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	381.	Lack of association between hepatocyte nuclear factor-1beta gene and common forms of type 2 diabetes in the Japanese population. [electronic resource] by Babaya, N Ikegami, H Fujisawa, T Hotta, M Ueda, H Shintani, M Nojima, K Kawabata, Y Ono, M Nishino, M Itoi-Babaya, M Taniguchi, H Noso, S Horiki, M Yamada, K Kawaguchi, Y Fukuda, M Ogihara, T Producer: 20020408 In: Diabetes, nutrition & metabolism vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	382.	Mutations and intronic variants in the HNF-1 beta gene in a group of German and Czech Caucasians with type 2 diabetes mellitus and progressive diabetic nephropathy. [electronic resource] by Selisko, T Vcelák, J Bendlová, B Graessler, J Schwarz, P E H Schulze, J Producer: 20020924 In: Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	383.	Identification of a new case of hepatocyte nuclear factor-1beta mutation with highly varied phenotypes. [electronic resource] by Shihara, N Horikawa, Y Onishi, T Ono, M Kashimada, K Takeda, J Producer: 20050215 In: Diabetologia vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	384.	Effect of mutations in HNF-1alpha and HNF-1beta on the transcriptional regulation of human sucrase-isomaltase in Caco-2 cells. [electronic resource] by Gu, Ning Suzuki, Naoko Takeda, Jun Adachi, Tetsuya Tsujimoto, Gozoh Aoki, Norihiko Ishihara, Akihiko Tsuda, Kinsuke Yasuda, Koichiro Producer: 20050125 In: Biochemical and biophysical research communications vol. 325 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	385.	Notch is required for the formation of all nephron segments and primes nephron progenitors for differentiation. [electronic resource] by Chung, Eunah Deacon, Patrick Park, Joo-Seop Producer: 20180102 In: Development (Cambridge, England) vol. 144 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	386.	A case of type-1 diabetes mellitus formerly diagnosed as maturity-onset diabetes of the young (MODY) carrying suggestive MODY3 gene. [electronic resource] by Miura, J Sanaka, M Ikeda, Y Watanabe, C Nakagami, T Iwasaki, N Uchigata, Y Takahashi, C Omori, Y Iwamoto, Y Producer: 19980417 In: Diabetes research and clinical practice vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	387.	Anatomy of a homeoprotein revealed by the analysis of human MODY3 mutations. [electronic resource] by Vaxillaire, M Abderrahmani, A Boutin, P Bailleul, B Froguel, P Yaniv, M Pontoglio, M Producer: 20000113 In: The Journal of biological chemistry vol. 274 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	388.	Mutation in hepatocyte nuclear factor-1alpha is not a common cause of MODY and early-onset type 2 diabetes in Korea. [electronic resource] by Lee, H J Ahn, C W Kim, S J Song, Y D Lim, S K Kim, K R Lee, H C Huh, K B Producer: 20020702 In: Acta diabetologica vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	389.	Common variants in maturity-onset diabetes of the young genes contribute to risk of type 2 diabetes in Finns. [electronic resource] by Bonnycastle, Lori L Willer, Cristen J Conneely, Karen N Jackson, Anne U Burrill, Cecily P Watanabe, Richard M Chines, Peter S Narisu, Narisu Scott, Laura J Enloe, Sareena T Swift, Amy J Duren, William L Stringham, Heather M Erdos, Michael R Riebow, Nancy L Buchanan, Thomas A Valle, Timo T Tuomilehto, Jaakko Bergman, Richard N Mohlke, Karen L Boehnke, Michael Collins, Francis S Producer: 20061024 In: Diabetes vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	390.	Genetic disorders of human congenital anomalies of the kidney and urinary tract (CAKUT). [electronic resource] by Nakanishi, Koichi Yoshikawa, Norishige Producer: 20050315 In: Pediatrics international : official journal of the Japan Pediatric Society vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	391.	Genetic polymorphisms in diabetes: influence on therapy with oral antidiabetics. [electronic resource] by Glamočlija, Una Jevrić-Čaušević, Adlija Producer: 20110621 In: Acta pharmaceutica (Zagreb, Croatia) vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	392.	HNF1β and S100A1 are useful biomarkers for distinguishing renal oncocytoma and chromophobe renal cell carcinoma in FNA and core needle biopsies. [electronic resource] by Conner, James R Hirsch, Michelle S Jo, Vickie Y Producer: 20150721 In: Cancer cytopathology vol. 123 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	393.	Hypomagnesemia as First Clinical Manifestation of ADTKD-HNF1B: A Case Series and Literature Review. [electronic resource] by van der Made, Cas I Hoorn, Ewout J de la Faille, Renaud Karaaslan, Huseyin Knoers, Nine V A M Hoenderop, Joost G J Vargas Poussou, Rosa de Baaij, Jeroen H F Producer: 20160614 In: American journal of nephrology vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	394.	Frequency and Characteristics of MODY 1 (HNF4A Mutation) and MODY 5 (HNF1B Mutation): Analysis From the DPV Database. [electronic resource] by Warncke, Katharina Kummer, Sebastian Raile, Klemens Grulich-Henn, Jürgen Woelfle, Joachim Steichen, Elisabeth Prinz, Nicole Holl, Reinhard W Producer: 20191217 In: The Journal of clinical endocrinology and metabolism vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	395.	HNF-1alpha G319S, a transactivation-deficient mutant, is associated with altered dynamics of diabetes onset in an Oji-Cree community. [electronic resource] by Triggs-Raine, Barbara L Kirkpatrick, Robert D Kelly, Sherrie L Norquay, Lisa D Cattini, Peter A Yamagata, Kazuya Hanley, Anthony J G Zinman, Bernard Harris, Stewart B Barrett, P Hugh Hegele, Robert A Producer: 20020425 In: Proceedings of the National Academy of Sciences of the United States of America vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	396.	[Development of prediction for NIDDM from a view point of genetics]. [electronic resource] by Sanke, T Producer: 19980316 In: Nihon rinsho. Japanese journal of clinical medicine vol. 55 Suppl Availability: No items available. Save to lists Add to cart (remove)
	397.	Neonatal diabetes mellitus and neonatal polycystic, dysplastic kidneys: Phenotypically discordant recurrence of a mutation in the hepatocyte nuclear factor-1beta gene due to germline mosaicism. [electronic resource] by Yorifuji, Tohru Kurokawa, Keiji Mamada, Mitsukazu Imai, Tsuyoshi Kawai, Masahiko Nishi, Yoshikazu Shishido, Seiichiro Hasegawa, Yukihiro Nakahata, Tatsutoshi Producer: 20040719 In: The Journal of clinical endocrinology and metabolism vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	398.	Chronic renal failure of unknown origin is caused by HNF1B mutations in 9% of adult patients: a single centre cohort analysis. [electronic resource] by Musetti, Claudio Quaglia, Marco Mellone, Simona Pagani, Alessia Fusco, Ileana Monzani, Alice Giordano, Mara Stratta, Piero Producer: 20141128 In: Nephrology (Carlton, Vic.) vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	399.	Transcribing diabetes. [electronic resource] by Todd, J A Producer: 19970106 In: Nature vol. 384 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	400.	Regulation of albumin gene expression in hepatoma cells of fetal phenotype: dominant inhibition of HNF1 function and role of ubiquitous transcription factors. [electronic resource] by Rollier, A DiPersio, C M Cereghini, S Stevens, K Tronche, F Zaret, K Weiss, M C Producer: 19930408 In: Molecular biology of the cell vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1139 results.