Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 22 entries
Sorted by: Best Match Show Resources per page
The Hepatocyte nuclear factor-1 alpha ( HNF1A) gene is associated with fatness and loin muscle area in the pig.

Animal : an international journal of animal bioscience

Fan B, Du ZQ, Rothschild MF.
PMID: 22445113
Animal. 2010 Oct;4(10):1619-27. doi: 10.1017/S175173111000087X.

The significance of hepatocyte nuclear factors (HNFs) in β-cell development and function has been generally recognized in humans, as evidenced by their associations with cases of maturity onset diabetes of the young (MODY). Common Hepatocyte nuclear factor-1 alpha (HNF1A),...

Cite
Fan B, Du ZQ, Rothschild MF. The Hepatocyte nuclear factor-1 alpha ( HNF1A) gene is associated with fatness and loin muscle area in the pig. Animal. 2010;4(10):1619-27doi: 10.1017/S175173111000087X.
Fan, B., Du, Z. Q., & Rothschild, M. F. (2010). The Hepatocyte nuclear factor-1 alpha ( HNF1A) gene is associated with fatness and loin muscle area in the pig. Animal : an international journal of animal bioscience, 4(10), 1619-27. https://doi.org/10.1017/S175173111000087X
Fan, B, et al. "The Hepatocyte nuclear factor-1 alpha ( HNF1A) gene is associated with fatness and loin muscle area in the pig." Animal : an international journal of animal bioscience vol. 4,10 (2010): 1619-27. doi: https://doi.org/10.1017/S175173111000087X
Fan B, Du ZQ, Rothschild MF. The Hepatocyte nuclear factor-1 alpha ( HNF1A) gene is associated with fatness and loin muscle area in the pig. Animal. 2010 Oct;4(10):1619-27. doi: 10.1017/S175173111000087X. PMID: 22445113.
Copy Download .nbib Format: NLM
The Hepatocyte nuclear factor-1 alpha ( HNF1A) gene is associated with fatness and loin muscle area in the pig.

Animal : an international journal of animal bioscience

Fan B, Du ZQ, Rothschild MF.
PMID: 22445113
Animal. 2010 Oct;4(10):1619-27. doi: 10.1017/S175173111000087X.

The significance of hepatocyte nuclear factors (HNFs) in β-cell development and function has been generally recognized in humans, as evidenced by their associations with cases of maturity onset diabetes of the young (MODY). Common Hepatocyte nuclear factor-1 alpha (HNF1A),...

Cite
Fan B, Du ZQ, Rothschild MF. The Hepatocyte nuclear factor-1 alpha ( HNF1A) gene is associated with fatness and loin muscle area in the pig. Animal. 2010;4(10):1619-27doi: 10.1017/S175173111000087X.
Fan, B., Du, Z. Q., & Rothschild, M. F. (2010). The Hepatocyte nuclear factor-1 alpha ( HNF1A) gene is associated with fatness and loin muscle area in the pig. Animal : an international journal of animal bioscience, 4(10), 1619-27. https://doi.org/10.1017/S175173111000087X
Fan, B, et al. "The Hepatocyte nuclear factor-1 alpha ( HNF1A) gene is associated with fatness and loin muscle area in the pig." Animal : an international journal of animal bioscience vol. 4,10 (2010): 1619-27. doi: https://doi.org/10.1017/S175173111000087X
Fan B, Du ZQ, Rothschild MF. The Hepatocyte nuclear factor-1 alpha ( HNF1A) gene is associated with fatness and loin muscle area in the pig. Animal. 2010 Oct;4(10):1619-27. doi: 10.1017/S175173111000087X. PMID: 22445113.
Copy Download .nbib Format: NLM
Molecular diagnosis of maturity onset diabetes of the young in Iranian patients: improving management.

Journal of diabetes and metabolic disorders

Davoudi F, Aminzadeh M, Shahbazian HB, Bijanzadeh M, Ghadiri AA, Ghandil P.
PMID: 34900788
J Diabetes Metab Disord. 2021 Aug 19;20(2):1369-1374. doi: 10.1007/s40200-021-00870-8. eCollection 2021 Dec.

