Fantini M, Vecchi M, Geginat J, Capriolia F.
PMID: 34850867
J Crohns Colitis. 2021 Nov 30; doi: 10.1093/ecco-jcc/jjab107. Epub 2021 Nov 30.

No abstract available.

Cite
Coletta M, Paroni M, Alvisi MF, et al. Corrigendum to: Immunological Variables Associated With Clinical and Endoscopic Response to Vedolizumab in Patients With Inflammatory Bowel Diseases. J Crohns Colitis. 2021;doi: 10.1093/ecco-jcc/jjab107.
Coletta, M., Paroni, M., Alvisi, M. F., De Luca, M., Rulli, E., Mazza, S., Facciotti, F., Lattanzi, G., Strati, F., Abrignani, S., Claudio Fantini, M., Vecchi, M., Geginat, J., & Capriolia, F. (2021). Corrigendum to: Immunological Variables Associated With Clinical and Endoscopic Response to Vedolizumab in Patients With Inflammatory Bowel Diseases. Journal of Crohn's & colitis, . https://doi.org/10.1093/ecco-jcc/jjab107
Coletta, Marina, et al. "Corrigendum to: Immunological Variables Associated With Clinical and Endoscopic Response to Vedolizumab in Patients With Inflammatory Bowel Diseases." Journal of Crohn's & colitis vol. (2021). doi: https://doi.org/10.1093/ecco-jcc/jjab107
Coletta M, Paroni M, Alvisi MF, De Luca M, Rulli E, Mazza S, Facciotti F, Lattanzi G, Strati F, Abrignani S, Claudio Fantini M, Vecchi M, Geginat J, Capriolia F. Corrigendum to: Immunological Variables Associated With Clinical and Endoscopic Response to Vedolizumab in Patients With Inflammatory Bowel Diseases. J Crohns Colitis. 2021 Nov 30; doi: 10.1093/ecco-jcc/jjab107. Epub 2021 Nov 30. PMID: 34850867.
Copy Download .nbib Format: NLM
Ex vivo microRNA and gene expression profiling of human Tr1-like cells suggests a role for miR-92a and -125a in the regulation of EOMES and IL-10R.

European journal of immunology

De Simone M, Chirichella M, Emming S, Mazzara S, Ranzani V, Gruarin P, Moschetti G, Pulvirenti N, Maglie S, Vasco C, Crosti MC, Rossetti G, Pagani M, Abrignani S, Monticelli S, Geginat J.
PMID: 34528258
Eur J Immunol. 2021 Sep 15; doi: 10.1002/eji.202149315. Epub 2021 Sep 15.

Ex vivo gene expression and miRNA profiling of Eomes

Cite
De Simone M, Chirichella M, Emming S, et al. Ex vivo microRNA and gene expression profiling of human Tr1-like cells suggests a role for miR-92a and -125a in the regulation of EOMES and IL-10R. Eur J Immunol. 2021;doi: 10.1002/eji.202149315.
De Simone, M., Chirichella, M., Emming, S., Mazzara, S., Ranzani, V., Gruarin, P., Moschetti, G., Pulvirenti, N., Maglie, S., Vasco, C., Crosti, M. C., Rossetti, G., Pagani, M., Abrignani, S., Monticelli, S., & Geginat, J. (2021). Ex vivo microRNA and gene expression profiling of human Tr1-like cells suggests a role for miR-92a and -125a in the regulation of EOMES and IL-10R. European journal of immunology, . https://doi.org/10.1002/eji.202149315
De Simone, Marco, et al. "Ex vivo microRNA and gene expression profiling of human Tr1-like cells suggests a role for miR-92a and -125a in the regulation of EOMES and IL-10R." European journal of immunology vol. (2021). doi: https://doi.org/10.1002/eji.202149315
De Simone M, Chirichella M, Emming S, Mazzara S, Ranzani V, Gruarin P, Moschetti G, Pulvirenti N, Maglie S, Vasco C, Crosti MC, Rossetti G, Pagani M, Abrignani S, Monticelli S, Geginat J. Ex vivo microRNA and gene expression profiling of human Tr1-like cells suggests a role for miR-92a and -125a in the regulation of EOMES and IL-10R. Eur J Immunol. 2021 Sep 15; doi: 10.1002/eji.202149315. Epub 2021 Sep 15. PMID: 34528258.
Copy Download .nbib Format: NLM
Clenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cells.

