Pages that link to "Q38502091"
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The following pages link to Mutations of the cystic fibrosis gene in patients with chronic pancreatitis (Q38502091):
Displaying 50 items.
- Hereditary chronic pancreatitis (Q21203019) (← links)
- Cystic Fibrosis Adult Care (Q22306058) (← links)
- Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping (Q24291081) (← links)
- Evaluating candidate agents of selective pressure for cystic fibrosis (Q24654240) (← links)
- Patterns of GI disease in adulthood associated with mutations in the CFTR gene (Q24673570) (← links)
- 'CFTR-opathies': disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations (Q24798831) (← links)
- A novel mutation of the calcium sensing receptor gene is associated with chronic pancreatitis in a family with heterozygous SPINK1 mutations (Q24805119) (← links)
- Epithelial Anion Transport as Modulator of Chemokine Signaling (Q26744381) (← links)
- Genetic predictors of human chronic pain conditions (Q26753046) (← links)
- Going MAD: development of a "matrix academic division" to facilitate translating research to personalized medicine (Q26851912) (← links)
- Genetics of pancreatitis (Q27000406) (← links)
- Loss of cftr function leads to pancreatic destruction in larval zebrafish. (Q27302962) (← links)
- Chymotrypsin C mutations in chronic pancreatitis (Q27693296) (← links)
- A signal peptide cleavage site mutation in the cationic trypsinogen gene is strongly associated with chronic pancreatitis (Q28138105) (← links)
- Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis (Q28145585) (← links)
- Mutational screening of the cationic trypsinogen gene in a large cohort of subjects with idiopathic chronic pancreatitis (Q28205812) (← links)
- Genetic issues in pediatric pancreatitis (Q28245133) (← links)
- Cystic fibrosis transmembrane regulator (CFTR) DeltaF508 mutation and 5T allele in patients with chronic pancreatitis and exocrine pancreatic cancer. PANKRAS II Study Group (Q28345126) (← links)
- A new polymorphism for the RI22H mutation in hereditary pancreatitis (Q28345956) (← links)
- Recent advances in cystic fibrosis (Q28367361) (← links)
- The absence of MIST1 leads to increased ethanol sensitivity and decreased activity of the unfolded protein response in mouse pancreatic acinar cells (Q28478610) (← links)
- A pharmacologic approach to acquired cystic fibrosis transmembrane conductance regulator dysfunction in smoking related lung disease (Q28727685) (← links)
- A conservative assessment of the major genetic causes of idiopathic chronic pancreatitis: data from a comprehensive analysis of PRSS1, SPINK1, CTRC and CFTR genes in 253 young French patients (Q30000783) (← links)
- Chronic Pancreatitis: Current Status and Challenges for Prevention and Treatment (Q30234471) (← links)
- What's unique about acute pancreatitis in children: risk factors, diagnosis and management (Q30235282) (← links)
- Environmental risk factors for pancreatic cancer: an update (Q30248417) (← links)
- Pathways to injury in chronic pancreatitis: decoding the role of the high-risk SPINK1 N34S haplotype using meta-analysis (Q33328503) (← links)
- Connections between genetics and clinical data: Role of MCP-1, CFTR, and SPINK-1 in the setting of acute, acute recurrent, and chronic pancreatitis (Q33511586) (← links)
- Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations and risk for pancreatic adenocarcinoma (Q33596314) (← links)
- Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice (Q33608587) (← links)
- The rod photoreceptor ATP-binding cassette transporter gene, ABCR, and retinal disease: from monogenic to multifactorial. (Q33682081) (← links)
- American Pancreatic Association Practice Guidelines in Chronic Pancreatitis: evidence-based report on diagnostic guidelines (Q33698421) (← links)
- The pathogenic consequences of a single mutated CFTR gene (Q33714004) (← links)
- New PRSS1 and common CFTR mutations in a child with acute recurrent pancreatitis, could be considered an "Hereditary" form of pancreatitis ? (Q33719943) (← links)
- Are mutations in the cystic fibrosis gene important in chronic pancreatitis? (Q33724438) (← links)
- Diagnosis of chronic pancreatitis. Is a gold standard necessary? (Q33724475) (← links)
- Early and late onset in idiopathic and alcoholic chronic pancreatitis. Different clinical courses (Q33724482) (← links)
- Pancreatitis and cystic fibrosis gene mutations (Q33741473) (← links)
- Pancreatic exocrine-endocrine interrelationship. Clinical implications (Q33741479) (← links)
- Molecular understanding of chronic pancreatitis: a perspective on the future (Q33756052) (← links)
- A synonymous mutation in the CFTR gene causes aberrant splicing in an italian patient affected by a mild form of cystic fibrosis. (Q33813887) (← links)
- Screening practices for mutations in the CFTR gene ABCC7. (Q33825439) (← links)
- Lack of association between UGT1A7, UGT1A9, ARP, SPINK1 and CFTR gene polymorphisms and pancreatic cancer in Italian patients (Q33869132) (← links)
- Assessment of oxidative stress in chronic pancreatitis patients (Q33869273) (← links)
- CFTR gene mutations and male infertility. (Q33885830) (← links)
- Genetic predispositions to acute and chronic pancreatitis (Q33953444) (← links)
- Genotype-phenotype relationships in cystic fibrosis (Q33953461) (← links)
- Cystic fibrosis mutations and genetic predisposition to idiopathic chronic pancreatitis (Q33953472) (← links)
- Mechanisms to explain pancreatic dysfunction in cystic fibrosis (Q33953488) (← links)
- The dangers of including nonclassical cystic fibrosis variants in population-based screening panels: p.L997F, further genotype/phenotype correlation data (Q33976441) (← links)