BACKGROUND: The purpose of this study is to identify the mutations of the most common form of maturity-onset diabetes of the young (MODY), also known as MODY3, in diabetic patients suspected of MODY. This can recommend appropriate medical surveillance...

Cite
Davoudi F, Aminzadeh M, Shahbazian HB, et al. Molecular diagnosis of maturity onset diabetes of the young in Iranian patients: improving management. J Diabetes Metab Disord. 2021;20(2):1369-1374doi: 10.1007/s40200-021-00870-8.
Davoudi, F., Aminzadeh, M., Shahbazian, H. B., Bijanzadeh, M., Ghadiri, A. A., & Ghandil, P. (2021). Molecular diagnosis of maturity onset diabetes of the young in Iranian patients: improving management. Journal of diabetes and metabolic disorders, 20(2), 1369-1374. https://doi.org/10.1007/s40200-021-00870-8
Davoudi, Fatemeh, et al. "Molecular diagnosis of maturity onset diabetes of the young in Iranian patients: improving management." Journal of diabetes and metabolic disorders vol. 20,2 (2021): 1369-1374. doi: https://doi.org/10.1007/s40200-021-00870-8
Davoudi F, Aminzadeh M, Shahbazian HB, Bijanzadeh M, Ghadiri AA, Ghandil P. Molecular diagnosis of maturity onset diabetes of the young in Iranian patients: improving management. J Diabetes Metab Disord. 2021 Aug 19;20(2):1369-1374. doi: 10.1007/s40200-021-00870-8. eCollection 2021 Dec. PMID: 34900788; PMCID: PMC8630313.
Copy Download .nbib Format: NLM
Clinicopathological analysis of hepatocellular adenoma according to new bordeaux classification: report of eight korean cases.

Korean journal of pathology

Kim H, Jang JJ, Kim DS, Yeom BW, Won NH.
PMID: 24255628
Korean J Pathol. 2013 Oct;47(5):411-7. doi: 10.4132/KoreanJPathol.2013.47.5.411. Epub 2013 Oct 25.

BACKGROUND: Hepatocellular adenoma (HCA) is a rare benign tumor of the liver. A subtype classification of HCA (hepatocyte nuclear factor 1α [HNF1α]-mutated, β-catenin-mutated HCA, inflammatory HCA, and unclassified HCA) has recently been established based on a single institutional review...

Cite
Kim H, Jang JJ, Kim DS, et al. Clinicopathological analysis of hepatocellular adenoma according to new bordeaux classification: report of eight korean cases. Korean J Pathol. 2013;47(5):411-7doi: 10.4132/KoreanJPathol.2013.47.5.411.
Kim, H., Jang, J. J., Kim, D. S., Yeom, B. W., & Won, N. H. (2013). Clinicopathological analysis of hepatocellular adenoma according to new bordeaux classification: report of eight korean cases. Korean journal of pathology, 47(5), 411-7. https://doi.org/10.4132/KoreanJPathol.2013.47.5.411
Kim, Hyunchul, et al. "Clinicopathological analysis of hepatocellular adenoma according to new bordeaux classification: report of eight korean cases." Korean journal of pathology vol. 47,5 (2013): 411-7. doi: https://doi.org/10.4132/KoreanJPathol.2013.47.5.411
Kim H, Jang JJ, Kim DS, Yeom BW, Won NH. Clinicopathological analysis of hepatocellular adenoma according to new bordeaux classification: report of eight korean cases. Korean J Pathol. 2013 Oct;47(5):411-7. doi: 10.4132/KoreanJPathol.2013.47.5.411. Epub 2013 Oct 25. PMID: 24255628; PMCID: PMC3830987.
Copy Download .nbib Format: NLM
Genetic markers of inflammation may not contribute to metabolic traits in Mexican children.

PeerJ

Vashi N, Stryjecki C, Peralta-Romero J, Suarez F, Gomez-Zamudio J, Burguete-Garcia AI, Cruz M, Meyre D.
PMID: 27366637
PeerJ. 2016 Jun 23;4:e2090. doi: 10.7717/peerj.2090. eCollection 2016.

