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B Pasini

Showing results (21-30 of 49) with videos related to

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European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|January 26, 2010
Laparoscopic unilateral adrenalectomy in children for isolated primary pigmented nodular adrenocortical disease (PPNAD): case report and literature reviewR Guanà, R Gesmundo, M Morino, et al.
Oncogene|December 11, 1997
The multiple endocrine neoplasia type 2B point mutation switches the specificity of the Ret tyrosine kinase towards cellular substrates that are susceptible to interact with Crk and NckR Bocciardi, B Mograbi, B Pasini, et al.
Genomics|November 1, 1992
Fine mapping and cloning of the breakpoint associated with Menkes syndrome in a female patientG Giacomo Consalez, J Gecz, C L Stayton, et al.
Nature Genetics|May 1, 1995
Loss of function effect of RET mutations causing Hirschsprung diseaseB Pasini, M G Borrello, A Greco, et al.
Human Molecular Genetics|November 1, 1993
Close linkage with the RET protooncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung diseaseY Luo, I Ceccherini, B Pasini, et al.
Gynecologic Oncology Reports|July 12, 2023
Lynch syndrome-associated endometrial cancer patient with a rare novel germline likely pathogenic variant of MSH2 gene: A case reportL Zumstein, V Tuninetti, M Vaira, et al.
Human Genetics|July 1, 1995
Ordering of markers in the pericentromeric region of chromosome 10R M Hofstra, T Stelwagen, B Pasini, et al.
Oncogene|November 2, 1995
The physical map of the human RET proto-oncogeneB Pasini, R M Hofstra, L Yin, et al.
Oncogene|December 7, 1995
RET activation by germline MEN2A and MEN2B mutationsM G Borrello, D P Smith, B Pasini, et al.
Gut|October 18, 2005
Association of a new cationic trypsinogen gene mutation (V39A) with chronic pancreatitis in an Italian familyC Arduino, P Salacone, B Pasini, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|January 26, 2010
Laparoscopic unilateral adrenalectomy in children for isolated primary pigmented nodular adrenocortical disease (PPNAD): case report and literature reviewR Guanà, R Gesmundo, M Morino, et al.
Oncogene|December 11, 1997
The multiple endocrine neoplasia type 2B point mutation switches the specificity of the Ret tyrosine kinase towards cellular substrates that are susceptible to interact with Crk and NckR Bocciardi, B Mograbi, B Pasini, et al.
Genomics|November 1, 1992
Fine mapping and cloning of the breakpoint associated with Menkes syndrome in a female patientG Giacomo Consalez, J Gecz, C L Stayton, et al.
Nature Genetics|May 1, 1995
Loss of function effect of RET mutations causing Hirschsprung diseaseB Pasini, M G Borrello, A Greco, et al.
Human Molecular Genetics|November 1, 1993
Close linkage with the RET protooncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung diseaseY Luo, I Ceccherini, B Pasini, et al.
Gynecologic Oncology Reports|July 12, 2023
Lynch syndrome-associated endometrial cancer patient with a rare novel germline likely pathogenic variant of MSH2 gene: A case reportL Zumstein, V Tuninetti, M Vaira, et al.
Human Genetics|July 1, 1995
Ordering of markers in the pericentromeric region of chromosome 10R M Hofstra, T Stelwagen, B Pasini, et al.
Oncogene|November 2, 1995
The physical map of the human RET proto-oncogeneB Pasini, R M Hofstra, L Yin, et al.
Oncogene|December 7, 1995
RET activation by germline MEN2A and MEN2B mutationsM G Borrello, D P Smith, B Pasini, et al.
Gut|October 18, 2005
Association of a new cationic trypsinogen gene mutation (V39A) with chronic pancreatitis in an Italian familyC Arduino, P Salacone, B Pasini, et al.
Pageof 5