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Monet șină Operă cfap410 rânjit acru expediție

CFAP410 DepMap Gene Summary
CFAP410 DepMap Gene Summary

CFAP410 Antibody (ABIN654737)
CFAP410 Antibody (ABIN654737)

CFAP410 Antibody - N-terminal region (ARP45819_P050) | Aviva Systems  Biology | Avivasysbio.com
CFAP410 Antibody - N-terminal region (ARP45819_P050) | Aviva Systems Biology | Avivasysbio.com

Frontiers | A polymorphic transcriptional regulatory domain in the  amyotrophic lateral sclerosis risk gene CFAP410 correlates with  differential isoform expression
Frontiers | A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene CFAP410 correlates with differential isoform expression

CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody

Frontiers | Pathogenicity and functional analysis of CFAP410 mutations  causing cone-rod dystrophy with macular staphyloma
Frontiers | Pathogenicity and functional analysis of CFAP410 mutations causing cone-rod dystrophy with macular staphyloma

Cfap410 MGI Mouse Gene Detail - MGI:1915134 - cilia and flagella associated  protein 410
Cfap410 MGI Mouse Gene Detail - MGI:1915134 - cilia and flagella associated protein 410

DYNC2H1 variants cause Leber congenital amaurosis without syndromic  features - Lee - 2021 - Clinical Genetics - Wiley Online Library
DYNC2H1 variants cause Leber congenital amaurosis without syndromic features - Lee - 2021 - Clinical Genetics - Wiley Online Library

Structural studies of cilia and flagella associated protein 410 (CFAP410)  reveal its bimodular organization with an N-terminal LRR motif and a  C-terminal tetrameric helical bundle | bioRxiv
Structural studies of cilia and flagella associated protein 410 (CFAP410) reveal its bimodular organization with an N-terminal LRR motif and a C-terminal tetrameric helical bundle | bioRxiv

CFAP410 Antibody - N-terminal region (ARP45819_P050) | Aviva Systems  Biology | Avivasysbio.com
CFAP410 Antibody - N-terminal region (ARP45819_P050) | Aviva Systems Biology | Avivasysbio.com

CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody

A) Pedigree chart of the affected family. Shaded boxes represent... |  Download Scientific Diagram
A) Pedigree chart of the affected family. Shaded boxes represent... | Download Scientific Diagram

CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody

Recombinant Human Cilia- and flagella-associated protein 410 (CFAP410) -  Cusabio
Recombinant Human Cilia- and flagella-associated protein 410 (CFAP410) - Cusabio

Structural studies of cilia and flagella associated protein 410 (CFAP410)  reveal its bimodular organization with an N-terminal LRR motif and a  C-terminal tetrameric helical bundle | bioRxiv
Structural studies of cilia and flagella associated protein 410 (CFAP410) reveal its bimodular organization with an N-terminal LRR motif and a C-terminal tetrameric helical bundle | bioRxiv

CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody

CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody

PDF) Pathogenicity and functional analysis of CFAP410 mutations causing  cone-rod dystrophy with macular staphyloma
PDF) Pathogenicity and functional analysis of CFAP410 mutations causing cone-rod dystrophy with macular staphyloma

CFAP410 protein (human) - STRING interaction network
CFAP410 protein (human) - STRING interaction network

Dong - Max Perutz Labs
Dong - Max Perutz Labs

Frontiers | A polymorphic transcriptional regulatory domain in the  amyotrophic lateral sclerosis risk gene CFAP410 correlates with  differential isoform expression
Frontiers | A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene CFAP410 correlates with differential isoform expression

C21orf2 variants causing inherited retinal disease: A review of what we  know and a report of two new suspected cases - Shinbashi - 2023 - Clinical  Case Reports - Wiley Online Library
C21orf2 variants causing inherited retinal disease: A review of what we know and a report of two new suspected cases - Shinbashi - 2023 - Clinical Case Reports - Wiley Online Library

Frontiers | Pathogenicity and functional analysis of CFAP410 mutations  causing cone-rod dystrophy with macular staphyloma
Frontiers | Pathogenicity and functional analysis of CFAP410 mutations causing cone-rod dystrophy with macular staphyloma

CFAP410 Antibody (ABIN654737)
CFAP410 Antibody (ABIN654737)