BACKGROUND: Low-grade chronic inflammation is a common feature of obesity and its cardio-metabolic complications. However, little is known about a possible causal role of inflammation in metabolic disorders. Mexico is among the countries with the highest obesity rates in...

Cite
Vashi N, Stryjecki C, Peralta-Romero J, et al. Genetic markers of inflammation may not contribute to metabolic traits in Mexican children. PeerJ. 2016;4:e2090doi: 10.7717/peerj.2090.
Vashi, N., Stryjecki, C., Peralta-Romero, J., Suarez, F., Gomez-Zamudio, J., Burguete-Garcia, A. I., Cruz, M., & Meyre, D. (2016). Genetic markers of inflammation may not contribute to metabolic traits in Mexican children. PeerJ, 4e2090. https://doi.org/10.7717/peerj.2090
Vashi, Neeti, et al. "Genetic markers of inflammation may not contribute to metabolic traits in Mexican children." PeerJ vol. 4 (2016): e2090. doi: https://doi.org/10.7717/peerj.2090
Vashi N, Stryjecki C, Peralta-Romero J, Suarez F, Gomez-Zamudio J, Burguete-Garcia AI, Cruz M, Meyre D. Genetic markers of inflammation may not contribute to metabolic traits in Mexican children. PeerJ. 2016 Jun 23;4:e2090. doi: 10.7717/peerj.2090. eCollection 2016. PMID: 27366637; PMCID: PMC4924140.
Copy Download .nbib Format: NLM
Malignant Transformation of an HNF1a-Inactivated Hepatocellular Adenoma to Hepatocellular Carcinoma.

Case reports in gastroenterology

Hepkema JT, Poelmann FB, Gouw ASH, de Haas RJ, Duiker EW, Blokzijl H, Klaase JM.
PMID: 33250700
Case Rep Gastroenterol. 2020 Nov 02;14(3):577-585. doi: 10.1159/000510215. eCollection 2020.

Hepatocellular adenomas (HCA) are rare benign tumors of the liver, occurring predominantly in females using oral contraceptives. Our case describes a 66-year-old woman presenting with a palpable mass in her upper abdomen. Contrast-enhanced computed tomography and magnetic resonance imaging...

Cite
Hepkema JT, Poelmann FB, Gouw ASH, et al. Malignant Transformation of an HNF1a-Inactivated Hepatocellular Adenoma to Hepatocellular Carcinoma. Case Rep Gastroenterol. 2020;14(3):577-585doi: 10.1159/000510215.
Hepkema, J. T., Poelmann, F. B., Gouw, A. S. H., de Haas, R. J., Duiker, E. W., Blokzijl, H., & Klaase, J. M. (2020). Malignant Transformation of an HNF1a-Inactivated Hepatocellular Adenoma to Hepatocellular Carcinoma. Case reports in gastroenterology, 14(3), 577-585. https://doi.org/10.1159/000510215
Hepkema, Joris T, et al. "Malignant Transformation of an HNF1a-Inactivated Hepatocellular Adenoma to Hepatocellular Carcinoma." Case reports in gastroenterology vol. 14,3 (2020): 577-585. doi: https://doi.org/10.1159/000510215
Hepkema JT, Poelmann FB, Gouw ASH, de Haas RJ, Duiker EW, Blokzijl H, Klaase JM. Malignant Transformation of an HNF1a-Inactivated Hepatocellular Adenoma to Hepatocellular Carcinoma. Case Rep Gastroenterol. 2020 Nov 02;14(3):577-585. doi: 10.1159/000510215. eCollection 2020. PMID: 33250700; PMCID: PMC7670361.
Copy Download .nbib Format: NLM
Development of an exoglycosidase plate-based assay for detecting α1-3,4 fucosylation biomarker in individuals with HNF1A-MODY.

Glycobiology

Demus D, Urbanowicz PA, Gardner RA, Wu H, Juszczak A, Štambuk T, Medvidović EP, Owen KR, Gornik O, Juge N, Spencer DIR.
PMID: 34939081
Glycobiology. 2021 Oct 25; doi: 10.1093/glycob/cwab107. Epub 2021 Oct 25.

