Results 41 to 50 of about 3,050,344 (306)

Molecular characterization, expression pattern and function analysis of the rice OsDUF866 family

Biotechnology & Biotechnological Equipment, 2017
Domain-of-unknown function (DUF) proteins represent a number of gene families with no functional annotation in the Pfam database. So far, the DUF866 family has not been characterized, and no member has been functionally studied.
Lihua Li, Chen Xie, Taozhi Ye, Jinghong Xu, Rongjun Chen, Xiaoling Gao, Jianqing Zhu, Zhengjun Xu   +7 more
doaj   +1 more source

Genome-wide identification of DnaJ gene family in Catalpa bungei and functional analysis of CbuDnaJ49 in leaf color formation

Frontiers in Plant Science, 2023
DnaJs are the common molecular chaperone proteins with strong structural and functional diversity. In recent years, only several DnaJ family members have been found to be able to regulate leaf color, and it remains to be explored whether there are other ...
Yingying Yang, Yingying Yang, Linjiao Zhao, Junhui Wang, Nan Lu, Wenjun Ma, Jiang Ma, Yu Zhang, Pengyue Fu, Chengcheng Yao, Jiwen Hu, Nan Wang   +11 more
doaj   +1 more source

A novel six3 mutation segregates with holoprosencephaly in a large family [PDF]

, 2009
Holoprosencephaly is the most common structural malformation of the forebrain in humans and has a complex etiology including chromosomal aberrations, single gene mutations and environmental components.
Abecasis, Barkovich, Bendavid, Bendavid, Brown, Cohen, Del Bene, Domené, Dubourg, Dubourg, El-Jaick, Geng, Gestri, Granadino, Gripp, Inbal, Kawakami, Kobayashi, Kobayashi, Kong, Kruglyak, Lagutin, Lazaro, Leoncini, Liu, Matsunaga, Ming, Ming, Muenke, Muenke, Nanni, O'Connell, Oliver, Pasquier, Pasquier, Ribeiro, Roessler, Roessler, Schell, Thiele, Wallis   +40 more
core   +1 more source

A real-world analysis of the impact of X-linked myotubular myopathy on caregivers in the United States

Orphanet Journal of Rare Diseases
Background X-linked myotubular myopathy (XLMTM) is a rare, life-threatening congenital myopathy with multisystem involvement, which often includes the need for invasive ventilator support, gastrostomy tube feeding, and wheelchair use in approximately 80%
Tina Duong, Tmirah Haselkorn, Beckley Miller, Julie Coats, Ivar Jensen, Erin Ward, Marie Wood, Robert J. Graham, Laurent Servais   +8 more
doaj   +1 more source

Genome-wide identification and expression analysis of BrAGC genes in Brassica rapa reveal their potential roles in sexual reproduction and abiotic stress tolerance

Frontiers in Genetics, 2022
AGC protein kinases play important roles in regulating plant growth, immunity, and cell death. However, the function of AGC in Brassica rapa has not yet been clarified. In this study, 62 BrAGC genes were identified, and these genes were distributed on 10
Xiaoyu Wu, Xiaoyu Wu, Lianhui Pan, Lianhui Pan, Xinping Guo, Xinping Guo, Ting Li, Ting Li, Jiali Li, Qiaohong Duan, Qiaohong Duan, Jiabao Huang, Jiabao Huang   +12 more
doaj   +1 more source

Changing the name of the NBPF/DUF1220 domain to the Olduvai domain [PDF]

, 2017
We are jointly proposing a new name for a protein domain of approximately 65 amino acids that has been previously termed NBPF or DUF1220. Our two labs independently reported the initial studies of this domain, which is encoded almost entirely within a ...
Sikela, James M, Van Roy, Frans
core   +2 more sources

European Standard Clinical Practice Guideline and EXPeRT Recommendations for the Diagnosis and Management of Gastroenteropancreatic Neuroendocrine Neoplasms in Children and Adolescents

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Pediatric gastroenteropancreatic neuroendocrine neoplasms (GEP‐NENs) are extremely rare and clinically heterogeneous. Management has largely been extrapolated from adult practice. This European Standard Clinical Practice Guideline (ESCP), developed by the EXPeRT network in collaboration with adult NEN experts, provides (adult) evidence ...
Michaela Kuhlen, Calogero Virgone, Antje Redlich, Michael Abele, Ricardo Lopez‐Almaraz, Tal Ben‐Ami, Ewa Bien, Gianni Bisogno, Maja Mazic Cesen, Andrea Ferrari, Malgorzata A. Krawczyk, Yves Reguerre, Dominik T. Schneider, Ines B. Brecht, Charlotte Rigaud, Bilgehan Yalcin, Rainer Claus, Christian Vokuhl, Constantin Lapa, Jörg Fuchs, Segolene Hescot, Thomas Walter, Julien Hadoux, Daniel Orbach   +23 more
wiley   +1 more source

The Carcinoembryonic Antigen Gene Family [PDF]

, 1988
The molecular cloning of carcinoembryonic antigen (CEA) and several cross-reacting antigens reveals a basic domain structure for the whole family, which shows structural similarities to the immunoglobulin superfamily.
Thompson, John A., Zimmermann, Wolfgang
core  

Clinical Insights Into Hypercalcemia of Malignancy in Childhood

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Hypercalcemia of malignancy (HCM) is a rare but life‐threatening metabolic emergency in children that occurs in less than 1% of pediatric cancer cases, with a reported incidence ranging from 0.4% to 1.0% across different studies. While it is observed in 10%–20% of adult malignancies, pediatric HCM remains relatively uncommon.
Hüseyin Anıl Korkmaz
wiley   +1 more source

Survival Outcomes and Complications Among Canadian Children With Retinoblastoma: A Population‐Based Report From CYP‐C

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Purpose Retinoblastoma (RB) is the most common pediatric ocular cancer, yet population‐based data on survival and risk factors remain limited. This study aimed to describe survival in a large national RB cohort and identify predictors of death and complications.
Samuel Sassine, Ofélie Trudeau‐Ferrin, Caroline Laverdière, Patrick Hamel, Rosanne Superstein, Bénédicte Koukoui, Carole Provost, Paul C. Nathan, Vijay Ramaswamy, Furqan Shaikh, Brenda Gallie, Ashwin Mallipatna, Stephanie Kletke, Helen Dimaras, Hallie Coltin   +14 more
wiley   +1 more source