UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Expression of ion transport-associated proteins in human efferent and epididymal ducts

Reproduction (Cambridge, England), 2007-04, Vol.133 (4), p.775-784

2007

Volltextzugriff (PDF)

Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD)

BMC gastroenterology, 2009-01, Vol.9 (1), p.8-8, Article 8

2009

Volltextzugriff (PDF)

Cl-Is Required for HCO3-Entry Necessary for Sperm Capacitation in Guinea Pig : Involvement of a Cl-/HCO3-Exchanger (SLC26A3) and CFTR

Biology of reproduction, 2009, Vol.80 (1), p.115-123

2009

Volltextzugriff (PDF)

Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea

American journal of physiology: Gastrointestinal and liver physiology, 1999-01, Vol.276 (1), p.G185-G192

1999

Volltextzugriff (PDF)

Cl− Is Required for HCO3− Entry Necessary for Sperm Capacitation in Guinea Pig: Involvement of a Cl−/HCO3− Exchanger (SLC26A3) and CFTR1

Biology of reproduction, 2009-01, Vol.80 (1), p.115-123

2009

Volltextzugriff (PDF)

Three cases of a rare disease, congenital chloride diarrhea, summons up the variation in the clinical course and significance of early diagnosis and adequate treatment in the prevention of intellectual disability

Turkish journal of pediatrics, 2011-03, Vol.53 (2), p.194-198

2011

Volltextzugriff (PDF)

Monoallelic Expression of HumanPEG1/MESTIs Paralleled by Parent-Specific Methylation in Fetuses

Genomics (San Diego, Calif.), 1997-06, Vol.42 (2), p.236-244

1997

Volltextzugriff (PDF)

SLC26A3 mutations in congenital chloride diarrhea: SLC26A3 MUTATIONS IN CLD

Human mutation, 2002-12, Vol.20 (6), p.425-438

2002

Volltextzugriff (PDF)

Inherited disorders of ion transport in the intestine

Current Opinion in Genetics & Development, 2000-06, Vol.10 (3), p.306-309

2000

Volltextzugriff (PDF)

Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses

Genomics (San Diego, Calif.), 1997-06, Vol.42 (2), p.236-244

1997

Volltextzugriff (PDF)

Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea

American journal of human genetics, 1994-10, Vol.55 (4), p.747-752

1994

Volltextzugriff (PDF)

Molecular characterization of deletion at 11q22.1‐23.3 in mantle cell lymphoma

British journal of haematology, 1999-03, Vol.104 (4), p.665-671

1999

Volltextzugriff (PDF)

Interstitial 1q25.3‐q31.3 deletion in a boy with mild manifestations

American journal of medical genetics. Part A, 2003-12, Vol.123A (3), p.290-295

2003

Volltextzugriff (PDF)

Maternal and Paternal Chromosomes 7 Show Differential Methylation of Many Genes in Lymphoblast DNA

Genomics (San Diego, Calif.), 2001-04, Vol.73 (1), p.1-9

2001

Volltextzugriff (PDF)

III. Congenital chloride diarrhea

American journal of physiology: Gastrointestinal and liver physiology, 1999-01, Vol.276 (1), p.G7-G13

1999

Volltextzugriff (PDF)

SLC26A3 and congenital chloride diarrhoea

Epithelial Anion Transport in Health and Disease, 2006, Vol.273, p.74-90

2006

Volltextzugriff (PDF)

Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3

Human molecular genetics, 1995-08, Vol.4 (8), p.1467-1469

1995

Volltextzugriff (PDF)

Four novel mutations in the lactase gene

BMC gastroenterology, 2009-01, Vol.9 (1), p.8

2009

Volltextzugriff (PDF)

MUTATION SPECTRUM OF DRA IN CONGENITAL CHLORIDE DIARRHEA

Journal of pediatric gastroenterology and nutrition, 1997-04, Vol.24 (4), p.472

1997

Volltextzugriff (PDF)

MUTATION SPECTRUM OF DRA IN CONGENITAL CHLORIDE DIARRHEA

Journal of pediatric gastroenterology and nutrition, 1997-04, Vol.24 (4), p.472-472