Maturity-onset diabetes of the young due to hepatocyte nuclear factor-1 alpha variants (HNF1A-MODY) causes monogenic diabetes. Individuals carrying damaging variants in HNF1A show decreased levels of α1-3,4 fucosylation, as demonstrated on antennary fucosylation of blood plasma N-glycans. The excellent...

Cite
Demus D, Urbanowicz PA, Gardner RA, et al. Development of an exoglycosidase plate-based assay for detecting α1-3,4 fucosylation biomarker in individuals with HNF1A-MODY. Glycobiology. 2021;doi: 10.1093/glycob/cwab107.
Demus, D., Urbanowicz, P. A., Gardner, R. A., Wu, H., Juszczak, A., Štambuk, T., Medvidović, E. P., Owen, K. R., Gornik, O., Juge, N., & Spencer, D. I. R. (2021). Development of an exoglycosidase plate-based assay for detecting α1-3,4 fucosylation biomarker in individuals with HNF1A-MODY. Glycobiology, . https://doi.org/10.1093/glycob/cwab107
Demus, Daniel, et al. "Development of an exoglycosidase plate-based assay for detecting α1-3,4 fucosylation biomarker in individuals with HNF1A-MODY." Glycobiology vol. (2021). doi: https://doi.org/10.1093/glycob/cwab107
Demus D, Urbanowicz PA, Gardner RA, Wu H, Juszczak A, Štambuk T, Medvidović EP, Owen KR, Gornik O, Juge N, Spencer DIR. Development of an exoglycosidase plate-based assay for detecting α1-3,4 fucosylation biomarker in individuals with HNF1A-MODY. Glycobiology. 2021 Oct 25; doi: 10.1093/glycob/cwab107. Epub 2021 Oct 25. PMID: 34939081.
Copy Download .nbib Format: NLM
Molecular and biochemical analysis of the MODY syndromes.

Pediatric diabetes

Winter WE.
PMID: 15016234
Pediatr Diabetes. 2000 Jun;1(2):88-117. doi: 10.1034/j.1399-5448.2000.010206.x.

Maturity onset diabetes of the young (MODY) is characterized by youth-onset diabetes that is inherited in an autosomal dominant (monogenic) pattern. Classic MODY accounts for less than 5% of cases of childhood diabetes in Caucasians, presents prior to age...

Cite
Winter WE. Molecular and biochemical analysis of the MODY syndromes. Pediatr Diabetes. 2000;1(2):88-117doi: 10.1034/j.1399-5448.2000.010206.x.
Winter, W. E. (2000). Molecular and biochemical analysis of the MODY syndromes. Pediatric diabetes, 1(2), 88-117. https://doi.org/10.1034/j.1399-5448.2000.010206.x
Winter, W E. "Molecular and biochemical analysis of the MODY syndromes." Pediatric diabetes vol. 1,2 (2000): 88-117. doi: https://doi.org/10.1034/j.1399-5448.2000.010206.x
Winter WE. Molecular and biochemical analysis of the MODY syndromes. Pediatr Diabetes. 2000 Jun;1(2):88-117. doi: 10.1034/j.1399-5448.2000.010206.x. PMID: 15016234.
Copy Download .nbib Format: NLM
Improved Progression-Free Survival in Irinotecan-Treated Metastatic Colorectal Cancer Patients Carrying the HNF1A Coding Variant p.I27L.

Frontiers in pharmacology

Labriet A, De Mattia E, Cecchin E, Lévesque É, Jonker D, Couture F, Buonadonna A, D'Andrea M, Villeneuve L, Toffoli G, Guillemette C.
PMID: 29066969
Front Pharmacol. 2017 Oct 10;8:712. doi: 10.3389/fphar.2017.00712. eCollection 2017.