Nature communications

Meister J, Bone DBJ, Knudsen JR, Barella LF, Velenosi TJ, Akhmedov D, Lee RJ, Cohen AH, Gavrilova O, Cui Y, Karsenty G, Chen M, Weinstein LS, Kleinert M, Berdeaux R, Jensen TE, Richter EA, Wess J.
PMID: 35013148
Nat Commun. 2022 Jan 10;13(1):22. doi: 10.1038/s41467-021-27540-w.

Activation of the sympathetic nervous system causes pronounced metabolic changes that are mediated by multiple adrenergic receptor subtypes. Systemic treatment with β

Cite
Meister J, Bone DBJ, Knudsen JR, et al. Clenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cells. Nat Commun. 2022;13(1):22doi: 10.1038/s41467-021-27540-w.
Meister, J., Bone, D. B. J., Knudsen, J. R., Barella, L. F., Velenosi, T. J., Akhmedov, D., Lee, R. J., Cohen, A. H., Gavrilova, O., Cui, Y., Karsenty, G., Chen, M., Weinstein, L. S., Kleinert, M., Berdeaux, R., Jensen, T. E., Richter, E. A., & Wess, J. (2022). Clenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cells. Nature communications, 13(1), 22. https://doi.org/10.1038/s41467-021-27540-w
Meister, Jaroslawna, et al. "Clenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cells." Nature communications vol. 13,1 (2022): 22. doi: https://doi.org/10.1038/s41467-021-27540-w
Meister J, Bone DBJ, Knudsen JR, Barella LF, Velenosi TJ, Akhmedov D, Lee RJ, Cohen AH, Gavrilova O, Cui Y, Karsenty G, Chen M, Weinstein LS, Kleinert M, Berdeaux R, Jensen TE, Richter EA, Wess J. Clenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cells. Nat Commun. 2022 Jan 10;13(1):22. doi: 10.1038/s41467-021-27540-w. PMID: 35013148.
Copy Download .nbib Format: NLM
High Yap and Mll1 promote a persistent regenerative cell state induced by Notch signaling and loss of p53.

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

Heuberger J, Grinat J, Kosel F, Liu L, Kunz S, Vidal RO, Keil M, Haybaeck J, Robine S, Louvard D, Regenbrecht C, Sporbert A, Sauer S, von Eyss B, Sigal M, Birchmeier W.
PMID: 34039707
Proc Natl Acad Sci U S A. 2021 Jun 01;118(22). doi: 10.1073/pnas.2019699118.

Specified intestinal epithelial cells reprogram and contribute to the regeneration and renewal of the epithelium upon injury. Mutations that deregulate such renewal processes may contribute to tumorigenesis. Using intestinal organoids, we show that concomitant activation of Notch signaling and...

Cite
Heuberger J, Grinat J, Kosel F, et al. High Yap and Mll1 promote a persistent regenerative cell state induced by Notch signaling and loss of p53. Proc Natl Acad Sci U S A. 2021;118(22)doi: 10.1073/pnas.2019699118.
Heuberger, J., Grinat, J., Kosel, F., Liu, L., Kunz, S., Vidal, R. O., Keil, M., Haybaeck, J., Robine, S., Louvard, D., Regenbrecht, C., Sporbert, A., Sauer, S., von Eyss, B., Sigal, M., & Birchmeier, W. (2021). High Yap and Mll1 promote a persistent regenerative cell state induced by Notch signaling and loss of p53. Proceedings of the National Academy of Sciences of the United States of America, 118(22), . https://doi.org/10.1073/pnas.2019699118
Heuberger, Julian, et al. "High Yap and Mll1 promote a persistent regenerative cell state induced by Notch signaling and loss of p53." Proceedings of the National Academy of Sciences of the United States of America vol. 118,22 (2021). doi: https://doi.org/10.1073/pnas.2019699118
Heuberger J, Grinat J, Kosel F, Liu L, Kunz S, Vidal RO, Keil M, Haybaeck J, Robine S, Louvard D, Regenbrecht C, Sporbert A, Sauer S, von Eyss B, Sigal M, Birchmeier W. High Yap and Mll1 promote a persistent regenerative cell state induced by Notch signaling and loss of p53. Proc Natl Acad Sci U S A. 2021 Jun 01;118(22). doi: 10.1073/pnas.2019699118. PMID: 34039707; PMCID: PMC8179171.
Copy Download .nbib Format: NLM
Ex vivo microRNA and gene expression profiling of human Tr1-like cells suggests a role for miR-92a and -125a in the regulation of EOMES and IL-10R.

