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Results for
""Zinc Finger Protein Gli3""[mesh_terms]

16 Results

Searching titles within these results

A translational approach to congenital non-obstructive hydronephrosis.

Norman D Rosenblum, Robyn P Thom

Pediatric nephrology (Berlin, Germany) 2014;28(9):1757-61

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Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review.

Kinga Kozma, Marius Bembea, Claudia M Jurca, Mihai Ioana, Ioana Streață, Simona Ş Şoşoi, Andrei Pirvu, Codruța D Petchesi, Ariana Szilágyi, Cristian N Sava, Alexandru Jurca, Anikó Ujfalusi, Zsuzsanna Szűcs, Katalin Szakszon

Genes 2022;12(11):1674

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Autistic symptoms in Greig cephalopolysyndactyly syndrome: a family case report.

Martina Siracusano, Assia Riccioni, Antonia Baratta, Maurizia Baldi, Paolo Curatolo, Luigi Mazzone

Journal of medical case reports 2019;13(1):100

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A multidisciplinary review of triphalangeal thumb.

Jacob W P Potuijt, Robert-Jan H Galjaard, Peter J van der Spek, Christianne A van Nieuwenhoven, Nadav Ahituv, Kerby C Oberg, Steven E R Hovius

The Journal of hand surgery, European volume 2020;44(1):59-68

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Novel GLI3 variant causing overlapped Greig cephalopolysyndactyly syndrome (GCPS) and Pallister-Hall syndrome (PHS) phenotype with agenesis of gallbladder and pancreas.

Saki Ito, Riko Kitazawa, Ryuma Haraguchi, Takeshi Kondo, Ayaka Ouchi, Yasuo Ueda, Sohei Kitazawa

Diagnostic pathology 2018;13(1):1

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The Greig cephalopolysyndactyly syndrome.

Leslie G Biesecker

Orphanet journal of rare diseases 2008;3():10

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Identification of the gene transcription repressor domain of Gli3.

Robert Tsanev, Piret Tiigimägi, Piret Michelson, Madis Metsis, Torben Østerlund, Priit Kogerman

FEBS letters 2009;583(1):224-8

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Developmental biology of the upper limb.

S Guéro

Hand surgery & rehabilitation 2019;37(5):265-274

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Novel GLI3 Mutations in Chinese Patients with Non-syndromic Post-axial Polydactyly.

X Chen, L Yuan, H Xu, P Hu, Y Yang, Y Guo, Z Guo, H Deng

Current molecular medicine 2020;19(3):228-235

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Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.

Elizabeth G Holliday, Albert V Smith, Belinda K Cornes, Gabriëlle H S Buitendijk, Richard A Jensen, Xueling Sim, Thor Aspelund, Tin Aung, Paul N Baird, Eric Boerwinkle, Ching Yu Cheng, Cornelia M van Duijn, Gudny Eiriksdottir, Vilmundur Gudnason, Tamara Harris, Alex W Hewitt, Michael Inouye, Fridbert Jonasson, Barbara E K Klein, Lenore Launer, Xiaohui Li, Gerald Liew, Thomas Lumley, Patrick McElduff, Barbara McKnight, Paul Mitchell, Bruce M Psaty, Elena Rochtchina, Jerome I Rotter, Rodney J Scott, Wanting Tay, Kent Taylor, Yik Ying Teo, André G Uitterlinden, Ananth Viswanathan, Sophia Xie, Johannes R Vingerling, Caroline C W Klaver, E Shyong Tai, David Siscovick, Ronald Klein, Mary Frances Cotch, Tien Y Wong, John Attia, Jie Jin Wang

PloS one 2013;8(1):e53830

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Pallister-Hall syndrome: unreported skeletal features of a GLI3 mutation.

T Roscioli, D Kennedy, J Cui, B Fonseca, G F Watson, J Pereira, Y-G Xie, D Mowat

American journal of medical genetics. Part A 2005;136A(4):390-4

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Genital abnormalities in Pallister-Hall syndrome: Report of two patients and review of the literature.

Yoko Narumi, Tomoki Kosho, Goro Tsuruta, Masaaki Shiohara, Ei Shimazaki, Tetsuo Mori, Ayako Shimizu, Yasuhiko Igawa, Shuji Nishizawa, Kimiyo Takagi, Rie Kawamura, Keiko Wakui, Yoshimitsu Fukushima

American journal of medical genetics. Part A 2011;152A(12):3143-7

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The transcriptional repressor domain of Gli3 is intrinsically disordered.

Robert Tsanev, Kalju Vanatalu, Jüri Jarvet, Risto Tanner, Kristi Laur, Piret Tiigimägi, Birthe B Kragelund, Torben Østerlund, Priit Kogerman

PloS one 2014;8(10):e76972

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Promotora assisted depression and self-care management among predominantly Latinos with concurrent chronic illness: Safety net care system clinical trial results.

Kathleen Ell, María P Aranda, Shinyi Wu, Hyunsung Oh, Pey-Jiuan Lee, Jeffrey Guterman

Contemporary clinical trials 2018;61():1-9

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BioBin: a bioinformatics tool for automating the binning of rare variants using publicly available biological knowledge.

Carrie B Moore, John R Wallace, Alex T Frase, Sarah A Pendergrass, Marylyn D Ritchie

BMC medical genomics 2013;6 Suppl 2(Suppl 2):S6

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Results: 1 – 15 / 16

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Results for ""Zinc Finger Protein Gli3""[mesh_terms]

A translational approach to congenital non-obstructive hydronephrosis.

Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review.

Autistic symptoms in Greig cephalopolysyndactyly syndrome: a family case report.

A multidisciplinary review of triphalangeal thumb.

Novel GLI3 variant causing overlapped Greig cephalopolysyndactyly syndrome (GCPS) and Pallister-Hall syndrome (PHS) phenotype with agenesis of gallbladder and pancreas.

The Greig cephalopolysyndactyly syndrome.

Identification of the gene transcription repressor domain of Gli3.

Developmental biology of the upper limb.

Novel GLI3 Mutations in Chinese Patients with Non-syndromic Post-axial Polydactyly.

Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.

Pallister-Hall syndrome: unreported skeletal features of a GLI3 mutation.

Genital abnormalities in Pallister-Hall syndrome: Report of two patients and review of the literature.

The transcriptional repressor domain of Gli3 is intrinsically disordered.

Promotora assisted depression and self-care management among predominantly Latinos with concurrent chronic illness: Safety net care system clinical trial results.

BioBin: a bioinformatics tool for automating the binning of rare variants using publicly available biological knowledge.

Results for
""Zinc Finger Protein Gli3""[mesh_terms]