Hepatocyte nuclear factor 1-alpha (HNF1A) is a liver-enriched transcription factor that plays a key role in many aspects of hepatic functions including detoxification processes. We examined whether

Cite
Labriet A, De Mattia E, Cecchin E, et al. Improved Progression-Free Survival in Irinotecan-Treated Metastatic Colorectal Cancer Patients Carrying the HNF1A Coding Variant p.I27L. Front Pharmacol. 2017;8:712doi: 10.3389/fphar.2017.00712.
Labriet, A., De Mattia, E., Cecchin, E., Lévesque, �. �., Jonker, D., Couture, F., Buonadonna, A., D'Andrea, M., Villeneuve, L., Toffoli, G., & Guillemette, C. (2017). Improved Progression-Free Survival in Irinotecan-Treated Metastatic Colorectal Cancer Patients Carrying the HNF1A Coding Variant p.I27L. Frontiers in pharmacology, 8712. https://doi.org/10.3389/fphar.2017.00712
Labriet, Adrien, et al. "Improved Progression-Free Survival in Irinotecan-Treated Metastatic Colorectal Cancer Patients Carrying the HNF1A Coding Variant p.I27L." Frontiers in pharmacology vol. 8 (2017): 712. doi: https://doi.org/10.3389/fphar.2017.00712
Labriet A, De Mattia E, Cecchin E, Lévesque É, Jonker D, Couture F, Buonadonna A, D'Andrea M, Villeneuve L, Toffoli G, Guillemette C. Improved Progression-Free Survival in Irinotecan-Treated Metastatic Colorectal Cancer Patients Carrying the HNF1A Coding Variant p.I27L. Front Pharmacol. 2017 Oct 10;8:712. doi: 10.3389/fphar.2017.00712. eCollection 2017. PMID: 29066969; PMCID: PMC5641335.
Copy Download .nbib Format: NLM
Genetic Study of Hepatocyte Nuclear Factor 1 Alpha Variants in Development of Early-Onset Diabetes Type 2 and Maturity-Onset Diabetes of the Young 3 in Iran.

Advanced biomedical research

Mohammadi A, Eskandari A, Sarmadi A, Rahimi M, Iraj B, Hashemipour M, Chaleshtori MH, Tabatabaiefar MA.
PMID: 31673528
Adv Biomed Res. 2019 Sep 23;8:55. doi: 10.4103/abr.abr_54_19. eCollection 2019.

BACKGROUND: Maturity-onset diabetes of the young (MODY) is a clinically and genetically heterogeneous group of diabetes characterized by noninsulin-dependent, autosomal-dominant disorder with strong familial history, early age of onset, and pancreatic beta-cell dysfunction. Mutations in at least 14 different...

Cite
Mohammadi A, Eskandari A, Sarmadi A, et al. Genetic Study of Hepatocyte Nuclear Factor 1 Alpha Variants in Development of Early-Onset Diabetes Type 2 and Maturity-Onset Diabetes of the Young 3 in Iran. Adv Biomed Res. 2019;8:55doi: 10.4103/abr.abr_54_19.
Mohammadi, A., Eskandari, A., Sarmadi, A., Rahimi, M., Iraj, B., Hashemipour, M., Chaleshtori, M. H., & Tabatabaiefar, M. A. (2019). Genetic Study of Hepatocyte Nuclear Factor 1 Alpha Variants in Development of Early-Onset Diabetes Type 2 and Maturity-Onset Diabetes of the Young 3 in Iran. Advanced biomedical research, 855. https://doi.org/10.4103/abr.abr_54_19
Mohammadi, Aliasgar, et al. "Genetic Study of Hepatocyte Nuclear Factor 1 Alpha Variants in Development of Early-Onset Diabetes Type 2 and Maturity-Onset Diabetes of the Young 3 in Iran." Advanced biomedical research vol. 8 (2019): 55. doi: https://doi.org/10.4103/abr.abr_54_19
Mohammadi A, Eskandari A, Sarmadi A, Rahimi M, Iraj B, Hashemipour M, Chaleshtori MH, Tabatabaiefar MA. Genetic Study of Hepatocyte Nuclear Factor 1 Alpha Variants in Development of Early-Onset Diabetes Type 2 and Maturity-Onset Diabetes of the Young 3 in Iran. Adv Biomed Res. 2019 Sep 23;8:55. doi: 10.4103/abr.abr_54_19. eCollection 2019. PMID: 31673528; PMCID: PMC6777141.
Copy Download .nbib Format: NLM
Genetic Testing of Maturity-Onset Diabetes of the Young Current Status and Future Perspectives.

