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Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation. [electronic resource] by
- Pilch, Jacek
- Koppolu, Agnieszka A
- Walczak, Anna
- Murcia Pienkowski, Victor A
- Biernacka, Anna
- Skiba, Paweł
- Machnik-Broncel, Joanna
- Gasperowicz, Piotr
- Kosińska, Joanna
- Rydzanicz, Małgorzata
- Emich-Widera, Ewa
- Płoski, Rafał
Producer: 20191028
In:
Clinical genetics vol. 94
Availability: No items available.
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Two additional males with X-linked, syndromic mental retardation carry de novo mutations in HNRNPH2. [electronic resource] by
- Jepsen, Wayne M
- Ramsey, Keri
- Szelinger, Szabolcs
- Llaci, Lorida
- Balak, Chris
- Belnap, Newell
- Bilagody, Cherae
- De Both, Matthew
- Gupta, Raj
- Naymik, Marcus
- Pandey, Richa
- Piras, Ignazio S
- Sanchez-Castillo, Meredith
- Rangasamy, Sampathkumar
- Narayanan, Vinodh
- Huentelman, Matthew J
Producer: 20200413
In:
Clinical genetics vol. 96
Availability: No items available.
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Antibodies to heterogeneous nuclear ribonucleoprotein H1 are directed to RNA recognition motif 3. [electronic resource] by
- Op de Beéck, Katrijn
- Van den Bergh, Karolien
- Westhovens, René
- Verschueren, Patrick
- Hooijkaas, Herbert
- van de Merwe, Joop P
- Michiels, Georges
- Schlumberger, Wolfgang
- Blockmans, Daniel
- Bossuyt, Xavier
Producer: 20120221
In:
Rheumatology (Oxford, England) vol. 50
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HnRNP F/H associate with hTERC and telomerase holoenzyme to modulate telomerase function and promote cell proliferation. [electronic resource] by
- Xu, Chenzhong
- Xie, Nan
- Su, Yuanyuan
- Sun, Zhaomeng
- Liang, Yao
- Zhang, Na
- Liu, Doudou
- Jia, Shuqin
- Xing, Xiaofang
- Han, Limin
- Li, Guodong
- Tong, Tanjun
- Chen, Jun
Producer: 20210908
In:
Cell death and differentiation vol. 27
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Missense variants in the Arg206 residue of HNRNPH2: Further evidence of causality and expansion of the phenotype. [electronic resource] by
- Peron, Angela
- Novara, Francesca
- La Briola, Francesca
- Merati, Elisabetta
- Giannusa, Emanuela
- Segalini, Elena
- Anniballi, Gloria
- Vignoli, Aglaia
- Ciccone, Roberto
- Canevini, Maria Paola
Producer: 20210203
In:
American journal of medical genetics. Part A vol. 182
Availability: No items available.
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Tubular Deficiency of Heterogeneous Nuclear Ribonucleoprotein F Elevates Systolic Blood Pressure and Induces Glycosuria in Mice. [electronic resource] by
- Lo, Chao-Sheng
- Miyata, Kana N
- Zhao, Shuiling
- Ghosh, Anindya
- Chang, Shiao-Ying
- Chenier, Isabelle
- Filep, Janos G
- Ingelfinger, Julie R
- Zhang, Shao-Ling
- Chan, John S D
Producer: 20201028
In:
Scientific reports vol. 9
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