European journal of immunology

De Simone M, Chirichella M, Emming S, Mazzara S, Ranzani V, Gruarin P, Moschetti G, Pulvirenti N, Maglie S, Vasco C, Crosti MC, Rossetti G, Pagani M, Abrignani S, Monticelli S, Geginat J.
PMID: 34528258
Eur J Immunol. 2021 Dec;51(12):3243-3246. doi: 10.1002/eji.202149315. Epub 2021 Sep 28.

Ex vivo gene expression and miRNA profiling of Eomes

Cite
De Simone M, Chirichella M, Emming S, et al. Ex vivo microRNA and gene expression profiling of human Tr1-like cells suggests a role for miR-92a and -125a in the regulation of EOMES and IL-10R. Eur J Immunol. 2021;51(12):3243-3246doi: 10.1002/eji.202149315.
De Simone, M., Chirichella, M., Emming, S., Mazzara, S., Ranzani, V., Gruarin, P., Moschetti, G., Pulvirenti, N., Maglie, S., Vasco, C., Crosti, M. C., Rossetti, G., Pagani, M., Abrignani, S., Monticelli, S., & Geginat, J. (2021). Ex vivo microRNA and gene expression profiling of human Tr1-like cells suggests a role for miR-92a and -125a in the regulation of EOMES and IL-10R. European journal of immunology, 51(12), 3243-3246. https://doi.org/10.1002/eji.202149315
De Simone, Marco, et al. "Ex vivo microRNA and gene expression profiling of human Tr1-like cells suggests a role for miR-92a and -125a in the regulation of EOMES and IL-10R." European journal of immunology vol. 51,12 (2021): 3243-3246. doi: https://doi.org/10.1002/eji.202149315
De Simone M, Chirichella M, Emming S, Mazzara S, Ranzani V, Gruarin P, Moschetti G, Pulvirenti N, Maglie S, Vasco C, Crosti MC, Rossetti G, Pagani M, Abrignani S, Monticelli S, Geginat J. Ex vivo microRNA and gene expression profiling of human Tr1-like cells suggests a role for miR-92a and -125a in the regulation of EOMES and IL-10R. Eur J Immunol. 2021 Dec;51(12):3243-3246. doi: 10.1002/eji.202149315. Epub 2021 Sep 28. PMID: 34528258.
Copy Download .nbib Format: NLM
Lactation Plays a Fundamental Role in Developmental Programming.

Endocrine, metabolic & immune disorders drug targets

Ramirez V, Montaño FA, Bautista RJ, Mummidi S, Alvarenga JC, Bautista CJ.
PMID: 33302843
Endocr Metab Immune Disord Drug Targets. 2020 Dec 09; doi: 10.2174/1871530320999201209223341. Epub 2020 Dec 09.

Breast milk has been considered the best source of nutrition for newborns. Several epidemiological and basic experimental studies have been conducted to understand the nutritional advantages of breast milk. Previous findings have emphasized the importance of a good maternal...

Cite
Ramirez V, Montaño FA, Bautista RJ, et al. Lactation Plays a Fundamental Role in Developmental Programming. Endocr Metab Immune Disord Drug Targets. 2020;doi: 10.2174/1871530320999201209223341.
Ramirez, V., Montaño, F. A., Bautista, R. J., Mummidi, S., Alvarenga, J. C., & Bautista, C. J. (2020). Lactation Plays a Fundamental Role in Developmental Programming. Endocrine, metabolic & immune disorders drug targets, . https://doi.org/10.2174/1871530320999201209223341
Ramirez, Victoria, et al. "Lactation Plays a Fundamental Role in Developmental Programming." Endocrine, metabolic & immune disorders drug targets vol. (2020). doi: https://doi.org/10.2174/1871530320999201209223341
Ramirez V, Montaño FA, Bautista RJ, Mummidi S, Alvarenga JC, Bautista CJ. Lactation Plays a Fundamental Role in Developmental Programming. Endocr Metab Immune Disord Drug Targets. 2020 Dec 09; doi: 10.2174/1871530320999201209223341. Epub 2020 Dec 09. PMID: 33302843.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 37 entries