1997

Volltextzugriff (PDF)

Genetic disorders of membrane transport. III. Congenital chloride diarrhea

American journal of physiology: Gastrointestinal and liver physiology, 1999, Vol.39 (1), p.G7-G13

1999

Volltextzugriff (PDF)

Interstitial 1q25.3-q31.3 deletion in a boy with mild manifestations

American Journal of Medical Genetics Part A, 2003, Vol.123A (3), p.290-295

2003

Volltextzugriff (PDF)

Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea

American journal of physiology: Gastrointestinal and liver physiology, 1999, Vol.39 (1), p.G185-G192

1999

Volltextzugriff (PDF)

Dental home care in dogs - a questionnaire study among Swedish dog owners, veterinarians and veterinary nurses

BMC veterinary research, 2020-03, Vol.16 (1), p.90-90, Article 90

2020

Volltextzugriff (PDF)

Development and validation of two questionnaires: Dental home care and dental health in Swedish dogs

PloS one, 2019-01, Vol.14 (1), p.e0204581-e0204581

2019

Volltextzugriff (PDF)

1 – 25 von 37

Suche als RSS-Feed

Aktive Filter

KollektionNature Journals

ThemaDiarrhea - Genetics

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(35)
Mit Volltextzugriff
(36)

Publikationsform

Sprache

Englisch
(37)
Japanisch
(5)

Erscheinungsjahr

n.n

Thema

Science & Technology
(24)
Life Sciences & Biomedicine
(23)
Humans
(17)
Male
(14)
Biological And Medical Sciences
(11)
Female
(9)
Adult
(8)
Medical Sciences
(8)
Genetics & Heredity
(6)
Aged
(5)
Medicin Och Hälsovetenskap
(5)
Middle Aged
(5)
Sweden
(5)
Animals
(4)
Clinical Science
(4)
Klinisk Vetenskap
(4)
Veterinary Sciences
(4)
Adolescent
(3)
Alleles
(3)
Biotechnology & Applied Microbiology
(3)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Expression of ion transport-associated proteins in human efferent and epididymal ducts

Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD)

Cl-Is Required for HCO3-Entry Necessary for Sperm Capacitation in Guinea Pig : Involvement of a Cl-/HCO3-Exchanger (SLC26A3) and CFTR

Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea

Cl− Is Required for HCO3− Entry Necessary for Sperm Capacitation in Guinea Pig: Involvement of a Cl−/HCO3− Exchanger (SLC26A3) and CFTR1

Three cases of a rare disease, congenital chloride diarrhea, summons up the variation in the clinical course and significance of early diagnosis and adequate treatment in the prevention of intellectual disability

Monoallelic Expression of HumanPEG1/MESTIs Paralleled by Parent-Specific Methylation in Fetuses

SLC26A3 mutations in congenital chloride diarrhea: SLC26A3 MUTATIONS IN CLD

Inherited disorders of ion transport in the intestine

Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses

Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea

Molecular characterization of deletion at 11q22.1‐23.3 in mantle cell lymphoma

Interstitial 1q25.3‐q31.3 deletion in a boy with mild manifestations

Maternal and Paternal Chromosomes 7 Show Differential Methylation of Many Genes in Lymphoblast DNA

III. Congenital chloride diarrhea

SLC26A3 and congenital chloride diarrhoea

Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3

Four novel mutations in the lactase gene

MUTATION SPECTRUM OF DRA IN CONGENITAL CHLORIDE DIARRHEA

MUTATION SPECTRUM OF DRA IN CONGENITAL CHLORIDE DIARRHEA

Genetic disorders of membrane transport. III. Congenital chloride diarrhea

Interstitial 1q25.3-q31.3 deletion in a boy with mild manifestations

Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea

Dental home care in dogs - a questionnaire study among Swedish dog owners, veterinarians and veterinary nurses

Development and validation of two questionnaires: Dental home care and dental health in Swedish dogs

Aktive Filter

Suchergebnisse filtern