Frontiers in endocrinology

Firdous P, Nissar K, Ali S, Ganai BA, Shabir U, Hassan T, Masoodi SR.
PMID: 29867778
Front Endocrinol (Lausanne). 2018 May 17;9:253. doi: 10.3389/fendo.2018.00253. eCollection 2018.

Diabetes is a global epidemic problem growing exponentially in Asian countries posing a serious threat. Among diabetes, maturity-onset diabetes of the young (MODY) is a heterogeneous group of monogenic disorders that occurs due to β cell dysfunction. Genetic defects...

Cite
Firdous P, Nissar K, Ali S, et al. Genetic Testing of Maturity-Onset Diabetes of the Young Current Status and Future Perspectives. Front Endocrinol (Lausanne). 2018;9:253doi: 10.3389/fendo.2018.00253.
Firdous, P., Nissar, K., Ali, S., Ganai, B. A., Shabir, U., Hassan, T., & Masoodi, S. R. (2018). Genetic Testing of Maturity-Onset Diabetes of the Young Current Status and Future Perspectives. Frontiers in endocrinology, 9253. https://doi.org/10.3389/fendo.2018.00253
Firdous, Parveena, et al. "Genetic Testing of Maturity-Onset Diabetes of the Young Current Status and Future Perspectives." Frontiers in endocrinology vol. 9 (2018): 253. doi: https://doi.org/10.3389/fendo.2018.00253
Firdous P, Nissar K, Ali S, Ganai BA, Shabir U, Hassan T, Masoodi SR. Genetic Testing of Maturity-Onset Diabetes of the Young Current Status and Future Perspectives. Front Endocrinol (Lausanne). 2018 May 17;9:253. doi: 10.3389/fendo.2018.00253. eCollection 2018. PMID: 29867778; PMCID: PMC5966560.
Copy Download .nbib Format: NLM
Molecular and disease association of gestational diabetes mellitus affected mother and placental datasets reveal a strong link between insulin growth factor (IGF) genes in amino acid transport pathway: A network biology approach.

Journal of cellular biochemistry

Rout M, Lulu S S.
PMID: 30335885
J Cell Biochem. 2018 Oct 18; doi: 10.1002/jcb.27418. Epub 2018 Oct 18.

Discerning the relationship between molecules involved in diseases based on their underlying biological mechanisms is one of the greatest challenges in therapeutic development today. Gestational diabetes mellitus (GDM) is one of the most common complications during pregnancy, which adversely...

Cite
Rout M, Lulu S S. Molecular and disease association of gestational diabetes mellitus affected mother and placental datasets reveal a strong link between insulin growth factor (IGF) genes in amino acid transport pathway: A network biology approach. J Cell Biochem. 2018;doi: 10.1002/jcb.27418.
Rout, M., & Lulu S, S. (2018). Molecular and disease association of gestational diabetes mellitus affected mother and placental datasets reveal a strong link between insulin growth factor (IGF) genes in amino acid transport pathway: A network biology approach. Journal of cellular biochemistry, . https://doi.org/10.1002/jcb.27418
Rout, Madhusmita, and Lulu S, Sajitha. "Molecular and disease association of gestational diabetes mellitus affected mother and placental datasets reveal a strong link between insulin growth factor (IGF) genes in amino acid transport pathway: A network biology approach." Journal of cellular biochemistry vol. (2018). doi: https://doi.org/10.1002/jcb.27418
Rout M, Lulu S S. Molecular and disease association of gestational diabetes mellitus affected mother and placental datasets reveal a strong link between insulin growth factor (IGF) genes in amino acid transport pathway: A network biology approach. J Cell Biochem. 2018 Oct 18; doi: 10.1002/jcb.27418. Epub 2018 Oct 18. PMID: 30335885.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 22 entries